Effects of moderate, voluntary ethanol consumption on the rat and human gut microbiome

失调 微生物群 肠道菌群 生物 基因组 粪便 人体微生物群 生理学 人类微生物组计划 微生物学 动物 生物信息学 遗传学 免疫学 基因
作者
Kassi L. Kosnicki,Jerrold C. Penprase,Patricia Cintora,Pedro J. Torres,Greg L. Harris,Susan M. Brasser,Scott T. Kelley
出处
期刊:Addiction Biology [Wiley]
卷期号:24 (4): 617-630 被引量:40
标识
DOI:10.1111/adb.12626
摘要

Abstract Many alcohol‐induced health complications are directly attributable to the toxicity of alcohol or its metabolites, but another potential health impact of alcohol may be on the microbial communities of the human gut. Clear distinctions between healthy and diseased‐state gut microbiota have been observed in subjects with metabolic diseases, and recent studies suggest that chronic alcoholism is linked to gut microbiome dysbiosis. Here, we investigated the effects of moderate levels of alcohol consumption on the gut microbiome in both rats and humans. The gut microbiota of rats voluntarily consuming a 20 percent ethanol solution, on alternate days, were compared with a non‐exposed control group to identify differential taxonomic and functional profiles. Gut microbial diversity profiles were determined using culture‐independent amplification, next‐generation sequencing and bioinformatic analysis of bacterial 16S ribosomal RNA gene sequence libraries. Our results showed that, compared with controls, ethanol‐consuming rats experienced a significant decline in the biodiversity of their gut microbiomes, a state generally associated with dysbiosis. We also observed significant shifts in the overall diversity of the gut microbial communities and a dramatic change in the relative abundance of particular microbes, such as the Lactobacilli . We also compared our results to human fecal microbiome data collected as part of the citizen science American Gut Project. In contrast to the rat data, human drinkers had significantly higher gut microbial biodiversity than non‐drinkers. However, we also observed that microbes that differed among the human subjects displayed similar trends in the rat model, including bacteria implicated in metabolic disease.
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