Condra J H, Lazzarini R A
J Virol. 1980 Dec;36(3):796-804. doi: 10.1128/JVI.36.3.796-804.1980.
A permeable-cell system has been developed to study the replication of vesicular stomatitis virus. When vesicular stomatitis virus-infected BHK cells were permeabilized by lysolecithin treatment, they incorporated nucleoside triphosphates into RNA and amino acids into proteins at nearly normal rates. The viral mRNA's synthesized appeared normal in polarity, size distribution, and polyadenylation, and all five viral proteins were synthesized. Replication of the viral genome proceeded, and full-length RNA strands were synthesized in amounts and polarities resembling those found in intact cells. These full-length RNAs associated with viral N proteins to form RNase-resistant nucleocapsids of normal buoyant density. Permeable cells appear to represent ideal hosts for studying vesicular stomatitis virus replication since they closely mimic in vivo conditions while retaining much of the experimental flexibility of current in vitro systems.
已开发出一种可渗透细胞系统来研究水疱性口炎病毒的复制。当用溶血卵磷脂处理使感染水疱性口炎病毒的BHK细胞通透化时,它们以接近正常的速率将核苷三磷酸掺入RNA,并将氨基酸掺入蛋白质。合成的病毒mRNA在极性、大小分布和多聚腺苷酸化方面看起来正常,并且所有五种病毒蛋白都被合成。病毒基因组的复制继续进行,全长RNA链的合成量和极性与完整细胞中发现的相似。这些全长RNA与病毒N蛋白结合形成具有正常浮力密度的抗核糖核酸酶核衣壳。可渗透细胞似乎是研究水疱性口炎病毒复制的理想宿主,因为它们紧密模拟体内条件,同时保留了当前体外系统的许多实验灵活性。