Hovi T, Huovilainen A, Murdin A, Wimmer E
Enterovirus Laboratory and Molecular Biology Programme, National Public Health Institute, Helsinki, Finland.
J Gen Virol. 1995 Jul;76 ( Pt 7):1861-5. doi: 10.1099/0022-1317-76-7-1861.
We constructed a hybrid type 1/type 3 poliovirus comprising the BC-loop of capsid protein VP1 of PV3/Finland/60212/84 and the rest derived from PV1/Mahoney, and cultured the virus in the presence of diluted rabbit antiserum to PV3/Finland/60212/84. Several strains isolated under this selection showed point mutations in the inserted type 3 poliovirus sequence but only in one case in the flanking PV1/Mahoney-derived RNA. These results indicate that, with the use of recombinant cDNA technology, it may be possible to study molecular interactions of defined regions of virus capsid proteins with neutralizing polyclonal antibodies.
我们构建了一种1型/3型杂交脊髓灰质炎病毒,其包含PV3/芬兰/60212/84衣壳蛋白VP1的BC环,其余部分源自PV1/马奥尼,并在稀释的抗PV3/芬兰/60212/84兔抗血清存在的情况下培养该病毒。在这种选择条件下分离出的几个毒株在插入的3型脊髓灰质炎病毒序列中显示出点突变,但仅在一例中侧翼的源自PV1/马奥尼的RNA中出现突变。这些结果表明,利用重组cDNA技术,有可能研究病毒衣壳蛋白特定区域与中和多克隆抗体的分子相互作用。