Mallipeddi S K, Samal S K, Mohanty S B
Virginia-Maryland Regional College of Veterinary Medicine, University of Maryland, College Park.
Arch Virol. 1990;115(1-2):23-36. doi: 10.1007/BF01310620.
Ten virus-specific polypeptides ranging in molecular weight from approximately 200k to 11k were identified in bovine respiratory syncytial virus (BRSV-)infected cells. Time course analysis of the induction of the viral polypeptides indicated that they could be detected as early as 30 min post-infection and their synthesis reached a plateau 12 h after infection. Cell free translation of total infected-cell mRNA in a rabbit reticulocyte system yielded 7 proteins corresponding in size to virus-specific proteins synthesized in BRSV-infected cells. The P protein was highly phosphorylated; G and F were identified as glycoproteins by [3H]glucosamine labeling. Glycosylation of G protein was largely resistant to tunicamycin, suggesting that the majority of the carbohydrate residues are attached via O-glycosidic bonds, whereas the F protein was N-linked glycosylated. Tunicamycin caused a drastic reduction in the yield of infectious virus titer indicating that the carbohydrate moieties serve a critical role in the infectious cycle of BRSV.
在感染牛呼吸道合胞病毒(BRSV)的细胞中鉴定出了十种病毒特异性多肽,其分子量约为200k至11k。对病毒多肽诱导的时间进程分析表明,它们在感染后30分钟即可检测到,并且其合成在感染后12小时达到平台期。在兔网织红细胞系统中对总感染细胞mRNA进行无细胞翻译,产生了7种大小与在BRSV感染细胞中合成的病毒特异性蛋白相对应的蛋白质。P蛋白高度磷酸化;通过[3H]葡糖胺标记将G和F鉴定为糖蛋白。G蛋白的糖基化对衣霉素具有很大的抗性,这表明大多数碳水化合物残基是通过O-糖苷键连接的,而F蛋白是N-连接糖基化的。衣霉素导致感染性病毒滴度的产量大幅降低,表明碳水化合物部分在BRSV的感染周期中起关键作用。