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丝状病毒进入细胞的机制——新的认识。

Filovirus entry into cells - new insights.

机构信息

Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, United States.

出版信息

Curr Opin Virol. 2012 Apr;2(2):206-14. doi: 10.1016/j.coviro.2012.02.015. Epub 2012 Mar 23.

DOI:10.1016/j.coviro.2012.02.015
PMID:22445965
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3322298/
Abstract

Filoviruses are hemorrhagic fever-causing agents that produce enveloped virions with a filamentous morphology. The viral surface glycoprotein, GP, orchestrates the surprisingly complex process by which filoviruses gain access to the cytoplasm of their host cells. GP mediates viral attachment to cells through multiple, redundant interactions with cell-surface factors. GP then induces virion internalization by a process that resembles cellular macropinocytosis. Within the endo/lysosomal pathway, GP undergoes a series of structural rearrangements, controlled by interactions with host factors, that prime and activate it to bring about fusion between the viral and cellular lipid bilayers. Membrane fusion delivers the viral nucleocapsid core into the cytoplasm, which is the site of filovirus replication. This review summarizes our understanding of the filovirus entry mechanism, with emphasis on recent findings.

摘要

丝状病毒是引起出血热的病原体,可产生带有丝状形态的包膜病毒。病毒表面糖蛋白 GP 通过多种冗余的与细胞表面因子相互作用,协调着丝状病毒进入宿主细胞细胞质的复杂过程。GP 通过类似于细胞巨胞饮的过程介导病毒与细胞的附着。在内涵体/溶酶体途径中,GP 经历一系列由与宿主因子相互作用控制的结构重排,使其启动并激活,从而导致病毒和细胞脂双层之间发生融合。膜融合将病毒核衣壳核心递送到细胞质中,这是丝状病毒复制的部位。本文综述了我们对丝状病毒进入机制的理解,重点介绍了最近的发现。

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本文引用的文献

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Ebola virus glycoprotein needs an additional trigger, beyond proteolytic priming for membrane fusion.埃博拉病毒糖蛋白需要除蛋白水解原激活以外的额外触发因素才能实现膜融合。
PLoS Negl Trop Dis. 2011 Nov;5(11):e1395. doi: 10.1371/journal.pntd.0001395. Epub 2011 Nov 15.
2
A shared structural solution for neutralizing ebolaviruses.中和埃博拉病毒的共享结构解决方案。
Nat Struct Mol Biol. 2011 Nov 20;18(12):1424-7. doi: 10.1038/nsmb.2150.
3
Cathepsin cleavage potentiates the Ebola virus glycoprotein to undergo a subsequent fusion-relevant conformational change.
Cell Rep. 2023 Oct 31;42(10):113254. doi: 10.1016/j.celrep.2023.113254. Epub 2023 Oct 17.
4
Unique Mode of Antiviral Action of a Marine Alkaloid against Ebola Virus and SARS-CoV-2.海洋生物碱抗埃博拉病毒和 SARS-CoV-2 的独特抗病毒作用模式。
Viruses. 2022 Apr 15;14(4):816. doi: 10.3390/v14040816.
5
Structure of the Core Postfusion Porcine Endogenous Retrovirus Fusion Protein.猪内源性逆转录病毒融合蛋白核心后融合结构。
mBio. 2022 Feb 22;13(1):e0292021. doi: 10.1128/mbio.02920-21. Epub 2022 Jan 25.
6
Inhibition of Viral Membrane Fusion by Peptides and Approaches to Peptide Design.肽对病毒膜融合的抑制作用及肽设计方法
Pathogens. 2021 Dec 9;10(12):1599. doi: 10.3390/pathogens10121599.
7
Pathogenicity and Virulence of Ebolaviruses with Species- and Variant-specificity.埃博拉病毒的物种和变体特异性的致病性和毒力。
Virulence. 2021 Dec;12(1):885-901. doi: 10.1080/21505594.2021.1898169.
8
Length of mucin-like domains enhances cell-Ebola virus adhesion by increasing binding probability.粘蛋白样结构域的长度通过增加结合概率增强了细胞与埃博拉病毒的黏附。
Biophys J. 2021 Mar 2;120(5):781-790. doi: 10.1016/j.bpj.2021.01.025. Epub 2021 Feb 2.
9
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J Virol. 2020 Aug 31;94(18). doi: 10.1128/JVI.00336-20.
10
Conformational and lipid bilayer-perturbing properties of Marburg virus GP2 segments containing the fusion loop and membrane-proximal external region/transmembrane domain.含有融合环和膜近端外部区域/跨膜结构域的马尔堡病毒GP2片段的构象及脂质双层扰动特性
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组织蛋白酶切割增强了埃博拉病毒糖蛋白发生随后的与融合相关的构象变化。
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4
Comparative analysis of Ebola virus glycoprotein interactions with human and bat cells.埃博拉病毒糖蛋白与人细胞和蝙蝠细胞相互作用的比较分析。
J Infect Dis. 2011 Nov;204 Suppl 3(Suppl 3):S840-9. doi: 10.1093/infdis/jir306.
5
Basic clinical and laboratory features of filoviral hemorrhagic fever.丝状病毒出血热的基本临床和实验室特征。
J Infect Dis. 2011 Nov;204 Suppl 3:S810-6. doi: 10.1093/infdis/jir299.
6
The Ebola virus glycoprotein mediates entry via a non-classical dynamin-dependent macropinocytic pathway.埃博拉病毒糖蛋白通过一种非经典的依赖于动力蛋白的巨胞饮途径介导进入。
Virology. 2011 Oct 25;419(2):72-83. doi: 10.1016/j.virol.2011.08.009. Epub 2011 Sep 9.
7
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EMBO J. 2011 Aug 31;30(17):3481-500. doi: 10.1038/emboj.2011.286.
8
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Protein Sci. 2011 Sep;20(9):1587-96. doi: 10.1002/pro.688. Epub 2011 Aug 3.