Protection from Clinical Disease Against Three Highly Virulent Strains of Newcastle Disease Virus After In Ovo Application of an Antibody–Antigen Complex Vaccine in Maternal Antibody–Positive Chickens

2012 ◽  
Vol 56 (3) ◽  
pp. 555-560 ◽  
Author(s):  
Darrell R. Kapczynski ◽  
Alison Martin ◽  
Eid E. Haddad ◽  
Daniel J. King
2020 ◽  
Vol 87 (1) ◽  
Author(s):  
Oday A. Aljumaili ◽  
Muhammad B. Bello ◽  
Swee K. Yeap ◽  
Abdul R. Omar ◽  
Aini Ideris

Despite the availability of Newcastle disease (ND) vaccines for more than six decades, disease outbreaks continue to occur with huge economic consequences to the global poultry industry. The aim of this study is to develop a safe and effective inactivated vaccine based on a recently isolated Newcastle disease virus (NDV) strain IBS025/13 and evaluate its protective efficacy in chicken following challenge with a highly virulent genotype VII isolate. Firstly, high titre of IBS025/13 was exposed to various concentrations of binary ethylenimine (BEI) to determine the optimal conditions for complete inactivation of the virus. The inactivated virus was then prepared in form of a stable water-in-oil emulsion of black seed oil (BSO) or Freund’s incomplete adjuvant (FIA) and used as vaccines in specific pathogen-free chicken. Efficacy of various vaccine preparations was also evaluated based on the ability of the vaccine to protect against clinical disease, mortality and virus shedding following challenge with highly virulent genotype\VII NDV isolate. The results indicate that exposure of NDV IBS025/13 to 10 mM of BEI for 21 h at 37 °C could completely inactivate the virus without tempering with the structural integrity of the viral hemagglutin-neuraminidase protein. More so, the inactivated vaccines adjuvanted with either BSO- or FIA-induced high hemagglutination inhibition antibody titre that protected the vaccinated birds against clinical disease and in some cases virus shedding, especially when used together with live attenuated vaccines. Thus, genotype VII-based NDV-inactivated vaccines formulated in BSO could substantially improve poultry disease control particularly when combined with live attenuated vaccines.


2016 ◽  
Vol 54 (5) ◽  
pp. 1228-1235 ◽  
Author(s):  
Kiril M. Dimitrov ◽  
Dong-Hun Lee ◽  
Dawn Williams-Coplin ◽  
Timothy L. Olivier ◽  
Patti J. Miller ◽  
...  

Virulent strains of Newcastle disease virus (NDV) cause Newcastle disease (ND), a devastating disease of poultry and wild birds. Phylogenetic analyses clearly distinguish historical isolates (obtained prior to 1960) from currently circulating viruses of class II genotypes V, VI, VII, and XII through XVIII. Here, partial and complete genomic sequences of recent virulent isolates of genotypes II and IX from China, Egypt, and India were found to be nearly identical to those of historical viruses isolated in the 1940s. Phylogenetic analysis, nucleotide distances, and rates of change demonstrate that these recent isolates have not evolved significantly from the most closely related ancestors from the 1940s. The low rates of change for these virulent viruses (7.05 × 10−5and 2.05 × 10−5per year, respectively) and the minimal genetic distances existing between these and historical viruses (0.3 to 1.2%) of the same genotypes indicate an unnatural origin. As with any other RNA virus, Newcastle disease virus is expected to evolve naturally; thus, these findings suggest that some recent field isolates should be excluded from evolutionary studies. Furthermore, phylogenetic analyses show that these recent virulent isolates are more closely related to virulent strains isolated during the 1940s, which have been and continue to be used in laboratory and experimental challenge studies. Since the preservation of viable viruses in the environment for over 6 decades is highly unlikely, it is possible that the source of some of the recent virulent viruses isolated from poultry and wild birds might be laboratory viruses.


PLoS ONE ◽  
2017 ◽  
Vol 12 (2) ◽  
pp. e0172812 ◽  
Author(s):  
Guoyuan Wen ◽  
Lintao Li ◽  
Qingzhong Yu ◽  
Hongling Wang ◽  
Qingping Luo ◽  
...  

Virology ◽  
1988 ◽  
Vol 165 (1) ◽  
pp. 291-295 ◽  
Author(s):  
Ulrike M. Schaper ◽  
Frederick J. Fuller ◽  
Marsha D.W. Ward ◽  
Yasmin Mehrotra ◽  
Henry O. Stone ◽  
...  

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