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黄热病17D病毒:E蛋白结构域II和III中的突变对缺陷病毒渗透和传播的假回复抑制作用

Yellow fever 17D virus: pseudo-revertant suppression of defective virus penetration and spread by mutations in domains II and III of the E protein.

作者信息

Vlaycheva Leonssia, Nickells Michael, Droll Deborah A, Chambers Thomas J

机构信息

Department of Molecular Microbiology and Immunology, Saint Louis University Health Sciences Center, St. Louis, MO 63104, USA.

出版信息

Virology. 2004 Sep 15;327(1):41-9. doi: 10.1016/j.virol.2004.06.015.

Abstract

A yellow fever (YFV) 17D virus variant, which causes persistent infection of mouse neuroblastoma cells associated with defective cell penetration and small plaque size, yielded plaque-revertant viruses from cells transfected with viral transcripts encoding the adaptive mutation (Gly360 in the E protein). Reconstruction of a plaque-purified revertant which contained Gly360 and additional substitutions (Asn for Lys303 and Val for Ala261) yielded a virus whose infectious center size, growth efficiency, and cell penetration rate similar to the parental YF5.2iv virus, whereas viruses with Asn303 or Val261 alone with Gly360 yielded either a small-plaque virus or a parental revertant. These data indicate that the YFV E protein is subject to suppression of mutations in domain III that are deleterious for viral entry and spread by a second-site mutation in domain II. Position 261 lies within the hydrophobic ligand-binding pocket at the domain I-II interface, a site believed to be involved in the hinge-like conformational change of domain II during activation of membrane fusion-activity. Results of this study provide genetic data consistent with findings on flavivirus structure and implicate domain III in functions beyond simply cell surface attachment.

摘要

一种黄热病(YFV)17D病毒变体,可导致小鼠神经母细胞瘤细胞持续感染,与细胞穿透缺陷和小蚀斑大小有关,从用编码适应性突变(E蛋白中的Gly360)的病毒转录本转染的细胞中产生了蚀斑回复病毒。对包含Gly360以及其他替代(Lys303突变为Asn和Ala261突变为Val)的蚀斑纯化回复病毒进行重建,得到一种病毒,其感染中心大小、生长效率和细胞穿透率与亲本YF5.2iv病毒相似,而单独含有Asn303或Val261与Gly360的病毒则产生小蚀斑病毒或亲本回复病毒。这些数据表明,YFV E蛋白在结构域III中的突变会受到抑制,这些突变对病毒进入和传播有害,原因是结构域II中的第二位点突变。261位位于结构域I-II界面处的疏水配体结合口袋内,该位点被认为在膜融合活性激活过程中参与结构域II的铰链样构象变化。本研究结果提供了与黄病毒结构研究结果一致的遗传数据,并表明结构域III的功能不仅仅是简单的细胞表面附着。

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