Baxt B, Vakharia V, Moore D M, Franke A J, Morgan D O
Department of Molecular Biology, Plum Island Animal Disease Center, Greenport, New York 11944-0848.
J Virol. 1989 May;63(5):2143-51. doi: 10.1128/JVI.63.5.2143-2151.1989.
A series of seven neutralizing monoclonal antibodies (nMAbs) directed against type A12 foot-and-mouth disease virus was used to generate neutralization-resistant variants. Both plaque reduction neutralization and microneutralization assays showed that the variants were no longer neutralized by the nMAbs used to generate them, although some of the variants still reacted with the nMAbs at high antibody concentrations. Results of cross-neutralization studies by both plaque reduction neutralization and microneutralization assays suggested the presence of at least one immunodominant antigenic site on the surface of type A12 foot-and-mouth disease virus, along with evidence of a second antigenic site on the viral surface. Two of the variants had reduced virulence in tissue culture as evidenced by their inability to inhibit cellular protein synthesis and a marked reduction in virus-induced cellular morphological alterations. Nucleotide sequencing of the variant genomes placed three epitopes of the major antigenic site on VP1 and the fourth epitope on VP3 and VP1. The one epitope of the minor site appears to reside only on VP1.
一系列七种针对A12型口蹄疫病毒的中和性单克隆抗体(nMAbs)被用于产生中和抗性变体。蚀斑减少中和试验和微量中和试验均表明,这些变体不再被用于产生它们的nMAbs中和,尽管一些变体在高抗体浓度下仍与nMAbs发生反应。蚀斑减少中和试验和微量中和试验的交叉中和研究结果表明,A12型口蹄疫病毒表面存在至少一个免疫显性抗原位点,同时有证据表明病毒表面存在第二个抗原位点。其中两个变体在组织培养中的毒力降低,这表现为它们无法抑制细胞蛋白质合成以及病毒诱导的细胞形态改变显著减少。变体基因组的核苷酸测序将主要抗原位点的三个表位定位在VP1上,第四个表位定位在VP3和VP1上。次要位点的一个表位似乎仅存在于VP1上。