Suzuki N, Ueno T, Yamashita T, Fujinaga K
Microbiol Immunol. 1981;25(12):1291-301. doi: 10.1111/j.1348-0421.1981.tb00138.x.
Simple and practical methods for grouping of adenoviruses and for identification of restriction endonuclease cleavage patterns of viral DNA were established by using infected cell DNA. DNA homology groupings of adenoviruses could be examined by spot hybridization, and restriction endonuclease cleavage patterns of viral DNAs could be obtained by Southern blot hybridization, by using infected cell DNA. The method was very sensitive and allowed the identification of the cleavage pattern of viral DNA of the inoculum by means of cell DNA extracted from infected cells with undetectable cytopathic effect (CPE). In ethidium bromide-stained gels without Southern blot hybridization, the restriction endonuclease cleavage pattern of viral DNA could be detected precisely in spite of background staining due to cellular DNA. The preparation of infected cell DNA used in these procedures was technically much easier than that of viral DNA. These methods require only a small number of infected cells and allow many isolates to be investigated with ease.
利用感染细胞DNA建立了腺病毒分组及病毒DNA限制性内切酶切割模式鉴定的简单实用方法。腺病毒的DNA同源性分组可通过斑点杂交检测,病毒DNA的限制性内切酶切割模式可通过Southern印迹杂交获得,使用的是感染细胞DNA。该方法非常灵敏,可通过从无明显细胞病变效应(CPE)的感染细胞中提取的细胞DNA鉴定接种物病毒DNA的切割模式。在未进行Southern印迹杂交的溴化乙锭染色凝胶中,尽管存在细胞DNA造成的背景染色,仍可精确检测病毒DNA的限制性内切酶切割模式。这些操作中使用的感染细胞DNA的制备在技术上比病毒DNA的制备要容易得多。这些方法只需要少量感染细胞,能够轻松对许多分离株进行研究。