Bond S B, Howley P M, Takemoto K K
J Virol. 1978 Oct;28(1):337-43. doi: 10.1128/JVI.28.1.337-343.1978.
The antigenic relationship between the two murine papovaviruses, K virus and polyoma virus, was examined by serological techniques to determine whether they shared any antigenic components. No cross-reactivity was found associated with the viral (V) antigens by the indirect immunofluorescence, neutralization, or hemagglutination-inhibition tests. The tumor (T) antigens expressed in transformed cells or cells productively infected by either K or polyoma virus did not cross-react by indirect immunofluorescence. An antigenic relationship was detected, however, among the late proteins of K virus, polyoma virus, simian virus 40, and the human papovavirus BKV, when tested with either hyperimmune sera prepared against polyoma virus and simian virus 40 or sera prepared against disrupted virions. The nucleic acids of K and polyoma viruses were compared by agarose gel electrophoresis and restriction endonuclease analysis. No nucleotide sequence homology between the genomes of these two viruses was detectable by DNA-DNA hybridization techniques under stringent conditions. The genome of K virus was found to be slightly smaller than that of polyoma virus, and the cleavage patterns of the viral DNAs with six restriction endonucleases were different. These findings indicate that there is little relationship between these two murine papovaviruses.
运用血清学技术检测了两种鼠乳头瘤病毒——K病毒和多瘤病毒之间的抗原关系,以确定它们是否共享任何抗原成分。通过间接免疫荧光、中和或血凝抑制试验,未发现与病毒(V)抗原相关的交叉反应。通过间接免疫荧光检测,在由K病毒或多瘤病毒转化的细胞或产生性感染的细胞中表达的肿瘤(T)抗原没有交叉反应。然而,当用针对多瘤病毒和猴病毒40制备的超免疫血清或针对破碎病毒粒子制备的血清进行检测时,在K病毒、多瘤病毒、猴病毒40和人乳头瘤病毒BKV的晚期蛋白之间检测到了抗原关系。通过琼脂糖凝胶电泳和限制性内切酶分析比较了K病毒和多瘤病毒的核酸。在严格条件下,通过DNA-DNA杂交技术未检测到这两种病毒基因组之间的核苷酸序列同源性。发现K病毒的基因组略小于多瘤病毒,并且这两种病毒DNA用六种限制性内切酶的切割模式不同。这些发现表明这两种鼠乳头瘤病毒之间关系不大。