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

被引:47
|
作者
Monaghan, Tanya [1 ,2 ]
Mullish, Benjamin H. [3 ]
Patterson, Jordan [4 ]
Wong, Gane K. S. [4 ,5 ,9 ]
Marchesi, Julian R. [3 ,6 ]
Xu, Huiping [7 ]
Jilani, Tahseen [8 ]
Kao, Dina [9 ,10 ]
机构
[1] Nottingham Univ Hosp NHS Trust, NIHR Nottingham Biomed Res Ctr BRC, Nottingham, England
[2] Univ Nottingham, Nottingham, England
[3] Imperial Coll London, Fac Med, Dept Surg & Canc, Div Integrat Syst Med & Digest Dis, London, England
[4] Univ Alberta, Dept Biol Sci, Edmonton, AB, Canada
[5] BGI Shenzhen, Shenzhen, Peoples R China
[6] Cardiff Univ, Sch Biosci, Cardiff, S Glam, Wales
[7] Indiana Univ Sch Med, Dept Biostat, Bloomington, IN USA
[8] Univ Nottingham, Adv Data Anal Ctr, Sch Comp Sci, Nottingham, England
[9] Univ Alberta, Dept Med, Div Gastroenterol, Edmonton, AB, Canada
[10] Ctr Excellence Gastrointestinal Inflammat & Immun, Edmonton, AB, Canada
基金
英国医学研究理事会; 英国工程与自然科学研究理事会;
关键词
Microbiota; fecal microbiota transplantation (FMT); recurrent Clostridium difficile infection (rCDI); bile acid metabolism; fibroblast growth factor (FGF)19; MASS;
D O I
10.1080/19490976.2018.1506667
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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 add 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.
引用
收藏
页码:142 / 148
页数:7
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