عنوان مقاله :
Evaluating the Immunogenicity of Avian Influenza Virus Nucleoprotein
پديد آورندگان :
Khademi Sayed Bonadaki, Zahra Sadat Department of Biochemistry - North Tehran Branch - Islamic Azad University, Tehran , Madani, Rasool Department of Proteomics and Biochemistry - Razi vaccine and serum research institute - Agricultural research education and extension organization (AREEO), Karaj , Pakzad, Parviz Department of Biochemistry - North Tehran Branch - Islamic Azad University, Tehran , Golchinfar, Fariba Department of Proteomics and Biochemistry - Razi vaccine and serum research institute - Agricultural research education and extension organization (AREEO), Karaj , Emami, Tara Department of Proteomics and Biochemistry - Razi vaccine and serum research institute - Agricultural research education and extension organization (AREEO), Karaj
كليدواژه :
Influenza virus , Avian influenza , Nucleoprotein , Western blot
چكيده فارسي :
اين مقاله فاقد چكيده فارسي است
چكيده لاتين :
Background: Influenza viruses cause Avian Influenza (AI) is a serious infectious disease belonging to type A Orthomyxovirus.
A viral RNA synthesis is due to an interaction of the nucleoprotein (NP) with the viral polymerase. In the present study, we
have evaluated the immunogenicity of avian influenza virus nucleoprotein.
Materials & Methods: An Influenza Virus N9H2 subtype A/Chicken Iran/259/2014 was selected. In order to perform
electrophoresis and purification of nucleoprotein, the protein concentration of the samples was determined. SDS-PAGE and
Native-PAGE electrophoresis on polyacrylamide gel were done and differences in gel bands in two methods were compared.
Purification of the virus nucleoprotein performed by electroelution method and purified nucleoprotein were assayed by ELISA
to obtain the produced antibody titers. Ouchterlony and western blot tests were used for final approval.
Results: By determining the molecular weight of each polypeptides, the molecular weights of H9N2 proteins were ranged from
30 to 140kDa and the molecular weight of the nucleoprotein was 60kDa. The nucleoprotein was purified by electroelution
method. Ouchterlony showed that in serum dilution of 1:2 and 1:4, the sediment lines were formed between the serum and
the NP antigen. The NP-ELISA enables rapid serological diagnosis in 1:20. Finally, the western blot test confirmed the 60kDa
nucleoprotein band.
Conclusion: The nucleoprotein which was purified by electroelution retained its antigenic property and it could be applied
in diagnostic kits.
عنوان نشريه :
ميكروب شناسي پزشكي ايران