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家蚕双顺反子病毒结构蛋白的表达分析及病毒样颗粒在昆虫细胞中的组装

Expression analysis of Bombyx mori bidensovirus structural proteins and assembly of virus-like particles in insect cells.

作者信息

Pan Xiaoli, Lü Peng, Zhang Miaomiao, Hu Zhaoyang, Li Guohui, Ma Shangshang, Feng Fan, Chen Keping, Yao Qin

机构信息

Institute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013, China,

出版信息

Curr Microbiol. 2014 Oct;69(4):567-73. doi: 10.1007/s00284-014-0613-9. Epub 2014 Jun 12.

Abstract

Bombyx mori bidensovirus (BmBDV) is a new designated species of the new genus Bidensovirus in the new family Bidnaviridae, which contains two single-stranded linear DNAs (VD1 and VD2) and causes the chronic densonucleosis disease of silkworm. Previous researches revealed that VD1-ORF3 encodes the major structural proteins VPs. In this work, through western blot, we found that VPs expressed from 48 h post-inoculation and kept increasing until 120 h post-inoculation in midgut of Bombyx mori. In order to further investigate the translation of vp gene, the ORFs (vp1 and vp2) of the VP started just up-stream of the first two candidate initiation codons were expressed in Sf9 cells by a baculovirus expression system. The expression products were purified by gradient density centrifugation and analyzed by Western blot and electron microscopy. The results showed that the expressions of vp1 yielded three proteins (VP1, VP1', and VP2), which are the same with the viral VPs expression in midgut of Bombyx mori, and vp2 generated two VPs with the molecular weights of about 51 kDa (VP2) and 37 kDa. The observation by electron microscopy indicated that these VPs can auto-assemble into virus-like particles that could not be distinguished from virus particles. These findings will provide materials for studying the structure of BmBDV and be helpful in the studies on BmBDV-based disease in silkworms.

摘要

家蚕双顺反子病毒(BmBDV)是双顺反子病毒科新属中的一个新指定物种,它含有两条单链线性DNA(VD1和VD2),可引发家蚕慢性浓核症疾病。先前的研究表明,VD1-ORF3编码主要结构蛋白VPs。在本研究中,通过蛋白质免疫印迹法,我们发现VPs在接种后48小时开始表达,并在家蚕中肠中持续增加,直至接种后120小时。为了进一步研究vp基因的翻译,通过杆状病毒表达系统在Sf9细胞中表达了VP前两个候选起始密码子上游起始的ORF(vp1和vp2)。表达产物通过梯度密度离心法纯化,并通过蛋白质免疫印迹法和电子显微镜进行分析。结果表明,vp1的表达产生了三种蛋白质(VP1、VP1'和VP2),这与家蚕中肠中的病毒VPs表达相同,vp2产生了两种分子量约为51 kDa(VP2)和37 kDa的VPs。电子显微镜观察表明,这些VPs可以自动组装成与病毒颗粒无法区分的病毒样颗粒。这些发现将为研究BmBDV的结构提供材料,并有助于对家蚕中基于BmBDV的疾病的研究。

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