Characterization of a trypsin-dependent avian influenza H5N1-pseudotyped HIV vector system for high throughput screening of inhibitory molecules

被引:25
作者
Ao, Zhujun [1 ,2 ]
Patel, Ami [2 ]
Tran, Kaylie
He, Xinying [3 ,4 ]
Fowke, Keith [2 ]
Coombs, Kevin [2 ]
Kobasa, Darwyn
Kobinger, Gary [2 ]
Yao, Xiaojian [1 ,2 ]
机构
[1] Univ Manitoba, Fac Med, Lab Mol Human Retrovirol, Winnipeg, MB R3T 2N2, Canada
[2] Univ Manitoba, Fac Med, Dept Med Microbiol, Winnipeg, MB R3T 2N2, Canada
[3] Montreal Childrens Hosp, Res Inst, Dept Histol, Montreal, PQ H3Z 2Z3, Canada
[4] McGill Univ, Ctr Hlth, Montreal, PQ H3Z 2Z3, Canada
关键词
avian influenza virus; hemagglutinin; neuraminidase; M2; protein; H5N1-pseudotyped HIV vector system;
D O I
10.1016/j.antiviral.2008.02.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, we have generated and characterized an avian influenza H5N1 hemagglutinin (HA), neuraminidase (NA) and M2 ion channel pseudotyped HIV-based vector system (HaNaM-pseudotyped HIV vector). The cleavage site of the HA protein was modified to necessitate trypsin-dependent maturation of the glycoprotein. HA, NA and M2 were efficiently incorporated in HIV vector particles which could transduce different cell lines in a trypsin-dependent manner. Results also showed that the presence of avian influenza M2 and NA proteins maximized both vector production and transduction and that transduction was highly sensitive to the specific NA inhibitor oseltamivir (Tamiflu). H5N1 HaNaM-pseudotyped HIV vector system was also adapted for cell-based high throughput screening of drug candidates against influenza virus infection, and its high sensitivity to the specific oseltamivir validates its potential utility in the identification of new influenza inhibitors. Overall, the trypsin-dependent H5N1-pseudotyped HIV vector can mimic avian influenza virus infection Processes with sufficient precision to allow for the identification of new antivirals and to study avian influenza virus biology in a lower biosafety level laboratory environment. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:12 / 18
页数:7
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