Kelly D C, Avery R J, Dimmock N J
J Virol. 1974 Jun;13(6):1155-61. doi: 10.1128/JVI.13.6.1155-1161.1974.
Studies employing indirect immunofluorescent staining, acrylamide gel electrophoresis of [(35)S]methionine-labeled cellular polypeptides, and RNA-RNA hybridization of [(3)H]uridine-labeled cellular RNA, failed to detect evidence of fowl plague virus infection of BHK cells enucleated with cytochalasin B, although virus-specific polypeptide and RNA synthesis was detected in nucleate BHK cells. The enucleate cells permitted the synthesis of Newcastle disease and vaccinia virus structural proteins. We conclude that influenza virus fails to initiate macromolecular synthesis in enucleate BHK cells, and the role of the nucleus in influenza virus replication is discussed.
采用间接免疫荧光染色、对[³⁵S]甲硫氨酸标记的细胞多肽进行丙烯酰胺凝胶电泳以及对[³H]尿苷标记的细胞RNA进行RNA-RNA杂交的研究,未能检测到用细胞松弛素B去核的BHK细胞感染禽瘟病毒的证据,尽管在有核的BHK细胞中检测到了病毒特异性多肽和RNA合成。去核细胞允许新城疫病毒和痘苗病毒结构蛋白的合成。我们得出结论,流感病毒无法在去核的BHK细胞中启动大分子合成,并讨论了细胞核在流感病毒复制中的作用。