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Recovery of ethanol-induced Akkermansia muciniphila depletion ameliorates alcoholic liver disease

某种肠道细菌 医学 势垒函数 内科学 微生物学 酒精性肝病 生物 化学 胃肠病学 肠道菌群 内分泌学 免疫学 肝硬化 细胞生物学
作者
Christoph Grander,Timon E. Adolph,Verena Wieser,Patrick Lowe,Laura Wrzosek,Benedek Gyöngyösi,Doyle V. Ward,Felix Grabherr,Romana R. Gerner,Alexandra Pfister,Barbara Enrich,Dragos Ciocan,S Macheiner,Lisa Mayr,Matthias Drach,Patrizia Moser,Alexander R. Moschen,Gabriel Perlemuter,Gyöngyi Szabó,Anne‐Marie Cassard
出处
期刊:Gut [BMJ]
卷期号:67 (5): 891-901 被引量:527
标识
DOI:10.1136/gutjnl-2016-313432
摘要

Objective Alcoholic liver disease (ALD) is a global health problem with limited therapeutic options. Intestinal barrier integrity and the microbiota modulate susceptibility to ALD. Akkermansia muciniphila , a Gram-negative intestinal commensal, promotes barrier function partly by enhancing mucus production. The aim of this study was to investigate microbial alterations in ALD and to define the impact of A. muciniphila administration on the course of ALD. Design The intestinal microbiota was analysed in an unbiased approach by 16S ribosomal DNA (rDNA) sequencing in a Lieber-DeCarli ALD mouse model, and faecal A. muciniphila abundance was determined in a cohort of patients with alcoholic steatohepatitis (ASH). The impact of A. muciniphila on the development of experimental acute and chronic ALD was determined in a preventive and therapeutic setting, and intestinal barrier integrity was analysed. Results Patients with ASH exhibited a decreased abundance of faecal A. muciniphila when compared with healthy controls that indirectly correlated with hepatic disease severity. Ethanol feeding of wild-type mice resulted in a prominent decline in A. muciniphila abundance. Ethanol-induced intestinal A. muciniphila depletion could be restored by oral A. muciniphila supplementation. Furthermore, A. muciniphila administration when performed in a preventive setting decreased hepatic injury, steatosis and neutrophil infiltration. A. muciniphila also protected against ethanol-induced gut leakiness, enhanced mucus thickness and tight-junction expression. In already established ALD, A. muciniphila used therapeutically ameliorated hepatic injury and neutrophil infiltration. Conclusion Ethanol exposure diminishes intestinal A. muciniphila abundance in both mice and humans and can be recovered in experimental ALD by oral supplementation. A. muciniphila promotes intestinal barrier integrity and ameliorates experimental ALD. Our data suggest that patients with ALD might benefit from A. muciniphila supplementation.
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