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Fecal Microbiota Transplant from Human to Mice Gives Insights into the Role of the Gut Microbiota in Non-Alcoholic Fatty Liver Disease (NAFLD)

Non-alcoholic fatty liver diseases (NAFLD) are associated with changes in the composition and metabolic activities of the gut microbiota. However, the causal role played by the gut microbiota in individual susceptibility to NAFLD and particularly at its early stage is still unclear. In this context,...

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Autores principales: Burz, Sebastian D., Monnoye, Magali, Philippe, Catherine, Farin, William, Ratziu, Vlad, Strozzi, Francesco, Paillarse, Jean-Michel, Chêne, Laurent, Blottière, Hervé M., Gérard, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7833443/
https://www.ncbi.nlm.nih.gov/pubmed/33477939
http://dx.doi.org/10.3390/microorganisms9010199
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author Burz, Sebastian D.
Monnoye, Magali
Philippe, Catherine
Farin, William
Ratziu, Vlad
Strozzi, Francesco
Paillarse, Jean-Michel
Chêne, Laurent
Blottière, Hervé M.
Gérard, Philippe
author_facet Burz, Sebastian D.
Monnoye, Magali
Philippe, Catherine
Farin, William
Ratziu, Vlad
Strozzi, Francesco
Paillarse, Jean-Michel
Chêne, Laurent
Blottière, Hervé M.
Gérard, Philippe
author_sort Burz, Sebastian D.
collection PubMed
description Non-alcoholic fatty liver diseases (NAFLD) are associated with changes in the composition and metabolic activities of the gut microbiota. However, the causal role played by the gut microbiota in individual susceptibility to NAFLD and particularly at its early stage is still unclear. In this context, we transplanted the microbiota from a patient with fatty liver (NAFL) and from a healthy individual to two groups of mice. We first showed that the microbiota composition in recipient mice resembled the microbiota composition of their respective human donor. Following administration of a high-fructose, high-fat diet, mice that received the human NAFL microbiota (NAFLR) gained more weight and had a higher liver triglycerides level and higher plasma LDL cholesterol than mice that received the human healthy microbiota (HR). Metabolomic analyses revealed that it was associated with lower and higher plasma levels of glycine and 3-Indolepropionic acid in NAFLR mice, respectively. Moreover, several bacterial genera and OTUs were identified as differently represented in the NAFLR and HR microbiota and therefore potentially responsible for the different phenotypes observed. Altogether, our results confirm that the gut bacteria play a role in obesity and steatosis development and that targeting the gut microbiota may be a preventive or therapeutic strategy in NAFLD management.
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spelling pubmed-78334432021-01-26 Fecal Microbiota Transplant from Human to Mice Gives Insights into the Role of the Gut Microbiota in Non-Alcoholic Fatty Liver Disease (NAFLD) Burz, Sebastian D. Monnoye, Magali Philippe, Catherine Farin, William Ratziu, Vlad Strozzi, Francesco Paillarse, Jean-Michel Chêne, Laurent Blottière, Hervé M. Gérard, Philippe Microorganisms Article Non-alcoholic fatty liver diseases (NAFLD) are associated with changes in the composition and metabolic activities of the gut microbiota. However, the causal role played by the gut microbiota in individual susceptibility to NAFLD and particularly at its early stage is still unclear. In this context, we transplanted the microbiota from a patient with fatty liver (NAFL) and from a healthy individual to two groups of mice. We first showed that the microbiota composition in recipient mice resembled the microbiota composition of their respective human donor. Following administration of a high-fructose, high-fat diet, mice that received the human NAFL microbiota (NAFLR) gained more weight and had a higher liver triglycerides level and higher plasma LDL cholesterol than mice that received the human healthy microbiota (HR). Metabolomic analyses revealed that it was associated with lower and higher plasma levels of glycine and 3-Indolepropionic acid in NAFLR mice, respectively. Moreover, several bacterial genera and OTUs were identified as differently represented in the NAFLR and HR microbiota and therefore potentially responsible for the different phenotypes observed. Altogether, our results confirm that the gut bacteria play a role in obesity and steatosis development and that targeting the gut microbiota may be a preventive or therapeutic strategy in NAFLD management. MDPI 2021-01-19 /pmc/articles/PMC7833443/ /pubmed/33477939 http://dx.doi.org/10.3390/microorganisms9010199 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Burz, Sebastian D.
Monnoye, Magali
Philippe, Catherine
Farin, William
Ratziu, Vlad
Strozzi, Francesco
Paillarse, Jean-Michel
Chêne, Laurent
Blottière, Hervé M.
Gérard, Philippe
Fecal Microbiota Transplant from Human to Mice Gives Insights into the Role of the Gut Microbiota in Non-Alcoholic Fatty Liver Disease (NAFLD)
title Fecal Microbiota Transplant from Human to Mice Gives Insights into the Role of the Gut Microbiota in Non-Alcoholic Fatty Liver Disease (NAFLD)
title_full Fecal Microbiota Transplant from Human to Mice Gives Insights into the Role of the Gut Microbiota in Non-Alcoholic Fatty Liver Disease (NAFLD)
title_fullStr Fecal Microbiota Transplant from Human to Mice Gives Insights into the Role of the Gut Microbiota in Non-Alcoholic Fatty Liver Disease (NAFLD)
title_full_unstemmed Fecal Microbiota Transplant from Human to Mice Gives Insights into the Role of the Gut Microbiota in Non-Alcoholic Fatty Liver Disease (NAFLD)
title_short Fecal Microbiota Transplant from Human to Mice Gives Insights into the Role of the Gut Microbiota in Non-Alcoholic Fatty Liver Disease (NAFLD)
title_sort fecal microbiota transplant from human to mice gives insights into the role of the gut microbiota in non-alcoholic fatty liver disease (nafld)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7833443/
https://www.ncbi.nlm.nih.gov/pubmed/33477939
http://dx.doi.org/10.3390/microorganisms9010199
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