PMID- 22956736 OWN - NLM STAT- MEDLINE DCOM- 20130125 LR - 20200226 IS - 1465-2099 (Electronic) IS - 0022-1317 (Linking) VI - 93 IP - Pt 12 DP - 2012 Dec TI - Incorporation of GP64 into Helicoverpa armigera nucleopolyhedrovirus enhances virus infectivity in vivo and in vitro. PG - 2705-2711 LID - 10.1099/vir.0.046458-0 [doi] AB - The envelope fusion proteins of baculoviruses, glycoprotein GP64 from group I nucleopolyhedrovirus (NPV) or the F protein from group II NPV and granulovirus, are essential for baculovirus morphogenesis and infectivity. The F protein is considered the ancestral baculovirus envelope fusion protein, while GP64 is a more recent evolutionary introduction into baculoviruses and exhibits higher fusogenic activity than the F protein. Each of the fusion proteins is required by the respective virus to spread infection within larval tissues. A recombinant Helicoverpa armigera NPV (HearNPV) expressing GP64 from Autographa californica multiple nucleopolyhedrovirus, vHaBac-gp64-egfp, was constructed, which still retained the native F protein, and its infectivity was assayed in vivo and in vitro. Analyses by one-step growth curve to determine viral titre and by quantitative PCR to determine viral DNA copy number showed that vHaBac-gp64-egfp was more infectious in vitro than the control, vHaBac-egfp. The polyhedrin gene (polh) was reintroduced into the recombinant viruses and bioassays showed that vHaBac-gp64-polh accelerated the mortality of infected larvae compared with the vHaBac-egfp-polh control, and the LC(50) (median lethal concentration) of vHaBac-gp64-polh was reduced to approximately 20 % of that of vHaBac-egfp-polh. Therefore, incorporation of GP64 into HearNPV budded virions improved virus infectivity both in vivo and in vitro. The construction of this bivalent virus with a more efficient fusion protein could improve the use of baculoviruses in different areas such as gene therapy and biocontrol. FAU - Shen, Shu AU - Shen S AD - State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China. FAU - Gan, Yinyin AU - Gan Y AD - State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China. FAU - Wang, Manli AU - Wang M AD - State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China. FAU - Hu, Zhihong AU - Hu Z AD - State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China. FAU - Wang, Hualin AU - Wang H AD - State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China. FAU - Deng, Fei AU - Deng F AD - State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20120905 PL - England TA - J Gen Virol JT - The Journal of general virology JID - 0077340 RN - 0 (Occlusion Body Matrix Proteins) RN - 0 (Viral Fusion Proteins) RN - 0 (Viral Structural Proteins) RN - 0 (polyhedrin protein, Nucleopolyhedrovirus) SB - IM MH - Animals MH - Cells, Cultured MH - Genes, Viral MH - Lepidoptera/*virology MH - Membrane Fusion/genetics/physiology MH - Nucleopolyhedroviruses/genetics/*pathogenicity/*physiology MH - Occlusion Body Matrix Proteins MH - Viral Fusion Proteins/genetics/*physiology MH - Viral Structural Proteins/genetics/physiology MH - Virulence/genetics/physiology MH - Virus Internalization MH - Virus Replication/genetics/physiology EDAT- 2012/09/08 06:00 MHDA- 2013/01/26 06:00 CRDT- 2012/09/08 06:00 PHST- 2012/09/08 06:00 [entrez] PHST- 2012/09/08 06:00 [pubmed] PHST- 2013/01/26 06:00 [medline] AID - 10.1099/vir.0.046458-0 [doi] PST - ppublish SO - J Gen Virol. 2012 Dec;93(Pt 12):2705-2711. doi: 10.1099/vir.0.046458-0. Epub 2012 Sep 5.