Burns J W, Chen D, Estes M K, Ramig R F
Department of Virology and Epidemiology, Baylor College of Medicine, Houston, Texas 77030.
Virology. 1989 Apr;169(2):427-35. doi: 10.1016/0042-6822(89)90168-2.
We have studied a variant virus isolated from a stock of SA11 virus (H. G. Pereira, R. S. Azeredo, A. M. Fialho, and M. N. P. Vidal, 1984, J. Gen. Virol. 65, 815-818). This virus, designated 4F, was initially identified by its faster electrophoretic mobility for genome segment 4. The variant was analyzed to determine if the altered electrophoretic mobility of genome segment 4 could be correlated with phenotypic changes. Comparison of our standard laboratory SA11 virus (clone 3) with the 4F variant showed the following: (i) The 4F variant possesses a viral hemagglutinin (VP4) with a higher apparent molecular weight than clone 3. (ii) The 4F variant produces large plaques when assayed in vitro, as compared to clone 3. (iii) The 4F variant produces plaques in the absence of proteolytic enzymes, whereas clone 3 does not. (iv) The 4F variant reacts with serotype-specific neutralizing monoclonal antibodies to VP7, but fails to react with several neutralizing anti-VP4 monoclonal antibodies generated to SA11 clone 3. (v) The 4F variant grows to a higher titer and is more stable than clone 3. (vi) The 4F variant produces a VP4 that appears to be more susceptible to cleavage by trypsin than is the VP4 of clone 3. Further analyses with the 4F variant may lead to an understanding of the molecular basis for these altered phenotypes that appear to be related, at least in part, to the product of genome segment 4.
我们研究了从一株SA11病毒毒株中分离出的变异病毒(H. G. 佩雷拉、R. S. 阿泽雷多、A. M. 菲亚略和M. N. P. 维达尔,1984年,《普通病毒学杂志》65卷,815 - 818页)。这种病毒被命名为4F,最初是通过其基因组片段4更快的电泳迁移率鉴定出来的。对该变异体进行了分析,以确定基因组片段4改变的电泳迁移率是否与表型变化相关。将我们的标准实验室SA11病毒(克隆3)与4F变异体进行比较,结果如下:(i)4F变异体的病毒血凝素(VP4)表观分子量比克隆3的高。(ii)与克隆3相比,4F变异体在体外测定时产生大的噬斑。(iii)4F变异体在没有蛋白水解酶的情况下产生噬斑,而克隆3则不能。(iv)4F变异体与针对VP7的血清型特异性中和单克隆抗体反应,但不与针对SA11克隆3产生的几种中和抗VP4单克隆抗体反应。(v)4F变异体生长到更高的滴度,并且比克隆3更稳定。(vi)4F变异体产生的VP4似乎比克隆3的VP4更容易被胰蛋白酶切割。对4F变异体的进一步分析可能会使我们了解这些改变的表型的分子基础,这些表型似乎至少部分与基因组片段4的产物有关。