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The Food Contaminant Deoxynivalenol Exacerbates the Genotoxicity of Gut Microbiota

An increasing number of human beings from developed countries are colonized by Escherichia coli strains producing colibactin, a genotoxin suspected to be associated with the development of colorectal cancers. Deoxynivalenol (DON) is the most prevalent mycotoxin that contaminates staple food—especial...

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Autores principales: Payros, Delphine, Dobrindt, Ulrich, Martin, Patricia, Secher, Thomas, Bracarense, Ana Paula F. L., Boury, Michèle, Laffitte, Joelle, Pinton, Philippe, Oswald, Eric, Oswald, Isabelle P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350463/
https://www.ncbi.nlm.nih.gov/pubmed/28292979
http://dx.doi.org/10.1128/mBio.00007-17
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author Payros, Delphine
Dobrindt, Ulrich
Martin, Patricia
Secher, Thomas
Bracarense, Ana Paula F. L.
Boury, Michèle
Laffitte, Joelle
Pinton, Philippe
Oswald, Eric
Oswald, Isabelle P.
author_facet Payros, Delphine
Dobrindt, Ulrich
Martin, Patricia
Secher, Thomas
Bracarense, Ana Paula F. L.
Boury, Michèle
Laffitte, Joelle
Pinton, Philippe
Oswald, Eric
Oswald, Isabelle P.
author_sort Payros, Delphine
collection PubMed
description An increasing number of human beings from developed countries are colonized by Escherichia coli strains producing colibactin, a genotoxin suspected to be associated with the development of colorectal cancers. Deoxynivalenol (DON) is the most prevalent mycotoxin that contaminates staple food—especially cereal products—in Europe and North America. This study investigates the effect of the food contaminant DON on the genotoxicity of the E. coli strains producing colibactin. In vitro, intestinal epithelial cells were coexposed to DON and E. coli producing colibactin. In vivo, newborn rats colonized at birth with E. coli producing colibactin were fed a DON-contaminated diet. Intestinal DNA damage was estimated by the phosphorylation of histone H2AX. DON exacerbates the genotoxicity of the E. coli producing colibactin in a time- and dose-dependent manner in vitro. Although DON had no effect on the composition of the gut microbiota, and especially on the number of E. coli, a significant increase in DNA damage was observed in intestinal epithelial cells of animals colonized by E. coli strains producing colibactin and coexposed to DON compared to animals colonized with E. coli strains unable to produce colibactin or animals exposed only to DON. In conclusion, our data demonstrate that the genotoxicity of E. coli strains producing colibactin, increasingly present in the microbiota of asymptomatic human beings, is modulated by the presence of DON in the diet. This raises questions about the synergism between food contaminants and gut microbiota with regard to intestinal carcinogenesis.
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spelling pubmed-53504632017-03-17 The Food Contaminant Deoxynivalenol Exacerbates the Genotoxicity of Gut Microbiota Payros, Delphine Dobrindt, Ulrich Martin, Patricia Secher, Thomas Bracarense, Ana Paula F. L. Boury, Michèle Laffitte, Joelle Pinton, Philippe Oswald, Eric Oswald, Isabelle P. mBio Research Article An increasing number of human beings from developed countries are colonized by Escherichia coli strains producing colibactin, a genotoxin suspected to be associated with the development of colorectal cancers. Deoxynivalenol (DON) is the most prevalent mycotoxin that contaminates staple food—especially cereal products—in Europe and North America. This study investigates the effect of the food contaminant DON on the genotoxicity of the E. coli strains producing colibactin. In vitro, intestinal epithelial cells were coexposed to DON and E. coli producing colibactin. In vivo, newborn rats colonized at birth with E. coli producing colibactin were fed a DON-contaminated diet. Intestinal DNA damage was estimated by the phosphorylation of histone H2AX. DON exacerbates the genotoxicity of the E. coli producing colibactin in a time- and dose-dependent manner in vitro. Although DON had no effect on the composition of the gut microbiota, and especially on the number of E. coli, a significant increase in DNA damage was observed in intestinal epithelial cells of animals colonized by E. coli strains producing colibactin and coexposed to DON compared to animals colonized with E. coli strains unable to produce colibactin or animals exposed only to DON. In conclusion, our data demonstrate that the genotoxicity of E. coli strains producing colibactin, increasingly present in the microbiota of asymptomatic human beings, is modulated by the presence of DON in the diet. This raises questions about the synergism between food contaminants and gut microbiota with regard to intestinal carcinogenesis. American Society for Microbiology 2017-03-14 /pmc/articles/PMC5350463/ /pubmed/28292979 http://dx.doi.org/10.1128/mBio.00007-17 Text en Copyright © 2017 Payros et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Payros, Delphine
Dobrindt, Ulrich
Martin, Patricia
Secher, Thomas
Bracarense, Ana Paula F. L.
Boury, Michèle
Laffitte, Joelle
Pinton, Philippe
Oswald, Eric
Oswald, Isabelle P.
The Food Contaminant Deoxynivalenol Exacerbates the Genotoxicity of Gut Microbiota
title The Food Contaminant Deoxynivalenol Exacerbates the Genotoxicity of Gut Microbiota
title_full The Food Contaminant Deoxynivalenol Exacerbates the Genotoxicity of Gut Microbiota
title_fullStr The Food Contaminant Deoxynivalenol Exacerbates the Genotoxicity of Gut Microbiota
title_full_unstemmed The Food Contaminant Deoxynivalenol Exacerbates the Genotoxicity of Gut Microbiota
title_short The Food Contaminant Deoxynivalenol Exacerbates the Genotoxicity of Gut Microbiota
title_sort food contaminant deoxynivalenol exacerbates the genotoxicity of gut microbiota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350463/
https://www.ncbi.nlm.nih.gov/pubmed/28292979
http://dx.doi.org/10.1128/mBio.00007-17
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