Strategies to improve Newcastle disease vaccines
Cardenas Garcia, Nany Stivalis
MetadataShow full item record
Despite decades of research, Newcastle disease (ND) persists as a continual threat to the poultry industry. Current vaccines have not been able to markedly reduce the global prevalence of disease and cannot prevent replication and shedding of the challenge virus; therefore, improved vaccines are required. To evaluate the effect of genotype-specific ND vaccines, a chimeric virus expressing the F and HN genes from a genotype XIII vNDV (rLS-PK33) was developed. Specific-pathogen-free chickens were vaccinated with LaSota or rLS-PK33 live vaccines at different doses, and challenged with virulent PK33 to evaluate and compare their performance on preventing mortality and challenge virus shedding. In addition, a plasmid and an attenuated ND virus expressing chicken IFN-γ (rZJ1*L/IFNγ), and an attenuated NDV expressing chicken IL-10 (rZJ1*L/IL-10) were developed to investigate their effect on modulating the immune response in chickens and their effect on protection and reduction of virus shedding after challenge with vZJ1. Cloning and reverse genetic techniques were utilized for the development of all recombinant viruses. These were characterized by sequencing of the fusion protein cleavage site and inserted genes, intracerebral pathogenicity index assay, mean death time assay in eggs, ELISA and Western blotting for cytokine determination, virus isolation and titration in eggs, hemagglutination inhibition assay for antibody quantification, and lymphocyte proliferation assays and flow cytometric analysis for evaluation of cellular immune response. Our results reveled that rLS-PK33 decreased viral shedding more efficiently than LaSota; additionally, it was able to increase survival rates better than LaSota when administered at suboptimal doses. Evaluation of the effects of chIFN-γ delivered by plasmid DNA, live or inactivated rZJ1*L/IFNγ, demonstrated that, regardless of the delivery system, chIFN-γ did not enhance the immune response. On the contrary, evaluation of the effect of chIL-10 delivered by inactivated rZJ1*L/IL-10, resulted in an increased antibody response and lower antigen-specific T cell response, without increasing morbidity and mortality after challenge. In conclusion, these results provide new strategies to improve ND vaccines, and provide new insights to better understand the chicken immune response, as well as the effects of two key avian cytokines on immune response modulation.
Showing items related by title, author, creator and subject.
Biochemical and immunological characterization of the immobilization antigens of Ichthyophthirius multifiliis Wang, Xuting (uga, 2001-12)The pathogenic ciliate Ichthyophthirius multifiliis (Fouquet) infects a wide range of freshwater fish and causes the disease Ichthyophthiriasis (Ich) or “white spot”. Fish that survive infection acquire immunity to subsequent ...
In ovo immunization of chickens for Newcastle disease virus using recombinant Newcastle disease viruses Marcano, Valerie C (uga, 2017-12)In ovo vaccination has been used commercially for over 20 years to control avian diseases due to its significant advantages over conventional vaccination. The advantages of in ovo vaccination include a significant reduction ...
Development of diagnostic methods and examination of vaccination failures for avian coronavirus infectious bronchitis virus Roh, Ha-Jung (uga, 2013-05)Infectious bronchitis virus (IBV) is an avian coronavirus with major economic importance to commercial chicken producers worldwide. Due to the existence of multiple serotypes and variants of the virus that do not cross ...