Adaptation of West Nile virus replicons to cells in culture and use of replicon-bearing cells to probe antiviral action

被引:58
作者
Rossi, SL
Zhao, QZ
O'Donnell, VK
Mason, PW
机构
[1] Univ Texas, Med Branch, Dept Pathol, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Sealy Ctr Vaccine Dev, Galveston, TX 77555 USA
关键词
West Nile virus; flavivirus; replicon; antivirals; ribavirin; interferon; persistent infection;
D O I
10.1016/j.virol.2004.10.046
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Flaviviruses are emerging threats to public health worldwide. Recently, one flavivirus, West Nile virus (WNV), has caused the largest epidemic of viral encephalitis in US history. Like other flaviviruses, WNV is thought to cause a persistent infection in insect cells, but an acute cytopathic infection of mammalian cells. To study adaptation of WNV to persistently replicate in cell Culture and generate a system capable of detecting antiviral compounds in the absence of live virus, we generated subgenomic replicons of WNV and adapted these to persistently replicate in mammalian cells. Here we report that adaptation of these replicons to cell culture results in a reduction of genome copy number, and demonstrate that hamster, monkey, and human cells that stably carry the replicons can be used as surrogates to detect the activity of anti-WNV compounds. Additionally, we have used these cells to investigate the interaction of WNV genomes with interferon (IFN). These studies demonstrated that IFN can cure cells of replicons and that replicon-bearing cells display lower responses to IFN than their IFN-cured derivatives. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:457 / 470
页数:14
相关论文
共 64 条
[1]   Efficacy of interferon alpha-2b and ribavirin against West Nile virus in vitro [J].
Anderson, JF ;
Rahal, JJ .
EMERGING INFECTIOUS DISEASES, 2002, 8 (01) :107-108
[2]   Highly permissive cell lines for subgenomic and genomic hepatitis C virus RNA replication [J].
Blight, KJ ;
McKeating, JA ;
Rice, CM .
JOURNAL OF VIROLOGY, 2002, 76 (24) :13001-13014
[3]   Efficient initiation of HCV RNA replication in cell culture [J].
Blight, KJ ;
Kolykhalov, AA ;
Rice, CM .
SCIENCE, 2000, 290 (5498) :1972-1974
[4]   A stable full-length yellow fever virus cDNA clone and the role of conserved RNA elements in flavivirus replication [J].
Bredenbeek, PJ ;
Kooi, EA ;
Lindenbach, B ;
Huijkman, N ;
Rice, CM ;
Spaan, WJM .
JOURNAL OF GENERAL VIROLOGY, 2003, 84 :1261-1268
[5]   Interferon-α protects mice against lethal infection with St Louis encephalitis virus delivered by the aerosol and subcutaneous routes [J].
Brooks, TJG ;
Phillpotts, RJ .
ANTIVIRAL RESEARCH, 1999, 41 (01) :57-64
[6]   West Nile virus [J].
Campbell, GL ;
Marfin, AA ;
Lanciotti, RS ;
Gubler, DJ .
LANCET INFECTIOUS DISEASES, 2002, 2 (09) :519-529
[7]   FLAVIVIRUS GENOME ORGANIZATION, EXPRESSION, AND REPLICATION [J].
CHAMBERS, TJ ;
HAHN, CS ;
GALLER, R ;
RICE, CM .
ANNUAL REVIEW OF MICROBIOLOGY, 1990, 44 :649-688
[8]   The mechanism of cell death during West Nile virus infection is dependent on initial infectious dose [J].
Chu, JJH ;
Ng, ML .
JOURNAL OF GENERAL VIROLOGY, 2003, 84 :3305-3314
[9]   Fine mapping of a cis-acting sequence element in yellow fever virus RNA that is required for RNA replication and cyclization [J].
Corver, J ;
Lenches, E ;
Smith, K ;
Robison, RA ;
Sando, T ;
Strauss, EG ;
Strauss, JH .
JOURNAL OF VIROLOGY, 2003, 77 (03) :2265-2270
[10]   Interferon, ribavirin, 6-azauridine and glycyrrhizin: antiviral compounds active against pathogenic flaviviruses [J].
Crance, JM ;
Scaramozzino, N ;
Jouan, A ;
Garin, D .
ANTIVIRAL RESEARCH, 2003, 58 (01) :73-79