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Metabolic adaptation of adherent-invasive Escherichia coli to exposure to bile salts

The adherent-invasive Escherichia coli (AIEC), which colonize the ileal mucosa of Crohn’s disease patients, adhere to intestinal epithelial cells, invade them and exacerbate intestinal inflammation. The high nutrient competition between the commensal microbiota and AIEC pathobiont requires the latte...

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Autores principales: Delmas, Julien, Gibold, Lucie, Faïs, Tiphanie, Batista, Sylvine, Leremboure, Martin, Sinel, Clara, Vazeille, Emilie, Cattoir, Vincent, Buisson, Anthony, Barnich, Nicolas, Dalmasso, Guillaume, Bonnet, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379400/
https://www.ncbi.nlm.nih.gov/pubmed/30778122
http://dx.doi.org/10.1038/s41598-019-38628-1
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author Delmas, Julien
Gibold, Lucie
Faïs, Tiphanie
Batista, Sylvine
Leremboure, Martin
Sinel, Clara
Vazeille, Emilie
Cattoir, Vincent
Buisson, Anthony
Barnich, Nicolas
Dalmasso, Guillaume
Bonnet, Richard
author_facet Delmas, Julien
Gibold, Lucie
Faïs, Tiphanie
Batista, Sylvine
Leremboure, Martin
Sinel, Clara
Vazeille, Emilie
Cattoir, Vincent
Buisson, Anthony
Barnich, Nicolas
Dalmasso, Guillaume
Bonnet, Richard
author_sort Delmas, Julien
collection PubMed
description The adherent-invasive Escherichia coli (AIEC), which colonize the ileal mucosa of Crohn’s disease patients, adhere to intestinal epithelial cells, invade them and exacerbate intestinal inflammation. The high nutrient competition between the commensal microbiota and AIEC pathobiont requires the latter to occupy their own metabolic niches to survive and proliferate within the gut. In this study, a global RNA sequencing of AIEC strain LF82 has been used to observe the impact of bile salts on the expression of metabolic genes. The results showed a global up-regulation of genes involved in degradation and a down-regulation of those implicated in biosynthesis. The main up-regulated degradation pathways were ethanolamine, 1,2-propanediol and citrate utilization, as well as the methyl-citrate pathway. Our study reveals that ethanolamine utilization bestows a competitive advantage of AIEC strains that are metabolically capable of its degradation in the presence of bile salts. We observed that bile salts activated secondary metabolism pathways that communicate to provide an energy benefit to AIEC. Bile salts may be used by AIEC as an environmental signal to promote their colonization.
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spelling pubmed-63794002019-02-21 Metabolic adaptation of adherent-invasive Escherichia coli to exposure to bile salts Delmas, Julien Gibold, Lucie Faïs, Tiphanie Batista, Sylvine Leremboure, Martin Sinel, Clara Vazeille, Emilie Cattoir, Vincent Buisson, Anthony Barnich, Nicolas Dalmasso, Guillaume Bonnet, Richard Sci Rep Article The adherent-invasive Escherichia coli (AIEC), which colonize the ileal mucosa of Crohn’s disease patients, adhere to intestinal epithelial cells, invade them and exacerbate intestinal inflammation. The high nutrient competition between the commensal microbiota and AIEC pathobiont requires the latter to occupy their own metabolic niches to survive and proliferate within the gut. In this study, a global RNA sequencing of AIEC strain LF82 has been used to observe the impact of bile salts on the expression of metabolic genes. The results showed a global up-regulation of genes involved in degradation and a down-regulation of those implicated in biosynthesis. The main up-regulated degradation pathways were ethanolamine, 1,2-propanediol and citrate utilization, as well as the methyl-citrate pathway. Our study reveals that ethanolamine utilization bestows a competitive advantage of AIEC strains that are metabolically capable of its degradation in the presence of bile salts. We observed that bile salts activated secondary metabolism pathways that communicate to provide an energy benefit to AIEC. Bile salts may be used by AIEC as an environmental signal to promote their colonization. Nature Publishing Group UK 2019-02-18 /pmc/articles/PMC6379400/ /pubmed/30778122 http://dx.doi.org/10.1038/s41598-019-38628-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Delmas, Julien
Gibold, Lucie
Faïs, Tiphanie
Batista, Sylvine
Leremboure, Martin
Sinel, Clara
Vazeille, Emilie
Cattoir, Vincent
Buisson, Anthony
Barnich, Nicolas
Dalmasso, Guillaume
Bonnet, Richard
Metabolic adaptation of adherent-invasive Escherichia coli to exposure to bile salts
title Metabolic adaptation of adherent-invasive Escherichia coli to exposure to bile salts
title_full Metabolic adaptation of adherent-invasive Escherichia coli to exposure to bile salts
title_fullStr Metabolic adaptation of adherent-invasive Escherichia coli to exposure to bile salts
title_full_unstemmed Metabolic adaptation of adherent-invasive Escherichia coli to exposure to bile salts
title_short Metabolic adaptation of adherent-invasive Escherichia coli to exposure to bile salts
title_sort metabolic adaptation of adherent-invasive escherichia coli to exposure to bile salts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379400/
https://www.ncbi.nlm.nih.gov/pubmed/30778122
http://dx.doi.org/10.1038/s41598-019-38628-1
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