Wigand R, Hassinger M
Med Microbiol Immunol. 1980;168(3):179-90. doi: 10.1007/BF02122852.
The inhibition of herpesvirus type 1 in cell cultures by seven inhibitors of DNA synthesis and by pactamycin was investigated by plaque inhibition in Vero cells with agarose overlay, and by yield reduction in one-step growth in HeLa cells. While the plaque inhibition method proved to be suitable to show inhibition by single substances, only the yield reduction procedure was reliable for investigating the interaction of two substances. Inhibition was evaluated by means of an inhibition quotient (number of PFU in uninhibited virus controls:number of PFU in test specimen); combined inhibition was related to results with single substances. Among the 28 substance pairs, 9 cases of indifference, 10 additive, and 9 synergistic interactions were found. Indifference was observed only with fluorodeoxyuridine and amethopterin as one of the partners, which by themselves inhibited herpesvirus multiplication incompletely.
通过在Vero细胞中使用琼脂糖覆盖物进行蚀斑抑制,以及在HeLa细胞中进行一步生长中的产量降低实验,研究了七种DNA合成抑制剂和放线菌酮对细胞培养物中1型疱疹病毒的抑制作用。虽然蚀斑抑制方法被证明适用于显示单一物质的抑制作用,但只有产量降低实验程序对于研究两种物质的相互作用是可靠的。通过抑制商(未抑制病毒对照中的空斑形成单位数:测试样品中的空斑形成单位数)来评估抑制作用;联合抑制与单一物质的结果相关。在28对物质中,发现了9例无差异、10例相加和9例协同相互作用。仅在氟脱氧尿苷和氨甲蝶呤作为其中一方时观察到无差异,它们自身对疱疹病毒增殖的抑制不完全。