Yuan Li, Zhang Xiaohua, Chang Mingxian, Jia Chensong, Hemmingsen Sean M, Dai Heping
Institute of Hydrobiology, Chinese Academy of Sciences, East Lake Southern Road #7, Wuhan 430072, Hubei, PR China.
J Virol Methods. 2007 Dec;146(1-2):96-103. doi: 10.1016/j.jviromet.2007.06.009. Epub 2007 Jul 23.
A fluorescent quantitative PCR (FQ-PCR) assay utilizing SYBR green I dye is described for quantitation of white spot syndrome virus (WSSV) particles isolated from infected crayfish, Cambarus clarkii. For this assay, a primer set was designed which amplifies, with high efficiency and specificity, a 129bp target sequence within ORF167 of the WSSV genome. Conveniently, WSSV particles can be added into the FQ-PCR assay with a simple and convenient method to release its DNA. To establish the basis for an in vitro neutralization test, primary cultures of shrimp cells were challenged with WSSV that had been incubated with a polyclonal anti-WSSV serum or with control proteins. The number of WSSV particles released from the cells after these treatments were assayed by FQ-PCR. This test may serve as a method to screen monoclonal antibody pools or recombinant antibody pools for neutralizing activity prior to in vivo animal experiments.
描述了一种利用SYBR Green I染料的荧光定量PCR(FQ-PCR)检测方法,用于定量从感染克氏原螯虾(Cambarus clarkii)中分离的白斑综合征病毒(WSSV)颗粒。对于该检测方法,设计了一组引物,可高效、特异性地扩增WSSV基因组ORF167内的129bp靶序列。方便的是,WSSV颗粒可以通过一种简单便捷的方法添加到FQ-PCR检测中以释放其DNA。为建立体外中和试验的基础,用与多克隆抗WSSV血清或对照蛋白孵育过的WSSV攻击对虾细胞原代培养物。通过FQ-PCR检测这些处理后从细胞中释放的WSSV颗粒数量。该试验可作为一种在体内动物实验之前筛选具有中和活性的单克隆抗体库或重组抗体库的方法。