in vivo experimental model to determine antigenic variations among infectious bursal disease viruses

• Published in: Avian pathology Vol. 42; no. 4; pp. 309 - 315
• Main Authors: Durairaj, Vijay, Linnemann, Erich, Icard, Alan H, Williams, Susan M, Sellers, Holly S, Mundt, Egbert
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis Group 01.08.2013; Taylor & Francis Ltd
• Subjects: Animal vaccines; Animals; antigenic variation; Antigens; Antigens, Viral - genetics; Avian flu; Birnaviridae Infections - veterinary; blood serum; bursa of Fabricius; Bursa of Fabricius - pathology; Chick Embryo; Chickens; Disease Models, Animal; double-stranded RNA; Immune Sera - immunology; in vivo studies; infectious bursal disease; Infectious bursal disease virus; Infectious bursal disease virus - immunology; intravenous injection; neutralization tests; Neutralization Tests - veterinary; Pathogens; Poultry; Poultry Diseases - virology; specific pathogen-free animals; Specific Pathogen-Free Organisms; vaccines; Viral Vaccines - genetics; viruses
• ISSN: 1465-3338; 0307-9457; 1465-3338
• DOI: 10.1080/03079457.2013.793783

Infectious bursal disease virus (IBDV) is a double-stranded RNA virus causing infectious bursal disease in chickens. IBDV undergoes antigenic drift, so characterizing the antigenicity of IBDV plays an important role for identification and selection of vaccine candidates. In this study, an in vivo experimental model was developed to differentiate a new antigenic variant of IBDV. To this end, a hyper-immune serum to IBDV E/Del-type virus was generated in specific pathogen-free chickens and a standard volume of the hyper-immune serum was serially diluted and injected in specific pathogen-free birds via intravenous, subcutaneous, or intramuscular routes. The chickens were bled at different time points in order to evaluate the dynamics of virus neutralization titres. Based on the results, chickens were injected with different serum dilutions by the subcutaneous route. Twenty-four hours later, chickens were bled and then challenged with 100 median chicken infectious doses of the E/Del virus and a new IBDV variant. Chickens were euthanized at 7 days post infection and the bursa of Fabricius was removed for microscopic evaluation to determine the bursal lesion score. The determined virus neutralization titre along with the bursal lesion score was used to determine the breakthrough titre in the in vivo chicken model. Based on the data obtained, an antigenic subtype of IBDV was identified and determined to be different from E/Del. This model is a sensitive model for determination of IBDV antigenicity of non-tissue culture adapted IBDV.