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Published in: Virology Journal 1/2010

Open Access 01-12-2010 | Research

Use of monoclonal antibodies against Hendra and Nipah viruses in an antigen capture ELISA

Authors: Cheng-Feng Chiang, Michael K Lo, Paul A Rota, Christina F Spiropoulou, Pierre E Rollin

Published in: Virology Journal | Issue 1/2010

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Abstract

Background

Outbreaks of Hendra (HeV) and Nipah (NiV) viruses have been reported starting in 1994 and 1998, respectively. Both viruses are capable of causing fatal disease in humans and effecting great economical loss in the livestock industry.

Results

Through screening of hybridomas derived from mice immunized with γ-irradiated Nipah virus, we identified two secreted antibodies; one reactive with the nucleocapsid (N) protein and the other, the phosphoprotein (P) of henipaviruses. Epitope mapping and protein sequence alignments between NiV and HeV suggest the last 14 amino acids of the carboxyl terminus of the N protein is the target of the anti-N antibody. The anti-P antibody recognizes an epitope in the amino-terminal half of P protein. These monoclonal antibodies were used to develop two antigen capture ELISAs, one for virus detection and the other for differentiation between NiV and HeV. The lower limit of detection of the capture assay with both monoclonal antibodies was 400 pfu. The anti-N antibody was used to successfully detect NiV in a lung tissue suspension from an infected pig.

Conclusion

The antigen capture ELISA developed is potentially affordable tool to provide rapid detection and differentiation between the henipaviruses.
Appendix
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Metadata
Title
Use of monoclonal antibodies against Hendra and Nipah viruses in an antigen capture ELISA
Authors
Cheng-Feng Chiang
Michael K Lo
Paul A Rota
Christina F Spiropoulou
Pierre E Rollin
Publication date
01-12-2010
Publisher
BioMed Central
Published in
Virology Journal / Issue 1/2010
Electronic ISSN: 1743-422X
DOI
https://doi.org/10.1186/1743-422X-7-115

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