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A New Strain of Christensenella minuta as a Potential Biotherapy for Obesity and Associated Metabolic Diseases

Obesity is associated with gut microbiota dysbiosis, characterized by a high Firmicutes/Bacteroidetes ratio. Gut-dwelling bacteria of the Christensenellaceae family have been proposed to act as keystones of the human gut ecosystem and to prevent adipogenesis. The objectives of the present study were...

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Autores principales: Mazier, Wilfrid, Le Corf, Katy, Martinez, Ccori, Tudela, Héloïse, Kissi, Déborah, Kropp, Camille, Coubard, Chrislain, Soto, Marion, Elustondo, Frédéric, Rawadi, Georges, Claus, Sandrine P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067450/
https://www.ncbi.nlm.nih.gov/pubmed/33917566
http://dx.doi.org/10.3390/cells10040823
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author Mazier, Wilfrid
Le Corf, Katy
Martinez, Ccori
Tudela, Héloïse
Kissi, Déborah
Kropp, Camille
Coubard, Chrislain
Soto, Marion
Elustondo, Frédéric
Rawadi, Georges
Claus, Sandrine P.
author_facet Mazier, Wilfrid
Le Corf, Katy
Martinez, Ccori
Tudela, Héloïse
Kissi, Déborah
Kropp, Camille
Coubard, Chrislain
Soto, Marion
Elustondo, Frédéric
Rawadi, Georges
Claus, Sandrine P.
author_sort Mazier, Wilfrid
collection PubMed
description Obesity is associated with gut microbiota dysbiosis, characterized by a high Firmicutes/Bacteroidetes ratio. Gut-dwelling bacteria of the Christensenellaceae family have been proposed to act as keystones of the human gut ecosystem and to prevent adipogenesis. The objectives of the present study were to demonstrate the antiobesity potential of a new strain of Christensenella minuta in preclinical models and explore related mechanisms of action. The antiobesity potential of C. minuta DSM33407 was assessed in a diet-induced obesity mouse model. Changes in hepatic lipid metabolism were explored using targeted transcriptomics. Effects on gut microbiota were further assessed in a humanized Simulator of the Human Intestinal Microbial Ecosystem (SHIME(®)) model inoculated with obese fecal samples. Shotgun metagenomics was applied to study microbial community structures in both models. C. minuta DSM33407 protected from diet-induced obesity and regulated associated metabolic markers such as glycemia and leptin. It also regulated hepatic lipid metabolism through a strong inhibition of de novo lipogenesis and maintained gut epithelial integrity. In the humanized SHIME(®) model, these effects were associated with modulations of the intestinal microbiota characterized by a decreased Firmicutes/Bacteroidetes ratio. These data indicate that C. minuta DSM33407 is a convincing therapeutic candidate for the management of obesity and associated metabolic disorders.
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spelling pubmed-80674502021-04-25 A New Strain of Christensenella minuta as a Potential Biotherapy for Obesity and Associated Metabolic Diseases Mazier, Wilfrid Le Corf, Katy Martinez, Ccori Tudela, Héloïse Kissi, Déborah Kropp, Camille Coubard, Chrislain Soto, Marion Elustondo, Frédéric Rawadi, Georges Claus, Sandrine P. Cells Article Obesity is associated with gut microbiota dysbiosis, characterized by a high Firmicutes/Bacteroidetes ratio. Gut-dwelling bacteria of the Christensenellaceae family have been proposed to act as keystones of the human gut ecosystem and to prevent adipogenesis. The objectives of the present study were to demonstrate the antiobesity potential of a new strain of Christensenella minuta in preclinical models and explore related mechanisms of action. The antiobesity potential of C. minuta DSM33407 was assessed in a diet-induced obesity mouse model. Changes in hepatic lipid metabolism were explored using targeted transcriptomics. Effects on gut microbiota were further assessed in a humanized Simulator of the Human Intestinal Microbial Ecosystem (SHIME(®)) model inoculated with obese fecal samples. Shotgun metagenomics was applied to study microbial community structures in both models. C. minuta DSM33407 protected from diet-induced obesity and regulated associated metabolic markers such as glycemia and leptin. It also regulated hepatic lipid metabolism through a strong inhibition of de novo lipogenesis and maintained gut epithelial integrity. In the humanized SHIME(®) model, these effects were associated with modulations of the intestinal microbiota characterized by a decreased Firmicutes/Bacteroidetes ratio. These data indicate that C. minuta DSM33407 is a convincing therapeutic candidate for the management of obesity and associated metabolic disorders. MDPI 2021-04-06 /pmc/articles/PMC8067450/ /pubmed/33917566 http://dx.doi.org/10.3390/cells10040823 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mazier, Wilfrid
Le Corf, Katy
Martinez, Ccori
Tudela, Héloïse
Kissi, Déborah
Kropp, Camille
Coubard, Chrislain
Soto, Marion
Elustondo, Frédéric
Rawadi, Georges
Claus, Sandrine P.
A New Strain of Christensenella minuta as a Potential Biotherapy for Obesity and Associated Metabolic Diseases
title A New Strain of Christensenella minuta as a Potential Biotherapy for Obesity and Associated Metabolic Diseases
title_full A New Strain of Christensenella minuta as a Potential Biotherapy for Obesity and Associated Metabolic Diseases
title_fullStr A New Strain of Christensenella minuta as a Potential Biotherapy for Obesity and Associated Metabolic Diseases
title_full_unstemmed A New Strain of Christensenella minuta as a Potential Biotherapy for Obesity and Associated Metabolic Diseases
title_short A New Strain of Christensenella minuta as a Potential Biotherapy for Obesity and Associated Metabolic Diseases
title_sort new strain of christensenella minuta as a potential biotherapy for obesity and associated metabolic diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067450/
https://www.ncbi.nlm.nih.gov/pubmed/33917566
http://dx.doi.org/10.3390/cells10040823
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