Abstract

Newcastle disease virus (NDV) is a prototype member of avian paramyxovirus serotype 1 (APMV-1), which causes severe and contagious disease in the commercial poultry and wild birds. Despite extensive vaccination programs and other control measures, the disease remains endemic around the globe especially in Asia, Africa, and the Middle East. Being a single serotype, genotype II based vaccines remained most acceptable means of immunization. However, the evidence is emerging on failures of vaccines mainly due to evolving nature of the virus and higher genetic gaps between vaccine and field strains of APMV-1. Most of the epidemiological and genetic characterizations of APMVs are based on conventional methods, which are prone to mask the diverse population of viruses in complex samples. In this study, we report the application of a simple, robust, and less resource-demanding methodology for the whole genome sequencing of NDV, using next-generation sequencing (NGS) on the Illumina MiSeq platform. Using this platform, we sequenced full genomes of five virulent Malaysian NDV strains collected during 2004–2013. All isolates clustered within highly prevalent lineage 5 (specifically in lineage 5a); however, a significantly greater genetic divergence was observed in isolates collected from 2004 to 2011. Interestingly, genetic characterization of one isolate collected in 2013 (IBS025/13) shown natural recombination between lineage 2 and lineage 5. In the event of recombination, the isolate (IBS025/13) carried nucleocapsid protein consist of 55–1801 nucleotides (nts) and near-complete phosphoprotein (1804–3254 nts) genes of lineage 2 whereas surface glycoproteins (fusion, hemagglutinin-neuraminidase) and large polymerase of lineage 5. Additionally, the recombinant virus has a genome size of 15,186 nts which is characteristics for the old genotypes I–IV isolated from 1930 to 1960. Taken together, we report the occurrence of a natural recombination in circulating strains of NDV in commercial poultry using NGS methodology. These findings will not only highlight the potential of RNA viruses to evolve but also to consider the application of NGS in revealing the genetic diversity of these viruses in clinical materials. Factors that drive these evolutionary events and subsequent impact of these divergences on clinical outcome of the disease warrant future investigations.

Highlights

  • Newcastle disease virus (NDV) is a type species of an avian paramyxovirus serotype 1 (APMV-(1), which belongs to genus Avulavirus in the family Paramyxoviridae

  • Since the analysis revealed that NP and P gene regions of isolate IBS025/13 have the highest genomic similarity toward lineage 2 viruses over lineage 5 (Figures 3A,B), we investigated the first 1/3 of NDV genome alignment to identify potential breakpoints by using recombinant detection program (RDP) (Martin et al, 2005)

  • Since adopted method used a unique combination of indexes to each NDV sample during multiplexing and raw sequenced data was filtered according to the tagged indexes, generated sequences are originated purely from the NDV isolates obtained from outbreaks

Read more

Summary

Introduction

Newcastle disease virus (NDV) is a type species of an avian paramyxovirus serotype 1 (APMV-(1), which belongs to genus Avulavirus in the family Paramyxoviridae. Depending on the pathogenicity in chicken, NDV strains are classified into highly virulent (velogenic), intermediate (mesogenic), and avirulent (lentogenic) strains (Alexander, 1997). The amino acid sequence of the F protein cleavage site has been used to determine the pathogenicity of NDV (Nagai et al, 1976). The sequence of the F protein cleavage site in mesogenic and velogenic strains of NDV consists of a polybasic cleavage site (R/K) RQ(R/K) R↓F, which is readily recognized by ubiquitous furin, an intracellular protease abundant in several cells and tissues, and cleaves in many tissues resulting in systematic infection. Initiation of viral infection by cleavage of the F protein in lentogenic strains is restricted to respiratory and enteric systems and limiting the infections in these organs (Collins et al, 1993)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call