St Jeor S, Rapp F
J Virol. 1973 Jun;11(6):986-90. doi: 10.1128/JVI.11.6.986-990.1973.
The replication of human cytomegalovirus (CMV) in cells pretreated with 5-iodo-2'-deoxyuridine (IUdR) was studied. Pretreatment of cells with IUdR enhanced several parameters of virus replication. Virus grown in drug-treated cells exhibited a shorter eclipse period and the cells produced more infectious virus sooner than did untreated cells. There was an approximate fivefold increase in virus yield per cell in the drug-treated samples when compared to control cultures. The time required for plaque development was shortened by 6 days in drug-treated cultures. Pretreatment of cells with IUdR also increased plaquing efficiency of the virus by approximately 10-fold. The enhancement of virus replication by IUdR was further demonstrated by varying the multiplicity of infection. In a 7-day period there was a 100-fold increase in sensitivity of the cultures for virus detection when the cells had been previously exposed to IUdR. The data presented indicate the possibility that IUdR interferes with the production of a cellular product inhibitory for CMV replication.
研究了人巨细胞病毒(CMV)在经5-碘-2'-脱氧尿苷(IUdR)预处理的细胞中的复制情况。用IUdR预处理细胞增强了病毒复制的几个参数。在药物处理细胞中生长的病毒表现出较短的隐蔽期,并且与未处理细胞相比,细胞更快产生更多有感染性的病毒。与对照培养物相比,药物处理样品中每个细胞的病毒产量增加了约五倍。药物处理培养物中噬斑形成所需的时间缩短了6天。用IUdR预处理细胞还使病毒的噬斑形成效率提高了约10倍。通过改变感染复数进一步证明了IUdR对病毒复制的增强作用。在7天的时间里,当细胞先前暴露于IUdR时,培养物对病毒检测的敏感性增加了100倍。所呈现的数据表明IUdR可能干扰了对CMV复制具有抑制作用的细胞产物的产生。