Stinski M F, Mocarski E S, Thomsen D R
J Virol. 1979 Jul;31(1):231-9. doi: 10.1128/JVI.31.1.231-239.1979.
The majority of DNA molecules associated with plaque-purified, low-multiplicity-passaged human cytomegalovirus (Towne strain) had a molecular weight of approximately 150 x 10(6) and a molecular complexity of approximately 140 x 10(6). Serial high-multiplicity passage resulted in the production of defective cytomegalovirions. An accumulation of smaller DNA molecules packaged into virions was directly correlated with a decrease in infectivity and an increase in the particle-to-PFU ratio. The majority of defective DNA molecules had a molecular weight of approximately 100 x 10(6). In addition, there were some viral DNA molecules of approximately 60 x 10(6). Restriction enzyme analysis of defective cytomegalovirus DNA detected unique DNA fragments, suggesting a specific alteration in the nucleotide sequence. Some reasons for the generation of defective cytomegalovirus DNA are discussed.
与蚀斑纯化、低传代倍数传代的人巨细胞病毒(Towne株)相关的大多数DNA分子的分子量约为150×10⁶,分子复杂度约为140×10⁶。连续高传代倍数传代导致产生有缺陷的巨细胞病毒粒子。包装到病毒粒子中的较小DNA分子的积累与感染力的降低和颗粒与空斑形成单位(PFU)比率的增加直接相关。大多数有缺陷的DNA分子的分子量约为100×10⁶。此外,还有一些约60×10⁶的病毒DNA分子。对有缺陷的巨细胞病毒DNA进行限制性酶切分析检测到独特的DNA片段,提示核苷酸序列发生了特异性改变。文中讨论了产生有缺陷的巨细胞病毒DNA的一些原因。