Vikhnovich E M, Zolotarskaia E E, Loparev V N, Dreĭzin R S
Vopr Virusol. 1982 May-Jun;27(3):365-9.
The clone KB-230 of simian adenovirus SA7(C8) is described differing from the reference SA7(C8) strain and clones KB-2 and MB-1 by the presence of additional recognition sites when treated with different endonucleases. The KB-230 clone differs antigenically in the neutralization test from the MB-1 clone. Some biological and molecular-biological properties of the KB-230 clone were studied. All the simian cell cultures under study were highly sensitive to the cytopathic effect and replication of the KB-230 clone. The reproduction cycle of the KB-230 clone was 12 h, that of KB-2 clone 16 h. The maximum accumulation of virus in the cells was observed by 27-29 h for both clones. The KB-230 clone differed from the KB-2 clone by early development of the CPE (by 9 h of cultivation against 19 h for the latter). The oncogenic activity of the KB-230 clone was less marked than that of the MB-1 clone. The methods of heteroduplex and polypeptide analysis established the difference of the KB-230 clone from the reference SA7(C8) strain and KB-2 and MB-1 clones.
描述了猿猴腺病毒SA7(C8)的克隆KB - 230,它在用不同核酸内切酶处理时,与参考SA7(C8)菌株以及克隆KB - 2和MB - 1不同,存在额外的识别位点。在中和试验中,KB - 230克隆在抗原性上与MB - 1克隆不同。对KB - 230克隆的一些生物学和分子生物学特性进行了研究。所有研究的猿猴细胞培养物对KB - 230克隆的细胞病变效应和复制都高度敏感。KB - 230克隆的复制周期为12小时,KB - 2克隆为16小时。两个克隆在27 - 29小时时在细胞中观察到病毒的最大积累量。KB - 230克隆与KB - 2克隆的不同之处在于CPE出现较早(培养9小时出现,而后者为19小时)。KB - 230克隆的致癌活性比MB - 1克隆弱。异源双链分析和多肽分析方法确定了KB - 230克隆与参考SA7(C8)菌株以及KB - 2和MB - 1克隆的差异。