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J Gen Virol 89 (2008), 1212-1219; DOI 10.1099/vir.0.83633-0

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Bombyx mori nucleopolyhedrovirus ORF56 encodes an occlusion-derived virus protein and is not essential for budded virus production

Hai-Jun Xu{dagger}, Zhang-Nv Yang{dagger}, Jin-Fang Zhao, Cai-Hong Tian, Jun-Qing Ge, Xu-Dong Tang, Yan-Yuan Bao and Chuan-Xi Zhang

Institute of Insect Science, Zhejiang University, Hangzhou 310029, PR China

Correspondence
Chuan-Xi Zhang
chxzhang{at}zju.edu.cn

Bombyx mori nucleopolyhedrovirus ORF56 (Bm56) is a baculovirus core gene that is highly conserved in all baculoviruses that have had their genomes sequenced to date. Its transcripts in BmNPV-infected cells could be detected from 12 h post-infection (p.i.) and the encoded protein could be detected at 16 h p.i. by using a polyclonal antibody against glutathione S-transferase–Bm56 fusion protein. Western blot analysis showed that Bm56 is a structural component of the occlusion-derived virus nucleocapsid. Subsequent confocal microscopy revealed that Bm56 was distributed in the outer nuclear membrane and the intranuclear region of infected cells. To investigate the role of Bm56 in virus replication, a Bm56-knockout bacmid of BmNPV was constructed via homologous recombination in Escherichia coli. The Bm56 deletion had no effect on budded virus (BV) production in cultured cells; however, the deletion affected occlusion-body morphogenesis. A larval bioassay demonstrated that the Bm56 deletion did not reduce infectivity, whereas it resulted in a 50 % lethal time that was 16–18 h longer than that of the wild-type bacmid at every dose used in this study. These results indicate that Bm56 facilitates efficient virus production in vivo; however, it is not essential for BV production in vitro.

{dagger}These authors contributed equally to this work.

A supplementary table showing oligonucleotide PCR primers that were designed for and used in this study is available with the online version of this paper.







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