Chnaiderman J, Diaz J, Magnusson G, Liprandi F, Spencer E
Departamento de Ciencias Biológicas, Facultad de Química y Biología, Universidad de Santiago de Chile, Chile.
Arch Virol. 1998;143(9):1711-22. doi: 10.1007/s007050050411.
The effect of replacement of gene 11 of rotavirus SA-11 by a gene carrying a head to tail duplication obtained from a swine rotavirus strain was studied. The swine rotavirus strain with a duplicated gene (CC86) exhibits both a phenotype that allows to overgrow other viral strains when coinfected and an increased plaque size when plated in both CV-1 and MA-104 monkey kidney cells. Using reassortment methods the duplicated gene of the swine rotavirus was introduced into the SA-11 virus, replacing the regular gene 11. The reassorted strain was characterized to find out the origin of each of the other viral gene segments. Based on electrophoretic mobilities segments 1, 2, 3, 5, 7, 8 and 10 were identified as of SA-11. The SA-11 origin of the segments 4, 6 and 9 was confirmed by neutralization with polyclonal and monoclonal antibodies and by ELISA. The results suggest that the new reassortant virus was a monoreassortant carrying SA-11 genes except the duplicated gene originated from the swine virus CC86. The ability to in vivo replicate and to synthesize viral proteins was identical in the reassorted virus and the parental strains. Sequence analysis indicates that the new phenotype does not originate in the duplication of gene 11 but possibly from mutations in the coding region of NSP5 gene that may result in different phosphorylation patterns of the protein.
研究了用从猪轮状病毒株获得的带有头尾重复序列的基因替换轮状病毒SA - 11的基因11的效果。带有重复基因的猪轮状病毒株(CC86)在共感染时表现出一种允许其在其他病毒株之上过度生长的表型,并且在CV - 1和MA - 104猴肾细胞中铺板时噬斑大小增加。使用重配方法将猪轮状病毒的重复基因引入SA - 11病毒中,取代常规的基因11。对重配株进行表征以确定其他病毒基因片段各自的来源。基于电泳迁移率,片段1、2、3、5、7、8和10被鉴定为来自SA - 11。通过用多克隆和单克隆抗体中和以及酶联免疫吸附测定(ELISA)证实了片段4、6和9来自SA - 11。结果表明,新的重配病毒是一种单重配病毒,除了源自猪病毒CC86的重复基因外,携带SA - 11基因。重配病毒和亲本株在体内复制和合成病毒蛋白的能力相同。序列分析表明,新表型并非源于基因11的重复,而是可能源于NSP5基因编码区的突变,这可能导致该蛋白不同的磷酸化模式。