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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6379400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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