中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Helicoverpa armigera nucleopolyhedrovirus occlusion-derived virus-associated protein, ha100, affects oral infectivity in vivo but not virus replication in vitro

文献类型:期刊论文

作者Luo, Sijiani1,2; Zhang, Yanfang1,2; Xu, Xushi1,2,3; Westenberg, Marcel4; Vlak, Just M.4; Wang, Hualin1,2; Hu, Zhihong1,2; Deng, Fei1,2
刊名Journal of general virology
出版日期2011-06-01
卷号92页码:1324-1331
ISSN号0022-1317
DOI10.1099/vir.0.029116-0
通讯作者Deng, fei(df@wh.iov.cn)
英文摘要Orf100 (ha100) of helicoverpa armigera nucleopolyhedrovirus (hearnpv) has been reported as one of the unique genes of group ii alphabaculoviruses encoding a protein located in the occlusion-derived virus (odv) envelope and nucleocapsid. the protein consists of 510 aa with a predicted mass of 58.1 kda and is a homologue of poly(adp ribose) glycohydrolase in eukaryotes. western blot analysis detected a 60 kda band in hearnpv-infected hzam1 cells starting at 18 h post-infection. transient expression of gfp-fused ha100 in hzam1 cells resulted in cytoplasmic localization of the protein, but after superinfection with hearnpv, gfp-fused ha100 was localized in the nucleus. to study the function of ha100 further, an ha100-null virus was constructed using bacmid technology. viral one-step growth curve analyses showed that the ha100-null virus had similar budded virus production kinetics to that of the parental virus. electron microscopy revealed that deletion of ha100 did not alter the morphology of odvs or occlusion bodies (obs). however, bioassays in larvae showed that the 50% lethal concentration (lc(50)) value of ha100-null obs was significantly higher than that of parental obs; the median lethal time (lt(50)) of ha 100-null obs was about 24 h later than control virus. these results indicate that ha100 is not essential for virus replication in vitro. however, it significantly affects the oral infectivity of obs in host insects, suggesting that the association ha100 with the odv contributes to the infectivity of obs in vivo.
WOS关键词SINGLE-NUCLEOCAPSID NUCLEOPOLYHEDROVIRUS ; NUCLEAR POLYHEDROSIS-VIRUS ; SPODOPTERA-FRUGIPERDA ; MULTIPLE NUCLEOPOLYHEDROVIRUS ; IDENTIFICATION ; HELIOTHIS ; SEQUENCE ; DELETION ; GENOMES ; GENE
WOS研究方向Biotechnology & Applied Microbiology ; Virology
WOS类目Biotechnology & Applied Microbiology ; Virology
语种英语
WOS记录号WOS:000291370100009
出版者SOC GENERAL MICROBIOLOGY
URI标识http://www.irgrid.ac.cn/handle/1471x/2375847
专题武汉病毒研究所
通讯作者Deng, Fei
作者单位1.Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
2.Chinese Acad Sci, Wuhan Inst Virol, CAS Key Lab Agr & Environm Microbiol, Wuhan 430071, Peoples R China
3.Nanjing Normal Univ, Fac Biosci, Nanjing 210097, Peoples R China
4.Wageningen Univ, Virol Lab, NL-6708 PB Wageningen, Netherlands
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Luo, Sijiani,Zhang, Yanfang,Xu, Xushi,et al. Helicoverpa armigera nucleopolyhedrovirus occlusion-derived virus-associated protein, ha100, affects oral infectivity in vivo but not virus replication in vitro[J]. Journal of general virology,2011,92:1324-1331.
APA Luo, Sijiani.,Zhang, Yanfang.,Xu, Xushi.,Westenberg, Marcel.,Vlak, Just M..,...&Deng, Fei.(2011).Helicoverpa armigera nucleopolyhedrovirus occlusion-derived virus-associated protein, ha100, affects oral infectivity in vivo but not virus replication in vitro.Journal of general virology,92,1324-1331.
MLA Luo, Sijiani,et al."Helicoverpa armigera nucleopolyhedrovirus occlusion-derived virus-associated protein, ha100, affects oral infectivity in vivo but not virus replication in vitro".Journal of general virology 92(2011):1324-1331.

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来源:武汉病毒研究所

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