Examination of some biological properties of glycoprotein subunits of PHY-LMV.42 strain of Newcastle disease virus

• Main Authors: Milić Nenad, Nišavić Jakov, Borozan Sunčica, Zorić Andrea, Lazić Sava, Petrović Tamaš, Rašić Zoran
• Format: Article
• Language: srp
• Published: Faculty of Veterinary Medicine, Belgrade 2015-01-01
• Series: Veterinarski Glasnik
• Subjects: Newcastle disease virus; glycoprotein subunits; SDS-PAGE; LC ESI-TOF-MS/MS; immunization
• Online Access: http://www.doiserbia.nb.rs/img/doi/0350-2457/2015/0350-24571506337M.pdf
• ISSN: 0350-2457; 2406-0771

The objective of our work was to investigate some biological characteristics of purified glycoprotein subunits of Newcastle disease virus strain PHY-LMV.42 isolated from pigeons for the purpose of vaccine production. PHY-LMV.42 strain of Newcastle disease virus was multiplied by successive passages in embryonated eggs and identified by the methods of Reverse transcriptase PCR and Real-Time PCR along with F gene sequencing. Proving the presence of HN and F antigene in the virus subunits samples was carried out by hemagglutination inhibition method with referent immune sera. Biochemical characterization of glycoprotein subunits was performed by SDS-PAGE method as well as liquid chromatography with mass spectrometry (LC ESI-TOF-MS/MS). Testing for the virus subunits immunogenicity was carried out in biological experiment on 75 laying hens Tetra-SSL and 25 chickens Isa Brown by inducing an artificial infection with Hertz 33 strain of the virus. Low concentrations of the virus antigens of 0.36 mg/ml along with glycoprotein fractions of 77 i 58 kDa manifested a strong hemagglutination activity of 4096 HJ/0,1ml. The subunit vaccines of 256 and 128 HJ/0.5 ml induced a protective immune response in all the vaccinated animals. Based on the obtained results it can be concluded that low concentrations of purified virus subunits of PHY-LMV.42 strain can be used for preparing of effective vaccines. [Projekat Ministarstva nauke Republike Srbije, br. TR 31008: Development and application of molecular methods based on polymerase chain reaction (PCR) in quick and direct identification of Newcastle disease virus strains and investigation of immunogenicity of subunit vaccine prepared of their antigens]