Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosis

The hallmark of Mycobacterium tuberculosis is its ability to persist for a long-term in host granulomas, in a non-replicating and drug-tolerant state, and later awaken to cause disease. To date, the cellular factors and the molecular mechanisms that mediate entry into the persistence phase are poorl...

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Main Authors: Ambre Sala, Patricia Bordes, Pierre Genevaux
Format: Article
Language:English
Published: MDPI AG 2014-03-01
Series:Toxins
Subjects:
Online Access:http://www.mdpi.com/2072-6651/6/3/1002
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author Ambre Sala
Patricia Bordes
Pierre Genevaux
author_facet Ambre Sala
Patricia Bordes
Pierre Genevaux
author_sort Ambre Sala
collection DOAJ
description The hallmark of Mycobacterium tuberculosis is its ability to persist for a long-term in host granulomas, in a non-replicating and drug-tolerant state, and later awaken to cause disease. To date, the cellular factors and the molecular mechanisms that mediate entry into the persistence phase are poorly understood. Remarkably, M. tuberculosis possesses a very high number of toxin-antitoxin (TA) systems in its chromosome, 79 in total, regrouping both well-known (68) and novel (11) families, with some of them being strongly induced in drug-tolerant persisters. In agreement with the capacity of stress-responsive TA systems to generate persisters in other bacteria, it has been proposed that activation of TA systems in M. tuberculosis could contribute to its pathogenesis. Herein, we review the current knowledge on the multiple TA families present in this bacterium, their mechanism, and their potential role in physiology and virulence.
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spelling doaj.art-f78f0bffd656410d865f8395167673762022-12-22T04:23:04ZengMDPI AGToxins2072-66512014-03-01631002102010.3390/toxins6031002toxins6031002Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosisAmbre Sala0Patricia Bordes1Pierre Genevaux2Laboratoire de Microbiologie et Génétique Moléculaire (LMGM), Centre National de la Recherche Scientifique (CNRS), Université Paul Sabatier, 118 route de Narbonne, Toulouse 31062, FranceLaboratoire de Microbiologie et Génétique Moléculaire (LMGM), Centre National de la Recherche Scientifique (CNRS), Université Paul Sabatier, 118 route de Narbonne, Toulouse 31062, FranceLaboratoire de Microbiologie et Génétique Moléculaire (LMGM), Centre National de la Recherche Scientifique (CNRS), Université Paul Sabatier, 118 route de Narbonne, Toulouse 31062, FranceThe hallmark of Mycobacterium tuberculosis is its ability to persist for a long-term in host granulomas, in a non-replicating and drug-tolerant state, and later awaken to cause disease. To date, the cellular factors and the molecular mechanisms that mediate entry into the persistence phase are poorly understood. Remarkably, M. tuberculosis possesses a very high number of toxin-antitoxin (TA) systems in its chromosome, 79 in total, regrouping both well-known (68) and novel (11) families, with some of them being strongly induced in drug-tolerant persisters. In agreement with the capacity of stress-responsive TA systems to generate persisters in other bacteria, it has been proposed that activation of TA systems in M. tuberculosis could contribute to its pathogenesis. Herein, we review the current knowledge on the multiple TA families present in this bacterium, their mechanism, and their potential role in physiology and virulence.http://www.mdpi.com/2072-6651/6/3/1002toxin-antitoxinsmolecular chaperonesproteasespersistence
spellingShingle Ambre Sala
Patricia Bordes
Pierre Genevaux
Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosis
Toxins
toxin-antitoxins
molecular chaperones
proteases
persistence
title Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosis
title_full Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosis
title_fullStr Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosis
title_full_unstemmed Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosis
title_short Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosis
title_sort multiple toxin antitoxin systems in mycobacterium tuberculosis
topic toxin-antitoxins
molecular chaperones
proteases
persistence
url http://www.mdpi.com/2072-6651/6/3/1002
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