Schlegel A, Giddings T H, Ladinsky M S, Kirkegaard K
Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder 80309, USA.
J Virol. 1996 Oct;70(10):6576-88. doi: 10.1128/JVI.70.10.6576-6588.1996.
Poliovirus RNA replicative complexes are associated with cytoplasmic membranous structures that accumulate during viral infection. These membranes were immunoisolated by using a monoclonal antibody against the viral nonstructural protein 2C. Biochemical analysis of the isolated membranes revealed that several organelles of the host cell (lysosomes, trans-Golgi stack and trans-Golgi network, and endoplasmic reticulum) contributed to the virus-induced membranous structures. Electron microscopy of infected cells preserved by high-pressure freezing revealed that the virus-induced membranes contain double lipid bilayers that surround apparently cytosolic material. Immunolabeling experiments showed that poliovirus proteins 2C and 3D were localized to the same membranes as the cellular markers tested. The morphological and biochemical data are consistent with the hypothesis that autophagy or a similar host process is involved in the formation of the poliovirus-induced membranes.
脊髓灰质炎病毒RNA复制复合物与病毒感染期间积累的细胞质膜结构相关。这些膜通过使用针对病毒非结构蛋白2C的单克隆抗体进行免疫分离。对分离出的膜进行生化分析表明,宿主细胞的几种细胞器(溶酶体、反式高尔基体堆叠和反式高尔基体网络以及内质网)参与了病毒诱导的膜结构的形成。通过高压冷冻保存的感染细胞的电子显微镜检查显示,病毒诱导的膜含有围绕明显胞质物质的双脂双层。免疫标记实验表明,脊髓灰质炎病毒蛋白2C和3D定位于与所测试的细胞标记相同的膜上。形态学和生化数据与自噬或类似的宿主过程参与脊髓灰质炎病毒诱导的膜形成的假设一致。