Virus-inducible reporter genes as a tool for detecting and quantifying influenza A virus replication

被引:81
作者
Lutz, A
Dyall, J
Olivo, PD
Pekosz, A
机构
[1] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[3] Apath LLC, St Louis, MO 63141 USA
关键词
influenza; diagnostics; reporter gene; cell culture;
D O I
10.1016/j.jviromet.2005.01.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The use of influenza A virus-inducible reporter gene segments in detecting influenza A virus replication was investigated. The RNA polymerase I promoter/terminator cassette was used to express RNA transcript, encoding green fluorescence protein or firefly luciferase flanked by the untranslated regions of the influenza A/WSN/33 nucleoprotein (NP) segment. Reporter gene activity was detected after reconstitution of the influenza A virus polymerase complex from cDNA or after virus infection, and was influenza A virus-specific. Reporter gene activity could be detected as early as 6 h post-infection and was virus dose-dependent. Inhibitory effects of antibodies or amantadine could be detected and quantified rapidly, providing a means of not only identifying influenza A virus-specific replication, but also of determining the antigenic Subtype as well as antiviral drug susceptibility. Induction of virus-specific reporter genes provides a rapid, sensitive method for detecting virus replication, quantifying virus titers and assessing antiviral sensitivity as well as antigenic subtype. (c) 2005 Elsevier B.V. All rights reserved.
引用
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页码:13 / 20
页数:8
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