共 33 条
Ebola virus VP35-VP40 interaction is sufficient for packaging 3E-5E minigenome RNA into virus-like particles
被引:54
作者:

Johnson, Reed F.
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Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

McCarthy, Sarah E.
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Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

Godlewski, Peter J.
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Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

Harty, Ronald N.
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机构:
Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA
机构:
[1] Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA
关键词:
D O I:
10.1128/JVI.01857-05
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
The packaging of viral genomic RNA into nucleocapsids and subsequently into virions is not completely understood. Phosphoprotein (P) and nucleoprotein (NP) interactions link NP-RNA complexes with P-L (polymerase) complexes to form viral nucleocapsids. The nucleocapsid then interacts with the viral matrix protein, leading to specific packaging of the nucleocapsid into the virion. A mammalian two-hybrid assay and confocal microscopy were used to demonstrate that Ebola virus VP35 and VP40 interact and colocalize in transfected cells. VP35 was packaged into budding virus-like particles (VLPs) as observed by protease protection assays. Moreover, VP40 and VP35 were sufficient for packaging an Ebola virus minignome RNA into VLPs. Results from immunoprecipitation-reverse transcriptase PCR experiments suggest that V-P35 confers specificity of the nucleocapsid for viral genomic RNA by direct VP35-RNA interactions.
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页码:5135 / 5144
页数:10
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