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The Streptococcus pneumoniae yefM-yoeB and relBE Toxin-Antitoxin Operons Participate in Oxidative Stress and Biofilm Formation

Type II (proteic) toxin-antitoxin systems (TAs) are widely distributed among bacteria and archaea. They are generally organized as operons integrated by two genes, the first encoding the antitoxin that binds to its cognate toxin to generate a harmless protein–protein complex. Under stress conditions...

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Autores principales: Chan, Wai Ting, Domenech, Mirian, Moreno-Córdoba, Inmaculada, Navarro-Martínez, Verónica, Nieto, Concha, Moscoso, Miriam, García, Ernesto, Espinosa, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162744/
https://www.ncbi.nlm.nih.gov/pubmed/30231554
http://dx.doi.org/10.3390/toxins10090378
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author Chan, Wai Ting
Domenech, Mirian
Moreno-Córdoba, Inmaculada
Navarro-Martínez, Verónica
Nieto, Concha
Moscoso, Miriam
García, Ernesto
Espinosa, Manuel
author_facet Chan, Wai Ting
Domenech, Mirian
Moreno-Córdoba, Inmaculada
Navarro-Martínez, Verónica
Nieto, Concha
Moscoso, Miriam
García, Ernesto
Espinosa, Manuel
author_sort Chan, Wai Ting
collection PubMed
description Type II (proteic) toxin-antitoxin systems (TAs) are widely distributed among bacteria and archaea. They are generally organized as operons integrated by two genes, the first encoding the antitoxin that binds to its cognate toxin to generate a harmless protein–protein complex. Under stress conditions, the unstable antitoxin is degraded by host proteases, releasing the toxin to achieve its toxic effect. In the Gram-positive pathogen Streptococcus pneumoniae we have characterized four TAs: pezAT, relBE, yefM-yoeB, and phD-doc, although the latter is missing in strain R6. We have assessed the role of the two yefM-yoeB and relBE systems encoded by S. pneumoniae R6 by construction of isogenic strains lacking one or two of the operons, and by complementation assays. We have analyzed the phenotypes of the wild type and mutants in terms of cell growth, response to environmental stress, and ability to generate biofilms. Compared to the wild-type, the mutants exhibited lower resistance to oxidative stress. Further, strains deleted in yefM-yoeB and the double mutant lacking yefM-yoeB and relBE exhibited a significant reduction in their ability for biofilm formation. Complementation assays showed that defective phenotypes were restored to wild type levels. We conclude that these two loci may play a relevant role in these aspects of the S. pneumoniae lifestyle and contribute to the bacterial colonization of new niches.
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spelling pubmed-61627442018-10-03 The Streptococcus pneumoniae yefM-yoeB and relBE Toxin-Antitoxin Operons Participate in Oxidative Stress and Biofilm Formation Chan, Wai Ting Domenech, Mirian Moreno-Córdoba, Inmaculada Navarro-Martínez, Verónica Nieto, Concha Moscoso, Miriam García, Ernesto Espinosa, Manuel Toxins (Basel) Article Type II (proteic) toxin-antitoxin systems (TAs) are widely distributed among bacteria and archaea. They are generally organized as operons integrated by two genes, the first encoding the antitoxin that binds to its cognate toxin to generate a harmless protein–protein complex. Under stress conditions, the unstable antitoxin is degraded by host proteases, releasing the toxin to achieve its toxic effect. In the Gram-positive pathogen Streptococcus pneumoniae we have characterized four TAs: pezAT, relBE, yefM-yoeB, and phD-doc, although the latter is missing in strain R6. We have assessed the role of the two yefM-yoeB and relBE systems encoded by S. pneumoniae R6 by construction of isogenic strains lacking one or two of the operons, and by complementation assays. We have analyzed the phenotypes of the wild type and mutants in terms of cell growth, response to environmental stress, and ability to generate biofilms. Compared to the wild-type, the mutants exhibited lower resistance to oxidative stress. Further, strains deleted in yefM-yoeB and the double mutant lacking yefM-yoeB and relBE exhibited a significant reduction in their ability for biofilm formation. Complementation assays showed that defective phenotypes were restored to wild type levels. We conclude that these two loci may play a relevant role in these aspects of the S. pneumoniae lifestyle and contribute to the bacterial colonization of new niches. MDPI 2018-09-18 /pmc/articles/PMC6162744/ /pubmed/30231554 http://dx.doi.org/10.3390/toxins10090378 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chan, Wai Ting
Domenech, Mirian
Moreno-Córdoba, Inmaculada
Navarro-Martínez, Verónica
Nieto, Concha
Moscoso, Miriam
García, Ernesto
Espinosa, Manuel
The Streptococcus pneumoniae yefM-yoeB and relBE Toxin-Antitoxin Operons Participate in Oxidative Stress and Biofilm Formation
title The Streptococcus pneumoniae yefM-yoeB and relBE Toxin-Antitoxin Operons Participate in Oxidative Stress and Biofilm Formation
title_full The Streptococcus pneumoniae yefM-yoeB and relBE Toxin-Antitoxin Operons Participate in Oxidative Stress and Biofilm Formation
title_fullStr The Streptococcus pneumoniae yefM-yoeB and relBE Toxin-Antitoxin Operons Participate in Oxidative Stress and Biofilm Formation
title_full_unstemmed The Streptococcus pneumoniae yefM-yoeB and relBE Toxin-Antitoxin Operons Participate in Oxidative Stress and Biofilm Formation
title_short The Streptococcus pneumoniae yefM-yoeB and relBE Toxin-Antitoxin Operons Participate in Oxidative Stress and Biofilm Formation
title_sort streptococcus pneumoniae yefm-yoeb and relbe toxin-antitoxin operons participate in oxidative stress and biofilm formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162744/
https://www.ncbi.nlm.nih.gov/pubmed/30231554
http://dx.doi.org/10.3390/toxins10090378
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