Properties of replication-competent vesicular stomatitis virus vectors expressing glycoproteins of filoviruses and arenaviruses

被引:294
作者
Garbutt, M
Liebscher, R
Wahl-Jensen, V
Jones, S
Möller, P
Wagner, R
Volchkov, V
Klenk, HD
Feldmann, H [1 ]
Ströher, U
机构
[1] Hlth Canada, Natl Microbiol Lab, Special Pathogens Program, Winnipeg, MB R3E 3R2, Canada
[2] Univ Manitoba, Dept Med Microbiol & Infect Dis, Winnipeg, MB R3T 2N2, Canada
[3] Univ Manitoba, Dept Immunol, Winnipeg, MB R3T 2N2, Canada
[4] Univ Marburg, Inst Virol, D-3550 Marburg, Germany
[5] Univ Lyon 1, INSERM, U412, Filovirus Lab, Lyon, France
关键词
D O I
10.1128/JVI.78.10.5458-5465.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Replication-competent recombinant vesicular stomatitis viruses (rVSVs) expressing the type 1 transmembrane glycoproteins and selected soluble glycoproteins of several viral hemorrhagic fever agents (Marburg virus, Ebola virus, and Lassa virus) were generated and characterized. All recombinant viruses exhibited rhabdovirus morphology and replicated cytolytically in tissue culture. Unlike the rVSVs with an additional transcription unit expressing the soluble glycoproteins, the viruses carrying the foreign transmembrane glycoproteins in replacement of the VSV glycoprotein were slightly attenuated in growth. Biosynthesis and processing of the foreign glycoproteins were authentic, and the cell tropism was defined by the transmembrane glycoprotein. None of the rVSVs displayed pathogenic potential in animals. The rVSV expressing the Zaire Ebola virus transmembrane glycoprotein mediated protection in mice against a lethal Zaire Ebola virus challenge. Our data suggest that the recombinant VSV can be used to study the role of the viral glycoproteins in virus replication, immune response, and pathogenesis.
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页码:5458 / 5465
页数:8
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