Phosphoglucomutase A-mediated metabolic adaptation is essential for antibiotic and disease persistence in Mycobacterium tuberculosis

ABSTRACT The long-term survival of Mycobacterium tuberculosis (Mtb) requires efficient use of host resources and uninterrupted access to host-derived nutrients. This is done by utilization of a highly flexible and integrated network of metabolic pathways. Phosphoglucomutase A (pgmA) is essential for...

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Main Authors: Taruna Sharma, Shaifali Tyagi, Rahul Pal, Jayendrajyoti Kundu, Sonu Kumar Gupta, Vishawjeet Barik, Vaibhav Kumar Nain, Manitosh Pandey, Prabhanjan Dwivedi, Bhishma Narayan Panda, Yashwant Kumar, Ranjan Kumar Nanda, Samrat Chatterjee, Amit Kumar Pandey
Format: Article
Language:English
Published: American Society for Microbiology 2025-07-01
Series:mSystems
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Online Access:https://journals.asm.org/doi/10.1128/msystems.00420-25
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author Taruna Sharma
Shaifali Tyagi
Rahul Pal
Jayendrajyoti Kundu
Sonu Kumar Gupta
Vishawjeet Barik
Vaibhav Kumar Nain
Manitosh Pandey
Prabhanjan Dwivedi
Bhishma Narayan Panda
Yashwant Kumar
Ranjan Kumar Nanda
Samrat Chatterjee
Amit Kumar Pandey
author_facet Taruna Sharma
Shaifali Tyagi
Rahul Pal
Jayendrajyoti Kundu
Sonu Kumar Gupta
Vishawjeet Barik
Vaibhav Kumar Nain
Manitosh Pandey
Prabhanjan Dwivedi
Bhishma Narayan Panda
Yashwant Kumar
Ranjan Kumar Nanda
Samrat Chatterjee
Amit Kumar Pandey
author_sort Taruna Sharma
collection DOAJ
description ABSTRACT The long-term survival of Mycobacterium tuberculosis (Mtb) requires efficient use of host resources and uninterrupted access to host-derived nutrients. This is done by utilization of a highly flexible and integrated network of metabolic pathways. Phosphoglucomutase A (pgmA) is essential for glycogen biosynthesis, which acts as a nutrient reservoir and is known to modulate carbon flux in various pathogens. We, for the first time, investigated the role of pgmA in Mtb by creating a strain lacking this gene. The absence of pgmA hinders the survival of pathogens under nutrient-limiting and reactivation conditions. Our study shows that the lack of cell membrane-associated glycolipids in ΔpgmA compromises cell wall integrity and increases susceptibility to stress. Interestingly, ΔpgmA exhibits an enhanced growth phenotype on cholesterol compared to the wild type due to low cyclic adenosine monophosphate (cAMP) levels. Differential gene expression and 13C3 carbon dilution analyses indicate that stored carbon as glycogen is crucial for Mtb survival under nutrient-limiting conditions. We demonstrate that pgmA is vital for Mtb growth within the host. This study highlights the critical role of pgmA in metabolic adaptation during nutrient starvation and reactivation and its implication on antibiotic and disease persistence. These insights are crucial for developing novel, shorter, and more effective anti-tuberculosis strategies.IMPORTANCEThis study for the first time investigated the role of metabolic enzyme phosphoglucomutase A (pgmA) in Mycobacterium tuberculosis (Mtb), revealing its crucial functions as a toggle switch between biosynthesis and growth. This work highlights the importance of pgmA in maintaining the metabolic flexibility of Mtb during the nutritional switch. The presence of pgmA is critical for the production of membrane-associated glycolipid, which helps maintain the cell wall integrity under various growth and stress conditions. This adaptability is pivotal for generating starvation-induced antibiotic tolerance in Mtb. In addition to the clinical context, these findings provide a mechanistic foundation for understanding adaptive strategies by Mtb to harsh environments and the development of drug-tolerant bacilli.
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spelling doaj-art-6ad90eb2f2f64f29b7ac0ff8f945ae152025-08-20T03:29:57ZengAmerican Society for MicrobiologymSystems2379-50772025-07-0110710.1128/msystems.00420-25Phosphoglucomutase A-mediated metabolic adaptation is essential for antibiotic and disease persistence in Mycobacterium tuberculosisTaruna Sharma0Shaifali Tyagi1Rahul Pal2Jayendrajyoti Kundu3Sonu Kumar Gupta4Vishawjeet Barik5Vaibhav Kumar Nain6Manitosh Pandey7Prabhanjan Dwivedi8Bhishma Narayan Panda9Yashwant Kumar10Ranjan Kumar Nanda11Samrat Chatterjee12Amit Kumar Pandey13Mycobacterial Pathogenesis Laboratory, Centre for Tuberculosis Research, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaMycobacterial Pathogenesis Laboratory, Centre for Tuberculosis Research, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaMycobacterial Pathogenesis Laboratory, Centre for Tuberculosis Research, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaComplex Analysis Group, Computational and Mathematical Biology Centre, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaBiomarker Discovery Laboratory, Non-communicable Disease Centre, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaMycobacterial Pathogenesis Laboratory, Centre for Tuberculosis Research, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaMycobacterial Pathogenesis Laboratory, Centre for Tuberculosis Research, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaMycobacterial Pathogenesis Laboratory, Centre for Tuberculosis Research, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaExperimental Animal Facility, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaExperimental Animal Facility, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaComplex Analysis Group, Computational and Mathematical Biology Centre, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaTranslational Health Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, Delhi, IndiaComplex Analysis Group, Computational and Mathematical Biology Centre, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaMycobacterial Pathogenesis Laboratory, Centre for Tuberculosis Research, Translational Health Science and Technology Institute, Faridabad, Haryana, IndiaABSTRACT The long-term survival of Mycobacterium tuberculosis (Mtb) requires efficient use of host resources and uninterrupted access to host-derived nutrients. This is done by utilization of a highly flexible and integrated network of metabolic pathways. Phosphoglucomutase A (pgmA) is essential for glycogen biosynthesis, which acts as a nutrient reservoir and is known to modulate carbon flux in various pathogens. We, for the first time, investigated the role of pgmA in Mtb by creating a strain lacking this gene. The absence of pgmA hinders the survival of pathogens under nutrient-limiting and reactivation conditions. Our study shows that the lack of cell membrane-associated glycolipids in ΔpgmA compromises cell wall integrity and increases susceptibility to stress. Interestingly, ΔpgmA exhibits an enhanced growth phenotype on cholesterol compared to the wild type due to low cyclic adenosine monophosphate (cAMP) levels. Differential gene expression and 13C3 carbon dilution analyses indicate that stored carbon as glycogen is crucial for Mtb survival under nutrient-limiting conditions. We demonstrate that pgmA is vital for Mtb growth within the host. This study highlights the critical role of pgmA in metabolic adaptation during nutrient starvation and reactivation and its implication on antibiotic and disease persistence. These insights are crucial for developing novel, shorter, and more effective anti-tuberculosis strategies.IMPORTANCEThis study for the first time investigated the role of metabolic enzyme phosphoglucomutase A (pgmA) in Mycobacterium tuberculosis (Mtb), revealing its crucial functions as a toggle switch between biosynthesis and growth. This work highlights the importance of pgmA in maintaining the metabolic flexibility of Mtb during the nutritional switch. The presence of pgmA is critical for the production of membrane-associated glycolipid, which helps maintain the cell wall integrity under various growth and stress conditions. This adaptability is pivotal for generating starvation-induced antibiotic tolerance in Mtb. In addition to the clinical context, these findings provide a mechanistic foundation for understanding adaptive strategies by Mtb to harsh environments and the development of drug-tolerant bacilli.https://journals.asm.org/doi/10.1128/msystems.00420-25Mycobacterium tuberculosisphosphoglucomutase ApgmAglycogen metabolismvirulenceantibiotic tolerance
spellingShingle Taruna Sharma
Shaifali Tyagi
Rahul Pal
Jayendrajyoti Kundu
Sonu Kumar Gupta
Vishawjeet Barik
Vaibhav Kumar Nain
Manitosh Pandey
Prabhanjan Dwivedi
Bhishma Narayan Panda
Yashwant Kumar
Ranjan Kumar Nanda
Samrat Chatterjee
Amit Kumar Pandey
Phosphoglucomutase A-mediated metabolic adaptation is essential for antibiotic and disease persistence in Mycobacterium tuberculosis
mSystems
Mycobacterium tuberculosis
phosphoglucomutase A
pgmA
glycogen metabolism
virulence
antibiotic tolerance
title Phosphoglucomutase A-mediated metabolic adaptation is essential for antibiotic and disease persistence in Mycobacterium tuberculosis
title_full Phosphoglucomutase A-mediated metabolic adaptation is essential for antibiotic and disease persistence in Mycobacterium tuberculosis
title_fullStr Phosphoglucomutase A-mediated metabolic adaptation is essential for antibiotic and disease persistence in Mycobacterium tuberculosis
title_full_unstemmed Phosphoglucomutase A-mediated metabolic adaptation is essential for antibiotic and disease persistence in Mycobacterium tuberculosis
title_short Phosphoglucomutase A-mediated metabolic adaptation is essential for antibiotic and disease persistence in Mycobacterium tuberculosis
title_sort phosphoglucomutase a mediated metabolic adaptation is essential for antibiotic and disease persistence in mycobacterium tuberculosis
topic Mycobacterium tuberculosis
phosphoglucomutase A
pgmA
glycogen metabolism
virulence
antibiotic tolerance
url https://journals.asm.org/doi/10.1128/msystems.00420-25
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