Mocarski E S, Stinski M F
J Virol. 1979 Sep;31(3):761-75. doi: 10.1128/JVI.31.3.761-775.1979.
A small percentage of human fibroblast cells survived high-multiplicity infection by cytomegalovirus and were isolated as persistently infected cultures. Approximately 30% of the cells were in the productive phase of infection, since virus-specific structural antigens and virions were associated with these cells. The remaining cells contained neither viral structural antigens nor particles. Nuclear DNA from these nonproductive cells contained approximately 120 genome equivalents of viral DNA per cell as determined by reassociation kinetics. In situ hybridization confirmed that nuclei from nonproductive cells contained a significant amount of viral DNA that was distributed in most of these cells. Early virus-induced proteins and antigens were also detected. Nonproductive cells continued to grow, and there was a slow, spontaneous transition of some of these cells to productive viral replication. The majority of the viral DNA in nonproductive cells persisted with restricted gene expression. When infectious virus production was eliminated by growing the persistently infected cultures in the presence of anticytomegalovirus serum, approximately 45 genome equivalents of the viral DNA persisted per cell. The reassociation reaction approached completion. After removal of the antiserum and subculturing, infectious virus production resumed. Therefore, it was assumed that all sequences of the viral genome remained associated with these cells. Restriction of cytomegalovirus gene expression in persistently infected cell cultures is discussed.
一小部分人成纤维细胞在巨细胞病毒高倍感染后存活下来,并被分离为持续感染培养物。大约30%的细胞处于感染的增殖期,因为病毒特异性结构抗原和病毒粒子与这些细胞相关联。其余细胞既不含有病毒结构抗原也不含有病毒颗粒。通过重缔合动力学测定,这些非增殖细胞的核DNA每个细胞含有约120个基因组当量的病毒DNA。原位杂交证实,非增殖细胞核含有大量分布于大多数此类细胞中的病毒DNA。还检测到早期病毒诱导的蛋白质和抗原。非增殖细胞继续生长,其中一些细胞缓慢、自发地转变为增殖性病毒复制。非增殖细胞中的大多数病毒DNA在基因表达受限的情况下持续存在。当在抗巨细胞病毒血清存在下培养持续感染培养物以消除感染性病毒产生时,每个细胞约有45个基因组当量的病毒DNA持续存在。重缔合反应接近完成。去除抗血清并传代培养后,感染性病毒产生恢复。因此,假定病毒基因组的所有序列仍与这些细胞相关联。文中讨论了巨细胞病毒在持续感染细胞培养物中基因表达的限制。