Abstract

BackgroundNewcastle disease (ND) is a devastating worldwide disease of poultry characterized by increased respiration, circulatory disturbances, hemorrhagic enteritis, and nervous signs. Sequence analysis shows several amino acid residue substitutions at neutralizing epitopes on the F and HN proteins of recent Shaanxi strains. Both Cross protection and cross serum neutralization tests revealed that the traditional vaccine strains were unable to provide full protection for the flocks.MethodsTo better understand the epidemiology of Newcastle disease outbreak, a portion of the F gene and the full-length HN gene were amplified from Shaanxi isolates by reverse transcription-polymerase chain reaction (RT-PCR) and then conducted sequence and phylogenetic analyzes. In pathogenicity analysis, both high intra-cerebral pathogenicity index (ICPI) and mean death time (MDT) tests of chicken embryo were carried out. Furthermore, a cross-protection experiment in which specific-pathogen-free chickens vaccinated with a LaSota vaccine strain were challenged by the recent Shaanxi strain was also performed.ResultsNine Newcastle disease (ND) virus (NDV) isolates which were recovered from ND outbreaks in chicken flocks in China were genotypically and pathotypically characterized. Amino acid sequence analysis revealed that all the recent Shaanxi-isolated NDVs have 112R-R-Q-K-R-F117 for the C-terminus of the F2 protein and exhibit high ICPI and MDT of chicken embryos, suggesting that they were all classified as velogenic type of NDVs. Phylogenetic analysis of these isolates showed that they belong to subgenotype VIId that have been implicated in the recent outbreaks in northwestern China. The percentage of amino acid sequence identity of F protein between recent Shaanxi stains and five vaccine strains was in the range of 81.9 %–88.1 %, while the percentage of amino acid sequence identity of HN protein between recent Shaanxi strains and vaccine strains was in the range of 87.4 %–91.2 %. Furthermore, a number of amino acid residue substitutions at neutralizing epitopes on the F and HN proteins of these isolates were observed, which may lead to the change of antibody recognition and neutralization capacity. A cross-protection experiment indicated that specific-pathogen-free chickens vaccinated with a LaSota vaccine strain was not capable of providing full protection for the flocks that were challenged by the recent Shaanxi strain.ConclusionsTaken together, our findings reveal that recent Shannxi NDVstrains exhibit antigenic variations that could be responsible for recent outbreaks of NDVs in northwestern China.

Highlights

  • Newcastle disease (ND) is a devastating worldwide disease of poultry characterized by increased respiration, circulatory disturbances, hemorrhagic enteritis, and nervous signs

  • Pathogenicity analysis and reverse transcription-polymerase chain reaction (RT-polymerase chain reaction (PCR)) Nine Newcastle disease virus (NDV) strains were isolated from NDV-infected chickens during 2011 and named NDV/Chicken/TC/1/ 2011, NDV/Chicken/TC/2/2011, NDV/Chicken/ TC/3 /2011, NDV/Chicken/TC/4/2011, NDV/Chicken/TC/5/ 2011, NDV/Chicken/ TC/6 /2011, NDV/Chicken/TC/7/ 2011, NDV/Chicken/TC/8/2011, and NDV/Chicken /TC/9/2011 (Table 1)

  • All Shaanxi strains of NDV with mean death time (MDT) of 38–50 h and with intra-cerebral pathogenicity index (ICPI) of 1.67-1.78 (Table 1) were classified as virulent NDVs

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Summary

Introduction

Newcastle disease (ND) is a devastating worldwide disease of poultry characterized by increased respiration, circulatory disturbances, hemorrhagic enteritis, and nervous signs. Sequence analysis shows several amino acid residue substitutions at neutralizing epitopes on the F and HN proteins of recent Shaanxi strains. Both Cross protection and cross serum neutralization tests revealed that the traditional vaccine strains were unable to provide full protection for the flocks. On the basis of restriction fragment length polymorphism (RFLP) analysis and partial nucleotide sequencing of the cleavage recognition sequence of the F gene, NDV strains are grouped into at least 10 genogroups, among which genogroup VII can be further divided into several sub-genotypes [5, 7, 8]. The F protein mediates the fusion of viral and cellular membranes during penetration and spread between infected and adjacent cells. Previous studies have suggested that there are at least five antigenic sites related to epitopes on the HN protein of NDV, which are related to antibody recognition [13, 14]

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