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Bilophila wadsworthia aggravates high fat diet induced metabolic dysfunctions in mice

Dietary lipids favor the growth of the pathobiont Bilophila wadsworthia, but the relevance of this expansion in metabolic syndrome pathogenesis is poorly understood. Here, we showed that B. wadsworthia synergizes with high fat diet (HFD) to promote higher inflammation, intestinal barrier dysfunction...

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Autores principales: Natividad, Jane M., Lamas, Bruno, Pham, Hang Phuong, Michel, Marie-Laure, Rainteau, Dominique, Bridonneau, Chantal, da Costa, Gregory, van Hylckama Vlieg, Johan, Sovran, Bruno, Chamignon, Celia, Planchais, Julien, Richard, Mathias L., Langella, Philippe, Veiga, Patrick, Sokol, Harry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052103/
https://www.ncbi.nlm.nih.gov/pubmed/30022049
http://dx.doi.org/10.1038/s41467-018-05249-7
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author Natividad, Jane M.
Lamas, Bruno
Pham, Hang Phuong
Michel, Marie-Laure
Rainteau, Dominique
Bridonneau, Chantal
da Costa, Gregory
van Hylckama Vlieg, Johan
Sovran, Bruno
Chamignon, Celia
Planchais, Julien
Richard, Mathias L.
Langella, Philippe
Veiga, Patrick
Sokol, Harry
author_facet Natividad, Jane M.
Lamas, Bruno
Pham, Hang Phuong
Michel, Marie-Laure
Rainteau, Dominique
Bridonneau, Chantal
da Costa, Gregory
van Hylckama Vlieg, Johan
Sovran, Bruno
Chamignon, Celia
Planchais, Julien
Richard, Mathias L.
Langella, Philippe
Veiga, Patrick
Sokol, Harry
author_sort Natividad, Jane M.
collection PubMed
description Dietary lipids favor the growth of the pathobiont Bilophila wadsworthia, but the relevance of this expansion in metabolic syndrome pathogenesis is poorly understood. Here, we showed that B. wadsworthia synergizes with high fat diet (HFD) to promote higher inflammation, intestinal barrier dysfunction and bile acid dysmetabolism, leading to higher glucose dysmetabolism and hepatic steatosis. Host-microbiota transcriptomics analysis reveal pathways, particularly butanoate metabolism, which may underlie the metabolic effects mediated by B. wadsworthia. Pharmacological suppression of B. wadsworthia-associated inflammation demonstrate the bacterium’s intrinsic capacity to induce a negative impact on glycemic control and hepatic function. Administration of the probiotic Lactobacillus rhamnosus CNCM I-3690 limits B. wadsworthia-induced immune and metabolic impairment by limiting its expansion, reducing inflammation and reinforcing intestinal barrier. Our results suggest a new avenue for interventions against western diet-driven inflammatory and metabolic diseases.
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spelling pubmed-60521032018-07-23 Bilophila wadsworthia aggravates high fat diet induced metabolic dysfunctions in mice Natividad, Jane M. Lamas, Bruno Pham, Hang Phuong Michel, Marie-Laure Rainteau, Dominique Bridonneau, Chantal da Costa, Gregory van Hylckama Vlieg, Johan Sovran, Bruno Chamignon, Celia Planchais, Julien Richard, Mathias L. Langella, Philippe Veiga, Patrick Sokol, Harry Nat Commun Article Dietary lipids favor the growth of the pathobiont Bilophila wadsworthia, but the relevance of this expansion in metabolic syndrome pathogenesis is poorly understood. Here, we showed that B. wadsworthia synergizes with high fat diet (HFD) to promote higher inflammation, intestinal barrier dysfunction and bile acid dysmetabolism, leading to higher glucose dysmetabolism and hepatic steatosis. Host-microbiota transcriptomics analysis reveal pathways, particularly butanoate metabolism, which may underlie the metabolic effects mediated by B. wadsworthia. Pharmacological suppression of B. wadsworthia-associated inflammation demonstrate the bacterium’s intrinsic capacity to induce a negative impact on glycemic control and hepatic function. Administration of the probiotic Lactobacillus rhamnosus CNCM I-3690 limits B. wadsworthia-induced immune and metabolic impairment by limiting its expansion, reducing inflammation and reinforcing intestinal barrier. Our results suggest a new avenue for interventions against western diet-driven inflammatory and metabolic diseases. Nature Publishing Group UK 2018-07-18 /pmc/articles/PMC6052103/ /pubmed/30022049 http://dx.doi.org/10.1038/s41467-018-05249-7 Text en © The Author(s) 2018 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
Natividad, Jane M.
Lamas, Bruno
Pham, Hang Phuong
Michel, Marie-Laure
Rainteau, Dominique
Bridonneau, Chantal
da Costa, Gregory
van Hylckama Vlieg, Johan
Sovran, Bruno
Chamignon, Celia
Planchais, Julien
Richard, Mathias L.
Langella, Philippe
Veiga, Patrick
Sokol, Harry
Bilophila wadsworthia aggravates high fat diet induced metabolic dysfunctions in mice
title Bilophila wadsworthia aggravates high fat diet induced metabolic dysfunctions in mice
title_full Bilophila wadsworthia aggravates high fat diet induced metabolic dysfunctions in mice
title_fullStr Bilophila wadsworthia aggravates high fat diet induced metabolic dysfunctions in mice
title_full_unstemmed Bilophila wadsworthia aggravates high fat diet induced metabolic dysfunctions in mice
title_short Bilophila wadsworthia aggravates high fat diet induced metabolic dysfunctions in mice
title_sort bilophila wadsworthia aggravates high fat diet induced metabolic dysfunctions in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052103/
https://www.ncbi.nlm.nih.gov/pubmed/30022049
http://dx.doi.org/10.1038/s41467-018-05249-7
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