Kobayashi N, Taniguchi K, Kojima K, Urasawa T, Urasawa S
Department of Hygiene, Sapporo Medical University School of Medicine, Japan.
Arch Virol. 1996;141(7):1167-76. doi: 10.1007/BF01718822.
We previously found the preferential selection of VP7 gene from a parent rotavirus strain SA11 with G serotype 3 (G3) in the sequential passages after mixed infection of simian rotavirus SA11 and SA11-human rotavirus single-VP7 gene-substitution reassortants with G1, G2, or G4 specificity. However, it has not been known whether or not VP7 genes derived from other strains with G3 specificity (G3-VP7 gene) are preferentially selected in the genetic background of SA11. To address this question, mixed infections followed by multiple passages were performed with a reassortant SA11-L2/KU-R1 (SKR1) (which possesses VP7 gene derived from G1 human rotavirus KU and other 10 genes of SA11 origin) and one of the five G3-rotaviruses, RRV, K9, YO, AK35, and S3. After the 10th passage, selection rates of SA11-L2/KU-R1 gene 9 (G1-VP7 gene) and gene 5 (NSP1 gene) reduced considerably (0 to 20.4%) in the clones obtained from all the coinfection experiments, while all or some of other segments were preferentially selected from SKR1 depending on the pairs of coinfection. When viral growth kinetics was examined, SKR1 exhibited better growth and reached a higher titer than any G3 viruses. Although the generated reassortants with VP7 gene and NSP1 gene derived from G3 viruses showed almost similar growth kinetics to that of SKR1 during the first 20 h of replication, the titers of these reassortants were higher than that of SKR1 after 36 h postinfection. The results obtained in this study suggested that G3-VP7 gene is functionally more adapted to the genetic background of SA11.
我们之前发现,在猿猴轮状病毒SA11与具有G1、G2或G4特异性的SA11-人轮状病毒单VP7基因替换重配体混合感染后的连续传代过程中,从G血清型为3(G3)的亲本轮状病毒株SA11中优先选择VP7基因。然而,尚不清楚源自其他具有G3特异性的毒株的VP7基因(G3-VP7基因)在SA11的遗传背景中是否会被优先选择。为了解决这个问题,我们用重配体SA11-L2/KU-R1(SKR1)(其具有源自G1人轮状病毒KU的VP7基因和其他10个源自SA11的基因)与五种G3轮状病毒之一RRV、K9、YO、AK35和S3进行混合感染并多次传代。在第10代传代后,从所有共感染实验获得的克隆中,SA11-L2/KU-R1的基因9(G1-VP7基因)和基因5(NSP1基因)的选择率大幅降低(0至20.4%),而根据共感染的配对情况,SKR1的所有或部分其他片段被优先选择。当检测病毒生长动力学时,SKR1表现出更好的生长情况,且达到的滴度高于任何G3病毒。尽管产生的具有源自G3病毒的VP7基因和NSP1基因的重配体在复制的前20小时内显示出与SKR1几乎相似的生长动力学,但这些重配体在感染后36小时的滴度高于SKR1。本研究获得的结果表明,G3-VP7基因在功能上更适应SA11的遗传背景。