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[Vaccination against Newcastle disease with variants and differentiation between post-vaccinal and post-infectious

V Jestin1, M Cherbonnel, G Bennejan

  • 1CNEVA, Laboratoire central de recherche avicole et porcine, Ploufragan, France.

Annales De Recherches Veterinaires. Annals of Veterinary Research
|January 1, 1991
PubMed

Insights

Newcastle disease virus (NDV) variants resistant to monoclonal antibody 3115 were evaluated as vaccines. These NDV variants provided protection comparable to the La Sota strain but induced lower antibody titers, aiding differentiation of vaccinated from infected birds.

Area of Science:

  • Veterinary Virology
  • Immunology
  • Vaccinology

Background:

  • Newcastle disease virus (NDV) is a significant avian pathogen.
  • Developing effective NDV vaccines is crucial for poultry health.
  • Differentiating between post-vaccinal and post-infectious antibodies is important for disease surveillance.

Purpose of the Study:

  • To select and characterize monoclonal antibody-resistant NDV variants.
  • To evaluate the efficacy of these variants as experimental vaccines in chickens.
  • To assess the antibody responses induced by these variants for diagnostic purposes.

Main Methods:

  • Selection and cloning of NDV La Sota strain variants resistant to anti-HN Mab 3115.
  • Characterization using haemagglutination inhibition, ELISA, and Western blot.
  • Vaccination of chickens with live or inactivated variants and challenge with virulent NDV.
  • Measurement of antibody titers using ELISA blocking tests.

Main Results:

  • Selected variants (a25, b23, a16) did not bind to Mab 3115.
  • Variants a25 and b23 showed low intracerebral pathogenicity index (ICPI).
  • Vaccination with variants provided protection comparable to La Sota strain.
  • Variants induced significantly lower antibody titers than post-challenge titers.
  • Variant b23 showed poor diffusion and stable antibody titers upon repeated exposure.

Conclusions:

  • NDV variants resistant to Mab 3115 can serve as effective experimental vaccines.
  • Lower antibody responses induced by these variants may aid in distinguishing vaccinated from infected birds.
  • Further studies are needed to confirm the stability and efficacy of these variants for differentiating immune responses.

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