太空飞行会改变宿主-肠道微生物群的相互作用

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
E Gonzalez, M D Lee, B T Tierney, N Lipieta, P Flores, M Mishra, L Beckett, A Finkelstein, A Mo, P Walton, F Karouia, R Barker, R J Jansen, S J Green, S Weging, J Kelliher, N K Singh, D Bezdan, J Galazska, N J B Brereton
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引用次数: 0

摘要

国际空间站啮齿动物栖息地为了解太空飞行对哺乳动物的影响提供了重要信息,这些啮齿动物会诱发肝病、胰岛素抵抗、骨质疏松和肌病等症状。虽然这些生理反应可能涉及地球上的微生物群,但太空飞行期间宿主与微生物群之间的相互作用仍有待阐明。我们利用多组学技术探索了小鼠在太空飞行 29 天和 56 天后的肠道微生物群以及结肠和肝脏中宿主基因的表达。元基因组学揭示了 44 种微生物群的显著变化,包括胆汁酸和丁酸代谢菌(如 Extibacter muris 和 Dysosmobacter welbionis)的相对减少。功能预测表明,脂肪酸和胆汁酸代谢、细胞外基质相互作用和抗生素耐药性基因的代表性过高。宿主基因表达描述了胆汁酸和能量代谢以及免疫抑制的相应变化。这些变化意味着宿主-肠道微生物组界面的相互作用导致了太空飞行病理学,这些相互作用可能会严重影响人类健康和长期太空飞行的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spaceflight alters host-gut microbiota interactions.

Spaceflight alters host-gut microbiota interactions.

The ISS rodent habitat has provided crucial insights into the impact of spaceflight on mammals, inducing symptoms characteristic of liver disease, insulin resistance, osteopenia, and myopathy. Although these physiological responses can involve the microbiome on Earth, host-microbiota interactions during spaceflight are still being elucidated. We explore murine gut microbiota and host gene expression in the colon and liver after 29 and 56 days of spaceflight using multiomics. Metagenomics revealed significant changes in 44 microbiome species, including relative reductions in bile acid and butyrate metabolising bacteria like Extibacter muris and Dysosmobacter welbionis. Functional prediction indicate over-representation of fatty acid and bile acid metabolism, extracellular matrix interactions, and antibiotic resistance genes. Host gene expression described corresponding changes to bile acid and energy metabolism, and immune suppression. These changes imply that interactions at the host-gut microbiome interface contribute to spaceflight pathology and that these interactions might critically influence human health and long-duration spaceflight feasibility.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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