• Title of article

    Cloning and Expression of Rabies Virus Glycoprotein Gene into Eukaryotic System

  • Author/Authors

    Borhani ، K Department of Virology - School of Medical Sciences - Tarbiat Modares University , Bamdad ، T Department of Virology - School of Medical Sciences - Tarbiat Modares University , Ajorloo ، M Department of Virology - School of Medical Sciences - Tarbiat Modares University , Mozhgani ، SHR Human Rabies Vaccine Laboratory - Institute of Iran , Miandehi ، N Viral Vaccines Production Department - Production and Research Complex Pasteur, - Institute of Iran , Moradi-Joshaghan ، A Viral Vaccines Production Department - Production and Research Complex Pasteur - Institute of Iran , Gholami ، AR Human Rabies Vaccine Laboratory, Viral Vaccines Production Department - Production and Research Complex Pasteur - Institute of Iran

  • From page
    8
  • To page
    11
  • Abstract
    Background and Aims: The aim of this study was cloning and expression of rabies virus glycoprotein by a eukaryotic expression plasmid pcDNA3.1(+) in BSR cell line. This construct might be used for a potential DNA vaccine. Materials and Methods: Glycoprotein gene was synthesized and cloned into pBluescript vector and then sub cloned into eukaryotic expression vector (pcDNA3.1(+)). After verification of the cloning, the recombinant plasmid was transfected into BSR cell line (a clone of BHK21 cell), and its expression was detected by RTPCR. Results: The authenticity of the recombinant plasmid pcDNA3.1(+)Gp has been confirmed by a quick check method and restriction endonuclease digestion analysis, and after transfection into eukaryotic cells, the presence of mRNA transcripts was verified by reverse transcriptasepolymerase chain reaction (RTPCR). Conclusion: This study demonstrated that the construction of eukaryotic expression plasmid for rabies virus glycoprotein is possible. Nevertheless, more work is necessary to develop this kind of vaccine for final use.
  • Keywords
    Rabies virus , glycoprotein , DNA vaccine , Reverse Transcriptase , Polymerase Chain Reaction (RT , PCR)
  • Journal title
    Iranian Journal of Virology
  • Journal title
    Iranian Journal of Virology
  • Record number

    2507547