مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

123
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

228
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Purification of Nucleoprotein of H9N2 Avian Influenza Virus Strain by Electroelution

Pages

  0-0

Abstract

 Background: Avian Influenza Virus (AIV) belongs to the family of Orthomyxoviruses typeAandcauses avian influenza (AI) infectious disease. Currently, serological diagnostic techniques such as agar gel propagation (AGP), Hemagglutination inhibition, and enzymelinked immunosorbent assay (ELISA) are considered as important tools for the antibodies detection against viral antigens. Due to antigenic variation in the surface of AIV glycoproteins (hemagglutinin and Neuraminidase), these proteins cannot be used in serological tests. Development of assays to detect AI surface glycoproteins is problematic because a great variety of combinations of these subtypes are found in nature. The internal antigen determinants on the nucleoprotein (NP) are highly conserved within influenza viruses, making this protein more appropriate for a serological test. Objectives: In the experimental present study, an effectual method was expanded to purify NP of H9N2 AIV based on Electroelution method. Methods: AIV strain A/flash chicken/Iran/772/1998 (H9N2) was acquired from the Department of Avian Influenza Reference Laboratory, Razi Vaccine and Serum Research Institute, Iran, about 2 cc, in 2017. Nucleoprotein of AIV (H9N2) was purified by an efficient and simple modified method directly from Native Polyacrylamide Gel Electrophoresis (PAGE) according to the Electroelution method. The purified protein concentration was defined by the Lowry method, and the purifiedNPprotein (60 KDa) was examined by Tricine-SDS-PAGE. Results: The protein concentration of the virus solution was 4. 62 mg/mL by the Lowry method. The purified Nucleoprotein concentration was 0. 296 mg/mL by Lowry method and the Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis results showed only a 60-KDa protein band in the gel. Conclusions: The current technique was simple and rapid and made it possible to isolate NP from the H9N2 virus. The Nucleoprotein antigen is an appropriate candidate potential to detect antibodies against all subtypes of AIV and used as the main target antigen for the diagnosis of influenza virus due to its very high scale of sequence preserved among exist strains.

Cites

  • No record.
  • References

    Cite

    APA: Copy

    HASHEMI, MARYAM, Aghamaali, Mahmoudreza, MADANI, RASOOL, & EMAMI, TARA. (2019). Purification of Nucleoprotein of H9N2 Avian Influenza Virus Strain by Electroelution. IRANIAN RED CRESCENT MEDICAL JOURNAL (IRCMJ), 21(10), 0-0. SID. https://sid.ir/paper/755621/en

    Vancouver: Copy

    HASHEMI MARYAM, Aghamaali Mahmoudreza, MADANI RASOOL, EMAMI TARA. Purification of Nucleoprotein of H9N2 Avian Influenza Virus Strain by Electroelution. IRANIAN RED CRESCENT MEDICAL JOURNAL (IRCMJ)[Internet]. 2019;21(10):0-0. Available from: https://sid.ir/paper/755621/en

    IEEE: Copy

    MARYAM HASHEMI, Mahmoudreza Aghamaali, RASOOL MADANI, and TARA EMAMI, “Purification of Nucleoprotein of H9N2 Avian Influenza Virus Strain by Electroelution,” IRANIAN RED CRESCENT MEDICAL JOURNAL (IRCMJ), vol. 21, no. 10, pp. 0–0, 2019, [Online]. Available: https://sid.ir/paper/755621/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button