Hansman Grant S, Natori Katsuro, Shirato-Horikoshi Haruko, Ogawa Satoko, Oka Tomoichiro, Katayama Kazuhiko, Tanaka Tomoyuki, Miyoshi Tatsuya, Sakae Kenji, Kobayashi Shinichi, Shinohara Michiyo, Uchida Kazue, Sakurai Nakao, Shinozaki Kuniko, Okada Mineyuki, Seto Yoshiyuki, Kamata Kunio, Nagata Noriyo, Tanaka Keiko, Miyamura Tatsuo, Takeda Naokazu
Department of Virology II, National Institute of Infectious Diseases, Gakuen 4-7-1, Musashi-Murayama, Tokyo 208-0011, Japan.
Sakai Institute of Public Health, Sakai, Osaka 590-0953, Japan.
J Gen Virol. 2006 Apr;87(Pt 4):909-919. doi: 10.1099/vir.0.81532-0.
Human norovirus (NoV) strains cause a considerable number of outbreaks of gastroenteritis worldwide. Based on their capsid gene (VP1) sequence, human NoV strains can be grouped into two genogroups (GI and GII) and at least 14 GI and 17 GII genotypes (GI/1-14 and GII/1-17). Human NoV strains cannot be propagated in cell-culture systems, but expression of recombinant VP1 in insect cells results in the formation of virus-like particles (VLPs). In order to understand NoV antigenic relationships better, cross-reactivity among 26 different NoV VLPs was analysed. Phylogenetic analyses grouped these NoV strains into six GI and 12 GII genotypes. An antibody ELISA using polyclonal antisera raised against these VLPs was used to determine cross-reactivity. Antisera reacted strongly with homologous VLPs; however, a number of novel cross-reactivities among different genotypes was observed. For example, GI/11 antiserum showed a broad-range cross-reactivity, detecting two GI and 10 GII genotypes. Likewise, GII/1, GII/10 and GII/12 antisera showed a broad-range cross-reactivity, detecting several other distinct GII genotypes. Alignment of VP1 amino acid sequences suggested that these broad-range cross-reactivities were due to conserved amino acid residues located within the shell and/or P1-1 domains. However, unusual cross-reactivities among different GII/3 antisera were found, with the results indicating that both conserved amino acid residues and VP1 secondary structures influence antigenicity.
人诺如病毒(NoV)毒株在全球引发了大量的肠胃炎暴发。根据其衣壳基因(VP1)序列,人NoV毒株可分为两个基因组(GI和GII)以及至少14个GI基因型和17个GII基因型(GI/1 - 14和GII/1 - 17)。人NoV毒株无法在细胞培养系统中增殖,但在昆虫细胞中表达重组VP1会导致病毒样颗粒(VLP)的形成。为了更好地了解NoV的抗原关系,分析了26种不同NoV VLP之间的交叉反应性。系统发育分析将这些NoV毒株分为6个GI基因型和12个GII基因型。使用针对这些VLP产生的多克隆抗血清进行抗体ELISA来确定交叉反应性。抗血清与同源VLP强烈反应;然而,观察到不同基因型之间存在一些新的交叉反应性。例如,GI/11抗血清显示出广泛的交叉反应性,可检测到2个GI基因型和10个GII基因型。同样,GII/1、GII/10和GII/12抗血清也显示出广泛的交叉反应性,可检测到其他几种不同的GII基因型。VP1氨基酸序列比对表明,这些广泛的交叉反应性是由于位于外壳和/或P1 - 1结构域内的保守氨基酸残基所致。然而,发现不同GII/3抗血清之间存在异常的交叉反应性,结果表明保守氨基酸残基和VP1二级结构均影响抗原性。