Construction of recombinant herpes simplex virus type I expressing green fluorescent protein without loss of any viral genes

被引:35
|
作者
Tanaka, M
Kodaira, H
Nishiyama, Y
Sata, T
Kawaguchi, Y
机构
[1] Natl Inst Infect Dis, Dept Pathol, Sinjyuku Ku, Tokyo 1628640, Japan
[2] Yakult Honsha Co Ltd, Dept Pharmaceut, Chuo Ku, Tokyo 1040061, Japan
[3] Japan Sci & Technol Agcy, PRESTO, Saitama 3320012, Japan
基金
日本学术振兴会;
关键词
simplex virus; green fluorescent protein; anti-viral agents;
D O I
10.1016/j.micinf.2004.01.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
For use in various applications in research on herpes simplex virus type 1, we attempted to generate recombinant HSV-1 expressing green fluorescent protein (GFP) without any loss of viral genes. Our results were as follows. (i) A recombinant HSV-1 (YK333), in which a GFP expression cassette driven by the Egr-1 promoter was inserted into the intergenic region between UL3 and UL4, was constructed. (ii) YK333 replicated as well as wild-type HSV-1 F strain in Vero cells. (iii) As one application of the recombinant YK333 for research on HSV-1, we developed a system to detect anti-herpetic activity, termed a fluorescence-based anti-viral assay. The 50% inhibitory concentration of ganciclovir for YK333 determined using our newly developed assay was comparable to that determined using a plaque reduction assay. YK333 will be a convenient tool for herpes simplex virus research, including such applications as monitoring of viral replication in vitro and in vivo, and rapid screening of potential anti-herpetic agents. (C) 2004 Elsevier SAS. All rights reserved.
引用
收藏
页码:485 / 493
页数:9
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