针对丝状病毒感染的抗病毒防御:靶点与逃逸机制
Antiviral defense against filovirus infections: targets and evasion mechanisms.
作者信息
Bodmer Bianca S, Wendt Lisa, Dupré Juliette, Groseth Allison, Hoenen Thomas
机构信息
Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Greifswald, Insel Riems, Germany.
Institute of Medical Virology, University Hospital Frankfurt, Goethe University Frankfurt, Frankfurt (Main), Germany.
出版信息
Future Microbiol. 2025 May-Jun;20(7-9):573-587. doi: 10.1080/17460913.2025.2501924. Epub 2025 May 7.
Filoviruses include a number of serious human pathogens, infections with which result in the development of hemorrhagic fevers with high case fatality rates. As for other RNA viruses, viral replication generates both protein and RNA species that can serve as danger signals, leading to the activation of antiviral defense pathways. However, in order to be able to efficiently infect humans these viruses have developed mechanisms that allow them to evade diverse host antiviral defense mechanisms. Consequently, in addition to their functions within the viral lifecycle many filovirus proteins have been shown to have accessory functions involved in the regulation of diverse host pathways. These include those of the type-I interferon response, other pathways involved in dsRNA-sensing, as well as the selective inhibition of interferon stimulated gene activities. Further, filoviruses have developed mechanisms to subvert recognition of infected cells and the generation of neutralizing antibodies. This review focuses on bringing together the evidence to date supporting the existence of diverse mechanisms aimed at regulating these pathways as well as providing details of the mechanisms involved.
丝状病毒包括一些严重的人类病原体,感染这些病原体会导致高病死率的出血热。与其他RNA病毒一样,病毒复制会产生可作为危险信号的蛋白质和RNA种类,从而导致抗病毒防御途径的激活。然而,为了能够有效感染人类,这些病毒已经进化出一些机制,使其能够逃避宿主的多种抗病毒防御机制。因此,除了在病毒生命周期中的功能外,许多丝状病毒蛋白还具有参与调节多种宿主途径的辅助功能。这些功能包括I型干扰素反应、参与双链RNA感应的其他途径,以及对干扰素刺激基因活性的选择性抑制。此外,丝状病毒还进化出了一些机制来颠覆对受感染细胞的识别和中和抗体的产生。本综述着重汇集迄今支持存在多种旨在调节这些途径的机制的证据,并详细介绍其中涉及的机制。
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