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Altered intestinal microbiota–host mitochondria crosstalk in new onset Crohn's disease
Intestinal microbial dysbiosis is associated with Crohn's disease (CD). However, the mechanisms leading to the chronic mucosal inflammation that characterizes this disease remain unclear. In this report, we use systems-level approaches to study the interactions between the gut microbiota and ho...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5122959/ https://www.ncbi.nlm.nih.gov/pubmed/27876802 http://dx.doi.org/10.1038/ncomms13419 |
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author | Mottawea, Walid Chiang, Cheng-Kang Mühlbauer, Marcus Starr, Amanda E. Butcher, James Abujamel, Turki Deeke, Shelley A. Brandel, Annette Zhou, Hu Shokralla, Shadi Hajibabaei, Mehrdad Singleton, Ruth Benchimol, Eric I. Jobin, Christian Mack, David R. Figeys, Daniel Stintzi, Alain |
author_facet | Mottawea, Walid Chiang, Cheng-Kang Mühlbauer, Marcus Starr, Amanda E. Butcher, James Abujamel, Turki Deeke, Shelley A. Brandel, Annette Zhou, Hu Shokralla, Shadi Hajibabaei, Mehrdad Singleton, Ruth Benchimol, Eric I. Jobin, Christian Mack, David R. Figeys, Daniel Stintzi, Alain |
author_sort | Mottawea, Walid |
collection | PubMed |
description | Intestinal microbial dysbiosis is associated with Crohn's disease (CD). However, the mechanisms leading to the chronic mucosal inflammation that characterizes this disease remain unclear. In this report, we use systems-level approaches to study the interactions between the gut microbiota and host in new-onset paediatric patients to evaluate causality and mechanisms of disease. We report an altered host proteome in CD patients indicative of impaired mitochondrial functions. In particular, mitochondrial proteins implicated in H(2)S detoxification are downregulated, while the relative abundance of H(2)S microbial producers is increased. Network correlation analysis reveals that Atopobium parvulum controls the central hub of H(2)S producers. A. parvulum induces pancolitis in colitis-susceptible interleukin-10-deficient mice and this phenotype requires the presence of the intestinal microbiota. Administrating the H(2)S scavenger bismuth mitigates A. parvulum-induced colitis in vivo. This study reveals that host–microbiota interactions are disturbed in CD and thus provides mechanistic insights into CD pathogenesis. |
format | Online Article Text |
id | pubmed-5122959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51229592016-11-29 Altered intestinal microbiota–host mitochondria crosstalk in new onset Crohn's disease Mottawea, Walid Chiang, Cheng-Kang Mühlbauer, Marcus Starr, Amanda E. Butcher, James Abujamel, Turki Deeke, Shelley A. Brandel, Annette Zhou, Hu Shokralla, Shadi Hajibabaei, Mehrdad Singleton, Ruth Benchimol, Eric I. Jobin, Christian Mack, David R. Figeys, Daniel Stintzi, Alain Nat Commun Article Intestinal microbial dysbiosis is associated with Crohn's disease (CD). However, the mechanisms leading to the chronic mucosal inflammation that characterizes this disease remain unclear. In this report, we use systems-level approaches to study the interactions between the gut microbiota and host in new-onset paediatric patients to evaluate causality and mechanisms of disease. We report an altered host proteome in CD patients indicative of impaired mitochondrial functions. In particular, mitochondrial proteins implicated in H(2)S detoxification are downregulated, while the relative abundance of H(2)S microbial producers is increased. Network correlation analysis reveals that Atopobium parvulum controls the central hub of H(2)S producers. A. parvulum induces pancolitis in colitis-susceptible interleukin-10-deficient mice and this phenotype requires the presence of the intestinal microbiota. Administrating the H(2)S scavenger bismuth mitigates A. parvulum-induced colitis in vivo. This study reveals that host–microbiota interactions are disturbed in CD and thus provides mechanistic insights into CD pathogenesis. Nature Publishing Group 2016-11-23 /pmc/articles/PMC5122959/ /pubmed/27876802 http://dx.doi.org/10.1038/ncomms13419 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Mottawea, Walid Chiang, Cheng-Kang Mühlbauer, Marcus Starr, Amanda E. Butcher, James Abujamel, Turki Deeke, Shelley A. Brandel, Annette Zhou, Hu Shokralla, Shadi Hajibabaei, Mehrdad Singleton, Ruth Benchimol, Eric I. Jobin, Christian Mack, David R. Figeys, Daniel Stintzi, Alain Altered intestinal microbiota–host mitochondria crosstalk in new onset Crohn's disease |
title | Altered intestinal microbiota–host mitochondria crosstalk in new onset Crohn's disease |
title_full | Altered intestinal microbiota–host mitochondria crosstalk in new onset Crohn's disease |
title_fullStr | Altered intestinal microbiota–host mitochondria crosstalk in new onset Crohn's disease |
title_full_unstemmed | Altered intestinal microbiota–host mitochondria crosstalk in new onset Crohn's disease |
title_short | Altered intestinal microbiota–host mitochondria crosstalk in new onset Crohn's disease |
title_sort | altered intestinal microbiota–host mitochondria crosstalk in new onset crohn's disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5122959/ https://www.ncbi.nlm.nih.gov/pubmed/27876802 http://dx.doi.org/10.1038/ncomms13419 |
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