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Autographa californica multiple nucleopolyhedrovirus gene ac81 is required for nucleocapsid envelopment
被引:15
作者:
Dong, Fang
[1
]
Wang, Jinwen
[1
]
Deng, Riqiang
[1
]
Wang, Xunzhang
[1
]
机构:
[1] Sun Yat Sen Univ, Sch Life Sci, Guangzhou 510275, Guangdong, Peoples R China
来源:
关键词:
ac81;
Core gene;
Nucleocapsid;
Budded virions;
Occlusion-derived virions;
Envelopment;
OCCLUSION-DERIVED-VIRUS;
NUCLEAR POLYHEDROSIS-VIRUS;
CORE GENE;
BUDDED-VIRUS;
BOMBYX-MORI;
PROTEIN;
DELETION;
VIRIONS;
BACULOVIRUSES;
REPLICATION;
D O I:
10.1016/j.virusres.2016.05.005
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is a highly pathogenic Baculoviridae that targets insects, whose core gene, ac81, has an unknown function. To determine the role of ac81 in the life cycle of AcMNPV, an ac81-knockout (Ac-81KO-GP) was constructed through homologous recombination in Escherichia coli. We determined that no budded virions were produced in Ac-81KO-GP-transfected Sf9 cells, while there was no effect on viral DNA replication. Electron microscopy (EM) analysis revealed that occlusion-derived virions (ODVs) envelopment and the subsequent embedding of virions into occlusion bodies (OBs) were aborted due to ac81 deletion. Interestingly, confocal microscopy and immunofluorescence analysis revealed that Ac81 was predominantly localized to the ring zone of nuclei during the late phase of infection. In addition, Ac81 was localized to the mature and premature ODVs in virus-infected cells within the ring zone as revealed by immuno-electron microscopy (IEM) analysis. Furthermore, we determined that Ac81 contained a functional hydrophobic transmembrane (TM) domain, whose deletion resulted in a phenotype similar to that of Ac-81KO-GP. These results suggest that Ac81 might be a TM protein that played an important role in nucleocapsid envelopment. (C) 2016 Elsevier B.V. All rights reserved.
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页码:47 / 57
页数:11
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