Bedaquiline reprograms central metabolism to reveal glycolytic vulnerability in Mycobacterium tuberculosis

Bedaquiline (BDQ) is a known tuberculosis treatment, but the precise mechanism of cell death is unclear. Here, the authors explore the metabolic profiles of M. tuberculosis upon BDQ treatment and find reliance on glycolysis and synergistic cell death when oxidative phosphorylation is also targeted.

Bibliographic Details
Main Authors: Jared S. Mackenzie, Dirk A. Lamprecht, Rukaya Asmal, John H. Adamson, Khushboo Borah, Dany J. V. Beste, Bei Shi Lee, Kevin Pethe, Simon Rousseau, Inna Krieger, James C. Sacchettini, Joel N. Glasgow, Adrie J. C. Steyn
Format: Article
Language:English
Published: Nature Portfolio 2020-11-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-020-19959-4
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author Jared S. Mackenzie
Dirk A. Lamprecht
Rukaya Asmal
John H. Adamson
Khushboo Borah
Dany J. V. Beste
Bei Shi Lee
Kevin Pethe
Simon Rousseau
Inna Krieger
James C. Sacchettini
Joel N. Glasgow
Adrie J. C. Steyn
author_facet Jared S. Mackenzie
Dirk A. Lamprecht
Rukaya Asmal
John H. Adamson
Khushboo Borah
Dany J. V. Beste
Bei Shi Lee
Kevin Pethe
Simon Rousseau
Inna Krieger
James C. Sacchettini
Joel N. Glasgow
Adrie J. C. Steyn
author_sort Jared S. Mackenzie
collection DOAJ
description Bedaquiline (BDQ) is a known tuberculosis treatment, but the precise mechanism of cell death is unclear. Here, the authors explore the metabolic profiles of M. tuberculosis upon BDQ treatment and find reliance on glycolysis and synergistic cell death when oxidative phosphorylation is also targeted.
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spelling doaj.art-d680f868a7c742a69cdc3f6e9206d15b2022-12-21T22:54:44ZengNature PortfolioNature Communications2041-17232020-11-0111111610.1038/s41467-020-19959-4Bedaquiline reprograms central metabolism to reveal glycolytic vulnerability in Mycobacterium tuberculosisJared S. Mackenzie0Dirk A. Lamprecht1Rukaya Asmal2John H. Adamson3Khushboo Borah4Dany J. V. Beste5Bei Shi Lee6Kevin Pethe7Simon Rousseau8Inna Krieger9James C. Sacchettini10Joel N. Glasgow11Adrie J. C. Steyn12Africa Health Research InstituteJanssen Pharmaceutica, Global Public HealthAfrica Health Research InstituteAfrica Health Research InstituteFaculty of Health and Medical Sciences, University of SurreyFaculty of Health and Medical Sciences, University of SurreySchool of Biological Sciences, Nanyang Technological UniversitySchool of Biological Sciences, Nanyang Technological UniversityTexas A&M University, Department of Biochemistry and BiophysicsTexas A&M University, Department of Biochemistry and BiophysicsTexas A&M University, Department of Biochemistry and BiophysicsDepartment of Microbiology, University of Alabama at BirminghamAfrica Health Research InstituteBedaquiline (BDQ) is a known tuberculosis treatment, but the precise mechanism of cell death is unclear. Here, the authors explore the metabolic profiles of M. tuberculosis upon BDQ treatment and find reliance on glycolysis and synergistic cell death when oxidative phosphorylation is also targeted.https://doi.org/10.1038/s41467-020-19959-4
spellingShingle Jared S. Mackenzie
Dirk A. Lamprecht
Rukaya Asmal
John H. Adamson
Khushboo Borah
Dany J. V. Beste
Bei Shi Lee
Kevin Pethe
Simon Rousseau
Inna Krieger
James C. Sacchettini
Joel N. Glasgow
Adrie J. C. Steyn
Bedaquiline reprograms central metabolism to reveal glycolytic vulnerability in Mycobacterium tuberculosis
Nature Communications
title Bedaquiline reprograms central metabolism to reveal glycolytic vulnerability in Mycobacterium tuberculosis
title_full Bedaquiline reprograms central metabolism to reveal glycolytic vulnerability in Mycobacterium tuberculosis
title_fullStr Bedaquiline reprograms central metabolism to reveal glycolytic vulnerability in Mycobacterium tuberculosis
title_full_unstemmed Bedaquiline reprograms central metabolism to reveal glycolytic vulnerability in Mycobacterium tuberculosis
title_short Bedaquiline reprograms central metabolism to reveal glycolytic vulnerability in Mycobacterium tuberculosis
title_sort bedaquiline reprograms central metabolism to reveal glycolytic vulnerability in mycobacterium tuberculosis
url https://doi.org/10.1038/s41467-020-19959-4
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