Kobayashi N, Kojima K, Taniguchi K, Urasawa T, Urasawa S
Department of Hygiene, School of Medicine, Sapporo Medical University, Japan.
Res Virol. 1994 Sep-Oct;145(5):303-11. doi: 10.1016/s0923-2516(07)80035-5.
A total of 200 clones of reassortants were generated in vitro between simian rotavirus SA11 (SA11-L2 strain) and each of five human rotavirus (HRV) strains with different antigenic specificities and RNA patterns. When culture fluid coinfected with parent viruses was subjected to repeated selection with anti-HRV-VP4 and anti-SA11-VP7 neutralizing monoclonal antibodies, all yielded progenies were antigenic mosaic reassortants possessing VP4 and VP7 derived from SA11 and HRV, respectively. In genomic analysis of viral RNA by PAGE, two and five different genotypes were identified in 40 clones, generated between SA11 and HRV strain Hochi (G serotype 4, G4) and between SA11 and KU (G1), respectively. In contrast, 11 and 17 genotypes were found in progenies between SA11 and subgroup I G2 HRV strain HN126 or DS-1, respectively. Although SA11 genes, except for the VP7 gene, were predominant in most reassortants, gene 5 was preferentially selected from HRV. Incorporation of HRV segments 1, 3 and 10 into progenies was more frequent in SA11 x HN126 and SA11 x DS-1 reassortants than in other reassortants. These results indicated that the extent of diversity of reassortant genotypes differs between the two groups of the parental HRV strain; one has subgroup I specificity and a short RNA pattern (DS-1 genogroup), while the other has subgroup II specificity and a long RNA pattern (Wa genogroup).
在体外,猿猴轮状病毒SA11(SA11-L2株)与五种具有不同抗原特异性和RNA模式的人类轮状病毒(HRV)毒株分别产生了总共200个重配体克隆。当用抗HRV-VP4和抗SA11-VP7中和单克隆抗体对与亲本病毒共感染的培养液进行反复筛选时,所有产生的子代都是抗原嵌合重配体,分别具有源自SA11和HRV的VP4和VP7。通过PAGE对病毒RNA进行基因组分析时,在分别由SA11与HRV毒株Hochi(G血清型4,G4)以及SA11与KU(G1)产生的40个克隆中,鉴定出了两种和五种不同的基因型。相比之下,在SA11与I组G2 HRV毒株HN126或DS-1产生的子代中分别发现了11种和17种基因型。尽管除VP7基因外,SA11基因在大多数重配体中占主导地位,但基因5优先从HRV中选择。在SA11×HN126和SA11×DS-1重配体中,HRV片段1、3和10掺入子代的频率比其他重配体更高。这些结果表明,两组亲本HRV毒株产生的重配体基因型的多样性程度有所不同;一组具有I组特异性和短RNA模式(DS-1基因组),而另一组具有II组特异性和长RNA模式(Wa基因组)。