Abstract

In-ovo vaccination is an attractive immunization approach for poultry industry. However, most of the Newcastle disease virus (NDV) vaccine strains used after hatch are unsafe, as in-ovo vaccines, due to their high pathogenicity for chicken embryos. In this study, we evaluated the safety and immunogenicity of a thermostable NDV strain TS09-C, derived from V4 strain, as in-ovo vaccine. Chickens in-ovo vaccinated with the parental V4 strain displayed greatly reduced hatchability and severe histopathological lesions in both trachea and intestine tissues, while the hatchability was not affected by in-ovo vaccination withTS09-C strain. The safe dose that infected all chicken embryos without obviously histopathological lesions was 103.0 EID50 per bird. In-ovo vaccination of chickens with TS09-C virus conferred complete protection against virulent NDV challenge. Results suggest that the thermostable NDV strain TS09-C is a safe and immunogenic in-ovo vaccine candidate that can be delivered quickly and uniformly, and induce earlier immune response.

Highlights

  • Newcastle disease (ND) is one of the most important infectious diseases of poultry

  • Newcastle disease virus (NDV), the causative agent of ND, is classified into lentogenic, mesogenic, and velogenic strains based on the pathogenicity for chickens[1]

  • We evaluated the thermostable NDV strain TS09-C as an in-ovo vaccine and focused on three criteria

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Summary

Introduction

Newcastle disease virus (NDV), the causative agent of ND, is classified into lentogenic, mesogenic, and velogenic strains based on the pathogenicity for chickens[1]. For NDV, the commercial live vaccines used after hatch are not safe for in-ovo vaccination, and can cause death of chicken embryos[7]. A recombinant attenuated avian influenza virus (AIV) expressing both hemagglutinin gene of H5 AIV and hemagglutinin-neuraminidase gene of NDV, was generated and evaluated [10]. This recombinant virus, when used as in-ovo vaccine, could confer90% and 80% protection against H5 AIV and NDV challenge, respectively, as early as 3 weeks post-hatch[10]. We evaluated the safety and efficacy of NDV strain TS09-C as an in-ovo vaccine against virulent NDV challenge

Materials and methods
Evaluation of safety profile
Evaluation of immunogenicity and protection efficacy
Ethics statement
Results and discussion
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