Rapid diagnosis and quantification of herpes simplex virus with a green fluorescent protein reporter system

被引:17
|
作者
Kung, SH
Wang, YC
Lin, CH
Kuo, RL
Liu, WT [1 ]
机构
[1] Natl Yang Ming Univ, Inst Biotechnol Med, Fac Med Technol, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Grad Inst Microbiol & Immunol, Taipei 112, Taiwan
[3] Vet Gen Hosp Taipei, Div Clin Virol, Taipei 112, Taiwan
关键词
herpes simplex virus; green fluorescent protein; ICP10; promoter;
D O I
10.1016/S0166-0934(00)00234-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A genetically modified cell line (Vero-ICP10-EGFP) was constructed for detection of herpes simplex virus (HSV) by a simple, rapid and direct method. The cell line was developed by stable transfection of Vero cell with a plasmid encoding the green fluorescent protein (GFP) driven by the promoter of the HSV-2 ICP10 gene. As early as 6 h after infection with HSV, fluorescence-emitting cells can be observed under a fluorescence microscope. A single infected cell emitting fluorescence can be observed with soft agar overlay by inverted fluorescence microscopy. No induction of detectable fluorescence was seen following infections with human cytomegalovirus (HCMV), varicella tester virus (VZV), coxsackievirus A16 and enterovirus 71. Analysis by flow cytometry also demonstrated that intensity of the triggered fluorescence is proportional to the titer of HSV inoculated. Taken together, this novel GFP reporter system could become a useful means for rapid detection and quantification of HSV in clinical specimens. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:205 / 212
页数:8
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