Bean W J, Simpson R W
J Virol. 1975 Sep;16(3):516-24. doi: 10.1128/JVI.16.3.516-524.1975.
A comparative study of the in vitro reaction kinetics of the virion RNA polymerase of influenza A strains WS and WSN was conducted to establish phenotypic differences for enzyme activity that might be exchanged as genetic markers among recombinants of these viruses. Characteristically, the RNA polymerase activity of WS virus showed an initial rate of synthesis about two- to threefold higher than that of WSN when assayed at 32 C. The two strains were also distinguishable by comparing the transcription rates of each strain at 32 and 37 C. The initial rate of WS was invariably higher at 37 than at 32 C, whereas the opposite was found with WSN. When a series of recombinants obtained from mixed infections with the WS and WSN viruses were examined for virion transcriptase activity, it was found that the two polymerase related markers behaved as properties which segregated independently of each other and of additional nonselective markers that were scored. Seven temperature-sensitive mutants of WSN virus representing distinct recombination-complementation groups were found to show a diminished transcriptase activity as compared to wild-type virus, and one of these clones (ts 24) was largely deficient for this function. None of these mutants appeared to possess a heat-liable virion polymerase.
对甲型流感病毒WS株和WSN株的病毒粒子RNA聚合酶的体外反应动力学进行了比较研究,以确定酶活性的表型差异,这些差异可能作为遗传标记在这些病毒的重组体之间进行交换。典型的是,在32℃下测定时,WS病毒的RNA聚合酶活性的初始合成速率比WSN病毒高约两到三倍。通过比较每种毒株在32℃和37℃下的转录速率,也可以区分这两种毒株。WS的初始速率在37℃时总是高于32℃,而WSN则相反。当检查从WS和WSN病毒混合感染获得的一系列重组体的病毒粒子转录酶活性时,发现这两个与聚合酶相关的标记表现为彼此独立分离的特性,并且与所计分的其他非选择性标记也是独立分离的。发现代表不同重组互补组的七个WSN病毒温度敏感突变体与野生型病毒相比,转录酶活性降低,并且其中一个克隆(ts 24)在很大程度上缺乏这种功能。这些突变体似乎都不具有热不稳定的病毒粒子聚合酶。