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Effective fecal microbiota transplantation for recurrent Clostridioides difficile infection in humans is associated with increased signalling in the bile acid-farnesoid X receptor-fibroblast growth factor pathway

The mechanisms of efficacy for fecal microbiota transplantation (FMT) in treating recurrent Clostridioides difficile infection (rCDI) remain poorly defined, with restored gut microbiota-bile acid interactions representing one possible explanation. Furthermore, the potential implications for host phy...

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Autores principales: Monaghan, Tanya, Mullish, Benjamin H, Patterson, Jordan, Wong, Gane KS, Marchesi, Julian R, Xu, Huiping, Jilani, Tahseen, Kao, Dina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546339/
https://www.ncbi.nlm.nih.gov/pubmed/30183484
http://dx.doi.org/10.1080/19490976.2018.1506667
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author Monaghan, Tanya
Mullish, Benjamin H
Patterson, Jordan
Wong, Gane KS
Marchesi, Julian R
Xu, Huiping
Jilani, Tahseen
Kao, Dina
author_facet Monaghan, Tanya
Mullish, Benjamin H
Patterson, Jordan
Wong, Gane KS
Marchesi, Julian R
Xu, Huiping
Jilani, Tahseen
Kao, Dina
author_sort Monaghan, Tanya
collection PubMed
description The mechanisms of efficacy for fecal microbiota transplantation (FMT) in treating recurrent Clostridioides difficile infection (rCDI) remain poorly defined, with restored gut microbiota-bile acid interactions representing one possible explanation. Furthermore, the potential implications for host physiology of these FMT-related changes in gut bile acid metabolism are also not well explored. In this study, we investigated the impact of FMT for rCDI upon signalling through the farnesoid X receptor (FXR)-fibroblast growth factor (FGF) pathway. Herein, we identify that in addition to restoration of gut microbiota and bile acid profiles, FMT for rCDI is accompanied by a significant, sustained increase in circulating levels of FGF19 and reduction in FGF21. These FGF changes were associated with weight gain post-FMT, to a level not exceeding the pre-rCDI baseline. Collectively, these data support the hypothesis that the restoration of gut microbial communities by FMT for rCDI is associated with an upregulated FXR-FGF pathway, and highlight the potential systemic effect of FMT.
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spelling pubmed-65463392019-06-14 Effective fecal microbiota transplantation for recurrent Clostridioides difficile infection in humans is associated with increased signalling in the bile acid-farnesoid X receptor-fibroblast growth factor pathway Monaghan, Tanya Mullish, Benjamin H Patterson, Jordan Wong, Gane KS Marchesi, Julian R Xu, Huiping Jilani, Tahseen Kao, Dina Gut Microbes Brief Report The mechanisms of efficacy for fecal microbiota transplantation (FMT) in treating recurrent Clostridioides difficile infection (rCDI) remain poorly defined, with restored gut microbiota-bile acid interactions representing one possible explanation. Furthermore, the potential implications for host physiology of these FMT-related changes in gut bile acid metabolism are also not well explored. In this study, we investigated the impact of FMT for rCDI upon signalling through the farnesoid X receptor (FXR)-fibroblast growth factor (FGF) pathway. Herein, we identify that in addition to restoration of gut microbiota and bile acid profiles, FMT for rCDI is accompanied by a significant, sustained increase in circulating levels of FGF19 and reduction in FGF21. These FGF changes were associated with weight gain post-FMT, to a level not exceeding the pre-rCDI baseline. Collectively, these data support the hypothesis that the restoration of gut microbial communities by FMT for rCDI is associated with an upregulated FXR-FGF pathway, and highlight the potential systemic effect of FMT. Taylor & Francis 2018-09-05 /pmc/articles/PMC6546339/ /pubmed/30183484 http://dx.doi.org/10.1080/19490976.2018.1506667 Text en © 2018 The Author(s). Published with license by Taylor & Francis Group, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Brief Report
Monaghan, Tanya
Mullish, Benjamin H
Patterson, Jordan
Wong, Gane KS
Marchesi, Julian R
Xu, Huiping
Jilani, Tahseen
Kao, Dina
Effective fecal microbiota transplantation for recurrent Clostridioides difficile infection in humans is associated with increased signalling in the bile acid-farnesoid X receptor-fibroblast growth factor pathway
title Effective fecal microbiota transplantation for recurrent Clostridioides difficile infection in humans is associated with increased signalling in the bile acid-farnesoid X receptor-fibroblast growth factor pathway
title_full Effective fecal microbiota transplantation for recurrent Clostridioides difficile infection in humans is associated with increased signalling in the bile acid-farnesoid X receptor-fibroblast growth factor pathway
title_fullStr Effective fecal microbiota transplantation for recurrent Clostridioides difficile infection in humans is associated with increased signalling in the bile acid-farnesoid X receptor-fibroblast growth factor pathway
title_full_unstemmed Effective fecal microbiota transplantation for recurrent Clostridioides difficile infection in humans is associated with increased signalling in the bile acid-farnesoid X receptor-fibroblast growth factor pathway
title_short Effective fecal microbiota transplantation for recurrent Clostridioides difficile infection in humans is associated with increased signalling in the bile acid-farnesoid X receptor-fibroblast growth factor pathway
title_sort effective fecal microbiota transplantation for recurrent clostridioides difficile infection in humans is associated with increased signalling in the bile acid-farnesoid x receptor-fibroblast growth factor pathway
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546339/
https://www.ncbi.nlm.nih.gov/pubmed/30183484
http://dx.doi.org/10.1080/19490976.2018.1506667
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