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痘病毒宿主范围基因。

Poxvirus host range genes.

作者信息

Werden Steven J, Rahman Masmudur M, McFadden Grant

机构信息

Department of Molecular Genetics and Microbiology, College of Medicine, University of Florida, Gainesville, FL 32610, USA.

出版信息

Adv Virus Res. 2008;71:135-71. doi: 10.1016/S0065-3527(08)00003-1.

Abstract

As a family of viruses, poxviruses collectively exhibit a broad host range and most of the individual members are capable of replicating in a wide array of cell types from various host species, at least in vitro. At the cellular level, poxvirus tropism is dependent not upon specific cell surface receptors, but rather upon: (1) the ability of the cell to provide intracellular complementing factors needed for productive virus replication, and (2) the ability of the specific virus to successfully manipulate intracellular signaling networks that regulate cellular antiviral processes downstream of virus entry. The large genomic coding capacity of poxviruses enables the virus to express a unique collection of viral proteins that function as host range factors, which specifically target and manipulate host signaling pathways to establish optimal cellular conditions for viral replication. Functionally, the known host range factors from poxviruses have been associated with manipulation of a diverse array of cellular targets, which includes cellular kinases and phosphatases, apoptosis, and various antiviral pathways. To date, only a small number of poxvirus host range genes have been identified and studied, and only a handful of these have been functionally characterized. For this reason, poxvirus host range factors represent a potential gold mine for the discovery of novel pathogen-host protein interactions. This review summarizes our current understanding of the mechanisms by which the known poxvirus host range genes, and their encoded factors, expand tropism through the manipulation of host cell intracellular signaling pathways.

摘要

作为一个病毒家族,痘病毒总体上表现出广泛的宿主范围,并且大多数个体成员至少在体外能够在来自各种宿主物种的多种细胞类型中复制。在细胞水平上,痘病毒嗜性并不取决于特定的细胞表面受体,而是取决于:(1)细胞提供有效病毒复制所需的细胞内互补因子的能力,以及(2)特定病毒成功操纵细胞内信号网络的能力,这些信号网络调节病毒进入下游的细胞抗病毒过程。痘病毒巨大的基因组编码能力使病毒能够表达一系列独特的病毒蛋白,这些蛋白作为宿主范围因子发挥作用,专门靶向和操纵宿主信号通路,以建立病毒复制的最佳细胞条件。在功能上,已知的来自痘病毒的宿主范围因子与多种细胞靶点的操纵有关,这些靶点包括细胞激酶和磷酸酶、细胞凋亡以及各种抗病毒途径。迄今为止,仅鉴定和研究了少数痘病毒宿主范围基因,其中只有少数已进行功能表征。因此,痘病毒宿主范围因子是发现新型病原体 - 宿主蛋白相互作用的潜在宝库。本综述总结了我们目前对已知痘病毒宿主范围基因及其编码因子通过操纵宿主细胞内信号通路来扩大嗜性的机制的理解。

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