Generation and evaluation of a recombinant Newcastle disease virus strain R2B with an altered fusion protein cleavage site as a vaccine candidate

Newcastle disease (ND) is a highly contagious and fatal disease of chickens. Newcastle disease virus (NDV) strain R2B is an Indian mesogenic strain used for secondary vaccination in chickens. Mesogenic strains have increased virulence and immunogenicity but may cause disease in vaccinated birds, thu...

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Veröffentlicht in:Microbial pathogenesis 2018-05, Vol.118, p.230-237
Hauptverfasser: Yadav, Kalpana, Pathak, Dinesh C., Saikia, Deep Prakash, Debnath, Ashis, Ramakrishnan, Saravanan, Dey, Sohini, Chellappa, Madhan Mohan
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Sprache:eng
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Zusammenfassung:Newcastle disease (ND) is a highly contagious and fatal disease of chickens. Newcastle disease virus (NDV) strain R2B is an Indian mesogenic strain used for secondary vaccination in chickens. Mesogenic strains have increased virulence and immunogenicity but may cause disease in vaccinated birds, thus rendering them ineffective for use. In this study, we generated a recombinant NDV by changing the fusion protein cleavage site of mesogenic rNDV-R2B from a polybasic amino acid motif RRQKRF to a dibasic amino acid motif GRQGRL leading to generation of an attenuated virus, rNDV-R2B-FPCS. The modified recombinant virus had similar growth characteristics as rNDV-R2B, but was less virulent in susceptible chickens. Immunization of the recombinant attenuated virus to one week of age SPF chickens generated a protective immune response with a substantial reduction in virus shed after challenge with virulent NDV. The results of the study indicate that the modified rNDV-R2B-FPCS virus can be used for primary immunization in birds without any adverse reactions. •The mesogenic NDV strain R2B was changed to an avirulent virus by reverse genetics.•Virulence of the modified virus was greatly reduced as indicated by MDT and ICPI analysis.•The modified virus generated a robust immune response on primary immunization in SPF chicks.
ISSN:0882-4010
1096-1208
DOI:10.1016/j.micpath.2018.03.038