Shah K V, Ozer H L, Ghazey H N, Kelly T J
J Virol. 1977 Jan;21(1):179-86. doi: 10.1128/JVI.21.1.179-186.1977.
An antigenic determinant common to the major capsid polypeptide (VP1) of simian virus 40 (SV40) and polyoma virus is described. Antisera prepared against intact viral particles reacted only with cells infected with the homologous virus by immunofluorescence tests (IF). However, antisera prepared against disrupted SV40 particles reacted in IF with both polyoma- and SV40-infected permissive cells. The cross-reaction with polyoma was localized to VP1 by the following evidence. (i) The IF cross-reaction was inhibited by preincubation of the antiserum with purified SV40 VP1; (ii) purified radiolabeled polyoma VP1 was precipitated by the cross-reactive serum, and this reaction was inhibited by unlabeled SV40 VP1; (iii) other antisera prepared against purified SV40 VP1 or polyoma VP1 reacted in IF with both SV40- and polyma-infected permissive cells. These cross-reacting antisera also reacted in IF with permissive cells infected with BK virus, rabbit kidney vacuolating virus, and the stumptailed macaque virus, suggesting that all members of the polyoma-SV40 subgroup share a common antigenic determinant located in their major capsid polypeptides.
描述了猴病毒40(SV40)和多瘤病毒主要衣壳多肽(VP1)共有的一个抗原决定簇。通过免疫荧光试验(IF),针对完整病毒颗粒制备的抗血清仅与感染同源病毒的细胞发生反应。然而,针对破碎的SV40颗粒制备的抗血清在IF中与感染多瘤病毒和SV40的允许细胞均发生反应。通过以下证据表明与多瘤病毒的交叉反应定位于VP1:(i)抗血清与纯化的SV40 VP1预孵育可抑制IF交叉反应;(ii)交叉反应血清可沉淀纯化的放射性标记多瘤病毒VP1,且该反应可被未标记的SV40 VP1抑制;(iii)针对纯化的SV40 VP1或多瘤病毒VP1制备的其他抗血清在IF中与感染SV40和多瘤病毒的允许细胞均发生反应。这些交叉反应抗血清在IF中也与感染BK病毒、兔肾空泡化病毒和断尾猕猴病毒的允许细胞发生反应,表明多瘤病毒 - SV40亚组的所有成员在其主要衣壳多肽中共享一个共同的抗原决定簇。