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病毒感染触发巨噬细胞诱导干扰素产生,从而将活的新型隐球菌排出。

Viral infection triggers interferon-induced expulsion of live Cryptococcus neoformans by macrophages.

机构信息

Institute of Microbiology & Infection and School of Biosciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom.

Division of Infection and Immunity, University College London, London, United Kingdom.

出版信息

PLoS Pathog. 2020 Feb 27;16(2):e1008240. doi: 10.1371/journal.ppat.1008240. eCollection 2020 Feb.

Abstract

Cryptococcus neoformans is an opportunistic human pathogen, which causes serious disease in immunocompromised hosts. Infection with this pathogen is particularly relevant in HIV+ patients, where it leads to around 200,000 deaths per annum. A key feature of cryptococcal pathogenesis is the ability of the fungus to survive and replicate within the phagosome of macrophages, as well as its ability to be expelled from host cells via a novel non-lytic mechanism known as vomocytosis. Here we show that cryptococcal vomocytosis from macrophages is strongly enhanced by viral coinfection, without altering phagocytosis or intracellular proliferation of the fungus. This effect occurs with distinct, unrelated human viral pathogens and is recapitulated when macrophages are stimulated with the anti-viral cytokines interferon alpha or beta (IFNα or IFNβ). Importantly, the effect is abrogated when type-I interferon signalling is blocked, thus underscoring the importance of type-I interferons in this phenomenon. Lastly, our data help resolve previous, contradictory animal studies on the impact of type I interferons on cryptococcal pathogenesis and suggest that secondary viral stimuli may alter patterns of cryptococcal dissemination in the host.

摘要

新生隐球菌是一种机会性人类病原体,可导致免疫功能低下宿主发生严重疾病。该病原体感染在 HIV+ 患者中尤为相关,每年导致约 20 万人死亡。隐球菌病发病机制的一个关键特征是真菌在巨噬细胞的吞噬体中存活和复制的能力,以及通过一种称为胞吐作用的新型非溶细胞机制从宿主细胞中排出的能力。在这里,我们表明,病毒共感染强烈增强了巨噬细胞中新生隐球菌的胞吐作用,而不改变真菌的吞噬作用或细胞内增殖。这种效应发生在不同的、不相关的人类病毒病原体中,并且当巨噬细胞被抗病毒细胞因子干扰素-α或-β(IFNα 或 IFNβ)刺激时也会重现。重要的是,当阻断 I 型干扰素信号时,该效应被消除,从而强调了 I 型干扰素在这一现象中的重要性。最后,我们的数据有助于解决先前关于 I 型干扰素对新生隐球菌病发病机制影响的动物研究中的矛盾,并表明继发性病毒刺激可能改变宿主中新生隐球菌传播的模式。

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