高脂肪饮食会损害微生物代谢物的产生,加重甲型流感感染。

IF 8.2 2区 生物学 Q1 CELL BIOLOGY
Franziska Hornung, Harini K SureshKumar, Laura Klement, Yasmina Reisser, Christoph Wernike, Vivien Nischang, Paul M Jordan, Oliver Werz, Carsten Hoffmann, Bettina Löffler, Stefanie Deinhardt-Emmer
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引用次数: 0

摘要

背景:肠道微生物群的改变可以显著影响人体的各个区域,包括肺部。本研究调查了高脂肪饮食(HFD)期间肠道微生物组的变化,特别是短链脂肪酸(SCFAs),以及这些代谢物如何影响甲型流感病毒(IAV)引起的肺部感染。方法:我们使用hfd小鼠模型来评估IAV感染后肠道微生物群组成、SCFA水平和肺部预后。通过分类和功能分析分析微生物变化,并测量非肥胖和肥胖血清供者的SCFA水平。最后,在人精确肺切片(PCLS)和体外肺上皮细胞中测试了乙酸盐的体外作用。机制研究探讨了SCFA受体游离脂肪酸受体2 (FFAR2)和细胞内抗病毒途径的参与。结果:我们的数据表明,肠道微生物群中厚壁菌门/拟杆菌门比例增加,碳水化合物代谢改变,导致短链脂肪酸产量减少。感染的HFD小鼠显示IAV滴度增加和持续的微生物改变。有趣的是,醋酸盐在人PCLS模型和病毒复制减少的肺细胞中都显示出抗病毒作用。这些作用依赖于FFAR2,它也作为IAV共受体,在我们的体外数据中,醋酸处理导致FFAR2内化并影响宿主细胞代谢。结论:HFD改变了SCFA的产生,降低了肠道微生物群中的醋酸水平。这种减少可能导致感染IAV的HFD小鼠的病毒载量升高和疾病恶化。我们的研究结果表明,醋酸盐在人离体肺模型和肺上皮细胞感染IAV期间具有抗病毒作用。在这里,醋酸酯阻止病毒进入并影响细胞代谢状态和抗病毒反应。了解这些机制可以为预防和治疗有饮食相关健康问题的人的病毒感染提供新的目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-fat diet impairs microbial metabolite production and aggravates influenza A infection.

High-fat diet impairs microbial metabolite production and aggravates influenza A infection.

High-fat diet impairs microbial metabolite production and aggravates influenza A infection.

High-fat diet impairs microbial metabolite production and aggravates influenza A infection.

Background: Alterations in the gut microbiom can significantly impact various regions in the human body, including the pulmonary tract. This study investigates alterations in the gut microbiome during a high-fat diet (HFD), particularly short-chain fatty acids (SCFAs), and how these metabolites affect lung infection caused by Influenza A virus (IAV).

Methods: We used a HFD-mouse model to evaluate gut microbiota composition, SCFA levels, and pulmonary outcomes following IAV infection. Microbial changes were analyzed via taxonomic and functional profiling and SCFA levels were measured from non-obese and obese serum donors. Ultimately, acetate's effects were tested ex vivo in human precision-cut lung slices (PCLS) and in vitro in pulmonary epithelial cells. Mechanistic studies investigated the involvement of the SCFA receptor free fatty acid receptor 2 (FFAR2) and intracellular antiviral pathways.

Results: Our data indicates an increased Firmicutes/Bacteroidetes ratio of the gut microbiome and an altered carbohydrate metabolism, leading to reduced SCFA production. Infected HFD mice showed increased IAV titers and sustained microbial alterations. Interestingly, acetate demonstrated antiviral effects in both the human PCLS model and pulmonary cells with an reduced viral replication. These effects depended on FFAR2, which also acts as an IAV co-receptor, as acetate treatment led to FFAR2 internalization and influenced host cell metabolism in our in vitro data.

Conclusion: HFD alters the SCFA production, reducing acetate levels in the gut microbiome. This reduction may lead to higher viral loads and worsened disease in HFD mice infected with IAV. Our findings indicate that acetate has antiviral effects during IAV infection in both a human ex vivo lung model and pulmonary epithelial cells. Here, acetate prevents viral entry and affects the cellular metabolic state and antiviral response. Understanding these mechanisms could provide new targets for preventing and treating viral infections in individuals with diet-related health issues.

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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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