Expression and antigenicity of virus-like particles of norovirus and their application for detection of noroviruses in stool samples

被引:18
|
作者
Kamata, K
Shinozaki, K
Okada, M
Seto, Y
Kobayashi, S
Sakae, KN
Oseto, M
Natori, K
Shirato-Horikoshi, H
Katayama, K
Tanaka, TK
Takeda, N
Taniguchi, K [1 ]
机构
[1] Fujita Hlth Univ, Sch Med, Dept Virol & Parasitol, Toyoake, Aichi 4701192, Japan
[2] Denka Seiken Co Ltd, Tech Mkt Dept, Niigata, Japan
[3] Publ Hlth Lab Chiba Prefecture, Virol Lab, Chuo Ku, Chiba, Japan
[4] Osaka City Univ, Sch Med, Dept Virol, Abeno Ku, Osaka 545, Japan
[5] Aichi Prefectural Inst Publ Hlth, Kita Ku, Nagoya, Aichi 462, Japan
[6] Ehime Prefectural Inst Publ Hlth & Environm Sci, Matsuyama, Ehime, Japan
[7] Natl Inst Infect Dis, Dept Virol 2, Musashimurayama, Tokyo, Japan
[8] Sakai City Inst Publ Hlth, Sakai, Osaka, Japan
关键词
norovirus; ELISA; gastroenteritis; virus-like particle; calicivirus;
D O I
10.1002/jmv.20334
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human noroviruses (NoVs), members of the genus Norovirus in the family Caliciviridae, are the leading agents of nonbacterial acute gastroenteritis worldwide. Human NoVs are currently divided into at least two genogroups, genogroup I (GI) and genogroup II (GII), each of which contains at least 14 and 17 genotypes. To explore the genetic and antigenic relationship among NoVs, we expressed the capsid protein of four genetically distinct NoVs, the GI/3 Kashiwa645 virus, the GII/3 Sanbu809 virus, the GII/5 lchikawa754 virus, and the GII/7 Osaka 10-25 virus in baculovirus expression system. An antigen enzyme-linked immunosorbent assay (ELISA) with hyperimmune serum against the four recombinant capsid proteins and characterized previously three capsid proteins derived from GI/1, GI/4, and GII/12 was developed to detect the NoVs antigen in stools. The antigen ELISA was highly specific to the homotypic strains, allowing assignment of a strain to a Norovirus genetic cluster within a genogroup. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:129 / 136
页数:8
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