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AsrR Is an Oxidative Stress Sensing Regulator Modulating Enterococcus faecium Opportunistic Traits, Antimicrobial Resistance, and Pathogenicity

Oxidative stress serves as an important host/environmental signal that triggers a wide range of responses in microorganisms. Here, we identified an oxidative stress sensor and response regulator in the important multidrug-resistant nosocomial pathogen Enterococcus faecium belonging to the MarR famil...

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Autores principales: Lebreton, François, van Schaik, Willem, Sanguinetti, Maurizio, Posteraro, Brunella, Torelli, Riccardo, Le Bras, Florian, Verneuil, Nicolas, Zhang, Xinglin, Giard, Jean-Christophe, Dhalluin, Anne, Willems, Rob J. L., Leclercq, Roland, Cattoir, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410868/
https://www.ncbi.nlm.nih.gov/pubmed/22876178
http://dx.doi.org/10.1371/journal.ppat.1002834
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author Lebreton, François
van Schaik, Willem
Sanguinetti, Maurizio
Posteraro, Brunella
Torelli, Riccardo
Le Bras, Florian
Verneuil, Nicolas
Zhang, Xinglin
Giard, Jean-Christophe
Dhalluin, Anne
Willems, Rob J. L.
Leclercq, Roland
Cattoir, Vincent
author_facet Lebreton, François
van Schaik, Willem
Sanguinetti, Maurizio
Posteraro, Brunella
Torelli, Riccardo
Le Bras, Florian
Verneuil, Nicolas
Zhang, Xinglin
Giard, Jean-Christophe
Dhalluin, Anne
Willems, Rob J. L.
Leclercq, Roland
Cattoir, Vincent
author_sort Lebreton, François
collection PubMed
description Oxidative stress serves as an important host/environmental signal that triggers a wide range of responses in microorganisms. Here, we identified an oxidative stress sensor and response regulator in the important multidrug-resistant nosocomial pathogen Enterococcus faecium belonging to the MarR family and called AsrR (antibiotic and stress response regulator). The AsrR regulator used cysteine oxidation to sense the hydrogen peroxide which results in its dissociation to promoter DNA. Transcriptome analysis showed that the AsrR regulon was composed of 181 genes, including representing functionally diverse groups involved in pathogenesis, antibiotic and antimicrobial peptide resistance, oxidative stress, and adaptive responses. Consistent with the upregulated expression of the pbp5 gene, encoding a low-affinity penicillin-binding protein, the asrR null mutant was found to be more resistant to β-lactam antibiotics. Deletion of asrR markedly decreased the bactericidal activity of ampicillin and vancomycin, which are both commonly used to treat infections due to enterococci, and also led to over-expression of two major adhesins, acm and ecbA, which resulted in enhanced in vitro adhesion to human intestinal cells. Additional pathogenic traits were also reinforced in the asrR null mutant including greater capacity than the parental strain to form biofilm in vitro and greater persistance in Galleria mellonella colonization and mouse systemic infection models. Despite overexpression of oxidative stress-response genes, deletion of asrR was associated with a decreased oxidative stress resistance in vitro, which correlated with a reduced resistance to phagocytic killing by murine macrophages. Interestingly, both strains showed similar amounts of intracellular reactive oxygen species. Finally, we observed a mutator phenotype and enhanced DNA transfer frequencies in the asrR deleted strain. These data indicate that AsrR plays a major role in antimicrobial resistance and adaptation for survival within the host, thereby contributes importantly to the opportunistic traits of E. faecium.
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spelling pubmed-34108682012-08-08 AsrR Is an Oxidative Stress Sensing Regulator Modulating Enterococcus faecium Opportunistic Traits, Antimicrobial Resistance, and Pathogenicity Lebreton, François van Schaik, Willem Sanguinetti, Maurizio Posteraro, Brunella Torelli, Riccardo Le Bras, Florian Verneuil, Nicolas Zhang, Xinglin Giard, Jean-Christophe Dhalluin, Anne Willems, Rob J. L. Leclercq, Roland Cattoir, Vincent PLoS Pathog Research Article Oxidative stress serves as an important host/environmental signal that triggers a wide range of responses in microorganisms. Here, we identified an oxidative stress sensor and response regulator in the important multidrug-resistant nosocomial pathogen Enterococcus faecium belonging to the MarR family and called AsrR (antibiotic and stress response regulator). The AsrR regulator used cysteine oxidation to sense the hydrogen peroxide which results in its dissociation to promoter DNA. Transcriptome analysis showed that the AsrR regulon was composed of 181 genes, including representing functionally diverse groups involved in pathogenesis, antibiotic and antimicrobial peptide resistance, oxidative stress, and adaptive responses. Consistent with the upregulated expression of the pbp5 gene, encoding a low-affinity penicillin-binding protein, the asrR null mutant was found to be more resistant to β-lactam antibiotics. Deletion of asrR markedly decreased the bactericidal activity of ampicillin and vancomycin, which are both commonly used to treat infections due to enterococci, and also led to over-expression of two major adhesins, acm and ecbA, which resulted in enhanced in vitro adhesion to human intestinal cells. Additional pathogenic traits were also reinforced in the asrR null mutant including greater capacity than the parental strain to form biofilm in vitro and greater persistance in Galleria mellonella colonization and mouse systemic infection models. Despite overexpression of oxidative stress-response genes, deletion of asrR was associated with a decreased oxidative stress resistance in vitro, which correlated with a reduced resistance to phagocytic killing by murine macrophages. Interestingly, both strains showed similar amounts of intracellular reactive oxygen species. Finally, we observed a mutator phenotype and enhanced DNA transfer frequencies in the asrR deleted strain. These data indicate that AsrR plays a major role in antimicrobial resistance and adaptation for survival within the host, thereby contributes importantly to the opportunistic traits of E. faecium. Public Library of Science 2012-08-02 /pmc/articles/PMC3410868/ /pubmed/22876178 http://dx.doi.org/10.1371/journal.ppat.1002834 Text en © 2012 Lebreton 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
Lebreton, François
van Schaik, Willem
Sanguinetti, Maurizio
Posteraro, Brunella
Torelli, Riccardo
Le Bras, Florian
Verneuil, Nicolas
Zhang, Xinglin
Giard, Jean-Christophe
Dhalluin, Anne
Willems, Rob J. L.
Leclercq, Roland
Cattoir, Vincent
AsrR Is an Oxidative Stress Sensing Regulator Modulating Enterococcus faecium Opportunistic Traits, Antimicrobial Resistance, and Pathogenicity
title AsrR Is an Oxidative Stress Sensing Regulator Modulating Enterococcus faecium Opportunistic Traits, Antimicrobial Resistance, and Pathogenicity
title_full AsrR Is an Oxidative Stress Sensing Regulator Modulating Enterococcus faecium Opportunistic Traits, Antimicrobial Resistance, and Pathogenicity
title_fullStr AsrR Is an Oxidative Stress Sensing Regulator Modulating Enterococcus faecium Opportunistic Traits, Antimicrobial Resistance, and Pathogenicity
title_full_unstemmed AsrR Is an Oxidative Stress Sensing Regulator Modulating Enterococcus faecium Opportunistic Traits, Antimicrobial Resistance, and Pathogenicity
title_short AsrR Is an Oxidative Stress Sensing Regulator Modulating Enterococcus faecium Opportunistic Traits, Antimicrobial Resistance, and Pathogenicity
title_sort asrr is an oxidative stress sensing regulator modulating enterococcus faecium opportunistic traits, antimicrobial resistance, and pathogenicity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410868/
https://www.ncbi.nlm.nih.gov/pubmed/22876178
http://dx.doi.org/10.1371/journal.ppat.1002834
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