Gut microbiota dysbiosis induced by alcohol exposure in pubertal and adult mice.

IF 5 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2024-12-17 Epub Date: 2024-11-27 DOI:10.1128/msystems.01366-24
Jinlong Yang, Haoyu Wang, Xiaoqian Lin, Jincen Liu, Yue Feng, Yuyin Bai, Hewei Liang, Tongyuan Hu, Zhinan Wu, Jianghua Lai, Jianmei Liu, Yuanqiang Zou, Shuguang Wei, Peng Yan
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Abstract

Alcohol intake causes many diseases including neuropsychiatric symptoms, nutritional deficiency, progressive pancreatitis, liver cirrhosis, and ischemic heart disease. The gut microbiota changes significantly after alcohol exposure. Alcohol consumption tends to increase in underage and young people, but the feature of the gut microbiota in puberty remains largely unexplored. In this study, we conducted alcohol-exposed pubertal and adult mice model to investigate the intestinal damage and gut microbiota change. Interestingly, the responses of pubertal mice and adult mice after alcohol exposure were different. We found that alcohol dehydrogenase decreased and aldehyde dehydrogenase increased in the liver of pubertal mice, thus reducing the accumulation of toxic acetaldehyde. Furthermore, alcohol exposure caused less intestinal injury in pubertal mice. Through the analysis of metagenome assembly genome, we obtained many unrecognized bacterial genomes. Limosillactobacillus reuteri (cluster_56) and Lactobacillus intestinalis (cluster_57) were assembled from the samples of pubertal mice, which were involved in the production of indole acetic acid and the transformation of bile acids in response to alcohol exposure. This study provided a new insight to investigate the gut microbiota change and explained the difference of the gut microbiota after alcohol exposure between pubertal mice and adult mice.

Importance: This study elucidates the significant impact of alcohol exposure on the gut microbiota and metabolic pathways in mice, highlighting the differential responses between adolescent and adult stages. Alcohol exposure was found to damage the intestinal barrier, alter the microbial composition by decreasing beneficial bacteria like Lactobacillus, and increase harmful bacteria such as Alistipes. The study also discovered unique microbial changes and resilience in pubertal mice. Species-level metagenomic analysis revealed specific microbial taxa and metabolic functions affected by alcohol. Metagenome-assembled genomes (MAGs) found many species that could not be annotated by conventional methods including many members of Lachnospiraceae, greatly expanding our understanding of the gut microbiota composition. These findings underscore the need for further research on alcohol's effects on various organs and the implications of microbial metabolites on disease progression.

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酒精暴露诱发青春期和成年小鼠肠道微生物菌群失调。
酒精摄入会导致多种疾病,包括神经精神症状、营养缺乏、进行性胰腺炎、肝硬化和缺血性心脏病。接触酒精后,肠道微生物群会发生明显变化。未成年和青少年的饮酒量呈上升趋势,但青春期肠道微生物群的特征在很大程度上仍未得到研究。在这项研究中,我们建立了暴露于酒精的青春期小鼠和成年小鼠模型,以研究肠道损伤和肠道微生物群的变化。有趣的是,酒精暴露后,青春期小鼠和成年小鼠的反应不同。我们发现,青春期小鼠肝脏中的乙醇脱氢酶减少,而醛脱氢酶增加,从而减少了有毒乙醛的积累。此外,酒精暴露对青春期小鼠肠道造成的损伤较小。通过分析元基因组组装基因组,我们获得了许多未被识别的细菌基因组。从青春期小鼠的样本中组装出了Limosillacillus reuteri(cluster_56)和Lactobacillus intestinalis(cluster_57),它们参与了酒精暴露下吲哚乙酸的产生和胆汁酸的转化。这项研究为研究肠道微生物群的变化提供了新的视角,并解释了青春期小鼠和成年小鼠在酒精暴露后肠道微生物群的差异:这项研究阐明了酒精暴露对小鼠肠道微生物群和代谢途径的重大影响,突出了青春期小鼠和成年小鼠之间的不同反应。研究发现,暴露于酒精会破坏肠道屏障,改变微生物组成,减少乳酸杆菌等有益细菌,增加阿利斯蒂普斯等有害细菌。研究还发现了青春期小鼠独特的微生物变化和恢复能力。物种级元基因组分析揭示了受酒精影响的特定微生物类群和代谢功能。元基因组组装基因组(MAGs)发现了许多无法用传统方法注释的物种,其中包括许多拉赫诺斯皮拉科(Lachnospiraceae)成员,这大大扩展了我们对肠道微生物群组成的了解。这些发现强调了进一步研究酒精对各种器官的影响以及微生物代谢物对疾病进展的影响的必要性。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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