Ogura T, Tanaka J, Kamiya S, Sato H, Ogura H, Hatano M
J Gen Virol. 1986 Dec;67 ( Pt 12):2605-16. doi: 10.1099/0022-1317-67-12-2605.
The susceptibility of human central nervous system cell lines to human cytomegalovirus (HCMV) and the fate of infected cultures were studied. Significant amounts of infectious progeny virus were produced in 118MGC glioma and IMR-32 neuroblastoma, but not in KGC oligodendroglioma cells when the cultures were infected with wild-type virus (HCMVwt) at an m.o.i. of 10 p.f.u. per cell. Further passage of infected 118MGC cells resulted in the establishment of a long-term persistent infection. This infection, designated 118MGC/Towne, continuously produced infectious virus (HCMVpi) with titres ranging from 10(2) to 10(5) p.f.u./10(6) cells up to 360 days post-infection (corresponding to 50 subcultures). Since no temperature-sensitive mutants, defective interfering particles or interferon-like activity were found in the 118MGC/Towne cultures, maintenance of the persistent infection seemed to be due to a balance between the release of infectious virus and the growth of uninfected cells. The HCMVpi produced in long-term persistently infected cultures was shown to be different from the HCMVwt originally used to infect by the following characteristics: HCMVpi replicated slowly and yielded lower amounts of progeny virus than HCMVwt; HCMVpi induced a 73,000 mol. wt. immediate early protein that was not synthesized in HCMVwt-infected cells; HCMVpi had a different DNA structure from that of HCMVwt. These results suggest that HCMVpi is a slower growing variant of HCMVwt and probably plays an important role in the maintenance of the persistent infection.
研究了人类中枢神经系统细胞系对人巨细胞病毒(HCMV)的易感性以及受感染培养物的命运。当以每细胞10个感染复数(m.o.i.)的野生型病毒(HCMVwt)感染培养物时,在118MGC胶质瘤和IMR - 32神经母细胞瘤细胞中产生了大量有感染性的子代病毒,但在KGC少突胶质细胞瘤细胞中未产生。感染的118MGC细胞进一步传代导致建立了长期持续性感染。这种感染被命名为118MGC/Towne,在感染后长达360天(相当于50次传代)持续产生滴度范围为10(2)至10(5)个感染复数/10(6)个细胞的有感染性病毒(HCMVpi)。由于在118MGC/Towne培养物中未发现温度敏感突变体、缺陷干扰颗粒或干扰素样活性,持续性感染的维持似乎是由于有感染性病毒的释放与未感染细胞的生长之间的平衡。长期持续性感染培养物中产生的HCMVpi在以下特征方面与最初用于感染的HCMVwt不同:HCMVpi复制缓慢,产生的子代病毒量比HCMVwt少;HCMVpi诱导产生一种73,000道尔顿的立即早期蛋白,而在HCMVwt感染的细胞中不合成该蛋白;HCMVpi的DNA结构与HCMVwt不同。这些结果表明,HCMVpi是HCMVwt生长较慢的变体,可能在持续性感染的维持中起重要作用。