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A Quantitative Assay for Measuring of Bovine Immunodeficiency Virus Using a Luciferase-based Indicator Cell Line

A Quantitative Assay for Measuring of Bovine Immunodeficiency Virus Using a Luciferase-based Indicator Cell Line
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摘要 In order to quantitate the bovine immunodeficiency virus (BIV) infection in vitro, a BIV indicator cell line (BIVL) was established by transfecting baby hamster kidney cells with reporter plasmids containing the firefly luciferase gene driven by a BIV long terminal repeat promoter. The BIV activates promoter activity of the LTR to express luciferase upon infection. BIV infection could therefore by quantified by detection of luciferase activity. Compared to standard assays used to detect BIV infection, the BIVL-based assay is 10 times more sensitive than the the CPE-based assay, and has similar sensitivity with the viral capsid protein Western blot assay. BIV indicator cell line could detect BIV infection specifically. Luciferase activity of BIV infected BIVL cells showed a time dependent manner, and 60 h post infection is the optimal time to detect BIV infection. Luciferase activity of BIVL cells correlates with the BIV capsid protein expression. Moreover, a linear relationship was found between MOI and the activated intensity of luciferase expression. In brief, the BIV indicator cell line is an easy, robust and quantitive method for monitoring BIV infection. In order to quantitate the bovine immunodeficiency virus line (BIVL) was established by transfecting baby hamster kidney (BIV) cells infection in vitro, a BIV indicator cell with reporter plasmids containing the firefly luciferase gene driven by a BIV long terminal repeat promoter. The BIV activates promoter activity of the LTR to express luciferase upon infection. BIV infection could therefore by quantified by detection of luciferase activity. Compared to standard assays used to detect BIV infection, the BIVL-based assay is 10 times more sensitive than the the CPE-based assay, and has similar sensitivity with the viral capsid protein Western blot assay BIV indicator cell line could detect BIV infection specifically. Luciferase activity of BIV infected BIVL cells showed a time dependent manner, and 60 h post infection is the optimal time to detect BIV infection. Luciferase activity of BIVL cells correlates with the BIV capsid protein expression. Moreover, a linear relationship was found between MOI and the activated intensity of luciferase expression. In brief, the BIV indicator cell line is an easy, robust and quantitive method for monitoring BIV infection.
出处 《Virologica Sinica》 SCIE CAS CSCD 2010年第2期137-144,共8页 中国病毒学(英文版)
基金 The General Foundation of Tianjin Science Committee for Applied Basic Research (08JCZDJC21000) Chinese Ministry of Education (30770081)
关键词 萤火虫荧光素酶基因 牛免疫缺陷病毒 定量检测 细胞株 感染细胞 蛋白免疫印迹法 启动子活性 基础 Bovine immunodeficiency virus (BIV) Bovine foamy virus (BFV) Luciferase Indicator cell line
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  • 1Gonda MA, Luther DG, Fong SE, et al. Bovine immunodeficiency virus: molecular biology and virus-host interactions. Virus Res, 1994,32 : 155-181.
  • 2Frankel AD, Young JA. HIV-I : fifteen proteins and an RNA. Annu Rev Biochem, 1998,67:1-25.
  • 3Barboric M, Taube R, Nekrep N, et al. Binding of Tat to TAR and recruitment of positive transcription elongation factor b occur independently in bovine immunodeficiency virus. J Virol, 2000, 74:6039-6044.
  • 4Bogerd HP, Wiegand HL, Bieniasz PD, et al. Functional differences between human and bovine immunodeficiency virus Tat transcription factors. J Virol, 2000, 74:4666-4671.
  • 5刘淑红,病毒学报

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