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Unraveling the mechanisms of intrinsic drug resistance in Mycobacterium tuberculosis

Tuberculosis (TB) is among the most difficult infections to treat, requiring several months of multidrug therapy to produce a durable cure. The reasons necessitating long treatment times are complex and multifactorial. However, one major difficulty of treating TB is the resistance of the infecting b...

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Detalles Bibliográficos
Autores principales: Poulton, Nicholas C., Rock, Jeremy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618640/
https://www.ncbi.nlm.nih.gov/pubmed/36325467
http://dx.doi.org/10.3389/fcimb.2022.997283
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author Poulton, Nicholas C.
Rock, Jeremy M.
author_facet Poulton, Nicholas C.
Rock, Jeremy M.
author_sort Poulton, Nicholas C.
collection PubMed
description Tuberculosis (TB) is among the most difficult infections to treat, requiring several months of multidrug therapy to produce a durable cure. The reasons necessitating long treatment times are complex and multifactorial. However, one major difficulty of treating TB is the resistance of the infecting bacterium, Mycobacterium tuberculosis (Mtb), to many distinct classes of antimicrobials. This review will focus on the major gaps in our understanding of intrinsic drug resistance in Mtb and how functional and chemical-genetics can help close those gaps. A better understanding of intrinsic drug resistance will help lay the foundation for strategies to disarm and circumvent these mechanisms to develop more potent antitubercular therapies.
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spelling pubmed-96186402022-11-01 Unraveling the mechanisms of intrinsic drug resistance in Mycobacterium tuberculosis Poulton, Nicholas C. Rock, Jeremy M. Front Cell Infect Microbiol Cellular and Infection Microbiology Tuberculosis (TB) is among the most difficult infections to treat, requiring several months of multidrug therapy to produce a durable cure. The reasons necessitating long treatment times are complex and multifactorial. However, one major difficulty of treating TB is the resistance of the infecting bacterium, Mycobacterium tuberculosis (Mtb), to many distinct classes of antimicrobials. This review will focus on the major gaps in our understanding of intrinsic drug resistance in Mtb and how functional and chemical-genetics can help close those gaps. A better understanding of intrinsic drug resistance will help lay the foundation for strategies to disarm and circumvent these mechanisms to develop more potent antitubercular therapies. Frontiers Media S.A. 2022-10-17 /pmc/articles/PMC9618640/ /pubmed/36325467 http://dx.doi.org/10.3389/fcimb.2022.997283 Text en Copyright © 2022 Poulton and Rock https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Poulton, Nicholas C.
Rock, Jeremy M.
Unraveling the mechanisms of intrinsic drug resistance in Mycobacterium tuberculosis
title Unraveling the mechanisms of intrinsic drug resistance in Mycobacterium tuberculosis
title_full Unraveling the mechanisms of intrinsic drug resistance in Mycobacterium tuberculosis
title_fullStr Unraveling the mechanisms of intrinsic drug resistance in Mycobacterium tuberculosis
title_full_unstemmed Unraveling the mechanisms of intrinsic drug resistance in Mycobacterium tuberculosis
title_short Unraveling the mechanisms of intrinsic drug resistance in Mycobacterium tuberculosis
title_sort unraveling the mechanisms of intrinsic drug resistance in mycobacterium tuberculosis
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618640/
https://www.ncbi.nlm.nih.gov/pubmed/36325467
http://dx.doi.org/10.3389/fcimb.2022.997283
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