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Infectious Bronchitis Virus Population Structure Defines Immune Response and Protection
R A Zegpi1, K S Joiner1, V L van Santen1
1Department of Pathobiology, Auburn University College of Veterinary Medicine, Auburn, AL 36830.
The genetic diversity of infectious bronchitis virus (IBV) vaccines impacts immune responses. A more homogeneous vaccine enhanced antibody avidity, while a diverse vaccine boosted innate immunity and reduced viral load.
Area of Science:
- Veterinary Virology
- Immunology
- Poultry Health
Background:
- Understanding the impact of vaccine population genetic structure on immune responses is crucial for improving poultry health.
- Arkansas (Ark) Delmarva Poultry Industry (DPI)-type vaccines and a homogeneous CEK-adapted variant (CEK-ArkDPI) were used to model these effects.
Purpose of the Study:
- To investigate how the genetic structure of infectious bronchitis virus (IBV) vaccines influences immune responses and protection against challenge.
- To compare the efficacy of a heterogeneous commercial vaccine versus a homogeneous adapted vaccine.
Main Methods:
- Chickens were vaccinated with either a commercial ArkDPI vaccine or a homogeneous CEK-ArkDPI vaccine.
- Vaccinated chickens were challenged with a virulent Ark99-type IBV strain (AL/4614/98).
- Viral loads, respiratory signs, tracheal lesions, antibody levels, antibody avidity, and innate immune gene expression were assessed.
Main Results:
- The heterogeneous commercial ArkDPI vaccine was more effective at reducing viral loads, while both vaccines similarly reduced respiratory signs and tracheal lesions.
- The homogeneous CEK-ArkDPI vaccine elicited greater antibody levels and antibody avidity.
- The heterogeneous commercial ArkDPI vaccine induced a stronger innate immune response, indicated by greater mRNA expression of immune genes.
Conclusions:
- Vaccine population structure significantly impacts both adaptive (antibody avidity) and innate immune responses.
- Homogeneous IBV vaccines may favor adaptive immunity, while diverse vaccines can enhance innate immunity and viral clearance.
- Immune pressure from vaccination selects for distinct subpopulations within the challenge virus.
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