Okada J, Kobayashi N, Taniguchi K, Urasawa S
Department of Hygiene, Sapporo Medical University School of Medicine, Japan.
Arch Virol. 1999;144(2):345-53. doi: 10.1007/s007050050508.
Rotavirus clones A5-10 and A5-16 isolated from a bovine rotavirus strain A5 possess NSP1 gene which has a point mutation generating a nonsense codon and a 500 base-deletion, respectively. As a result, the two A5 clones encode truncated NSP1 product which lacks cysteine-rich region forming zinc finger motif. In order to analyze reassortment of these mutated NSP1 gene with RNA segments from heterologous strains, we investigated a number of reassortant clones derived from coinfection with either A5-10, A5-16 or a reference strain A5-13 (possessing intact NSP1 gene) and either simian rotavirus SA11 or human rotavirus KU. In coinfection with SA11 and A5-13, selection rates of A5-13 segments in reassortants ranged approximately from 20 to 70% (46% for NSP1 gene). In contrast, in the reassortment between SA11 and A5-10 or between SA11 and A5-16, selection rates of NSP1 gene from A5-10 and A5-16 were only 1% (one clone) and 0%, respectively. In reassortants from crosses KU x A5-clones, selection rate of A5-13 NSP1 gene decreased to 15%, while 11 reassortants with A5-10 NSP1 gene (31%) and one reassortant with A5-16 NSP1 gene (2%) were isolated. Reassortants with A5-10 NSP1 possessed a single gene (segment 9 or 11) from KU in the genetic background of A5-10. One reassortant clone (cl-55) with A5-16 NSP1 gene possessed KU gene segments 3, 4, and 8-11. When single-step growth curves were compared, the reassortant cl-55 showed almost identical growth curve to that of KU, while KU showed a better replication than A5-16. These results indicated that although A5-10 or A5-16 NSP1 gene encoding the truncated NSP1 is selected into reassortants much less efficiently than normal NSP1 gene, the reassortants with the mutated NSP1 gene and RNA segments from heterologous strains normally replicated in cultured cells. Thus, cysteine-rich region of NSP1 was not considered essential for genome segment reassortment with heterologous virus.
从牛轮状病毒A5株分离出的轮状病毒克隆A5-10和A5-16,其NSP1基因分别发生了产生无义密码子的点突变和500个碱基的缺失。结果,这两个A5克隆编码截短的NSP1产物,该产物缺乏形成锌指基序的富含半胱氨酸区域。为了分析这些突变的NSP1基因与来自异源毒株的RNA片段的重配情况,我们研究了许多由A5-10、A5-16或参考毒株A5-13(具有完整的NSP1基因)与猿猴轮状病毒SA11或人轮状病毒KU共感染产生的重配克隆。在与SA11和A5-13共感染时,重配体中A5-13片段的选择率约为20%至70%(NSP1基因为46%)。相比之下,在SA11与A5-10或SA11与A5-16的重配中,来自A5-10和A5-16的NSP1基因的选择率分别仅为1%(一个克隆)和0%。在KU与A5克隆杂交产生的重配体中,A5-13 NSP1基因的选择率降至15%,同时分离出11个具有A5-10 NSP1基因的重配体(31%)和1个具有A5-16 NSP1基因的重配体(2%)。具有A5-10 NSP1的重配体在A5-10的遗传背景中拥有来自KU的单个基因(第9或11节段)。一个具有A5-16 NSP基因的重配克隆(cl-55)拥有KU基因节段3、4和8至11。当比较单步生长曲线时,重配体cl-55的生长曲线与KU几乎相同,而KU的复制能力比A5-16更好。这些结果表明,尽管编码截短NSP1的A5-10或A5-16 NSP1基因被选入重配体的效率远低于正常NSP1基因,但具有突变NSP1基因和来自异源毒株的RNA片段的重配体通常在培养细胞中复制。因此,NSP1的富含半胱氨酸区域对于与异源病毒的基因组节段重配并非必不可少。