• Title of article

    Expression, Purification and Characterization of Three Overlapping Immunodominant Recombinant Fragments from Bordetella pertussis Filamentous Hemagglutinin

  • Author/Authors

    Asgarian Omran، Hossein نويسنده , , Amirzargar، Ali Akbar نويسنده , , Arjmand، Mohammad نويسنده Department of Biochemistry, Pasteur Institute of Iran , , Eshraghian ، Mohammadreza نويسنده Department of Biostatistics and Epidemiology, School of Public Health, Tehran University of Medical Sciences , , Nikbin، Behrooz نويسنده , , Eshraghi، Saeid نويسنده Department of Microbiology, School of Public Health, Tehran University of Medical Sciences , , Mahdavi، Marzieh نويسنده Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR , , Khoshnoodi، Jalal نويسنده Department of Immunology, School of Public Health, Tehran University of Medical Sciences , , Jeddi Tehrani]، Mahmood نويسنده , , Rabbani، Hodjattallah نويسنده Immune and Gene Therapy Laboratory, CCK, Karolinska University Hospital Solna Department of Antigen and Antibody Engineering, Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR , , Shokri، Fazel نويسنده ,

  • Issue Information
    فصلنامه با شماره پیاپی 16 سال 2013
  • Pages
    9
  • From page
    20
  • To page
    28
  • Abstract
    Background: Filamentous hemagglutinin (FHA) is one of the most important immunoprotective antigens of Bordetella pertussis (B.pertussis) and a major component of the acellular pertussis vaccine. In the present study, three overlapping recombinant fragments from the immunodominant region of FHA were produced and their immunogenicity was investigated. Methods: Three overlapping coding sequences of FHA antigen were amplified from B.pertussis genomic DNA by PCR. Amplified fragments were expressed in Escherichia coli (E. coli) BL21(DE3) strain and purified through His-tag using Nickel-based chromatography. Purified fragments were characterized by SDS-PAGE and Western blotting techniques. In vitro peripheral blood mononuclear cells (PBMC) proliferation and IFN-γ production were assessed in a limited number of healthy adults vaccinated with a commercial acellular pertussis vaccine in response to all purified FHA fragments by H3-Thymidine incorporation and ELISA, respectively. Results: Recombinant FHA segments were successfully cloned and produced at high levels in E. coli BL21(DE3). SDS-PAGE and Western blot analyses confirmed their purity and reactivity. All three recombinant fragments together with a commercial native FHA were able to induce in vitro PBMC proliferation and IFN-γ production. Conclusion: Our preliminary results suggest that these overlapping recombinant FHA fragments are immunogenic and may prove to be immuno-protective.
  • Journal title
    AJMB Avicenna Journal of Medical Biotechnology
  • Serial Year
    2013
  • Journal title
    AJMB Avicenna Journal of Medical Biotechnology
  • Record number

    1983022