Lambert D M, Pons M W, Mbuy G N, Dorsch-Hasler K
J Virol. 1980 Dec;36(3):837-46. doi: 10.1128/JVI.36.3.837-846.1980.
Analysis of purified respiratory syncytial virus revealed that the virion RNA was composed of 50S, 28S, 18S, and 4S species. The 18S and 28S species were presumed to represent host rRNA since virus grown in actinomycin D-treated cells contained only 50S and 4S RNAs. Actinomycin D treatment stimulated production of infectious respiratory syncytial virus 5- to 10-fold. The 50S virion RNA was shown to hybridize with polyadenylated mRNA's isolated from infected cells, indicating that respiratory syncytial virus RNA is of negative-strand sense. Six mRNA's were identified by polyacrylamide gel electrophoresis.
对纯化的呼吸道合胞病毒的分析表明,病毒粒子RNA由50S、28S、18S和4S组分组成。18S和28S组分被推测代表宿主rRNA,因为在放线菌素D处理的细胞中生长的病毒仅含有50S和4S RNA。放线菌素D处理刺激传染性呼吸道合胞病毒的产生达5至10倍。50S病毒粒子RNA被证明与从感染细胞中分离的聚腺苷酸化mRNA杂交,表明呼吸道合胞病毒RNA为负链。通过聚丙烯酰胺凝胶电泳鉴定出六种mRNA。