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Rhodococcus equi’s Extreme Resistance to Hydrogen Peroxide Is Mainly Conferred by One of Its Four Catalase Genes

Rhodococcus equi is one of the most widespread causes of disease in foals aged from 1 to 6 months. R. equi possesses antioxidant defense mechanisms to protect it from reactive oxygen metabolites such as hydrogen peroxide (H(2)O(2)) generated during the respiratory burst of phagocytic cells. These de...

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Autores principales: Bidaud, Pauline, Hébert, Laurent, Barbey, Corinne, Appourchaux, Anne-Cécile, Torelli, Riccardo, Sanguinetti, Maurizio, Laugier, Claire, Petry, Sandrine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412833/
https://www.ncbi.nlm.nih.gov/pubmed/22879963
http://dx.doi.org/10.1371/journal.pone.0042396
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author Bidaud, Pauline
Hébert, Laurent
Barbey, Corinne
Appourchaux, Anne-Cécile
Torelli, Riccardo
Sanguinetti, Maurizio
Laugier, Claire
Petry, Sandrine
author_facet Bidaud, Pauline
Hébert, Laurent
Barbey, Corinne
Appourchaux, Anne-Cécile
Torelli, Riccardo
Sanguinetti, Maurizio
Laugier, Claire
Petry, Sandrine
author_sort Bidaud, Pauline
collection PubMed
description Rhodococcus equi is one of the most widespread causes of disease in foals aged from 1 to 6 months. R. equi possesses antioxidant defense mechanisms to protect it from reactive oxygen metabolites such as hydrogen peroxide (H(2)O(2)) generated during the respiratory burst of phagocytic cells. These defense mechanisms include enzymes such as catalase, which detoxify hydrogen peroxide. Recently, an analysis of the R. equi 103 genome sequence revealed the presence of four potential catalase genes. We first constructed ΔkatA-, ΔkatB-, ΔkatC-and ΔkatD -deficient mutants to study the ability of R. equi to survive exposure to H(2)O(2) in vitro and within mouse peritoneal macrophages. Results showed that ΔkatA and, to a lesser extent ΔkatC, were affected by 80 mM H(2)O(2). Moreover, katA deletion seems to significantly affect the ability of R. equi to survive within murine macrophages. We finally investigated the expression of the four catalases in response to H(2)O(2) assays with a real time PCR technique. Results showed that katA is overexpressed 367.9 times (±122.6) in response to exposure to 50 mM of H(2)O(2) added in the stationary phase, and 3.11 times (±0.59) when treatment was administered in the exponential phase. In untreated bacteria, katB, katC and katD were overexpressed from 4.3 to 17.5 times in the stationary compared to the exponential phase. Taken together, our results show that KatA is the major catalase involved in the extreme H(2)O(2) resistance capability of R. equi.
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spelling pubmed-34128332012-08-09 Rhodococcus equi’s Extreme Resistance to Hydrogen Peroxide Is Mainly Conferred by One of Its Four Catalase Genes Bidaud, Pauline Hébert, Laurent Barbey, Corinne Appourchaux, Anne-Cécile Torelli, Riccardo Sanguinetti, Maurizio Laugier, Claire Petry, Sandrine PLoS One Research Article Rhodococcus equi is one of the most widespread causes of disease in foals aged from 1 to 6 months. R. equi possesses antioxidant defense mechanisms to protect it from reactive oxygen metabolites such as hydrogen peroxide (H(2)O(2)) generated during the respiratory burst of phagocytic cells. These defense mechanisms include enzymes such as catalase, which detoxify hydrogen peroxide. Recently, an analysis of the R. equi 103 genome sequence revealed the presence of four potential catalase genes. We first constructed ΔkatA-, ΔkatB-, ΔkatC-and ΔkatD -deficient mutants to study the ability of R. equi to survive exposure to H(2)O(2) in vitro and within mouse peritoneal macrophages. Results showed that ΔkatA and, to a lesser extent ΔkatC, were affected by 80 mM H(2)O(2). Moreover, katA deletion seems to significantly affect the ability of R. equi to survive within murine macrophages. We finally investigated the expression of the four catalases in response to H(2)O(2) assays with a real time PCR technique. Results showed that katA is overexpressed 367.9 times (±122.6) in response to exposure to 50 mM of H(2)O(2) added in the stationary phase, and 3.11 times (±0.59) when treatment was administered in the exponential phase. In untreated bacteria, katB, katC and katD were overexpressed from 4.3 to 17.5 times in the stationary compared to the exponential phase. Taken together, our results show that KatA is the major catalase involved in the extreme H(2)O(2) resistance capability of R. equi. Public Library of Science 2012-08-06 /pmc/articles/PMC3412833/ /pubmed/22879963 http://dx.doi.org/10.1371/journal.pone.0042396 Text en © 2012 Bidaud 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
Bidaud, Pauline
Hébert, Laurent
Barbey, Corinne
Appourchaux, Anne-Cécile
Torelli, Riccardo
Sanguinetti, Maurizio
Laugier, Claire
Petry, Sandrine
Rhodococcus equi’s Extreme Resistance to Hydrogen Peroxide Is Mainly Conferred by One of Its Four Catalase Genes
title Rhodococcus equi’s Extreme Resistance to Hydrogen Peroxide Is Mainly Conferred by One of Its Four Catalase Genes
title_full Rhodococcus equi’s Extreme Resistance to Hydrogen Peroxide Is Mainly Conferred by One of Its Four Catalase Genes
title_fullStr Rhodococcus equi’s Extreme Resistance to Hydrogen Peroxide Is Mainly Conferred by One of Its Four Catalase Genes
title_full_unstemmed Rhodococcus equi’s Extreme Resistance to Hydrogen Peroxide Is Mainly Conferred by One of Its Four Catalase Genes
title_short Rhodococcus equi’s Extreme Resistance to Hydrogen Peroxide Is Mainly Conferred by One of Its Four Catalase Genes
title_sort rhodococcus equi’s extreme resistance to hydrogen peroxide is mainly conferred by one of its four catalase genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412833/
https://www.ncbi.nlm.nih.gov/pubmed/22879963
http://dx.doi.org/10.1371/journal.pone.0042396
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