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家蚕细胞质型多角体病毒第9片段核苷酸序列的测定及其在BmN4细胞中的表达

Determination of the nucleotide sequence of Bombyx mori cytoplasmic polyhedrosis virus segment 9 and its expression in BmN4 cells.

作者信息

Hagiwara K, Tomita M, Nakai K, Kobayashi J, Miyajima S, Yoshimura T

机构信息

Faculty of Engineering, Mie University, Tsu, Mie 514-8507, Japan.

出版信息

J Virol. 1998 Jul;72(7):5762-8. doi: 10.1128/JVI.72.7.5762-5768.1998.

Abstract

Cloning and sequencing of segment 9 of Bombyx mori cytoplasmic polyhedrosis virus (BmCPV) strains H and I were performed. The segment consisted of 1,186 bp harboring 5' and 3' noncoding regions and an open reading frame from positions 75 to 1037, encoding a protein with 320 amino acids, termed NS5. Comparison of the nucleotide sequences of NS5 for the two strains indicated 37 point differences resulting in only six amino acid replacements. Homology search showed that NS5 has localized similarities to human poliovirus RNA-dependent RNA polymerase and human rotavirus NS26. By Western blot analysis, NS5 was found in BmCPV-infected midgut cells, but not in polyhedra or virus virions, and was mainly detectable in the nucleus in BmCPV-infected BmN4 cells. Immunoblot analysis with anti-NS5 and antipolyhedrin antibodies displayed marked differences in the period of expression of NS5 and polyhedrin: the polyhedrin molecule was first detected 2 or 3 days after infection with BmCPV, whereas the expression of NS5 was initiated within a few hours. In addition, the level of polyhedrin increased as the infection developed, whereas the amount of NS5 remained essentially constant. When segment 9 was expressed with a baculovirus expression system, the resulting NS5 protein possessed the ability to bind to the double-stranded RNA genome. These results suggest that NS5 is expressed in early stages of infection and contributes to regulation of genomic RNA function.

摘要

对家蚕细胞质型多角体病毒(BmCPV)H株和I株的第9节段进行了克隆和测序。该节段由1186个碱基对组成,包含5'和3'非编码区以及一个从第75位到1037位的开放阅读框,编码一个含有320个氨基酸的蛋白质,称为NS5。对这两个毒株的NS5核苷酸序列进行比较,发现有37个位点差异,仅导致6个氨基酸替换。同源性搜索表明,NS5与人脊髓灰质炎病毒RNA依赖的RNA聚合酶和人轮状病毒NS26存在局部相似性。通过蛋白质免疫印迹分析发现,NS5存在于受BmCPV感染的中肠细胞中,但不存在于多角体或病毒粒子中,并且在受BmCPV感染的BmN4细胞中主要在细胞核中可检测到。用抗NS5抗体和抗多角体蛋白抗体进行的免疫印迹分析显示,NS5和多角体蛋白的表达时期存在明显差异:多角体蛋白分子在感染BmCPV后2或3天首次检测到,而NS5的表达在数小时内就开始了。此外,随着感染的发展,多角体蛋白的水平升高,而NS5的量基本保持不变。当用杆状病毒表达系统表达第9节段时,产生的NS5蛋白具有与双链RNA基因组结合的能力。这些结果表明,NS5在感染早期表达,并有助于调节基因组RNA的功能。

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