Okazaki K, Chiya S, Ideguchi S, Kimura S
Department of Microbiology, Kochi Medical School, Japan.
J Virol Methods. 1987 Nov;18(2-3):169-78. doi: 10.1016/0166-0934(87)90122-4.
Herpes simplex virus (HSV) isolates were differentiated by immunoblotting analysis using a mixture of polyclonal antisera directed against HSV type 1 (HSV-1) and HSV type 2 (HSV-2) glycoprotein fractions (gB/gC of HSV-1 and gC/gE/84-kDa protein of HSV-2), since the mixed antisera recognized viral polypeptides with different molecular weights in HSV-1- and HSV-2-infected cells. Results of typing by immunoblotting analysis were consistent with those obtained by restriction endonuclease analysis of DNAs extracted from 10 HSV isolates. These results suggest that the immunoblotting technique will be applicable to reliable typing of HSV isolates using polyclonal antisera showing the difference in reaction patterns between HSV-1- and HSV-2-infected cells.
单纯疱疹病毒(HSV)分离株通过免疫印迹分析进行区分,该分析使用了针对1型单纯疱疹病毒(HSV-1)和2型单纯疱疹病毒(HSV-2)糖蛋白组分(HSV-1的gB/gC和HSV-2的gC/gE/84 kDa蛋白)的多克隆抗血清混合物,因为该混合抗血清能识别HSV-1和HSV-2感染细胞中具有不同分子量的病毒多肽。免疫印迹分析的分型结果与从10株HSV分离株中提取的DNA进行限制性内切酶分析所获得的结果一致。这些结果表明,免疫印迹技术将适用于使用多克隆抗血清对HSV分离株进行可靠分型,该多克隆抗血清显示出HSV-1和HSV-2感染细胞之间反应模式的差异。