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Influenza Virus Affects Intestinal Microbiota and Secondary Salmonella Infection in the Gut through Type I Interferons

机译:流感病毒通过I型干扰素影响肠道肠道菌群和肠道沙门氏菌继发感染。

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摘要

Human influenza viruses replicate almost exclusively in the respiratory tract, yet infected individuals may also develop gastrointestinal symptoms, such as vomiting and diarrhea. However, the molecular mechanisms remain incompletely defined. Using an influenza mouse model, we found that influenza pulmonary infection can significantly alter the intestinal microbiota profile through a mechanism dependent on type I interferons (IFN-Is). Notably, influenza-induced IFN-Is produced in the lungs promote the depletion of obligate anaerobic bacteria and the enrichment of Proteobacteria in the gut, leading to a “dysbiotic” microenvironment. Additionally, we provide evidence that IFN-Is induced in the lungs during influenza pulmonary infection inhibit the antimicrobial and inflammatory responses in the gut during Salmonella-induced colitis, further enhancing Salmonella intestinal colonization and systemic dissemination. Thus, our studies demonstrate a systemic role for IFN-Is in regulating the host immune response in the gut during Salmonella-induced colitis and in altering the intestinal microbial balance after influenza infection.
机译:人类流感病毒几乎只能在呼吸道中复制,但受感染的人也可能会出现胃肠道症状,例如呕吐和腹泻。但是,分子机制仍未完全确定。使用流感小鼠模型,我们发现流感肺部感染可以通过依赖于I型干扰素(IFN-Is)的机制显着改变肠道菌群特征。值得注意的是,在肺中产生的流感诱导的IFN-γ促进了专性厌氧细菌的枯竭和肠道中变形杆菌的富集,从而导致了“不良生物”微环境。此外,我们提供的证据表明,在流感肺部感染期间在肺中诱导的IFN-Is抑制了沙门氏菌引起的结肠炎期间肠道中的抗菌和炎症反应,从而进一步增强了沙门氏菌在肠道的定植和全身性传播。因此,我们的研究表明,IFN-γ在调节沙门氏菌诱发的结肠炎期间肠道中的宿主免疫反应以及在流感感染后改变肠道微生物平衡方面具有系统性作用。

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