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本文引用的文献

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Antiviral Res. 2018 Jan;149:58-74. doi: 10.1016/j.antiviral.2017.11.001. Epub 2017 Nov 8.
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Seneca Valley Virus Suppresses Host Type I Interferon Production by Targeting Adaptor Proteins MAVS, TRIF, and TANK for Cleavage.塞内卡谷病毒通过靶向衔接蛋白MAVS、TRIF和TANK进行切割来抑制宿主I型干扰素的产生。
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Encephalomyocarditis virus 3C protease attenuates type I interferon production through disrupting the TANK-TBK1-IKKε-IRF3 complex.脑心肌炎病毒3C蛋白酶通过破坏TANK-TBK1-IKKε-IRF3复合物来减弱I型干扰素的产生。
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Broad-spectrum agents for flaviviral infections: dengue, Zika and beyond.用于黄病毒感染的广谱药物:登革热、寨卡病毒及其他。
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Enterovirus 71 suppresses interferon responses by blocking Janus kinase (JAK)/signal transducer and activator of transcription (STAT) signaling through inducing karyopherin-α1 degradation.肠道病毒71型通过诱导核转运蛋白α1降解来阻断Janus激酶(JAK)/信号转导子和转录激活子(STAT)信号通路,从而抑制干扰素反应。
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Changes to taxonomy and the International Code of Virus Classification and Nomenclature ratified by the International Committee on Taxonomy of Viruses (2017).病毒分类学的变化以及由国际病毒分类委员会批准的《国际病毒分类和命名法典》(2017年)。
Arch Virol. 2017 Aug;162(8):2505-2538. doi: 10.1007/s00705-017-3358-5. Epub 2017 Apr 22.
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Disruption of MDA5-Mediated Innate Immune Responses by the 3C Proteins of Coxsackievirus A16, Coxsackievirus A6, and Enterovirus D68.柯萨奇病毒A16、柯萨奇病毒A6和肠道病毒D68的3C蛋白对MDA5介导的固有免疫反应的破坏
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Importin β1 targeting by hepatitis C virus NS3/4A protein restricts IRF3 and NF-κB signaling of IFNB1 antiviral response.丙型肝炎病毒NS3/4A蛋白靶向输入蛋白β1会限制IFNB1抗病毒反应的IRF3和NF-κB信号传导。
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Porcine Deltacoronavirus nsp5 Antagonizes Type I Interferon Signaling by Cleaving STAT2.猪德尔塔冠状病毒nsp5通过切割信号转导和转录激活因子2(STAT2)来拮抗I型干扰素信号传导。
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对抗宿主先天免疫的RNA病毒蛋白酶

RNA-virus proteases counteracting host innate immunity.

作者信息

Lei Jian, Hilgenfeld Rolf

机构信息

Institute of Biochemistry, Center for Structural and Cell Biology in Medicine, University of Lübeck, Germany.

German Center for Infection Research (DZIF), Hamburg - Lübeck - Borstel - Riems Site, University of Lübeck, Germany.

出版信息

FEBS Lett. 2017 Oct;591(20):3190-3210. doi: 10.1002/1873-3468.12827. Epub 2017 Sep 15.

DOI:10.1002/1873-3468.12827
PMID:28850669
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7163997/
Abstract

Virus invasion triggers host immune responses, in particular, innate immune responses. Pathogen-associated molecular patterns of viruses (such as dsRNA, ssRNA, or viral proteins) released during virus replication are detected by the corresponding pattern-recognition receptors of the host, and innate immune responses are induced. Through production of type-I and type-III interferons as well as various other cytokines, the host innate immune system forms the frontline to protect host cells and inhibit virus infection. Not surprisingly, viruses have evolved diverse strategies to counter this antiviral system. In this review, we discuss the multiple strategies used by proteases of positive-sense single-stranded RNA viruses of the families Picornaviridae, Coronaviridae, and Flaviviridae, when counteracting host innate immune responses.

摘要

病毒入侵会触发宿主的免疫反应,尤其是先天免疫反应。病毒复制过程中释放的病毒病原体相关分子模式(如双链RNA、单链RNA或病毒蛋白)会被宿主相应的模式识别受体检测到,从而诱导先天免疫反应。宿主先天免疫系统通过产生I型和III型干扰素以及各种其他细胞因子,形成保护宿主细胞和抑制病毒感染的第一道防线。毫不奇怪,病毒已经进化出多种策略来对抗这种抗病毒系统。在这篇综述中,我们讨论了小RNA病毒科、冠状病毒科和黄病毒科的正链单链RNA病毒的蛋白酶在对抗宿主先天免疫反应时所使用的多种策略。