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杆状病毒核心基因Bm67缺失的核型多角体病毒的特性分析

Characterization of a nucleopolyhedrovirus with a deletion of the baculovirus core gene Bm67.

作者信息

Ge Jun-Qing, Yang Zhang-Nv, Tang Xu-Dong, Xu Hai-Jun, Hong Jian, Chen Jian-Guo, Zhang Chuan-Xi

机构信息

Institute of Insect Science, Zhejiang University, Kaixuan Road 268, Hangzhou 310029, PR China.

College of Life Sciences, Peking University, Beijing 100087, PR China.

出版信息

J Gen Virol. 2008 Mar;89(Pt 3):766-774. doi: 10.1099/vir.0.83398-0.

DOI:10.1099/vir.0.83398-0
PMID:18272769
Abstract

Open reading frame (ORF) 67 (Bm67) of the Bombyx mori nucleopolyhedrovirus (BmNPV) is a highly conserved gene that is found in all completely sequenced baculoviruses; its function is unknown. In the present study, a Bm67-knockout virus was generated for studying the role of Bm67 in the BmNPV infection cycle. Furthermore, a Bm67-repair bacmid was constructed by transposing the Bm67 native promoter-promoted Bm67 ORF into the polyhedrin locus of the Bm67-knockout bacmid. After these recombinant bacmids were transfected into BmN cells, the Bm67-knockout bacmid caused defects in the production of infectious budded viruses. However, the Bm67-repair bacmid could rescue the defect, and budded virus titres reached wild-type levels. Quantitative real-time PCR analysis indicated that Bm67 is required for normal levels of DNA synthesis or for the stability of nascent viral DNA at the early stage. Electron microscopic analysis revealed that the formation of normal-appearing nucleocapsids is reduced in Bm67-knockout bacmid-transfected cells, and nucleocapsids are rarely found in the cytoplasm. The presence of 'enveloped' nucleocapsids at the nucleoplasm bilayer indicated that they are enveloped abnormally. These results indicated that Bm67 is required for the production of infectious budded viruses and for assembly of envelope and nucleocapsids.

摘要

家蚕核型多角体病毒(BmNPV)的开放阅读框(ORF)67(Bm67)是一个高度保守的基因,在所有已完成全序列测序的杆状病毒中均有发现;其功能尚不清楚。在本研究中,构建了一种Bm67基因敲除病毒,用于研究Bm67在家蚕核型多角体病毒感染周期中的作用。此外,通过将Bm67天然启动子驱动的Bm67开放阅读框转座到Bm67基因敲除杆粒的多角体蛋白基因座中,构建了一个Bm67修复杆粒。将这些重组杆粒转染到家蚕BmN细胞后,Bm67基因敲除杆粒导致感染性出芽病毒的产生出现缺陷。然而,Bm67修复杆粒能够挽救该缺陷,出芽病毒滴度达到野生型水平。实时定量PCR分析表明,Bm67在早期对于正常水平的DNA合成或新生病毒DNA的稳定性是必需的。电子显微镜分析显示,在转染了Bm67基因敲除杆粒的细胞中,正常形态核衣壳的形成减少,在细胞质中很少发现核衣壳。在核质双层处出现“包膜”核衣壳表明它们的包膜过程异常。这些结果表明,Bm67对于感染性出芽病毒的产生以及包膜和核衣壳的组装是必需的。

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