抗原性
生物
抗血清
衣壳
病毒学
基因型
多克隆抗体
交叉反应性
诺如病毒
表位
系统发育树
血清型
抗原
病毒
基因
遗传学
交叉反应
作者
Grant S. Hansman,Katsuro Natori,Haruko Shirato-Horikoshi,Satoko Ogawa,Oka T,Kazuhiko Katayama,Tomoyuki Tanaka,Tatsuya Miyoshi,Kenji Sakae,Shinichi Kobayashi,Michiyo Shinohara,Kazue Uchida,Nakao Sakurai,Kuniko Shinozaki,Mineyuki Okada,Yoshiyuki Seto,Kunio Kamata,Noriyo Nagata,Keiko Tanaka,Tatsuo Miyamura
标识
DOI:10.1099/vir.0.81532-0
摘要
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.
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