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Toxin–antitoxin systems and their role in disseminating and maintaining antimicrobial resistance

Toxin–antitoxin systems (TAs) are ubiquitous among bacteria and play a crucial role in the dissemination and evolution of antibiotic resistance, such as maintaining multi-resistant plasmids and inducing persistence formation. Generally, activities of the toxins are neutralised by their conjugate ant...

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Detalles Bibliográficos
Autores principales: Yang, Qiu E., Walsh, Timothy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812544/
https://www.ncbi.nlm.nih.gov/pubmed/28449040
http://dx.doi.org/10.1093/femsre/fux006
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author Yang, Qiu E.
Walsh, Timothy R.
author_facet Yang, Qiu E.
Walsh, Timothy R.
author_sort Yang, Qiu E.
collection PubMed
description Toxin–antitoxin systems (TAs) are ubiquitous among bacteria and play a crucial role in the dissemination and evolution of antibiotic resistance, such as maintaining multi-resistant plasmids and inducing persistence formation. Generally, activities of the toxins are neutralised by their conjugate antitoxins. In contrast, antitoxins are more liable to degrade under specific conditions such as stress, and free active toxins interfere with essential cellular processes including replication, translation and cell-wall synthesis. TAs have also been shown to be responsible for plasmid maintenance, stress management, bacterial persistence and biofilm formation. We discuss here the recent findings of these multifaceted TAs (type I–VI) and in particular examine the role of TAs in augmenting the dissemination and maintenance of multi-drug resistance in bacteria.
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spelling pubmed-58125442018-02-23 Toxin–antitoxin systems and their role in disseminating and maintaining antimicrobial resistance Yang, Qiu E. Walsh, Timothy R. FEMS Microbiol Rev Review Article Toxin–antitoxin systems (TAs) are ubiquitous among bacteria and play a crucial role in the dissemination and evolution of antibiotic resistance, such as maintaining multi-resistant plasmids and inducing persistence formation. Generally, activities of the toxins are neutralised by their conjugate antitoxins. In contrast, antitoxins are more liable to degrade under specific conditions such as stress, and free active toxins interfere with essential cellular processes including replication, translation and cell-wall synthesis. TAs have also been shown to be responsible for plasmid maintenance, stress management, bacterial persistence and biofilm formation. We discuss here the recent findings of these multifaceted TAs (type I–VI) and in particular examine the role of TAs in augmenting the dissemination and maintenance of multi-drug resistance in bacteria. Oxford University Press 2017-03-16 2017-05 /pmc/articles/PMC5812544/ /pubmed/28449040 http://dx.doi.org/10.1093/femsre/fux006 Text en © FEMS 2017. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Yang, Qiu E.
Walsh, Timothy R.
Toxin–antitoxin systems and their role in disseminating and maintaining antimicrobial resistance
title Toxin–antitoxin systems and their role in disseminating and maintaining antimicrobial resistance
title_full Toxin–antitoxin systems and their role in disseminating and maintaining antimicrobial resistance
title_fullStr Toxin–antitoxin systems and their role in disseminating and maintaining antimicrobial resistance
title_full_unstemmed Toxin–antitoxin systems and their role in disseminating and maintaining antimicrobial resistance
title_short Toxin–antitoxin systems and their role in disseminating and maintaining antimicrobial resistance
title_sort toxin–antitoxin systems and their role in disseminating and maintaining antimicrobial resistance
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812544/
https://www.ncbi.nlm.nih.gov/pubmed/28449040
http://dx.doi.org/10.1093/femsre/fux006
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