Gibadulin R A, Denisova T S, Zavgorodniĭ S G, Florent'ev V L, Zhdanov V M
Vopr Virusol. 1983 Jul-Aug;28(4):59-63.
By successive passages and triple cloning of herpes simplex virus type 1 (HSV-1) in Vero cell culture in the presence of increasing concentrations of phosphonoacetic acid (PAA) a mutant of HSV-1 resistant to PAA (PAAr) was derived and characterized. The resistance to the inhibitor was transmitted from PAAr-mutant to a sensitive strain (L2) by recombination performed by the marker rescue method using DNA fragmented by Hpa-1 restrictase. The resulting recombinant (R-551) was resistant to the inhibitor and had an altered primary structure of DNA.
通过在不断增加浓度的膦甲酸(PAA)存在下,将1型单纯疱疹病毒(HSV-1)在Vero细胞培养物中连续传代和三次克隆,获得并鉴定了一株对PAA具有抗性的HSV-1突变体(PAAr)。通过使用经Hpa-1限制性内切酶切割的DNA,采用标记拯救法进行重组,将对该抑制剂的抗性从PAAr突变体传递给敏感菌株(L2)。产生的重组体(R-551)对该抑制剂具有抗性,并且其DNA的一级结构发生了改变。