Yang Jinlong, Wang Haoyu, Lin Xiaoqian, Liu Jincen, Feng Yue, Bai Yuyin, Liang Hewei, Hu Tongyuan, Wu Zhinan, Lai Jianghua, Liu Jianmei, Zou Yuanqiang, Wei Shuguang, Yan Peng
College of Forensic Science, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
BGI Research, Kunming, China.
mSystems. 2024 Dec 17;9(12):e0136624. doi: 10.1128/msystems.01366-24. Epub 2024 Nov 27.
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. (cluster_56) and (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.
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 , and increase harmful bacteria such as . 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 , 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.
酒精摄入会引发多种疾病,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。酒精暴露后肠道微生物群会发生显著变化。未成年人和年轻人的酒精消费量往往会增加,但青春期肠道微生物群的特征在很大程度上仍未得到探索。在本研究中,我们构建了酒精暴露的青春期和成年小鼠模型,以研究肠道损伤和肠道微生物群的变化。有趣的是,青春期小鼠和成年小鼠在酒精暴露后的反应有所不同。我们发现青春期小鼠肝脏中的乙醇脱氢酶减少,而乙醛脱氢酶增加,从而减少了有毒乙醛的积累。此外,酒精暴露对青春期小鼠造成的肠道损伤较小。通过宏基因组组装基因组分析,我们获得了许多未被识别的细菌基因组。(簇56)和(簇57)是从青春期小鼠的样本中组装出来的,它们参与了吲哚乙酸的产生以及对酒精暴露的胆汁酸转化。本研究为研究肠道微生物群的变化提供了新的见解,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。
本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,突出了青少年和成年阶段之间的不同反应。研究发现酒精暴露会损害肠道屏障,通过减少有益细菌(如 )来改变微生物组成,并增加有害细菌(如 )。该研究还发现了青春期小鼠独特的微生物变化和恢复力。物种水平的宏基因组分析揭示了受酒精影响的特定微生物分类群和代谢功能。宏基因组组装基因组(MAGs)发现了许多无法通过传统方法注释的物种,包括许多 成员,极大地扩展了我们对肠道微生物群组成的理解。这些发现强调了进一步研究酒精对各个器官的影响以及微生物代谢产物对疾病进展的影响的必要性。