Peränen J, Kääriäinen L
Institute of Biotechnology, University of Helsinki, Finland.
J Virol. 1991 Mar;65(3):1623-7. doi: 10.1128/JVI.65.3.1623-1627.1991.
We investigated the biogenesis of type I cytopathic vacuoles (CPVIs) in Semliki Forest virus (SFV)-infected cells by immunofluorescence and electron microscopy. By using the ts1 mutant of SFV at the restrictive temperature to avoid superinfection, we showed that the multiplicity of infection affects the time of appearance but not the number of CPVIs in a cell. Formation of CPVIs did not require incoming virus particles, because they were found in BHK cells transfected with infectious RNA from the SFV prototype strain or ts1 mutant. When the SFV gene for nsP3 was expressed alone in BHK cells, the nsP3 protein was localized to numerous vesiclelike structures and large vacuoles. The nsP3 protein may function as an anchoring protein for the RNA replication complex of SFV.
我们通过免疫荧光和电子显微镜研究了感染塞米基森林病毒(SFV)的细胞中I型细胞病变空泡(CPVI)的生物发生。通过在限制温度下使用SFV的ts1突变体来避免超感染,我们发现感染复数影响CPVI在细胞中出现的时间,但不影响其数量。CPVI的形成不需要进入的病毒颗粒,因为在转染了来自SFV原型株或ts1突变体的感染性RNA的BHK细胞中发现了它们。当SFV的nsP3基因单独在BHK细胞中表达时,nsP3蛋白定位于许多囊泡样结构和大空泡中。nsP3蛋白可能作为SFV RNA复制复合体的锚定蛋白发挥作用。