Epitope mapping of canine distemper virus phosphoprotein by monoclonal antibodies

被引:5
|
作者
Sugai, Akihiro [1 ]
Kooriyama, Takanori [1 ]
Sato, Hiroki [1 ]
Yoneda, Misako [1 ]
Kai, Chieko [1 ]
机构
[1] Univ Tokyo, Lab Anim Res Ctr, Inst Med Sci, Minato Ku, Tokyo 1088639, Japan
关键词
canine distemper virus; epitope; monoclonal antibody; phosphoprotein; C-TERMINAL DOMAIN; MEASLES-VIRUS; P-PROTEIN; NUCLEOCAPSID BINDING; GENOME REPLICATION; MESSENGER-RNA; HOST-RANGE; NUCLEOPROTEIN; EXPRESSION; INFECTION;
D O I
10.1111/j.1348-0421.2009.00176.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The gene for phosphoprotein (P) of CDV encodes three different proteins, P, V, and C. The P protein is involved in viral gene transcription and replication. In the present study, we produced MAbs against a unique domain of the CDV-P protein, from aa 232 to 507, and determined their antigenic sites. By immunizing BALB/c mice with the recombinant P protein-specific fragment, we obtained six MAbs. Competitive binding inhibition assays revealed that they recognized two distinct regions of the P protein. Western blot analysis and immunofluorescence assays using deletion mutants of the unique C-terminus of the CDV-P protein revealed that all MAbs recognized a central short region (aa 233-303) of the CDV-P protein. In addition, linear and conformational epitopes have been determined, and at least four antigenic sites exist in the P protein central region. Furthermore, four of the MAbs were found to react with the P protein of recent Japanese field isolates but not with that of the older CDV strains, including a vaccine strain. Thus, these MAbs could be clinically useful for quick diagnosis during the CDV outbreaks.
引用
收藏
页码:667 / 674
页数:8
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