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本文引用的文献

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Virus entry paradigms.病毒进入模式。
Amino Acids. 2011 Nov;41(5):1147-57. doi: 10.1007/s00726-009-0363-3. Epub 2009 Oct 15.
2
Functional analysis of the Bunyamwera orthobunyavirus Gc glycoprotein.布尼亚姆韦拉正布尼亚病毒Gc糖蛋白的功能分析
J Gen Virol. 2009 Oct;90(Pt 10):2483-2492. doi: 10.1099/vir.0.013540-0. Epub 2009 Jul 1.
3
Characterization and subcellular localization of an RNA silencing suppressor encoded by Rice stripe tenuivirus.水稻条纹叶枯病毒编码的一种RNA沉默抑制子的特性及亚细胞定位
Virology. 2009 Apr 25;387(1):29-40. doi: 10.1016/j.virol.2009.01.045. Epub 2009 Feb 28.
4
Identification of a movement protein of the tenuivirus rice stripe virus.水稻条纹病毒(纤细病毒属)运动蛋白的鉴定
J Virol. 2008 Dec;82(24):12304-11. doi: 10.1128/JVI.01696-08. Epub 2008 Sep 25.
5
The P2 capsid protein of the nonenveloped rice dwarf phytoreovirus induces membrane fusion in insect host cells.非包膜水稻矮缩植物呼肠孤病毒的P2衣壳蛋白在昆虫宿主细胞中诱导膜融合。
Proc Natl Acad Sci U S A. 2007 Dec 4;104(49):19547-52. doi: 10.1073/pnas.0708946104. Epub 2007 Nov 27.
6
Role of the cytoplasmic tail domains of Bunyamwera orthobunyavirus glycoproteins Gn and Gc in virus assembly and morphogenesis.布尼亚姆韦拉正布尼亚病毒糖蛋白Gn和Gc的胞质尾域在病毒组装和形态发生中的作用
J Virol. 2007 Sep;81(18):10151-60. doi: 10.1128/JVI.00573-07. Epub 2007 Jul 3.
7
Development and characterization of a Rift Valley fever virus cell-cell fusion assay using alphavirus replicon vectors.使用甲病毒复制子载体的裂谷热病毒细胞-细胞融合测定法的开发与特性研究
Virology. 2006;356(1-2):155-64. doi: 10.1016/j.virol.2006.07.035. Epub 2006 Aug 30.
8
Detection and localization of Rice stripe virus gene products in vivo.水稻条纹病毒基因产物在体内的检测与定位
Virus Genes. 2005 Oct;31(2):211-21. doi: 10.1007/s11262-005-1798-6.
9
California serogroup Gc (G1) glycoprotein is the principal determinant of pH-dependent cell fusion and entry.加利福尼亚血清群Gc(G1)糖蛋白是pH依赖性细胞融合和进入的主要决定因素。
Virology. 2005 Jul 20;338(1):121-32. doi: 10.1016/j.virol.2005.04.026.
10
Tomato spotted wilt virus glycoprotein G(C) is cleaved at acidic pH.番茄斑萎病毒糖蛋白G(C)在酸性pH条件下会被切割。
Virus Res. 2005 Jun;110(1-2):183-6. doi: 10.1016/j.virusres.2005.01.007.

水稻条纹病毒 NSvc2 的表面展示及其膜融合活性分析。

Surface display of rice stripe virus NSvc2 and analysis of its membrane fusion activity.

机构信息

College of Bioscience and Biotechnology, Yangzhou University, Yangzhou 225009, China.

出版信息

Virol Sin. 2012 Apr;27(2):100-8. doi: 10.1007/s12250-012-3237-x. Epub 2012 Apr 11.

DOI:10.1007/s12250-012-3237-x
PMID:22492001
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8218033/
Abstract

Rice stripe virus (RSV) infects rice and is transmitted in a propagative manner by the small brown planthopper. How RSV enters an insect cell to initiate the infection cycle is poorly understood. Sequence analysis revealed that the RSV NSvc2 protein was similar to the membrane glycoproteins of several members in the family Bunyaviridae and might induce cell membrane fusion. To conveniently study the membrane fusion activity of NSvc2, we constructed cell surface display vectors for expressing Nsvc2 on the insect cell surface as the membrane glycoproteins of the enveloped viruses. Our results showed that NSvc2 was successfully expressed and displayed on the surface of insect Sf9 cells. When induced by low pH, the membrane fusion was not observed in the cells that expressed NSvc2. Additionally, the membrane fusion was also not detected when co-expressing Nsvc2 and the viral capsid protein on insect cell surface. Thus, RSV NSvc2 is probably different from the phlebovirus counterparts, which could suggest different functions. RSV might enter insect cells other than by fusion with plasma or endosome membrane.

摘要

水稻条纹病毒(RSV)感染水稻,并通过褐飞虱以增殖的方式传播。RSV 如何进入昆虫细胞启动感染周期,目前还知之甚少。序列分析表明,RSV NSvc2 蛋白与 Bunyaviridae 家族的几种膜糖蛋白相似,可能诱导细胞膜融合。为了方便研究 NSvc2 的膜融合活性,我们构建了细胞表面展示载体,用于将 NSvc2 作为包膜病毒的膜糖蛋白表达在昆虫细胞表面。我们的结果表明,NSvc2 成功地在昆虫 Sf9 细胞表面表达和展示。当用低 pH 值诱导时,表达 NSvc2 的细胞中没有观察到膜融合。此外,当在昆虫细胞表面共表达 NSvc2 和病毒衣壳蛋白时,也没有检测到膜融合。因此,RSV NSvc2 可能与黄病毒不同,这可能表明其具有不同的功能。RSV 可能通过与质膜或内体膜融合以外的其他方式进入昆虫细胞。