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Antimicrobial Treatment Improves Mycobacterial Survival in Nonpermissive Growth Conditions
Antimicrobials targeting cell wall biosynthesis are generally considered inactive against nonreplicating bacteria. Paradoxically, we found that under nonpermissive growth conditions, exposure of Mycobacterium bovis BCG bacilli to such antimicrobials enhanced their survival. We identified a transcrip...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3993263/ https://www.ncbi.nlm.nih.gov/pubmed/24590482 http://dx.doi.org/10.1128/AAC.02774-13 |
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author | Turapov, Obolbek Waddell, Simon J. Burke, Bernard Glenn, Sarah Sarybaeva, Asel A. Tudo, Griselda Labesse, Gilles Young, Danielle I. Young, Michael Andrew, Peter W. Butcher, Philip D. Cohen-Gonsaud, Martin Mukamolova, Galina V. |
author_facet | Turapov, Obolbek Waddell, Simon J. Burke, Bernard Glenn, Sarah Sarybaeva, Asel A. Tudo, Griselda Labesse, Gilles Young, Danielle I. Young, Michael Andrew, Peter W. Butcher, Philip D. Cohen-Gonsaud, Martin Mukamolova, Galina V. |
author_sort | Turapov, Obolbek |
collection | PubMed |
description | Antimicrobials targeting cell wall biosynthesis are generally considered inactive against nonreplicating bacteria. Paradoxically, we found that under nonpermissive growth conditions, exposure of Mycobacterium bovis BCG bacilli to such antimicrobials enhanced their survival. We identified a transcriptional regulator, RaaS (for regulator of antimicrobial-assisted survival), encoded by bcg1279 (rv1219c) as being responsible for the observed phenomenon. Induction of this transcriptional regulator resulted in reduced expression of specific ATP-dependent efflux pumps and promoted long-term survival of mycobacteria, while its deletion accelerated bacterial death under nonpermissive growth conditions in vitro and during macrophage or mouse infection. These findings have implications for the design of antimicrobial drug combination therapies for persistent infectious diseases, such as tuberculosis. |
format | Online Article Text |
id | pubmed-3993263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-39932632014-05-17 Antimicrobial Treatment Improves Mycobacterial Survival in Nonpermissive Growth Conditions Turapov, Obolbek Waddell, Simon J. Burke, Bernard Glenn, Sarah Sarybaeva, Asel A. Tudo, Griselda Labesse, Gilles Young, Danielle I. Young, Michael Andrew, Peter W. Butcher, Philip D. Cohen-Gonsaud, Martin Mukamolova, Galina V. Antimicrob Agents Chemother Mechanisms of Action: Physiological Effects Antimicrobials targeting cell wall biosynthesis are generally considered inactive against nonreplicating bacteria. Paradoxically, we found that under nonpermissive growth conditions, exposure of Mycobacterium bovis BCG bacilli to such antimicrobials enhanced their survival. We identified a transcriptional regulator, RaaS (for regulator of antimicrobial-assisted survival), encoded by bcg1279 (rv1219c) as being responsible for the observed phenomenon. Induction of this transcriptional regulator resulted in reduced expression of specific ATP-dependent efflux pumps and promoted long-term survival of mycobacteria, while its deletion accelerated bacterial death under nonpermissive growth conditions in vitro and during macrophage or mouse infection. These findings have implications for the design of antimicrobial drug combination therapies for persistent infectious diseases, such as tuberculosis. American Society for Microbiology 2014-05 /pmc/articles/PMC3993263/ /pubmed/24590482 http://dx.doi.org/10.1128/AAC.02774-13 Text en Copyright © 2014 Turapov et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license (http://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Mechanisms of Action: Physiological Effects Turapov, Obolbek Waddell, Simon J. Burke, Bernard Glenn, Sarah Sarybaeva, Asel A. Tudo, Griselda Labesse, Gilles Young, Danielle I. Young, Michael Andrew, Peter W. Butcher, Philip D. Cohen-Gonsaud, Martin Mukamolova, Galina V. Antimicrobial Treatment Improves Mycobacterial Survival in Nonpermissive Growth Conditions |
title | Antimicrobial Treatment Improves Mycobacterial Survival in Nonpermissive Growth Conditions |
title_full | Antimicrobial Treatment Improves Mycobacterial Survival in Nonpermissive Growth Conditions |
title_fullStr | Antimicrobial Treatment Improves Mycobacterial Survival in Nonpermissive Growth Conditions |
title_full_unstemmed | Antimicrobial Treatment Improves Mycobacterial Survival in Nonpermissive Growth Conditions |
title_short | Antimicrobial Treatment Improves Mycobacterial Survival in Nonpermissive Growth Conditions |
title_sort | antimicrobial treatment improves mycobacterial survival in nonpermissive growth conditions |
topic | Mechanisms of Action: Physiological Effects |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3993263/ https://www.ncbi.nlm.nih.gov/pubmed/24590482 http://dx.doi.org/10.1128/AAC.02774-13 |
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