Genetic and antigenic diversity among noroviruses

被引:127
作者
Hansman, GS
Natori, K
Shirato-Horikoshi, H
Ogawa, S
Oka, T
Katayama, K
Tanaka, T
Miyoshi, T
Sakae, K
Kobayashi, S
Shinohara, M
Uchida, K
Sakurai, N
Shinozaki, K
Okada, M
Seto, Y
Kamata, K
Nagata, N
Tanaka, K
Miyamura, T
Takeda, N
机构
[1] Natl Inst Infect Dis, Dept Virol 2, Tokyo 2080011, Japan
[2] Sakai Inst Publ Hlth, Sakai, Osaka 5900953, Japan
[3] Aichi Prefectural Inst Publ Hlth, Virol Lab, Kita Ku, Nagoya, Aichi 4628576, Japan
[4] Mie Pref Sci & Technol Promot Ctr, Publ Hlth & Environm Res Div, Yokaichi, Mie 5121211, Japan
[5] Chiba Prefectural Inst Publ Hlth, Div Virol, Chiba 2608715, Japan
[6] Osaka Prefecture Univ, Grad Sch Life & Environm Sci, Osaka 5998531, Japan
[7] Denka Seiken Co Ltd, Tech Mkt Dept, Niigata 9591695, Japan
[8] Natl Inst Infect Dis, Dept Pathol, Tokyo 2080011, Japan
关键词
D O I
10.1099/vir.0.81532-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
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 Gill 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, Gl/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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页码:909 / 919
页数:11
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