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Highly active antiretroviral therapies are effective against HIV-1 cell-to-cell transmission.高效抗逆转录病毒疗法可有效抑制 HIV-1 细胞间传播。
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Coxsackievirus A9 infects cells via nonacidic multivesicular bodies.柯萨奇病毒 A9 通过非酸性多泡体感染细胞。
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The Rac1 inhibitor NSC23766 exerts anti-influenza virus properties by affecting the viral polymerase complex activity.Rac1抑制剂NSC23766通过影响病毒聚合酶复合物活性发挥抗流感病毒特性。
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Ubiquitin-proteasome-dependent slingshot 1 downregulation in neuronal cells inactivates cofilin to facilitate HSV-1 replication.泛素蛋白酶体依赖性弹弓 1 在神经元细胞中的下调使丝切蛋白失活,从而促进 HSV-1 的复制。
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HIV-1 triggers WAVE2 phosphorylation in primary CD4 T cells and macrophages, mediating Arp2/3-dependent nuclear migration.HIV-1 触发原代 CD4 T 细胞和巨噬细胞中 WAVE2 的磷酸化,介导 Arp2/3 依赖性核迁移。
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The formin FHOD1 and the small GTPase Rac1 promote vaccinia virus actin-based motility.formin FHOD1 和小 GTP 酶 Rac1 促进痘苗病毒基于肌动蛋白的运动。
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病毒对肌动蛋白的利用:病毒感染中的力产生和支架功能

Viral exploitation of actin: force-generation and scaffolding functions in viral infection.

作者信息

Spear Mark, Wu Yuntao

机构信息

National Center for Biodefense and Infectious Diseases, Department of Molecular and Microbiology, George Mason University, Manassas, VA, 20110, USA.

出版信息

Virol Sin. 2014 Jun;29(3):139-47. doi: 10.1007/s12250-014-3476-0. Epub 2014 Jun 6.

DOI:10.1007/s12250-014-3476-0
PMID:24938714
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4373664/
Abstract

As a fundamental component of the host cellular cytoskeleton, actin is routinely engaged by infecting viruses. Furthermore, viruses from diverse groups, and infecting diverse hosts, have convergently evolved an array of mechanisms for manipulating the actin cytoskeleton for efficacious infection. An ongoing chorus of research now indicates that the actin cytoskeleton is critical for viral replication at many stages of the viral life cycle, including binding, entry, nuclear localization, genomic transcription and reverse transcription, assembly, and egress/dissemination. Specifically, viruses subvert the force-generating and macromolecular scaffolding properties of the actin cytoskeleton to propel viral surfing, internalization, and migration within the cell. Additionally, viruses utilize the actin cytoskeleton to support and organize assembly sites, and eject budding virions for cell-to-cell transmission. It is the purpose of this review to provide an overview of current research, focusing on the various mechanisms and themes of virus-mediated actin modulation described therein.

摘要

作为宿主细胞细胞骨架的基本组成部分,肌动蛋白经常被感染病毒所利用。此外,来自不同病毒组、感染不同宿主的病毒已经趋同进化出一系列操纵肌动蛋白细胞骨架以实现有效感染的机制。目前不断涌现的大量研究表明,肌动蛋白细胞骨架在病毒生命周期的许多阶段对病毒复制至关重要,包括结合、进入、核定位、基因组转录和逆转录、组装以及释放/传播。具体而言,病毒颠覆肌动蛋白细胞骨架的力产生和大分子支架特性,以推动病毒在细胞内的冲浪、内化和迁移。此外,病毒利用肌动蛋白细胞骨架来支持和组织组装位点,并排出出芽的病毒粒子以进行细胞间传播。本综述的目的是概述当前的研究,重点关注其中描述的病毒介导的肌动蛋白调节的各种机制和主题。