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A Clostridia-rich microbiota enhances bile acid excretion in diarrhea-predominant irritable bowel syndrome
Ling Zhao, … , Wei Jia, Zhaoxiang Bian
Ling Zhao, … , Wei Jia, Zhaoxiang Bian
Published December 9, 2019
Citation Information: J Clin Invest. 2020;130(1):438-450. https://doi.org/10.1172/JCI130976.
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Research Article Gastroenterology Microbiology

A Clostridia-rich microbiota enhances bile acid excretion in diarrhea-predominant irritable bowel syndrome

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Abstract

An excess of fecal bile acids (BAs) is thought to be one of the mechanisms for diarrhea-predominant irritable bowel syndrome (IBS-D). However, the factors causing excessive BA excretion remain incompletely studied. Given the importance of gut microbiota in BA metabolism, we hypothesized that gut dysbiosis might contribute to excessive BA excretion in IBS-D. By performing BA-related metabolic and metagenomic analyses in 290 IBS-D patients and 89 healthy volunteers, we found that 24.5% of IBS-D patients exhibited excessive excretion of total BAs and alteration of BA-transforming bacteria in feces. Notably, the increase in Clostridia bacteria (e.g., C. scindens) was positively associated with the levels of fecal BAs and serum 7α-hydroxy-4-cholesten-3-one (C4), but negatively correlated with serum fibroblast growth factor 19 (FGF19) concentration. Furthermore, colonization with Clostridia-rich IBS-D fecal microbiota or C. scindens individually enhanced serum C4 and hepatic conjugated BAs but reduced ileal FGF19 expression in mice. Inhibition of Clostridium species with vancomycin yielded opposite results. Clostridia-derived BAs suppressed the intestinal FGF19 expression in vitro and in vivo. In conclusion, this study demonstrates that the Clostridia-rich microbiota contributes to excessive BA excretion in IBS-D patients, which provides a mechanistic hypothesis with testable clinical implications.

Authors

Ling Zhao, Wei Yang, Yang Chen, Fengjie Huang, Lin Lu, Chengyuan Lin, Tao Huang, Ziwan Ning, Lixiang Zhai, Linda L.D. Zhong, Waiching Lam, Zhen Yang, Xuan Zhang, Chungwah Cheng, Lijuan Han, Qinwei Qiu, Xiaoxiao Shang, Runyue Huang, Haitao Xiao, Zhenxing Ren, Dongfeng Chen, Silong Sun, Hani El-Nezami, Zongwei Cai, Aiping Lu, Xiaodong Fang, Wei Jia, Zhaoxiang Bian

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Figure 1

Alteration of fecal BA profiles and serum BA synthetic indicators in IBS-D patients.

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Alteration of fecal BA profiles and serum BA synthetic indicators in IBS...
(A) Histogram of the distribution of total fecal BA levels in healthy controls (n = 89) and IBS-D patients (n = 290). Based on the 90th percentile of healthy total fecal BA level, 25% of IBS-D patients (n = 71) with excessive BA excretion were grouped as BA+IBS-D and the other patients (n = 219) were classified as BA–IBS-D. (B and C) Concentrations of serum 7α-hydroxy-4-cholesten-3-one (C4) and fibroblast growth factor 19 (FGF19). (D–F) The severity of bowel symptoms between IBS-D subgroups assessed by defecation frequency (D), Bristol stool scale (E), and IBS severity scoring system (IBS-SSS) (F). (G and H) Absolute contents of fecal dominant BAs. (I) Proportions of fecal dominant BAs. Only BAs constituting greater than 1% of the total BA pool are shown in the legend. Differences in phenotypic scores between IBS-D subgroups were analyzed by the Mann-Whitney test, and BA-related indices were evaluated among 3 groups by the Kruskal-Wallis test. The box-and-whisker plots show the mean (horizontal lines), 5th–95th percentile values (boxes), and SEM (whiskers). *P < 0.05, ***P < 0.005 compared with the HC group; #P < 0.05, ##P < 0.01, ###P < 0.005 compared with the BA–IBS-D group. TCA, taurocholic acid; TCDCA, taurochenodeoxycholic acid; GCA, glycocholic acid; GCDCA, glycocheno-deoxycholic acid; GUDCA, glycoursodeoxycholic acid; GHDCA, glycohyodeoxycholic acid; GDCA, glycodeoxycholic acid; CA, cholic acid; CDCA, chenodeoxycholic acid; DCA, deoxycholic acid; LCA, lithocholic acid; 7-KDCA, 7-ketodeoxycholic acid; UDCA, ursodeoxycholic acid; HDCA, hyodeoxycholic acid; KLCA, ketolithocholic acid; HCA, hyocholic acid; ωMCA, ω-muricholic acid; isoLCA, isolithocholic acid; ACA, allocholic acid.

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