Identification and subgrouping of pigeon type Newcastle disease virus strains by restriction enzyme cleavage site analysis

• Published in: Journal of virological methods 2006-02, Vol.131 (2), p.115-121
• Main Authors: Ujvári, Dorina, Wehmann, Enikő, Herczeg, József, Lomniczi, Béla
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Columbidae - virology; Deoxyribonucleases, Type II Site-Specific - metabolism; DNA, Viral - genetics; DNA, Viral - metabolism; Electrophoresis, Agar Gel; F gene; Fundamental and applied biological sciences. Psychology; Microbiology; Newcastle Disease - virology; Newcastle disease virus; Newcastle disease virus - classification; Newcastle disease virus - genetics; Newcastle disease virus - isolation & purification; Paramyxovirus; Phylogeny; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; PPMV1; Restriction site analysis; Reverse Transcriptase Polymerase Chain Reaction; Techniques used in virology; Viral Envelope Proteins - genetics; Virology
• ISSN: 0166-0934; 1879-0984
• DOI: 10.1016/j.jviromet.2005.07.012

A host variant of Newcastle disease virus (NDV, genus Avulavirus, family Paramyxoviridae) is responsible for an autonomous disease in pigeons. It emerged in the late 1970s in the Mediterranean region. Despite great genetic diversity the vast majority of strains belong to a monophyletic group (sublineage VIb) within genotype VI of NDV strains that were indigenous in the region at that time. To date only a monoclonal antibody assay is available for the specific identification of pigeon type strains. A specific genetic assay is described suitable for the identification of pigeon isolates. Cleavage site analysis of a 1349 bp amplicon of the fusion protein gene was carried out using restriction enzymes (RE) HinfI, BstOI and RsaI. RE analysis of over 100 strains isolated between 1978 and 2002 deriving from 16 countries has revealed nine RE-patterns, which were progressive site variants of the parental (group VI) genotype. In spite of substantial site variation, extant pigeon viruses lacked a BstOI cleavage site at nucleotide 1601 shared by other NDV strains of chicken origin. RE analysis is a simple and reliable method both for the identification and subgrouping of pigeon type viruses.