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Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosis

Laboratoire de Microbiologie et Génétique Moléculaire (LMGM), Centre National de la Recherche Scientifique (CNRS), Université Paul Sabatier, 118 route de Narbonne, Toulouse 31062, France
Author to whom correspondence should be addressed.
Toxins 2014, 6(3), 1002-1020;
Received: 19 December 2013 / Revised: 20 February 2014 / Accepted: 24 February 2014 / Published: 6 March 2014
(This article belongs to the Special Issue Toxin-Antitoxin System)
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. View Full-Text
Keywords: toxin-antitoxins; molecular chaperones; proteases; persistence toxin-antitoxins; molecular chaperones; proteases; persistence
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MDPI and ACS Style

Sala, A.; Bordes, P.; Genevaux, P. Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosis. Toxins 2014, 6, 1002-1020.

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