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传染性法氏囊病病毒病毒蛋白 5 的结构与功能建模。

Structural and functional modeling of viral protein 5 of Infectious Bursal Disease Virus.

机构信息

Animal Biotechnology Center, Department of Veterinary Physiology and Biochemistry, College of Veterinary and Animal Sciences, G. B. Pant University of Agriculture and Technology, Pantnagar, Uttarakhand, 263145, India.

Animal Biotechnology Center, Department of Veterinary Physiology and Biochemistry, College of Veterinary and Animal Sciences, G. B. Pant University of Agriculture and Technology, Pantnagar, Uttarakhand, 263145, India.

出版信息

Virus Res. 2018 Mar 2;247:55-60. doi: 10.1016/j.virusres.2018.01.017. Epub 2018 Feb 7.

DOI:10.1016/j.virusres.2018.01.017
PMID:29427596
Abstract

Infectious Bursal Disease (IBD) is an acute, highly contagious and immunosuppressive disease of young chicken. The causative virus (IBDV) is a bi-segmented, double-stranded RNA virus. The virus encodes five major proteins, viral protein (VP) 1-5. VPs 1-3 have been characterized crystallographically. Albeit a rise in the number of studies reporting successful heterologous expression of VP5 in recent times, challenging the notion that rapid death of host cells overexpressing VP5 disallows obtaining sufficiently pure preparations of the protein for crystallographic studies, the structure of VP5 remains unknown and its function controversial. Our study describes the first 3D model of IBD VP5 obtained through an elaborate computational workflow. Based on the results of the study, IBD VP5 can be predicted to be a structural analog of the leucine-rich repeat (LRR) family of proteins. Functional implications arising from structural similarity of VP5 with host Toll-like receptor (Tlr) 3 also satisfy the previously reported opposing roles of the protein in first abolishing and later inducing host-cell apoptosis.

摘要

传染性法氏囊病(IBD)是一种急性、高度传染性和免疫抑制性疾病,主要发生于雏鸡。病原体(IBDV)是一种双片段、双链 RNA 病毒。该病毒编码 5 种主要蛋白,即病毒蛋白(VP)1-5。VP1-3 已通过晶体学进行了表征。尽管最近有越来越多的研究报告成功异源表达 VP5,但挑战了“过度表达 VP5 的宿主细胞快速死亡不允许获得足够纯的蛋白质用于晶体学研究”的观点,但 VP5 的结构仍然未知,其功能也存在争议。我们的研究描述了通过精心计算工作流程获得的 IBD VP5 的第一个 3D 模型。根据研究结果,IBD VP5 可以预测为富含亮氨酸重复(LRR)蛋白家族的结构类似物。VP5 与宿主 Toll 样受体(Tlr)3 的结构相似性所产生的功能影响也满足了该蛋白在最初抑制和随后诱导宿主细胞凋亡的相反作用的先前报道。

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Structural and functional modeling of viral protein 5 of Infectious Bursal Disease Virus.传染性法氏囊病病毒病毒蛋白 5 的结构与功能建模。
Virus Res. 2018 Mar 2;247:55-60. doi: 10.1016/j.virusres.2018.01.017. Epub 2018 Feb 7.
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The VP5 protein of infectious bursal disease virus promotes virion release from infected cells and is not involved in cell death.传染性法氏囊病病毒的 VP5 蛋白促进感染细胞中的病毒粒子释放,而不参与细胞死亡。
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[Cloning of infectious bursal disease virus (Gt strain) lack of VP5 gene].[传染性法氏囊病病毒(Gt株)缺失VP5基因的克隆]
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VP5, the nonstructural polypeptide of infectious bursal disease virus, accumulates within the host plasma membrane and induces cell lysis.传染性法氏囊病病毒的非结构多肽VP5在宿主质膜内积聚并诱导细胞裂解。
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VP5 of infectious bursal disease virus is not essential for viral replication in cell culture.传染性法氏囊病病毒的VP5对于病毒在细胞培养中的复制并非必需。
J Virol. 1997 Jul;71(7):5647-51. doi: 10.1128/JVI.71.7.5647-5651.1997.

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