Monoclonal antibodies against the nucleocapsid proteins of henipaviruses: production, epitope mapping and application in immunohistochemistry

被引:7
|
作者
Xiao, C. [1 ]
Liu, Y. [1 ]
Jiang, Y. [1 ]
Magoffin, D. E. [2 ,3 ]
Guo, H. [1 ]
Xuan, H. [4 ]
Wang, G. [4 ]
Wang, L. -F. [2 ,3 ]
Tu, C. [1 ]
机构
[1] Acad Mil Med Sci, Inst Vet Sci, Changchun 130062, Peoples R China
[2] Australian Biosecurity Cooperat Res Ctr Emerging, Geelong, Vic, Australia
[3] CSIRO, Livestock Ind, Australian Anim Hlth Lab, Geelong, Vic, Australia
[4] Guangdong Acad Agr Sci, Vet Res Inst, Guangzhou, Peoples R China
关键词
D O I
10.1007/s00705-007-1079-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Four monoclonal antibodies (mAbs) were generated by immunizing BALB/C mice with recombinant nucleocapsid protein (N) of Nipah virus (NiV) and Hendra virus (HeV) expressed in E. coli. Two mAbs each were obtained for the HeV N and NiV N, respectively. All four mAbs displayed specific reactivity with the recombinant N proteins of both viruses by western blot, which was further confirmed by immunofluorescent antibody assay using fixed insect cells infected with recombinant baculoviruses expressing either the HeV or NiV N protein. Epitope mapping using a 12-mer random peptide phage display library revealed two linear antigenic sites of the henipavirus N proteins, KLxR (aa 17-20) and FKREM (aa 446-450), which have not been reported previously. Two of the mAbs were able to specifically recognize HeV antigens by immunohistochemical staining of lung tissue sections of a horse experimentally infected with HeV. These reagents will be a useful addition to the collection of tools essential for further research and improvement in diagnosis of henipaviruses.
引用
收藏
页码:273 / 281
页数:9
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