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Mycobacterium tuberculosis Exploits Asparagine to Assimilate Nitrogen and Resist Acid Stress during Infection

Mycobacterium tuberculosis is an intracellular pathogen. Within macrophages, M. tuberculosis thrives in a specialized membrane-bound vacuole, the phagosome, whose pH is slightly acidic, and where access to nutrients is limited. Understanding how the bacillus extracts and incorporates nutrients from...

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Autores principales: Gouzy, Alexandre, Larrouy-Maumus, Gérald, Bottai, Daria, Levillain, Florence, Dumas, Alexia, Wallach, Joshua B., Caire-Brandli, Irène, de Chastellier, Chantal, Wu, Ting-Di, Poincloux, Renaud, Brosch, Roland, Guerquin-Kern, Jean-Luc, Schnappinger, Dirk, Sório de Carvalho, Luiz Pedro, Poquet, Yannick, Neyrolles, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930563/
https://www.ncbi.nlm.nih.gov/pubmed/24586151
http://dx.doi.org/10.1371/journal.ppat.1003928
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author Gouzy, Alexandre
Larrouy-Maumus, Gérald
Bottai, Daria
Levillain, Florence
Dumas, Alexia
Wallach, Joshua B.
Caire-Brandli, Irène
de Chastellier, Chantal
Wu, Ting-Di
Poincloux, Renaud
Brosch, Roland
Guerquin-Kern, Jean-Luc
Schnappinger, Dirk
Sório de Carvalho, Luiz Pedro
Poquet, Yannick
Neyrolles, Olivier
author_facet Gouzy, Alexandre
Larrouy-Maumus, Gérald
Bottai, Daria
Levillain, Florence
Dumas, Alexia
Wallach, Joshua B.
Caire-Brandli, Irène
de Chastellier, Chantal
Wu, Ting-Di
Poincloux, Renaud
Brosch, Roland
Guerquin-Kern, Jean-Luc
Schnappinger, Dirk
Sório de Carvalho, Luiz Pedro
Poquet, Yannick
Neyrolles, Olivier
author_sort Gouzy, Alexandre
collection PubMed
description Mycobacterium tuberculosis is an intracellular pathogen. Within macrophages, M. tuberculosis thrives in a specialized membrane-bound vacuole, the phagosome, whose pH is slightly acidic, and where access to nutrients is limited. Understanding how the bacillus extracts and incorporates nutrients from its host may help develop novel strategies to combat tuberculosis. Here we show that M. tuberculosis employs the asparagine transporter AnsP2 and the secreted asparaginase AnsA to assimilate nitrogen and resist acid stress through asparagine hydrolysis and ammonia release. While the role of AnsP2 is partially spared by yet to be identified transporter(s), that of AnsA is crucial in both phagosome acidification arrest and intracellular replication, as an M. tuberculosis mutant lacking this asparaginase is ultimately attenuated in macrophages and in mice. Our study provides yet another example of the intimate link between physiology and virulence in the tubercle bacillus, and identifies a novel pathway to be targeted for therapeutic purposes.
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spelling pubmed-39305632014-02-25 Mycobacterium tuberculosis Exploits Asparagine to Assimilate Nitrogen and Resist Acid Stress during Infection Gouzy, Alexandre Larrouy-Maumus, Gérald Bottai, Daria Levillain, Florence Dumas, Alexia Wallach, Joshua B. Caire-Brandli, Irène de Chastellier, Chantal Wu, Ting-Di Poincloux, Renaud Brosch, Roland Guerquin-Kern, Jean-Luc Schnappinger, Dirk Sório de Carvalho, Luiz Pedro Poquet, Yannick Neyrolles, Olivier PLoS Pathog Research Article Mycobacterium tuberculosis is an intracellular pathogen. Within macrophages, M. tuberculosis thrives in a specialized membrane-bound vacuole, the phagosome, whose pH is slightly acidic, and where access to nutrients is limited. Understanding how the bacillus extracts and incorporates nutrients from its host may help develop novel strategies to combat tuberculosis. Here we show that M. tuberculosis employs the asparagine transporter AnsP2 and the secreted asparaginase AnsA to assimilate nitrogen and resist acid stress through asparagine hydrolysis and ammonia release. While the role of AnsP2 is partially spared by yet to be identified transporter(s), that of AnsA is crucial in both phagosome acidification arrest and intracellular replication, as an M. tuberculosis mutant lacking this asparaginase is ultimately attenuated in macrophages and in mice. Our study provides yet another example of the intimate link between physiology and virulence in the tubercle bacillus, and identifies a novel pathway to be targeted for therapeutic purposes. Public Library of Science 2014-02-20 /pmc/articles/PMC3930563/ /pubmed/24586151 http://dx.doi.org/10.1371/journal.ppat.1003928 Text en © 2014 Gouzy et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gouzy, Alexandre
Larrouy-Maumus, Gérald
Bottai, Daria
Levillain, Florence
Dumas, Alexia
Wallach, Joshua B.
Caire-Brandli, Irène
de Chastellier, Chantal
Wu, Ting-Di
Poincloux, Renaud
Brosch, Roland
Guerquin-Kern, Jean-Luc
Schnappinger, Dirk
Sório de Carvalho, Luiz Pedro
Poquet, Yannick
Neyrolles, Olivier
Mycobacterium tuberculosis Exploits Asparagine to Assimilate Nitrogen and Resist Acid Stress during Infection
title Mycobacterium tuberculosis Exploits Asparagine to Assimilate Nitrogen and Resist Acid Stress during Infection
title_full Mycobacterium tuberculosis Exploits Asparagine to Assimilate Nitrogen and Resist Acid Stress during Infection
title_fullStr Mycobacterium tuberculosis Exploits Asparagine to Assimilate Nitrogen and Resist Acid Stress during Infection
title_full_unstemmed Mycobacterium tuberculosis Exploits Asparagine to Assimilate Nitrogen and Resist Acid Stress during Infection
title_short Mycobacterium tuberculosis Exploits Asparagine to Assimilate Nitrogen and Resist Acid Stress during Infection
title_sort mycobacterium tuberculosis exploits asparagine to assimilate nitrogen and resist acid stress during infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930563/
https://www.ncbi.nlm.nih.gov/pubmed/24586151
http://dx.doi.org/10.1371/journal.ppat.1003928
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