Gut microbiota from green tea polyphenol-dosed mice improves intestinal epithelial homeostasis and ameliorates experimental colitis

被引:645
作者
Wu, Zhenhua [1 ]
Huang, Shimeng [1 ]
Li, Tiantian [1 ]
Li, Na [1 ]
Han, Dandan [1 ]
Zhang, Bing [2 ]
Xu, Zhenjiang Zech [3 ]
Zhang, Shiyi [1 ]
Pang, Jiaman [1 ]
Wang, Shilan [1 ]
Zhang, Guolong [4 ]
Zhao, Jiangchao [5 ]
Wang, Junjun [1 ]
机构
[1] China Agr Univ, Coll Anim Sci & Technol, State Key Lab Anim Nutr, Beijing 100193, Peoples R China
[2] China Agr Univ, Coll Vet Med, Minist Agr, Key Lab Anim Epidemiol, Beijing 100193, Peoples R China
[3] Nanchang Univ, State Key Lab Food Sci & Technol, Nanchang 214122, Jiangxi, Peoples R China
[4] Oklahoma State Univ, Dept Anim & Food Sci, Stillwater, OK 74078 USA
[5] Univ Arkansas, Dept Anim Sci, Div Agr, Fayetteville, AR 72701 USA
基金
中国国家自然科学基金;
关键词
Green tea polyphenol; Colitis; Gut microbiota; Fecal microbiota transplantation; Sterile fecal filtrate; INFLAMMATORY-BOWEL-DISEASE; HOST; INTEGRITY; MODEL;
D O I
10.1186/s40168-021-01115-9
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Background: Alteration of the gut microbiota may contribute to the development of inflammatory bowel disease (IBD). Epigallocatechin-3-gallate (EGCG), a major bioactive constituent of green tea, is known to be beneficial in IBD alleviation. However, it is unclear whether the gut microbiota exerts an effect when EGCG attenuates IBD. Results: We first explored the effect of oral or rectal EGCG delivery on the DSS-induced murine colitis. Our results revealed that anti-inflammatory effect and colonic barrier integrity were enhanced by oral, but not rectal, EGCG. We observed a distinct EGCG-mediated alteration in the gut microbiome by increasing Akkermansia abundance and butyrate production. Next, we demonstrated that the EGCG pre-supplementation induced similar beneficial outcomes to oral EGCG administration. Prophylactic EGCG attenuated colitis and significantly enriched short-chain fatty acids (SCFAs)-producing bacteria such as Akkermansia and SCFAs production in DSS-induced mice. To validate these discoveries, we performed fecal microbiota transplantation (FMT) and sterile fecal filtrate (SFF) to inoculate DSS-treated mice. Microbiota from EGCG-dosed mice alleviated the colitis over microbiota from control mice and SFF shown by superiorly anti-inflammatory effect and colonic barrier integrity, and also enriched bacteria such as Akkermansia and SCFAs. Collectively, the attenuation of colitis by oral EGCG suggests an intimate involvement of SCFAs-producing bacteria Akkermansia, and SCFAs, which was further demonstrated by prophylaxis and FMT. Conclusions: This study provides the first data indicating that oral EGCG ameliorated the colonic inflammation in a gut microbiota-dependent manner. Our findings provide novel insights into EGCG-mediated remission of IBD and EGCG as a potential modulator for gut microbiota to prevent and treat IBD.
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页数:22
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