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Cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice
Increasing evidence point to the relevance of intestinal disfunction and changes in the microbiome composition during chronic liver disease. More specifically, recent studies have highlighted that cholestatic diseases associate with a reduction in the microbiome diversity in patients. Still, the dyn...
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/PMC6707139/ https://www.ncbi.nlm.nih.gov/pubmed/31444478 http://dx.doi.org/10.1038/s41598-019-48784-z |
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author | Cabrera-Rubio, Raul Patterson, Angela M. Cotter, Paul D. Beraza, Naiara |
author_facet | Cabrera-Rubio, Raul Patterson, Angela M. Cotter, Paul D. Beraza, Naiara |
author_sort | Cabrera-Rubio, Raul |
collection | PubMed |
description | Increasing evidence point to the relevance of intestinal disfunction and changes in the microbiome composition during chronic liver disease. More specifically, recent studies have highlighted that cholestatic diseases associate with a reduction in the microbiome diversity in patients. Still, the dynamics of the changes in the microbiome composition observed, as well as their implication in contributing to the pathogenesis of this disease remain largely undefined. Hence, experimental mouse models resembling the human pathogenesis are crucial to move forward our understanding on the mechanisms underpinning cholestatic disease and to enable the development of effective therapeutics. Our results show that the bile duct ligation (BDL) experimental model of cholestasis leads to rapid and significant changes in the microbiome diversity, with more than 100 OTUs being significantly different in faecal samples obtained from WT mice at 3 days and 7 days after BDL when compared to control animals. Changes in the microbial composition in mice after BDL included the enrichment of Akkermansia, Prevotella, Bacteroides and unclassified Ruminococcaceae in parallel with a drastic reduction of the presence of Faecalibacterium prausnitzii. In conclusion, our results support that bile duct ligation induces changes in the microbiome that partly resemble the gut microbial changes observed during human cholestatic disease. |
format | Online Article Text |
id | pubmed-6707139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67071392019-09-08 Cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice Cabrera-Rubio, Raul Patterson, Angela M. Cotter, Paul D. Beraza, Naiara Sci Rep Article Increasing evidence point to the relevance of intestinal disfunction and changes in the microbiome composition during chronic liver disease. More specifically, recent studies have highlighted that cholestatic diseases associate with a reduction in the microbiome diversity in patients. Still, the dynamics of the changes in the microbiome composition observed, as well as their implication in contributing to the pathogenesis of this disease remain largely undefined. Hence, experimental mouse models resembling the human pathogenesis are crucial to move forward our understanding on the mechanisms underpinning cholestatic disease and to enable the development of effective therapeutics. Our results show that the bile duct ligation (BDL) experimental model of cholestasis leads to rapid and significant changes in the microbiome diversity, with more than 100 OTUs being significantly different in faecal samples obtained from WT mice at 3 days and 7 days after BDL when compared to control animals. Changes in the microbial composition in mice after BDL included the enrichment of Akkermansia, Prevotella, Bacteroides and unclassified Ruminococcaceae in parallel with a drastic reduction of the presence of Faecalibacterium prausnitzii. In conclusion, our results support that bile duct ligation induces changes in the microbiome that partly resemble the gut microbial changes observed during human cholestatic disease. Nature Publishing Group UK 2019-08-23 /pmc/articles/PMC6707139/ /pubmed/31444478 http://dx.doi.org/10.1038/s41598-019-48784-z 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 Cabrera-Rubio, Raul Patterson, Angela M. Cotter, Paul D. Beraza, Naiara Cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice |
title | Cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice |
title_full | Cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice |
title_fullStr | Cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice |
title_full_unstemmed | Cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice |
title_short | Cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice |
title_sort | cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707139/ https://www.ncbi.nlm.nih.gov/pubmed/31444478 http://dx.doi.org/10.1038/s41598-019-48784-z |
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