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  4. Development of an antigen-capture enzyme-linked immunosorbent assay using monoclonal antibodies for detecting H6 avian influenza viruses
 
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Development of an antigen-capture enzyme-linked immunosorbent assay using monoclonal antibodies for detecting H6 avian influenza viruses

Journal
Journal of Microbiology, Immunology and Infection
Journal Volume
45
Journal Issue
3
Pages
243-247
Date Issued
2012
Author(s)
Chen, Y.-T.
Tsao, Z.
Chang, S.-T.
Juang, R.-H.
Wang, L.-C.
Chang, C.-M.
Wang, C.-H.
LIH-CHIANN WANG  
RONG-HUAY JUANG  
DOI
10.1016/j.jmii.2011.11.012
URI
http://www.scopus.com/inward/record.url?eid=2-s2.0-84861234262&partnerID=MN8TOARS
http://scholars.lib.ntu.edu.tw/handle/123456789/371433
Abstract
The H6 subtype of avian influenza virus (AIV) infection occurs frequently in wild and domestic birds. AIV antigen detection is preferred for controlling AIV as birds are infected before they produce antibodies. The purpose of this study was to develop an early diagnostic method for AIV detection. Six monoclonal antibodies (mAbs) developed from a field H6N1 AIV strain were tested for their ability to bind to viruses. The two that showed the greatest binding ability to AIVs were used for antigen detection. An antigen-capture enzyme-linked immunosorbent assay (ELISA) to detect H6 AIVs was developed using these mAbs. One mAb was coated onto an ELISA plate as the capture antibody. The other mAb was used as the detector antibody after labeling with horseradish peroxidase. The antigen-capture ELISA detected H6N1 AIVs but not H5 AIVs, human H1N1, H3N2 influenza or other viruses. This antigen-capture ELISA could be used to specifically detect H6N1 AIV.
Type
journal article

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