Skip Navigation
Skip to contents

J Bacteriol Virol.  2008 Sep;38(3):139-147. 10.4167/jbv.2008.38.3.139.

Detection of Infectious Bursal Disease Virus by Double Antibody Sandwich ELISA

Affiliations
  • 1National Veterinary Research Institute, National Veterinary Research and Quarantine ServiceAnyang, Gyeonggi, Korea. choiks@nvrqs.go.kr
  • 2JenoBiotech Inc, Chuncheon, Gangwon, Korea.

Abstract

Infectious bursal disease virus (IBDV) is responsible for a highly contagious disease of poultry causing severe immunosuppression in chickens. A double antibody sandwich ELISA (DAS-ELISA) was developed to detect IBDV from clinical samples. Two kinds of anti-IBDV antibodies, monoclonal antibody R63 and chicken anti-IBDV sera, were used for DAS-ELISA. Detection limit of IBDV by DAS-ELISA was approximately 10(2.7) EID(50)/ml. The DAS-ELISA detected IBDV from most (13/14) of vaccine products including mild, intermediate and intermediate-plus types. The DAS-ELISA also detected IBDV from all (19/19) of field Korean isolates including very virulent and intermediate-plus phenotypes. Our results indicate that the DAS-ELISA would provide useful diagnostic tool to detect IBDV from clinical samples as well as rapid quantitative detection of IBDV.

Keyword

Antigen detection; Diagnosis; ELISA; Infectious bursal disease

MeSH Terms

Antibodies, Monoclonal
Chickens
Enzyme-Linked Immunosorbent Assay
Immunosuppression
Infectious bursal disease virus
Limit of Detection
Phenotype
Poultry
Viruses
Antibodies, Monoclonal
Full Text Links
  • JBV
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2026 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr