Hansman Grant S, Oka Tomoichiro, Sakon Naomi, Takeda Naokazu
National Institute of Infectious Diseases, Tokyo, Japan.
Emerg Infect Dis. 2007 Oct;13(10):1519-25. doi: 10.3201/eid1310.070402.
Sapovirus (SaV) is a causative agent of gastroenteritis. On the basis of capsid protein (VP1) nucleotide sequences, SaV can be divided into 5 genogroups (GI-GV), of which the GI, GII, GIV, and GV strains infect humans. SaV is uncultivable, but expression of recombinant VP1 in insect cells results in formation of viruslike particles (VLPs) that are antigenically similar to native SaV. In this study, we newly expressed SaV GII and GIV VLPs to compare genetic and antigenic relationships among all human SaV genogroups. Hyperimmune antiserum samples against VLPs reacted strongly with homologous VLPs. However, several antiserum samples weakly cross-reacted against heterologous VLPs in an antibody ELISA. Conversely, an antigen ELISA showed that VLPs of SaV in all human genogroups were antigenically distinct. These findings indicate a likely correspondence between SaV antigenicity and VP1 genogrouping and genotyping.
札幌病毒(SaV)是肠胃炎的病原体。基于衣壳蛋白(VP1)核苷酸序列,SaV可分为5个基因组(GI - GV),其中GI、GII、GIV和GV株感染人类。SaV无法培养,但在昆虫细胞中重组VP1的表达会导致形成与天然SaV抗原相似的病毒样颗粒(VLP)。在本研究中,我们新表达了SaV GII和GIV VLP,以比较所有人类SaV基因组之间的遗传和抗原关系。针对VLP的超免疫抗血清样本与同源VLP反应强烈。然而,在抗体ELISA中,几个抗血清样本与异源VLP有弱交叉反应。相反,抗原ELISA表明,所有人类基因组中的SaV VLP在抗原性上是不同的。这些发现表明SaV抗原性与VP1基因组分类和基因分型之间可能存在对应关系。