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肥胖重塑小鼠肠道-肝脏-肺轴沿线的微生物种群结构。

Obesity Reshapes the Microbial Population Structure along the Gut-Liver-Lung Axis in Mice.

作者信息

Galaris Apostolos, Fanidis Dionysios, Stylianaki Elli-Anna, Harokopos Vaggelis, Kalantzi Alexandra-Styliani, Moulos Panagiotis, Dimas Antigone S, Hatzis Pantelis, Aidinis Vassilis

机构信息

Institute of Bioinnovation, Biomedical Sciences Research Center Alexander Fleming, 16672 Athens, Greece.

Institute for Fundamental Biomedical Research, Biomedical Sciences Research Center Alexander Fleming, 16672 Athens, Greece.

出版信息

Biomedicines. 2022 Feb 19;10(2):494. doi: 10.3390/biomedicines10020494.

Abstract

The microbiome is emerging as a major player in tissue homeostasis in health and disease. Gut microbiome dysbiosis correlates with several autoimmune and metabolic diseases, while high-fat diets and ensuing obesity are known to affect the complexity and diversity of the microbiome, thus modulating pathophysiology. Moreover, the existence of a gut-liver microbial axis has been proposed, which may extend to the lung. In this context, we systematically compared the microbiomes of the gut, liver, and lung of mice fed a high-fat diet to those of littermates fed a matched control diet. We carried out deep sequencing of seven hypervariable regions of the 16S rRNA microbial gene to examine microbial diversity in the tissues of interest. Comparison of the local microbiomes indicated that lung tissue has the least diverse microbiome under healthy conditions, while microbial diversity in the healthy liver clustered closer to the gut. Obesity increased microbial complexity in all three tissues, with lung microbial diversity being the most modified. Obesity promoted the expansion of Firmicutes along the gut-liver-lung axis, highlighting staphylococcus as a possible pathologic link between obesity and systemic pathophysiology, especially in the lungs.

摘要

微生物群正在成为健康和疾病状态下组织稳态的主要参与者。肠道微生物群失调与多种自身免疫性疾病和代谢性疾病相关,而高脂饮食及随之而来的肥胖已知会影响微生物群的复杂性和多样性,进而调节病理生理学过程。此外,有人提出存在肠-肝微生物轴,这一轴可能延伸至肺部。在此背景下,我们系统地比较了高脂饮食喂养的小鼠与喂食匹配对照饮食的同窝小鼠的肠道、肝脏和肺部微生物群。我们对16S rRNA微生物基因的七个高变区进行了深度测序,以检测目标组织中的微生物多样性。局部微生物群的比较表明,在健康条件下,肺组织的微生物群多样性最低,而健康肝脏中的微生物多样性聚类更接近肠道。肥胖增加了所有三个组织中的微生物复杂性,其中肺部微生物多样性变化最大。肥胖促进了厚壁菌门沿肠-肝-肺轴的扩张,突出了葡萄球菌作为肥胖与全身病理生理学之间可能的病理联系,尤其是在肺部。

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