Project

Project uploaded by:	Yashwant
Project ID:	IMP_100052
Title:	A genome-scale metabolic model for deciphering the host metabolic perturbations during Mycobacterium tuberculosis infection
Project Description:	Conventional tuberculosis (TB) research predominantly relies on forward-designed experiments, such as studying host responses to Mycobacterium tuberculosis (Mtb) gene knockouts. While informative, these approaches offer only a partial view of host-pathogen interactions and often overlook the broader alterations in the host microenvironment during infection. To address this limitation, we adopted a backtracing strategy to retrospectively identify host metabolic modulators and link them to specific Mtb virulence factors. Using RNA-seq data from Mtb-infected mouse lung tissue, we integrated transcriptomic profiles into a genome-scale metabolic model to predict host metabolic genes essential for Mtb survival. This analysis identified 18 host proteins as putative modulators. We then constructed a host-pathogen protein interaction network, which connected these host factors to 9 Mtb proteins. Experimental validation using Mtb knockdown strains confirmed that three genes Rv1970, Rv0243, and Rv2234 play key roles in manipulating host responses rather than supporting intrinsic bacterial viability. Further, we employed targeted proteomics and untargeted metabolomics analyses on THP-1 macrophages infected with these KD strains to dissect the host-pathogen interaction mechanisms in greater detail. These findings in troduce a novel framework for decoding host-pathogen interactions and lay the groundwork for future host-directed therapy (HDT) strategies targeting Mtb-induced host vulnerabilities.
Research Area:	Biological Sciences
Funding Source:	Translational Research Program (TRP) (No. BT/PR30159/MED/15/188/2018) of Department of Biotechnology (DBT), Govt. of India.
Project Contributors:	Yashwant Kumar

Study

Study uploaded by:	Yashwant
Study ID:	IMS_100047
Title:	A genome-scale metabolic model for deciphering the host metabolic perturbations during Mycobacterium tuberculosis infection
Summary:	Conventional tuberculosis (TB) research predominantly relies on forward-designed experiments, such as studying host responses to Mycobacterium tuberculosis (Mtb) gene knockouts. While informative, these approaches offer only a partial view of host-pathogen interactions and often overlook the broader alterations in the host microenvironment during infection. To address this limitation, we adopted a backtracing strategy to retrospectively identify host metabolic modulators and link them to specific Mtb virulence factors. Using RNA-seq data from Mtb-infected mouse lung tissue, we integrated transcriptomic profiles into a genome-scale metabolic model to predict host metabolic genes essential for Mtb survival. This analysis identified 18 host proteins as putative modulators. We then constructed a host-pathogen protein interaction network, which connected these host factors to 9 Mtb proteins. Experimental validation using Mtb knockdown strains confirmed that three genes Rv1970, Rv0243, and Rv2234 play key roles in manipulating host responses rather than supporting intrinsic bacterial viability. Further, we employed targeted proteomics and untargeted metabolomics analyses on THP-1 macrophages infected with these KD strains to dissect the host-pathogen interaction mechanisms in greater detail. These findings in troduce a novel framework for decoding host-pathogen interactions and lay the groundwork for future host-directed therapy (HDT) strategies targeting Mtb-induced host vulnerabilities.
Publication:
Release Date:	Dec. 25, 2025
Study Type:	Mass Spectrometry (MS)
Data Type:	Targeted
IEC/IBSC Approval Number :

Sample (Total Count:66)

Sr.No	Sample ID	Sample Name	Organism	Source	Sample Preparation Protocol	Sample Type	Experimental Condition	Time of treatment	Variant/Variety	Gender	Age	Replicates	Storage Conditions	Extraction Protocol	Number of files per sample
1	IMSM_103669	Rv0243+Atc1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0243+Atc1)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
2	IMSM_103670	Rv0243-Atc1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0243-Atc1)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
3	IMSM_103671	Rv0243+Atc2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0243+Atc2)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
4	IMSM_103672	Rv0243-Atc2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0243-Atc2)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
5	IMSM_103673	Rv0243+Atc3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0243+Atc3)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
6	IMSM_103674	Rv0243-Atc3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0243-Atc3)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
7	IMSM_103675	Rv0243+Atc4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0243+Atc4)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
8	IMSM_103676	Rv0243-Atc4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0243-Atc4)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
9	IMSM_103677	Rv0243+Atc5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0243+Atc5)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
10	IMSM_103678	Rv0243-Atc5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0243-Atc5)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
11	IMSM_103679	Rv0243+Atc6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0243+Atc6)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
12	IMSM_103680	Rv0243-Atc6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0243-Atc6)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
13	IMSM_103681	Rv0410+Atc1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0410+Atc1)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
14	IMSM_103682	Rv0410-Atc1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0410-Atc1)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
15	IMSM_103683	Rv0410+Atc2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0410+Atc2)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
16	IMSM_103684	Rv0410-Atc2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0410-Atc2)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
17	IMSM_103685	Rv0410+Atc3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0410+Atc3)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
18	IMSM_103686	Rv0410-Atc3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0410-Atc3)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
19	IMSM_103687	Rv0410+Atc4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0410+Atc4)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
20	IMSM_103688	Rv0410-Atc4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0410-Atc4)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
21	IMSM_103689	Rv0410+Atc5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0410+Atc5)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
22	IMSM_103690	Rv0410-Atc5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0410-Atc5)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
23	IMSM_103691	Rv0410+Atc6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv0410+Atc6)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
24	IMSM_103692	Rv0410-Atc6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv0410-Atc6)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
25	IMSM_103693	Rv1970+Atc1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv1970+Atc1)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
26	IMSM_103694	Rv1970-Atc1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv1970-Atc1)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
27	IMSM_103695	Rv1970+Atc2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv1970+Atc2)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
28	IMSM_103696	Rv1970-Atc2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv1970-Atc2)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
29	IMSM_103697	Rv1970+Atc3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv1970+Atc3)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
30	IMSM_103698	Rv1970-Atc3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv1970-Atc3)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
31	IMSM_103699	Rv1970+Atc4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv1970+Atc4)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
32	IMSM_103700	Rv1970-Atc4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv1970-Atc4)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
33	IMSM_103701	Rv1970+Atc5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv1970+Atc5)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
34	IMSM_103702	Rv1970-Atc5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv1970-Atc5)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
35	IMSM_103703	Rv1970+Atc6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv1970+Atc6)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
36	IMSM_103704	Rv1970-Atc6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv1970-Atc6)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
37	IMSM_103705	Rv2234+Atc1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv2234+Atc1)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
38	IMSM_103706	Rv2234-Atc1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv2234-Atc1)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
39	IMSM_103707	Rv2234+Atc2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv2234+Atc2)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
40	IMSM_103708	Rv2234-Atc2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv2234-Atc2)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
41	IMSM_103709	Rv2234+Atc3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv2234+Atc3)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
42	IMSM_103710	Rv2234-Atc3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv2234-Atc3)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
43	IMSM_103711	Rv2234+Atc4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv2234+Atc4)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
44	IMSM_103712	Rv2234-Atc4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv2234-Atc4)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
45	IMSM_103713	Rv2234+Atc5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv2234+Atc5)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
46	IMSM_103714	Rv2234-Atc5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv2234-Atc5)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
47	IMSM_103715	Rv2234+Atc6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv2234+Atc6)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
48	IMSM_103716	Rv2234-Atc6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv2234-Atc6)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
49	IMSM_103717	Rv3774+Atc1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv3774+Atc1)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
50	IMSM_103718	Rv3774-Atc1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv3774-Atc1)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
51	IMSM_103719	Rv3774+Atc2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv3774+Atc2)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
52	IMSM_103720	Rv3774-Atc2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv3774-Atc2)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
53	IMSM_103721	Rv3774+Atc3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv3774+Atc3)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
54	IMSM_103722	Rv3774-Atc3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv3774-Atc3)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
55	IMSM_103723	Rv3774+Atc4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv3774+Atc4)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
56	IMSM_103724	Rv3774-Atc4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv3774-Atc4)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
57	IMSM_103725	Rv3774+Atc5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv3774+Atc5)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
58	IMSM_103726	Rv3774-Atc5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv3774-Atc5)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
59	IMSM_103727	Rv3774+Atc6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	knockdown(Rv3774+Atc6)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
60	IMSM_103728	Rv3774-Atc6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	control(Rv3774-Atc6)	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
61	IMSM_103729	Uninfected1	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	Uninfected	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
62	IMSM_103730	Uninfected2	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	Uninfected	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
63	IMSM_103731	Uninfected3	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	Uninfected	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
64	IMSM_103732	Uninfected4	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	Uninfected	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
65	IMSM_103733	Uninfected5	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	Uninfected	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4
66	IMSM_103734	Uninfected6	Homo sapiens	Human acute monocytic leukemia cell line	THP-1 cells (2x10^6) were seeded in 6-well plates and treated with 50 ng/mL PMA for 36 hours to induce differentiation. After PMA treatment, the medium was replaced with fresh RPMI, and the cells were allowed to mature for an additional 24 hours. Mtb infection was performed at a MOI of 5 and un-infected cells were maintained in parallel culture as control. After 4 hours of infection, extracellular bacteria were removed by three washes with pre-warmed PBS. A complete RPMI medium supplemented with 400 ng/mL ATc was added to the wells to induce the knockdown effect. The infected cells were incubated for 48 hours before being washed again with pre-warmed PBS.	Human THP-1 Macrophages	Uninfected	48 hours	NA	NA	NA	Yes	NA	To quench metabolism and extract metabolites, 1 mL of chilled methanol (HPLC grade; Sigma) was added to the cells. The cells were harvested on ice using a scraper, and the resulting extracts were transferred to pre-cooled microcentrifuge tubes (MCTs) maintained at 4°C. The extracts were vortexed for 15 minutes and centrifuged at 12000 rpm for 10 minutes at 4°C. After centrifugation, the supernatants were transferred to fresh pre-cooled MCTs (4°C), dried under vacuum, and reconstituted. The reconstituted samples were stored at -80°C until further analysis by liquid chromatography-mass spectrometry (LC-MS).	4

Mass Spectrometry

Sr.No	MS Exp ID	Sample Name/ID	Mass Spectrometer Type	MS Instrument Name	MS Instrument type	MS Ionization Method	Ion Mode/Scan Polarity	Data Transformation (Software/s Used)
1	IME_101708	Rv0243+Atc1 / IMSM_103669	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
2	IME_101709	Rv0243-Atc1 / IMSM_103670	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
3	IME_101710	Rv0243+Atc2 / IMSM_103671	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
4	IME_101711	Rv0243-Atc2 / IMSM_103672	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
5	IME_101712	Rv0243+Atc3 / IMSM_103673	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
6	IME_101713	Rv0243-Atc3 / IMSM_103674	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
7	IME_101714	Rv0243+Atc4 / IMSM_103675	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
8	IME_101715	Rv0243-Atc4 / IMSM_103676	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
9	IME_101716	Rv0243+Atc5 / IMSM_103677	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
10	IME_101717	Rv0243-Atc5 / IMSM_103678	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
11	IME_101718	Rv0243+Atc6 / IMSM_103679	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
12	IME_101719	Rv0243-Atc6 / IMSM_103680	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
13	IME_101720	Rv0410+Atc1 / IMSM_103681	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
14	IME_101721	Rv0410-Atc1 / IMSM_103682	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
15	IME_101722	Rv0410+Atc2 / IMSM_103683	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
16	IME_101723	Rv0410-Atc2 / IMSM_103684	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
17	IME_101724	Rv0410+Atc3 / IMSM_103685	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
18	IME_101725	Rv0410-Atc3 / IMSM_103686	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
19	IME_101726	Rv0410+Atc4 / IMSM_103687	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
20	IME_101727	Rv0410-Atc4 / IMSM_103688	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
21	IME_101728	Rv0410+Atc5 / IMSM_103689	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
22	IME_101729	Rv0410-Atc5 / IMSM_103690	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
23	IME_101730	Rv0410+Atc6 / IMSM_103691	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
24	IME_101731	Rv0410-Atc6 / IMSM_103692	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
25	IME_101732	Rv1970+Atc1 / IMSM_103693	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
26	IME_101733	Rv1970-Atc1 / IMSM_103694	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
27	IME_101734	Rv1970+Atc2 / IMSM_103695	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
28	IME_101735	Rv1970-Atc2 / IMSM_103696	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
29	IME_101736	Rv1970+Atc3 / IMSM_103697	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
30	IME_101737	Rv1970-Atc3 / IMSM_103698	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
31	IME_101738	Rv1970+Atc4 / IMSM_103699	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
32	IME_101739	Rv1970-Atc4 / IMSM_103700	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
33	IME_101740	Rv1970+Atc5 / IMSM_103701	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
34	IME_101741	Rv1970-Atc5 / IMSM_103702	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
35	IME_101742	Rv1970+Atc6 / IMSM_103703	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
36	IME_101743	Rv1970-Atc6 / IMSM_103704	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
37	IME_101744	Rv2234+Atc1 / IMSM_103705	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
38	IME_101745	Rv2234-Atc1 / IMSM_103706	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
39	IME_101746	Rv2234+Atc2 / IMSM_103707	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
40	IME_101747	Rv2234-Atc2 / IMSM_103708	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
41	IME_101748	Rv2234+Atc3 / IMSM_103709	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
42	IME_101749	Rv2234-Atc3 / IMSM_103710	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
43	IME_101750	Rv2234+Atc4 / IMSM_103711	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
44	IME_101751	Rv2234-Atc4 / IMSM_103712	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
45	IME_101752	Rv2234+Atc5 / IMSM_103713	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
46	IME_101753	Rv2234-Atc5 / IMSM_103714	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
47	IME_101754	Rv2234+Atc6 / IMSM_103715	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
48	IME_101755	Rv2234-Atc6 / IMSM_103716	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
49	IME_101756	Rv3774+Atc1 / IMSM_103717	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
50	IME_101757	Rv3774-Atc1 / IMSM_103718	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
51	IME_101758	Rv3774+Atc2 / IMSM_103719	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
52	IME_101759	Rv3774-Atc2 / IMSM_103720	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
53	IME_101760	Rv3774+Atc3 / IMSM_103721	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
54	IME_101761	Rv3774-Atc3 / IMSM_103722	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
55	IME_101762	Rv3774+Atc4 / IMSM_103723	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
56	IME_101763	Rv3774-Atc4 / IMSM_103724	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
57	IME_101764	Rv3774+Atc5 / IMSM_103725	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
58	IME_101765	Rv3774-Atc5 / IMSM_103726	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
59	IME_101766	Rv3774+Atc6 / IMSM_103727	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
60	IME_101767	Rv3774-Atc6 / IMSM_103728	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
61	IME_101768	Uninfected1 / IMSM_103729	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
62	IME_101769	Uninfected2 / IMSM_103730	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
63	IME_101770	Uninfected3 / IMSM_103731	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
64	IME_101771	Uninfected4 / IMSM_103732	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
65	IME_101772	Uninfected5 / IMSM_103733	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
66	IME_101773	Uninfected6 / IMSM_103734	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
67	IME_101774	Rv0243+Atc1 / IMSM_103669	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
68	IME_101775	Rv0243-Atc1 / IMSM_103670	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
69	IME_101776	Rv0243+Atc2 / IMSM_103671	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
70	IME_101777	Rv0243-Atc2 / IMSM_103672	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
71	IME_101778	Rv0243+Atc3 / IMSM_103673	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
72	IME_101779	Rv0243-Atc3 / IMSM_103674	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
73	IME_101780	Rv0243+Atc4 / IMSM_103675	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
74	IME_101781	Rv0243-Atc4 / IMSM_103676	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
75	IME_101782	Rv0243+Atc5 / IMSM_103677	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
76	IME_101783	Rv0243-Atc5 / IMSM_103678	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
77	IME_101784	Rv0243+Atc6 / IMSM_103679	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
78	IME_101785	Rv0243-Atc6 / IMSM_103680	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
79	IME_101786	Rv0410+Atc1 / IMSM_103681	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
80	IME_101787	Rv0410-Atc1 / IMSM_103682	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
81	IME_101788	Rv0410+Atc2 / IMSM_103683	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
82	IME_101789	Rv0410-Atc2 / IMSM_103684	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
83	IME_101790	Rv0410+Atc3 / IMSM_103685	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
84	IME_101791	Rv0410-Atc3 / IMSM_103686	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
85	IME_101792	Rv0410+Atc4 / IMSM_103687	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
86	IME_101793	Rv0410-Atc4 / IMSM_103688	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
87	IME_101794	Rv0410+Atc5 / IMSM_103689	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
88	IME_101795	Rv0410-Atc5 / IMSM_103690	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
89	IME_101796	Rv0410+Atc6 / IMSM_103691	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
90	IME_101797	Rv0410-Atc6 / IMSM_103692	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
91	IME_101798	Rv1970+Atc1 / IMSM_103693	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
92	IME_101799	Rv1970-Atc1 / IMSM_103694	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
93	IME_101800	Rv1970+Atc2 / IMSM_103695	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
94	IME_101801	Rv1970-Atc2 / IMSM_103696	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
95	IME_101802	Rv1970+Atc3 / IMSM_103697	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
96	IME_101803	Rv1970-Atc3 / IMSM_103698	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
97	IME_101804	Rv1970+Atc4 / IMSM_103699	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
98	IME_101805	Rv1970-Atc4 / IMSM_103700	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
99	IME_101806	Rv1970+Atc5 / IMSM_103701	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
100	IME_101807	Rv1970-Atc5 / IMSM_103702	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
101	IME_101808	Rv1970+Atc6 / IMSM_103703	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
102	IME_101809	Rv1970-Atc6 / IMSM_103704	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
103	IME_101810	Rv2234+Atc1 / IMSM_103705	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
104	IME_101811	Rv2234-Atc1 / IMSM_103706	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
105	IME_101812	Rv2234+Atc2 / IMSM_103707	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
106	IME_101813	Rv2234-Atc2 / IMSM_103708	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
107	IME_101814	Rv2234+Atc3 / IMSM_103709	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
108	IME_101815	Rv2234-Atc3 / IMSM_103710	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
109	IME_101816	Rv2234+Atc4 / IMSM_103711	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
110	IME_101817	Rv2234-Atc4 / IMSM_103712	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
111	IME_101818	Rv2234+Atc5 / IMSM_103713	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
112	IME_101819	Rv2234-Atc5 / IMSM_103714	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
113	IME_101820	Rv2234+Atc6 / IMSM_103715	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
114	IME_101821	Rv2234-Atc6 / IMSM_103716	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
115	IME_101822	Rv3774+Atc1 / IMSM_103717	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
116	IME_101823	Rv3774-Atc1 / IMSM_103718	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
117	IME_101824	Rv3774+Atc2 / IMSM_103719	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
118	IME_101825	Rv3774-Atc2 / IMSM_103720	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
119	IME_101826	Rv3774+Atc3 / IMSM_103721	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
120	IME_101827	Rv3774-Atc3 / IMSM_103722	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
121	IME_101828	Rv3774+Atc4 / IMSM_103723	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
122	IME_101829	Rv3774-Atc4 / IMSM_103724	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
123	IME_101830	Rv3774+Atc5 / IMSM_103725	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
124	IME_101831	Rv3774-Atc5 / IMSM_103726	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
125	IME_101832	Rv3774+Atc6 / IMSM_103727	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
126	IME_101833	Rv3774-Atc6 / IMSM_103728	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
127	IME_101834	Uninfected1 / IMSM_103729	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
128	IME_101835	Uninfected2 / IMSM_103730	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
129	IME_101836	Uninfected3 / IMSM_103731	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
130	IME_101837	Uninfected4 / IMSM_103732	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
131	IME_101838	Uninfected5 / IMSM_103733	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
132	IME_101839	Uninfected6 / IMSM_103734	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
133	IME_101840	Rv0243+Atc1 / IMSM_103669	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
134	IME_101841	Rv0243-Atc1 / IMSM_103670	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
135	IME_101842	Rv0243+Atc2 / IMSM_103671	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
136	IME_101843	Rv0243-Atc2 / IMSM_103672	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
137	IME_101844	Rv0243+Atc3 / IMSM_103673	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
138	IME_101845	Rv0243-Atc3 / IMSM_103674	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
139	IME_101846	Rv0243+Atc4 / IMSM_103675	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
140	IME_101847	Rv0243-Atc4 / IMSM_103676	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
141	IME_101848	Rv0243+Atc5 / IMSM_103677	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
142	IME_101849	Rv0243-Atc5 / IMSM_103678	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
143	IME_101850	Rv0243+Atc6 / IMSM_103679	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
144	IME_101851	Rv0243-Atc6 / IMSM_103680	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
145	IME_101852	Rv0410+Atc1 / IMSM_103681	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
146	IME_101853	Rv0410-Atc1 / IMSM_103682	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
147	IME_101854	Rv0410+Atc2 / IMSM_103683	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
148	IME_101855	Rv0410-Atc2 / IMSM_103684	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
149	IME_101856	Rv0410+Atc3 / IMSM_103685	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
150	IME_101857	Rv0410-Atc3 / IMSM_103686	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
151	IME_101858	Rv0410+Atc4 / IMSM_103687	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
152	IME_101859	Rv0410-Atc4 / IMSM_103688	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
153	IME_101860	Rv0410+Atc5 / IMSM_103689	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
154	IME_101861	Rv0410-Atc5 / IMSM_103690	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
155	IME_101862	Rv0410+Atc6 / IMSM_103691	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
156	IME_101863	Rv0410-Atc6 / IMSM_103692	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
157	IME_101864	Rv1970+Atc1 / IMSM_103693	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
158	IME_101865	Rv1970-Atc1 / IMSM_103694	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
159	IME_101866	Rv1970+Atc2 / IMSM_103695	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
160	IME_101867	Rv1970-Atc2 / IMSM_103696	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
161	IME_101868	Rv1970+Atc3 / IMSM_103697	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
162	IME_101869	Rv1970-Atc3 / IMSM_103698	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
163	IME_101870	Rv1970+Atc4 / IMSM_103699	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
164	IME_101871	Rv1970-Atc4 / IMSM_103700	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
165	IME_101872	Rv1970+Atc5 / IMSM_103701	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
166	IME_101873	Rv1970-Atc5 / IMSM_103702	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
167	IME_101874	Rv1970+Atc6 / IMSM_103703	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
168	IME_101875	Rv1970-Atc6 / IMSM_103704	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
169	IME_101876	Rv2234+Atc1 / IMSM_103705	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
170	IME_101877	Rv2234-Atc1 / IMSM_103706	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
171	IME_101878	Rv2234+Atc2 / IMSM_103707	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
172	IME_101879	Rv2234-Atc2 / IMSM_103708	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
173	IME_101880	Rv2234+Atc3 / IMSM_103709	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
174	IME_101881	Rv2234-Atc3 / IMSM_103710	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
175	IME_101882	Rv2234+Atc4 / IMSM_103711	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
176	IME_101883	Rv2234-Atc4 / IMSM_103712	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
177	IME_101884	Rv2234+Atc5 / IMSM_103713	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
178	IME_101885	Rv2234-Atc5 / IMSM_103714	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
179	IME_101886	Rv2234+Atc6 / IMSM_103715	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
180	IME_101887	Rv2234-Atc6 / IMSM_103716	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
181	IME_101888	Rv3774+Atc1 / IMSM_103717	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
182	IME_101889	Rv3774-Atc1 / IMSM_103718	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
183	IME_101890	Rv3774+Atc2 / IMSM_103719	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
184	IME_101891	Rv3774-Atc2 / IMSM_103720	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
185	IME_101892	Rv3774+Atc3 / IMSM_103721	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
186	IME_101893	Rv3774-Atc3 / IMSM_103722	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
187	IME_101894	Rv3774+Atc4 / IMSM_103723	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
188	IME_101895	Rv3774-Atc4 / IMSM_103724	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
189	IME_101896	Rv3774+Atc5 / IMSM_103725	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
190	IME_101897	Rv3774-Atc5 / IMSM_103726	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
191	IME_101898	Rv3774+Atc6 / IMSM_103727	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
192	IME_101899	Rv3774-Atc6 / IMSM_103728	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
193	IME_101900	Uninfected1 / IMSM_103729	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
194	IME_101901	Uninfected2 / IMSM_103730	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
195	IME_101902	Uninfected3 / IMSM_103731	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
196	IME_101903	Uninfected4 / IMSM_103732	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
197	IME_101904	Uninfected5 / IMSM_103733	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
198	IME_101905	Uninfected6 / IMSM_103734	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	NEGATIVE	NA
199	IME_101906	Rv0243+Atc1 / IMSM_103669	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
200	IME_101907	Rv0243-Atc1 / IMSM_103670	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
201	IME_101908	Rv0243+Atc2 / IMSM_103671	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
202	IME_101909	Rv0243-Atc2 / IMSM_103672	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
203	IME_101910	Rv0243+Atc3 / IMSM_103673	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
204	IME_101911	Rv0243-Atc3 / IMSM_103674	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
205	IME_101912	Rv0243+Atc4 / IMSM_103675	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
206	IME_101913	Rv0243-Atc4 / IMSM_103676	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
207	IME_101914	Rv0243+Atc5 / IMSM_103677	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
208	IME_101915	Rv0243-Atc5 / IMSM_103678	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
209	IME_101916	Rv0243+Atc6 / IMSM_103679	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
210	IME_101917	Rv0243-Atc6 / IMSM_103680	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
211	IME_101918	Rv0410+Atc1 / IMSM_103681	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
212	IME_101919	Rv0410-Atc1 / IMSM_103682	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
213	IME_101920	Rv0410+Atc2 / IMSM_103683	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
214	IME_101921	Rv0410-Atc2 / IMSM_103684	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
215	IME_101922	Rv0410+Atc3 / IMSM_103685	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
216	IME_101923	Rv0410-Atc3 / IMSM_103686	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
217	IME_101924	Rv0410+Atc4 / IMSM_103687	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
218	IME_101925	Rv0410-Atc4 / IMSM_103688	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
219	IME_101926	Rv0410+Atc5 / IMSM_103689	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
220	IME_101927	Rv0410-Atc5 / IMSM_103690	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
221	IME_101928	Rv0410+Atc6 / IMSM_103691	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
222	IME_101929	Rv0410-Atc6 / IMSM_103692	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
223	IME_101930	Rv1970+Atc1 / IMSM_103693	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
224	IME_101931	Rv1970-Atc1 / IMSM_103694	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
225	IME_101932	Rv1970+Atc2 / IMSM_103695	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
226	IME_101933	Rv1970-Atc2 / IMSM_103696	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
227	IME_101934	Rv1970+Atc3 / IMSM_103697	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
228	IME_101935	Rv1970-Atc3 / IMSM_103698	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
229	IME_101936	Rv1970+Atc4 / IMSM_103699	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
230	IME_101937	Rv1970-Atc4 / IMSM_103700	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
231	IME_101938	Rv1970+Atc5 / IMSM_103701	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
232	IME_101939	Rv1970-Atc5 / IMSM_103702	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
233	IME_101940	Rv1970+Atc6 / IMSM_103703	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
234	IME_101941	Rv1970-Atc6 / IMSM_103704	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
235	IME_101942	Rv2234+Atc1 / IMSM_103705	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
236	IME_101943	Rv2234-Atc1 / IMSM_103706	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
237	IME_101944	Rv2234+Atc2 / IMSM_103707	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
238	IME_101945	Rv2234-Atc2 / IMSM_103708	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
239	IME_101946	Rv2234+Atc3 / IMSM_103709	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
240	IME_101947	Rv2234-Atc3 / IMSM_103710	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
241	IME_101948	Rv2234+Atc4 / IMSM_103711	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
242	IME_101949	Rv2234-Atc4 / IMSM_103712	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
243	IME_101950	Rv2234+Atc5 / IMSM_103713	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
244	IME_101951	Rv2234-Atc5 / IMSM_103714	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
245	IME_101952	Rv2234+Atc6 / IMSM_103715	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
246	IME_101953	Rv2234-Atc6 / IMSM_103716	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
247	IME_101954	Rv3774+Atc1 / IMSM_103717	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
248	IME_101955	Rv3774-Atc1 / IMSM_103718	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
249	IME_101956	Rv3774+Atc2 / IMSM_103719	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
250	IME_101957	Rv3774-Atc2 / IMSM_103720	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
251	IME_101958	Rv3774+Atc3 / IMSM_103721	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
252	IME_101959	Rv3774-Atc3 / IMSM_103722	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
253	IME_101960	Rv3774+Atc4 / IMSM_103723	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
254	IME_101961	Rv3774-Atc4 / IMSM_103724	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
255	IME_101962	Rv3774+Atc5 / IMSM_103725	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
256	IME_101963	Rv3774-Atc5 / IMSM_103726	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
257	IME_101964	Rv3774+Atc6 / IMSM_103727	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
258	IME_101965	Rv3774-Atc6 / IMSM_103728	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
259	IME_101966	Uninfected1 / IMSM_103729	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
260	IME_101967	Uninfected2 / IMSM_103730	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
261	IME_101968	Uninfected3 / IMSM_103731	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
262	IME_101969	Uninfected4 / IMSM_103732	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
263	IME_101970	Uninfected5 / IMSM_103733	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA
264	IME_101971	Uninfected6 / IMSM_103734	LCMS (Liquid Chromatography- Mass Spectrometry)	Thermo Fusion Tribrid Orbitrap	Orbitrap	Electrospray Ionization - ESI	POSITIVE	NA

Author List

Sr.No	First name	Last name	Email	Organization	Designation
1	Yashwant	Kumar	y.kumar@thsti.res.in	Translational Health Science And Technology Institute (THSTI)	principal_investigator

File Details

Sr.No	ftprun ID	MS Exp ID	MS Data Files
1	IMR_102312	IME_101708	HILIC_NEG_Rv0243+Atc1.mzXML
2	IMR_102313	IME_101709	HILIC_NEG_Rv0243-Atc1.mzXML
3	IMR_102314	IME_101710	HILIC_NEG_Rv0243+Atc2.mzXML
4	IMR_102315	IME_101711	HILIC_NEG_Rv0243-Atc2.mzXML
5	IMR_102316	IME_101712	HILIC_NEG_Rv0243+Atc3.mzXML
6	IMR_102317	IME_101713	HILIC_NEG_Rv0243-Atc3.mzXML
7	IMR_102318	IME_101714	HILIC_NEG_Rv0243+Atc4.mzXML
8	IMR_102319	IME_101715	HILIC_NEG_Rv0243-Atc4.mzXML
9	IMR_102320	IME_101716	HILIC_NEG_Rv0243+Atc5.mzXML
10	IMR_102321	IME_101717	HILIC_NEG_Rv0243-Atc5.mzXML
11	IMR_102322	IME_101718	HILIC_NEG_Rv0243+Atc6.mzXML
12	IMR_102323	IME_101719	HILIC_NEG_Rv0243-Atc6.mzXML
13	IMR_102324	IME_101720	HILIC_NEG_Rv0410+Atc1.mzXML
14	IMR_102325	IME_101721	HILIC_NEG_Rv0410-Atc1.mzXML
15	IMR_102326	IME_101722	HILIC_NEG_Rv0410+Atc2.mzXML
16	IMR_102327	IME_101723	HILIC_NEG_Rv0410-Atc2.mzXML
17	IMR_102328	IME_101724	HILIC_NEG_Rv0410+Atc3.mzXML
18	IMR_102329	IME_101725	HILIC_NEG_Rv0410-Atc3.mzXML
19	IMR_102330	IME_101726	HILIC_NEG_Rv0410+Atc4.mzXML
20	IMR_102331	IME_101727	HILIC_NEG_Rv0410-Atc4.mzXML
21	IMR_102332	IME_101728	HILIC_NEG_Rv0410+Atc5.mzXML
22	IMR_102333	IME_101729	HILIC_NEG_Rv0410-Atc5.mzXML
23	IMR_102334	IME_101730	HILIC_NEG_Rv0410+Atc6.mzXML
24	IMR_102335	IME_101731	HILIC_NEG_Rv0410-Atc6.mzXML
25	IMR_102336	IME_101732	HILIC_NEG_Rv1970+Atc1.mzXML
26	IMR_102337	IME_101733	HILIC_NEG_Rv1970-Atc1.mzXML
27	IMR_102338	IME_101734	HILIC_NEG_Rv1970+Atc2.mzXML
28	IMR_102339	IME_101735	HILIC_NEG_Rv1970-Atc2.mzXML
29	IMR_102340	IME_101736	HILIC_NEG_Rv1970+Atc3.mzXML
30	IMR_102341	IME_101737	HILIC_NEG_Rv1970-Atc3.mzXML
31	IMR_102342	IME_101738	HILIC_NEG_Rv1970+Atc4.mzXML
32	IMR_102343	IME_101739	HILIC_NEG_Rv1970-Atc4.mzXML
33	IMR_102344	IME_101740	HILIC_NEG_Rv1970+Atc5.mzXML
34	IMR_102345	IME_101741	HILIC_NEG_Rv1970-Atc5.mzXML
35	IMR_102346	IME_101742	HILIC_NEG_Rv1970+Atc6.mzXML
36	IMR_102347	IME_101743	HILIC_NEG_Rv1970-Atc6.mzXML
37	IMR_102348	IME_101744	HILIC_NEG_Rv2234+Atc1.mzXML
38	IMR_102349	IME_101745	HILIC_NEG_Rv2234-Atc1.mzXML
39	IMR_102350	IME_101746	HILIC_NEG_Rv2234+Atc2.mzXML
40	IMR_102351	IME_101747	HILIC_NEG_Rv2234-Atc2.mzXML
41	IMR_102352	IME_101748	HILIC_NEG_Rv2234+Atc3.mzXML
42	IMR_102353	IME_101749	HILIC_NEG_Rv2234-Atc3.mzXML
43	IMR_102354	IME_101750	HILIC_NEG_Rv2234+Atc4.mzXML
44	IMR_102355	IME_101751	HILIC_NEG_Rv2234-Atc4.mzXML
45	IMR_102356	IME_101752	HILIC_NEG_Rv2234+Atc5.mzXML
46	IMR_102357	IME_101753	HILIC_NEG_Rv2234-Atc5.mzXML
47	IMR_102358	IME_101754	HILIC_NEG_Rv2234+Atc6.mzXML
48	IMR_102359	IME_101755	HILIC_NEG_Rv2234-Atc6.mzXML
49	IMR_102360	IME_101756	HILIC_NEG_Rv3774+Atc1.mzXML
50	IMR_102361	IME_101757	HILIC_NEG_Rv3774-Atc1.mzXML
51	IMR_102362	IME_101758	HILIC_NEG_Rv3774+Atc2.mzXML
52	IMR_102363	IME_101759	HILIC_NEG_Rv3774-Atc2.mzXML
53	IMR_102364	IME_101760	HILIC_NEG_Rv3774+Atc3.mzXML
54	IMR_102365	IME_101761	HILIC_NEG_Rv3774-Atc3.mzXML
55	IMR_102366	IME_101762	HILIC_NEG_Rv3774+Atc4.mzXML
56	IMR_102367	IME_101763	HILIC_NEG_Rv3774-Atc4.mzXML
57	IMR_102368	IME_101764	HILIC_NEG_Rv3774+Atc5.mzXML
58	IMR_102369	IME_101765	HILIC_NEG_Rv3774-Atc5.mzXML
59	IMR_102370	IME_101766	HILIC_NEG_Rv3774+Atc6.mzXML
60	IMR_102371	IME_101767	HILIC_NEG_Rv3774-Atc6.mzXML
61	IMR_102372	IME_101768	HILIC_NEG_Uninfected1.mzXML
62	IMR_102373	IME_101769	HILIC_NEG_Uninfected2.mzXML
63	IMR_102374	IME_101770	HILIC_NEG_Uninfected3.mzXML
64	IMR_102375	IME_101771	HILIC_NEG_Uninfected4.mzXML
65	IMR_102376	IME_101772	HILIC_NEG_Uninfected5.mzXML
66	IMR_102377	IME_101773	HILIC_NEG_Uninfected6.mzXML
67	IMR_102378	IME_101774	HILIC_POS_Rv0243+Atc1.mzXML
68	IMR_102379	IME_101775	HILIC_POS_Rv0243-Atc1.mzXML
69	IMR_102380	IME_101776	HILIC_POS_Rv0243+Atc2.mzXML
70	IMR_102381	IME_101777	HILIC_POS_Rv0243-Atc2.mzXML
71	IMR_102382	IME_101778	HILIC_POS_Rv0243+Atc3.mzXML
72	IMR_102383	IME_101779	HILIC_POS_Rv0243-Atc3.mzXML
73	IMR_102384	IME_101780	HILIC_POS_Rv0243+Atc4.mzXML
74	IMR_102385	IME_101781	HILIC_POS_Rv0243-Atc4.mzXML
75	IMR_102386	IME_101782	HILIC_POS_Rv0243+Atc5.mzXML
76	IMR_102387	IME_101783	HILIC_POS_Rv0243-Atc5.mzXML
77	IMR_102388	IME_101784	HILIC_POS_Rv0243+Atc6.mzXML
78	IMR_102389	IME_101785	HILIC_POS_Rv0243-Atc6.mzXML
79	IMR_102390	IME_101786	HILIC_POS_Rv0410+Atc1.mzXML
80	IMR_102391	IME_101787	HILIC_POS_Rv0410-Atc1.mzXML
81	IMR_102392	IME_101788	HILIC_POS_Rv0410+Atc2.mzXML
82	IMR_102393	IME_101789	HILIC_POS_Rv0410-Atc2.mzXML
83	IMR_102394	IME_101790	HILIC_POS_Rv0410+Atc3.mzXML
84	IMR_102395	IME_101791	HILIC_POS_Rv0410-Atc3.mzXML
85	IMR_102396	IME_101792	HILIC_POS_Rv0410+Atc4.mzXML
86	IMR_102397	IME_101793	HILIC_POS_Rv0410-Atc4.mzXML
87	IMR_102398	IME_101794	HILIC_POS_Rv0410+Atc5.mzXML
88	IMR_102399	IME_101795	HILIC_POS_Rv0410-Atc5.mzXML
89	IMR_102400	IME_101796	HILIC_POS_Rv0410+Atc6.mzXML
90	IMR_102401	IME_101797	HILIC_POS_Rv0410-Atc6.mzXML
91	IMR_102402	IME_101798	HILIC_POS_Rv1970+Atc1.mzXML
92	IMR_102403	IME_101799	HILIC_POS_Rv1970-Atc1.mzXML
93	IMR_102404	IME_101800	HILIC_POS_Rv1970+Atc2.mzXML
94	IMR_102405	IME_101801	HILIC_POS_Rv1970-Atc2.mzXML
95	IMR_102406	IME_101802	HILIC_POS_Rv1970+Atc3.mzXML
96	IMR_102407	IME_101803	HILIC_POS_Rv1970-Atc3.mzXML
97	IMR_102408	IME_101804	HILIC_POS_Rv1970+Atc4.mzXML
98	IMR_102409	IME_101805	HILIC_POS_Rv1970-Atc4.mzXML
99	IMR_102410	IME_101806	HILIC_POS_Rv1970+Atc5.mzXML
100	IMR_102411	IME_101807	HILIC_POS_Rv1970-Atc5.mzXML
101	IMR_102412	IME_101808	HILIC_POS_Rv1970+Atc6.mzXML
102	IMR_102413	IME_101809	HILIC_POS_Rv1970-Atc6.mzXML
103	IMR_102414	IME_101810	HILIC_POS_Rv2234+Atc1.mzXML
104	IMR_102415	IME_101811	HILIC_POS_Rv2234-Atc1.mzXML
105	IMR_102416	IME_101812	HILIC_POS_Rv2234+Atc2.mzXML
106	IMR_102417	IME_101813	HILIC_POS_Rv2234-Atc2.mzXML
107	IMR_102418	IME_101814	HILIC_POS_Rv2234+Atc3.mzXML
108	IMR_102419	IME_101815	HILIC_POS_Rv2234-Atc3.mzXML
109	IMR_102420	IME_101816	HILIC_POS_Rv2234+Atc4.mzXML
110	IMR_102421	IME_101817	HILIC_POS_Rv2234-Atc4.mzXML
111	IMR_102422	IME_101818	HILIC_POS_Rv2234+Atc5.mzXML
112	IMR_102423	IME_101819	HILIC_POS_Rv2234-Atc5.mzXML
113	IMR_102424	IME_101820	HILIC_POS_Rv2234+Atc6.mzXML
114	IMR_102425	IME_101821	HILIC_POS_Rv2234-Atc6.mzXML
115	IMR_102426	IME_101822	HILIC_POS_Rv3774+Atc1.mzXML
116	IMR_102427	IME_101823	HILIC_POS_Rv3774-Atc1.mzXML
117	IMR_102428	IME_101824	HILIC_POS_Rv3774+Atc2.mzXML
118	IMR_102429	IME_101825	HILIC_POS_Rv3774-Atc2.mzXML
119	IMR_102430	IME_101826	HILIC_POS_Rv3774+Atc3.mzXML
120	IMR_102431	IME_101827	HILIC_POS_Rv3774-Atc3.mzXML
121	IMR_102432	IME_101828	HILIC_POS_Rv3774+Atc4.mzXML
122	IMR_102433	IME_101829	HILIC_POS_Rv3774-Atc4.mzXML
123	IMR_102434	IME_101830	HILIC_POS_Rv3774+Atc5.mzXML
124	IMR_102435	IME_101831	HILIC_POS_Rv3774-Atc5.mzXML
125	IMR_102436	IME_101832	HILIC_POS_Rv3774+Atc6.mzXML
126	IMR_102437	IME_101833	HILIC_POS_Rv3774-Atc6.mzXML
127	IMR_102438	IME_101834	HILIC_POS_Uninfected1.mzXML
128	IMR_102439	IME_101835	HILIC_POS_Uninfected2.mzXML
129	IMR_102440	IME_101836	HILIC_POS_Uninfected3.mzXML
130	IMR_102441	IME_101837	HILIC_POS_Uninfected4.mzXML
131	IMR_102442	IME_101838	HILIC_POS_Uninfected5.mzXML
132	IMR_102443	IME_101839	HILIC_POS_Uninfected6.mzXML
133	IMR_102444	IME_101840	RP_NEG_Rv0243+Atc1.mzXML
134	IMR_102445	IME_101841	RP_NEG_Rv0243-Atc1.mzXML
135	IMR_102446	IME_101842	RP_NEG_Rv0243+Atc2.mzXML
136	IMR_102447	IME_101843	RP_NEG_Rv0243-Atc2.mzXML
137	IMR_102448	IME_101844	RP_NEG_Rv0243+Atc3.mzXML
138	IMR_102449	IME_101845	RP_NEG_Rv0243-Atc3.mzXML
139	IMR_102450	IME_101846	RP_NEG_Rv0243+Atc4.mzXML
140	IMR_102451	IME_101847	RP_NEG_Rv0243-Atc4.mzXML
141	IMR_102452	IME_101848	RP_NEG_Rv0243+Atc5.mzXML
142	IMR_102453	IME_101849	RP_NEG_Rv0243-Atc5.mzXML
143	IMR_102454	IME_101850	RP_NEG_Rv0243+Atc6.mzXML
144	IMR_102455	IME_101851	RP_NEG_Rv0243-Atc6.mzXML
145	IMR_102456	IME_101852	RP_NEG_Rv0410+Atc1.mzXML
146	IMR_102457	IME_101853	RP_NEG_Rv0410-Atc1.mzXML
147	IMR_102458	IME_101854	RP_NEG_Rv0410+Atc2.mzXML
148	IMR_102459	IME_101855	RP_NEG_Rv0410-Atc2.mzXML
149	IMR_102460	IME_101856	RP_NEG_Rv0410+Atc3.mzXML
150	IMR_102461	IME_101857	RP_NEG_Rv0410-Atc3.mzXML
151	IMR_102462	IME_101858	RP_NEG_Rv0410+Atc4.mzXML
152	IMR_102463	IME_101859	RP_NEG_Rv0410-Atc4.mzXML
153	IMR_102464	IME_101860	RP_NEG_Rv0410+Atc5.mzXML
154	IMR_102465	IME_101861	RP_NEG_Rv0410-Atc5.mzXML
155	IMR_102466	IME_101862	RP_NEG_Rv0410+Atc6.mzXML
156	IMR_102467	IME_101863	RP_NEG_Rv0410-Atc6.mzXML
157	IMR_102468	IME_101864	RP_NEG_Rv1970+Atc1.mzXML
158	IMR_102469	IME_101865	RP_NEG_Rv1970-Atc1.mzXML
159	IMR_102470	IME_101866	RP_NEG_Rv1970+Atc2.mzXML
160	IMR_102471	IME_101867	RP_NEG_Rv1970-Atc2.mzXML
161	IMR_102472	IME_101868	RP_NEG_Rv1970+Atc3.mzXML
162	IMR_102473	IME_101869	RP_NEG_Rv1970-Atc3.mzXML
163	IMR_102474	IME_101870	RP_NEG_Rv1970+Atc4.mzXML
164	IMR_102475	IME_101871	RP_NEG_Rv1970-Atc4.mzXML
165	IMR_102476	IME_101872	RP_NEG_Rv1970+Atc5.mzXML
166	IMR_102477	IME_101873	RP_NEG_Rv1970-Atc5.mzXML
167	IMR_102478	IME_101874	RP_NEG_Rv1970+Atc6.mzXML
168	IMR_102479	IME_101875	RP_NEG_Rv1970-Atc6.mzXML
169	IMR_102480	IME_101876	RP_NEG_Rv2234+Atc1.mzXML
170	IMR_102481	IME_101877	RP_NEG_Rv2234-Atc1.mzXML
171	IMR_102482	IME_101878	RP_NEG_Rv2234+Atc2.mzXML
172	IMR_102483	IME_101879	RP_NEG_Rv2234-Atc2.mzXML
173	IMR_102484	IME_101880	RP_NEG_Rv2234+Atc3.mzXML
174	IMR_102485	IME_101881	RP_NEG_Rv2234-Atc3.mzXML
175	IMR_102486	IME_101882	RP_NEG_Rv2234+Atc4.mzXML
176	IMR_102487	IME_101883	RP_NEG_Rv2234-Atc4.mzXML
177	IMR_102488	IME_101884	RP_NEG_Rv2234+Atc5.mzXML
178	IMR_102489	IME_101885	RP_NEG_Rv2234-Atc5.mzXML
179	IMR_102490	IME_101886	RP_NEG_Rv2234+Atc6.mzXML
180	IMR_102491	IME_101887	RP_NEG_Rv2234-Atc6.mzXML
181	IMR_102492	IME_101888	RP_NEG_Rv3774+Atc1.mzXML
182	IMR_102493	IME_101889	RP_NEG_Rv3774-Atc1.mzXML
183	IMR_102494	IME_101890	RP_NEG_Rv3774+Atc2.mzXML
184	IMR_102495	IME_101891	RP_NEG_Rv3774-Atc2.mzXML
185	IMR_102496	IME_101892	RP_NEG_Rv3774+Atc3.mzXML
186	IMR_102497	IME_101893	RP_NEG_Rv3774-Atc3.mzXML
187	IMR_102498	IME_101894	RP_NEG_Rv3774+Atc4.mzXML
188	IMR_102499	IME_101895	RP_NEG_Rv3774-Atc4.mzXML
189	IMR_102500	IME_101896	RP_NEG_Rv3774+Atc5.mzXML
190	IMR_102501	IME_101897	RP_NEG_Rv3774-Atc5.mzXML
191	IMR_102502	IME_101898	RP_NEG_Rv3774+Atc6.mzXML
192	IMR_102503	IME_101899	RP_NEG_Rv3774-Atc6.mzXML
193	IMR_102504	IME_101900	RP_NEG_Uninfected1.mzXML
194	IMR_102505	IME_101901	RP_NEG_Uninfected2.mzXML
195	IMR_102506	IME_101902	RP_NEG_Uninfected3.mzXML
196	IMR_102507	IME_101903	RP_NEG_Uninfected4.mzXML
197	IMR_102508	IME_101904	RP_NEG_Uninfected5.mzXML
198	IMR_102509	IME_101905	RP_NEG_Uninfected6.mzXML
199	IMR_102510	IME_101906	RP_POS_Rv0243+Atc1.mzXML
200	IMR_102511	IME_101907	RP_POS_Rv0243-Atc1.mzXML
201	IMR_102512	IME_101908	RP_POS_Rv0243+Atc2.mzXML
202	IMR_102513	IME_101909	RP_POS_Rv0243-Atc2.mzXML
203	IMR_102514	IME_101910	RP_POS_Rv0243+Atc3.mzXML
204	IMR_102515	IME_101911	RP_POS_Rv0243-Atc3.mzXML
205	IMR_102516	IME_101912	RP_POS_Rv0243+Atc4.mzXML
206	IMR_102517	IME_101913	RP_POS_Rv0243-Atc4.mzXML
207	IMR_102518	IME_101914	RP_POS_Rv0243+Atc5.mzXML
208	IMR_102519	IME_101915	RP_POS_Rv0243-Atc5.mzXML
209	IMR_102520	IME_101916	RP_POS_Rv0243+Atc6.mzXML
210	IMR_102521	IME_101917	RP_POS_Rv0243-Atc6.mzXML
211	IMR_102522	IME_101918	RP_POS_Rv0410+Atc1.mzXML
212	IMR_102523	IME_101919	RP_POS_Rv0410-Atc1.mzXML
213	IMR_102524	IME_101920	RP_POS_Rv0410+Atc2.mzXML
214	IMR_102525	IME_101921	RP_POS_Rv0410-Atc2.mzXML
215	IMR_102526	IME_101922	RP_POS_Rv0410+Atc3.mzXML
216	IMR_102527	IME_101923	RP_POS_Rv0410-Atc3.mzXML
217	IMR_102528	IME_101924	RP_POS_Rv0410+Atc4.mzXML
218	IMR_102529	IME_101925	RP_POS_Rv0410-Atc4.mzXML
219	IMR_102530	IME_101926	RP_POS_Rv0410+Atc5.mzXML
220	IMR_102531	IME_101927	RP_POS_Rv0410-Atc5.mzXML
221	IMR_102532	IME_101928	RP_POS_Rv0410+Atc6.mzXML
222	IMR_102533	IME_101929	RP_POS_Rv0410-Atc6.mzXML
223	IMR_102534	IME_101930	RP_POS_Rv1970+Atc1.mzXML
224	IMR_102535	IME_101931	RP_POS_Rv1970-Atc1.mzXML
225	IMR_102536	IME_101932	RP_POS_Rv1970+Atc2.mzXML
226	IMR_102537	IME_101933	RP_POS_Rv1970-Atc2.mzXML
227	IMR_102538	IME_101934	RP_POS_Rv1970+Atc3.mzXML
228	IMR_102539	IME_101935	RP_POS_Rv1970-Atc3.mzXML
229	IMR_102540	IME_101936	RP_POS_Rv1970+Atc4.mzXML
230	IMR_102541	IME_101937	RP_POS_Rv1970-Atc4.mzXML
231	IMR_102542	IME_101938	RP_POS_Rv1970+Atc5.mzXML
232	IMR_102543	IME_101939	RP_POS_Rv1970-Atc5.mzXML
233	IMR_102544	IME_101940	RP_POS_Rv1970+Atc6.mzXML
234	IMR_102545	IME_101941	RP_POS_Rv1970-Atc6.mzXML
235	IMR_102546	IME_101942	RP_POS_Rv2234+Atc1.mzXML
236	IMR_102547	IME_101943	RP_POS_Rv2234-Atc1.mzXML
237	IMR_102548	IME_101944	RP_POS_Rv2234+Atc2.mzXML
238	IMR_102549	IME_101945	RP_POS_Rv2234-Atc2.mzXML
239	IMR_102550	IME_101946	RP_POS_Rv2234+Atc3.mzXML
240	IMR_102551	IME_101947	RP_POS_Rv2234-Atc3.mzXML
241	IMR_102552	IME_101948	RP_POS_Rv2234+Atc4.mzXML
242	IMR_102553	IME_101949	RP_POS_Rv2234-Atc4.mzXML
243	IMR_102554	IME_101950	RP_POS_Rv2234+Atc5.mzXML
244	IMR_102555	IME_101951	RP_POS_Rv2234-Atc5.mzXML
245	IMR_102556	IME_101952	RP_POS_Rv2234+Atc6.mzXML
246	IMR_102557	IME_101953	RP_POS_Rv2234-Atc6.mzXML
247	IMR_102558	IME_101954	RP_POS_Rv3774+Atc1.mzXML
248	IMR_102559	IME_101955	RP_POS_Rv3774-Atc1.mzXML
249	IMR_102560	IME_101956	RP_POS_Rv3774+Atc2.mzXML
250	IMR_102561	IME_101957	RP_POS_Rv3774-Atc2.mzXML
251	IMR_102562	IME_101958	RP_POS_Rv3774+Atc3.mzXML
252	IMR_102563	IME_101959	RP_POS_Rv3774-Atc3.mzXML
253	IMR_102564	IME_101960	RP_POS_Rv3774+Atc4.mzXML
254	IMR_102565	IME_101961	RP_POS_Rv3774-Atc4.mzXML
255	IMR_102566	IME_101962	RP_POS_Rv3774+Atc5.mzXML
256	IMR_102567	IME_101963	RP_POS_Rv3774-Atc5.mzXML
257	IMR_102568	IME_101964	RP_POS_Rv3774+Atc6.mzXML
258	IMR_102569	IME_101965	RP_POS_Rv3774-Atc6.mzXML
259	IMR_102570	IME_101966	RP_POS_Uninfected1.mzXML
260	IMR_102571	IME_101967	RP_POS_Uninfected2.mzXML
261	IMR_102572	IME_101968	RP_POS_Uninfected3.mzXML
262	IMR_102573	IME_101969	RP_POS_Uninfected4.mzXML
263	IMR_102574	IME_101970	RP_POS_Uninfected5.mzXML
264	IMR_102575	IME_101971	RP_POS_Uninfected6.mzXML

MS Study

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Study

Sample (Total Count:66)

Mass Spectrometry

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