Grimley P M, Levin J G, Berezesky I K, Friedman R M
J Virol. 1972 Sep;10(3):492-503. doi: 10.1128/JVI.10.3.492-503.1972.
Semliki Forest virus (SFV), Sindbis virus, or Western equine encephalomyelitis virus. The structures, referred to as type 1 cytopathic vacuoles (CPV-1), were membrane-limited and characteristically lined by regular membranous spherules measuring 50 nm in diameter. The membranous spherules typically contained a fine central density, but were neither virus cores nor virions. Detection of CPV-1 by electron microscopy at 3 to 6 hr postinfection coincided with the time of rapid virus growth and preceded the accumulation of virus nucleocapsids. A range of 20 to 100 CPV-1 profiles were counted per 100 ultrathin cell sections at 6 to 9 hr postinfection when viruses were grown in chick embryo, baby hamster kidney, or mouse L cells. Maximum counts remained in the same range even when the multiplicity of infection was varied over 100-fold. Inhibition of cellular ribonucleic acid (RNA) and protein synthesis by actinomycin D during SFV infection did not decrease the counts of CPV-1; however, biogenesis of CPV-1 was decreased when viral replication was limited by inhibitors of viral RNA synthesis (guanidine) or of viral protein synthesis (cycloheximide). On the basis of present and earlier findings, we concluded that formation of CPV-1 must result from a virus-specified modification of pre-existing host cell macromolecules.
一种独特类型的胞质内膜性结构与三种A组虫媒病毒的复制相关:Semliki森林病毒(SFV)、辛德毕斯病毒或西部马脑炎病毒。这些结构被称为1型细胞病变空泡(CPV-1),由膜包被,其特征是内衬有直径为50nm的规则膜性小球。膜性小球通常含有细小的中央致密物质,但既不是病毒核心也不是病毒粒子。感染后3至6小时通过电子显微镜检测到CPV-1,这与病毒快速生长的时间一致,且先于病毒核衣壳的积累。当病毒在鸡胚、幼仓鼠肾或小鼠L细胞中生长时,感染后6至9小时,每100个超薄细胞切片中可计数到20至100个CPV-1形态。即使感染复数变化超过100倍,最大计数仍保持在同一范围内。在SFV感染期间,放线菌素D对细胞核糖核酸(RNA)和蛋白质合成的抑制作用并未降低CPV-1的计数;然而,当病毒复制受到病毒RNA合成抑制剂(胍)或病毒蛋白质合成抑制剂(环己酰亚胺)的限制时,CPV-1的生物发生减少。根据目前和早期的研究结果,我们得出结论,CPV-1的形成必定是由病毒指定的对预先存在的宿主细胞大分子的修饰所致。