Autographa californica multiple nucleopolyhedrovirus odv-e66 is an essential gene required for oral infectivity

被引:35
作者
Xiang, Xingwei [1 ]
Chen, Lin [1 ]
Hu, Xiaolong [1 ]
Yu, Shaofang [1 ]
Yang, Rui [1 ]
Wu, Xiaofeng [1 ]
机构
[1] Zhejiang Univ, Coll Anim Sci, Hangzhou 310029, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Autographa californica multiple nucleopolyhedrovirus (AcMNPV); ODV-E66; Polyhedron; Oral infectivity; OCCLUSION-DERIVED VIRUS; PER-OS INFECTIVITY; NUCLEAR POLYHEDROSIS-VIRUS; ENVELOPE PROTEIN; BACULOVIRUS; IDENTIFICATION; PATHWAY; BINDING; CELLS; FORM;
D O I
10.1016/j.virusres.2011.03.012
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Autographa californica multiple nucleopolyhedrovirus (AcMNPV) odv-e66 is a core gene and encodes an occlusion-derived virus (ODV)-specific envelope protein, ODV-E66. The N-terminal 23 amino acid of the envelope protein ODV-E66 are sufficient to direct native and fusion proteins to induced membrane microvesicles and the viral envelope during infection with AcMNPV. In this study, an odv-e66-knockout bacmid can not express N-terminal hydrophobic domains was constructed via homologous recombination in Escherichia coli. The odv-e66 deletion had no effect on budded virus (BV) production and viral DNA replication in infected Sf9 cells. Larval bioassays demonstrated that injection of odv-e66 deletion BV into the hemocoel could kill P. xylostella larvae as efficiently as repaired and control viruses; however, odv-e66 deletion mutant resulted in a 50% lethal dose that was 10(3) higher than that of the repaired and control viruses when inoculated per as. These results indicated that ODV-E66 envelope protein most likely played an important role in the oral infectivity of AcMNPV, but is not essential for virus replication. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:72 / 78
页数:7
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