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Cell. 2023 Jan 19;186(2):287-304.e26. doi: 10.1016/j.cell.2022.12.017. Epub 2023 Jan 6.
2
Bile acids and the gut microbiota: metabolic interactions and impacts on disease.胆汁酸与肠道微生物群:代谢相互作用及其对疾病的影响。
Nat Rev Microbiol. 2023 Apr;21(4):236-247. doi: 10.1038/s41579-022-00805-x. Epub 2022 Oct 17.
3
Phage delivered CRISPR-Cas system to combat multidrug-resistant pathogens in gut microbiome.噬菌体递送 CRISPR-Cas 系统以对抗肠道微生物组中的多药耐药病原体。
Biomed Pharmacother. 2022 Jul;151:113122. doi: 10.1016/j.biopha.2022.113122. Epub 2022 May 17.
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The gut microbiome as a modulator of healthy ageing.肠道微生物组作为健康衰老的调节剂。
Nat Rev Gastroenterol Hepatol. 2022 Sep;19(9):565-584. doi: 10.1038/s41575-022-00605-x. Epub 2022 Apr 25.
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Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort.宿主遗传学和饮食对单个人群队列中人类肠道微生物群和疾病发病的综合影响。
Nat Genet. 2022 Feb;54(2):134-142. doi: 10.1038/s41588-021-00991-z. Epub 2022 Feb 3.
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Phage-delivered CRISPR-Cas9 for strain-specific depletion and genomic deletions in the gut microbiome.噬菌体递送 CRISPR-Cas9 用于肠道微生物组中特定菌株的耗竭和基因组缺失。
Cell Rep. 2021 Nov 2;37(5):109930. doi: 10.1016/j.celrep.2021.109930.
7
The microbiome extends host evolutionary potential.微生物组扩展了宿主的进化潜力。
Nat Commun. 2021 Aug 26;12(1):5141. doi: 10.1038/s41467-021-25315-x.
8
Response of the microbiome-gut-brain axis in Drosophila to amino acid deficit.果蝇中微生物群-肠道-大脑轴对氨基酸缺乏的反应。
Nature. 2021 May;593(7860):570-574. doi: 10.1038/s41586-021-03522-2. Epub 2021 May 5.
9
Association Between Gut Microbiome and Frailty in the Older Adult Population in Korea.韩国老年人群体中肠道微生物组与虚弱的关联。
J Gerontol A Biol Sci Med Sci. 2021 Jul 13;76(8):1362-1368. doi: 10.1093/gerona/glaa319.
10
CRISPR RNA-guided integrases for high-efficiency, multiplexed bacterial genome engineering.CRISPR RNA 引导的整合酶用于高效、多重的细菌基因组工程。
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肠道微生物遗传变异调节宿主寿命、睡眠和运动表现。

Gut microbial genetic variation modulates host lifespan, sleep, and motor performance.

机构信息

Medical Technology College, Xuzhou Medical University, Xuzhou, China.

Department of Biological Sciences, Faculty of Science, National University of Singapore, Singapore, 117543, Singapore.

出版信息

ISME J. 2023 Oct;17(10):1733-1740. doi: 10.1038/s41396-023-01478-x. Epub 2023 Aug 7.

DOI:10.1038/s41396-023-01478-x
PMID:37550381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10504343/
Abstract

Recent studies have shown that gut microorganisms can modulate host lifespan and activities, including sleep quality and motor performance. However, the role of gut microbial genetic variation in regulating host phenotypes remains unclear. In this study, we investigated the links between gut microbial genetic variation and host phenotypes using Saccharomyces cerevisiae and Drosophila melanogaster as research models. Our result suggested a novel role for peroxisome-related genes in yeast in regulating host lifespan and activities by modulating gut oxidative stress. Specifically, we found that deficiency in catalase A (CTA1) in yeast reduced both the sleep duration and lifespan of fruit flies significantly. Furthermore, our research also expanded our understanding of the relationship between sleep and longevity. Using a large sample size and excluding individual genetic background differences, we found that lifespan is associated with sleep duration, but not sleep fragmentation or motor performance. Overall, our study provides novel insights into the role of gut microbial genetic variation in regulating host phenotypes and offers potential new avenues for improving health and longevity.

摘要

最近的研究表明,肠道微生物可以调节宿主的寿命和活动,包括睡眠质量和运动性能。然而,肠道微生物遗传变异在调节宿主表型中的作用尚不清楚。在这项研究中,我们使用酿酒酵母和黑腹果蝇作为研究模型,研究了肠道微生物遗传变异与宿主表型之间的联系。我们的结果表明,过氧化物酶体相关基因在酵母中通过调节肠道氧化应激来调节宿主寿命和活动方面发挥着新的作用。具体来说,我们发现酵母中过氧化氢酶 A(CTA1)的缺乏显著降低了果蝇的睡眠时间和寿命。此外,我们的研究还扩展了我们对睡眠与长寿之间关系的理解。使用大样本量并排除个体遗传背景差异,我们发现寿命与睡眠时间有关,但与睡眠片段化或运动性能无关。总的来说,我们的研究为肠道微生物遗传变异在调节宿主表型中的作用提供了新的见解,并为改善健康和长寿提供了潜在的新途径。