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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
来源:
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.
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页码:294 / 304
页数:11
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