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Activation of class 1 integron integrase is promoted in the intestinal environment

Class 1 integrons are widespread genetic elements playing a major role in the dissemination of antibiotic resistance. They allow bacteria to capture, express and exchange antibiotic resistance genes embedded within gene cassettes. Acquisition of gene cassettes is catalysed by the class 1 integron in...

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Autores principales: Baltazar, Murielle, Bourgeois-Nicolaos, Nadège, Larroudé, Macarena, Couet, William, Uwajeneza, Solange, Doucet-Populaire, Florence, Ploy, Marie-Cécile, Da Re, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090394/
https://www.ncbi.nlm.nih.gov/pubmed/35482826
http://dx.doi.org/10.1371/journal.pgen.1010177
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author Baltazar, Murielle
Bourgeois-Nicolaos, Nadège
Larroudé, Macarena
Couet, William
Uwajeneza, Solange
Doucet-Populaire, Florence
Ploy, Marie-Cécile
Da Re, Sandra
author_facet Baltazar, Murielle
Bourgeois-Nicolaos, Nadège
Larroudé, Macarena
Couet, William
Uwajeneza, Solange
Doucet-Populaire, Florence
Ploy, Marie-Cécile
Da Re, Sandra
author_sort Baltazar, Murielle
collection PubMed
description Class 1 integrons are widespread genetic elements playing a major role in the dissemination of antibiotic resistance. They allow bacteria to capture, express and exchange antibiotic resistance genes embedded within gene cassettes. Acquisition of gene cassettes is catalysed by the class 1 integron integrase, a site-specific recombinase playing a key role in the integron system. In in vitro planktonic culture, expression of intI1 is controlled by the SOS response, a regulatory network which mediates the repair of DNA damage caused by a wide range of bacterial stress, including antibiotics. However, in vitro experimental conditions are far from the real lifestyle of bacteria in natural environments such as the intestinal tract which is known to be a reservoir of integrons. In this study, we developed an in vivo model of intestinal colonization in gnotobiotic mice and used a recombination assay and quantitative real-time PCR, to investigate the induction of the SOS response and expression and activity of the class 1 integron integrase, IntI1. We found that the basal activity of IntI1 was higher in vivo than in vitro. In addition, we demonstrated that administration of a subinhibitory concentration of ciprofloxacin rapidly induced both the SOS response and intI1 expression that was correlated with an increase of the activity of IntI1. Our findings show that the gut is an environment in which the class 1 integron integrase is induced and active, and they highlight the potential role of integrons in the acquisition and/or expression of resistance genes in the gut, particularly during antibiotic therapy.
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spelling pubmed-90903942022-05-11 Activation of class 1 integron integrase is promoted in the intestinal environment Baltazar, Murielle Bourgeois-Nicolaos, Nadège Larroudé, Macarena Couet, William Uwajeneza, Solange Doucet-Populaire, Florence Ploy, Marie-Cécile Da Re, Sandra PLoS Genet Research Article Class 1 integrons are widespread genetic elements playing a major role in the dissemination of antibiotic resistance. They allow bacteria to capture, express and exchange antibiotic resistance genes embedded within gene cassettes. Acquisition of gene cassettes is catalysed by the class 1 integron integrase, a site-specific recombinase playing a key role in the integron system. In in vitro planktonic culture, expression of intI1 is controlled by the SOS response, a regulatory network which mediates the repair of DNA damage caused by a wide range of bacterial stress, including antibiotics. However, in vitro experimental conditions are far from the real lifestyle of bacteria in natural environments such as the intestinal tract which is known to be a reservoir of integrons. In this study, we developed an in vivo model of intestinal colonization in gnotobiotic mice and used a recombination assay and quantitative real-time PCR, to investigate the induction of the SOS response and expression and activity of the class 1 integron integrase, IntI1. We found that the basal activity of IntI1 was higher in vivo than in vitro. In addition, we demonstrated that administration of a subinhibitory concentration of ciprofloxacin rapidly induced both the SOS response and intI1 expression that was correlated with an increase of the activity of IntI1. Our findings show that the gut is an environment in which the class 1 integron integrase is induced and active, and they highlight the potential role of integrons in the acquisition and/or expression of resistance genes in the gut, particularly during antibiotic therapy. Public Library of Science 2022-04-28 /pmc/articles/PMC9090394/ /pubmed/35482826 http://dx.doi.org/10.1371/journal.pgen.1010177 Text en © 2022 Baltazar et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Baltazar, Murielle
Bourgeois-Nicolaos, Nadège
Larroudé, Macarena
Couet, William
Uwajeneza, Solange
Doucet-Populaire, Florence
Ploy, Marie-Cécile
Da Re, Sandra
Activation of class 1 integron integrase is promoted in the intestinal environment
title Activation of class 1 integron integrase is promoted in the intestinal environment
title_full Activation of class 1 integron integrase is promoted in the intestinal environment
title_fullStr Activation of class 1 integron integrase is promoted in the intestinal environment
title_full_unstemmed Activation of class 1 integron integrase is promoted in the intestinal environment
title_short Activation of class 1 integron integrase is promoted in the intestinal environment
title_sort activation of class 1 integron integrase is promoted in the intestinal environment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090394/
https://www.ncbi.nlm.nih.gov/pubmed/35482826
http://dx.doi.org/10.1371/journal.pgen.1010177
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