Jolicoeur P, Baltimore D
J Virol. 1975 Dec;16(6):1593-8. doi: 10.1128/JVI.16.6.1593-1598.1975.
Titration of N- and B-tropic murine leukemia viruses on sensitive and resistant cell lines has been studied by direct XC plaque assay and infective center assay. The titration of cloned B-tropic virus by infective center assay on BALB/3T3 (Fv-1b/b) and NIH/3T3 (Fv-1n/n) cells gave one-hit patterns, with 100-fold less infected NIH/3T3 cells than BALB/3T3 cells. The titration of B-tropic virus on DBA/2 cells (Fv-1n/n) was also a one-hit. The titration of a one-hit curve, and there were about 100-fold less infected BALB/3T3 cells than NIH/3T3 cells. Comparable results were obtained by titrating the cloned N-tropic virus on congenic SIM (Fv-1n/n) and SIM.R (Fv-1b/b) cells or the Gross N-tropic virus on BALB/3T3 cells. Therefore, our data indicate that the multiple-hit phenomenon described previously may not be an essential part of the Fv-1 gene restriction.
通过直接XC空斑试验和感染中心试验,研究了N-嗜性和B-嗜性鼠白血病病毒在敏感和抗性细胞系上的滴定。通过感染中心试验在BALB/3T3(Fv-1b/b)和NIH/3T3(Fv-1n/n)细胞上对克隆的B-嗜性病毒进行滴定,得到了单次打击模式,感染的NIH/3T3细胞比BALB/3T3细胞少100倍。在DBA/2细胞(Fv-1n/n)上对B-嗜性病毒进行滴定也是单次打击。对单次打击曲线进行滴定,感染的BALB/3T3细胞比NIH/3T3细胞少约100倍。通过在同基因的SIM(Fv-1n/n)和SIM.R(Fv-1b/b)细胞上滴定克隆的N-嗜性病毒,或在BALB/3T3细胞上滴定格罗斯N-嗜性病毒,也得到了类似的结果。因此,我们的数据表明,先前描述的多次打击现象可能不是Fv-1基因限制的必要组成部分。