An infectious clone of the West Nile flavivirus

被引:88
作者
Yamshchikov, VF [1 ]
Wengler, G
Perelygin, AA
Brinton, MA
Compans, RW
机构
[1] Univ Virginia, Dept Internal Med, Charlottesville, VA 22908 USA
[2] Univ Giessen, Inst Virol, D-6300 Giessen, Germany
[3] Georgia State Univ, Dept Biol, Atlanta, GA 30302 USA
[4] Emory Univ, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
关键词
West Nile virus; infectious clone; flavivirus; RNA; replication; genome; end repair; ribozyme; chimeric virus;
D O I
10.1006/viro.2000.0795
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
West Nile (WN) virus is the most widespread among flaviviruses, but until recently it was not known on the American continent. We describe here design of a subgenomic replicon, as well as a full-length infectious clone of the lineage II WN strain, which appeared surprisingly stable compared to other flavivirus infectious clones. This infectious clone was used to investigate effects of 5'- and 3'-nonrelated sequences on virus replication and infectivity of synthetic RNA. While a long nonrelated sequence at the 3'-end delayed but did not prevent establishment of the productive infectious cycle, a much shorter extra sequence at the 5'-end completely abrogated virus replication. Replacement of the conserved 5'-adenosine residue substantially delayed, but did not prevent, establishment of virus infection. In all cases, the recovered Virus had restored its authentic 5'- and 3'-end genome sequences. However, the presence of extensive nonrelated sequences at both 5'- and 3'-ends could not be repaired. (C) 2001 Academic Press.
引用
收藏
页码:294 / 304
页数:11
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