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Development of a rabies vaccine seed with high productivity and immunogenicity by modification of glycosylation

Research Project

Project/Area Number 24658258
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeSingle-year Grants
Research Field Applied veterinary science
Research InstitutionOita University

Principal Investigator

YAMADA Kentaro  大分大学, 医学部, 助教 (70458280)

Project Period (FY) 2012-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2013: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2012: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Keywords狂犬病 / ウイルス / ワクチン / N型糖鎖 / 免疫原性 / 狂犬病ウイルス
Research Abstract

In this work, we aimed to identify the rabies virus G protein applicative for an effective rabies vaccine by modification of the N-glycosylation. We found that the street virus G proteins with the multiple N-glycosylation additions did not enhance virus production compared with the G proteins with the single addition. The G protein with five additional N-glycosylation sites was able to produce few progeny viruses, but it recovered the function to produce progeny viruses in the presence of an inhibitor of cellular enzymes associated with N-glycosylation, indicating that this modified G protein may be applicative for development of a safe live vaccine strain with limited replication. Moreover, we found that the N-glycan addition, especially addition at position 194, enhanced the immunogenicity of the street virus G protein.

Report

(3 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • Research Products

    (5 results)

All 2014 2013

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (4 results)

  • [Journal Article] Efficient N-glycosylation at position 37, but not at position 146, in the street rabies virus glycoprotein reduces pathogenicity2014

    • Author(s)
      Yamada K., Noguchi K., Nishizono A
    • Journal Title

      Virus Research

      Volume: 179 Pages: 169-176

    • DOI

      10.1016/j.virusres.2013.10.015

    • Related Report
      2013 Annual Research Report 2013 Final Research Report
    • Peer Reviewed
  • [Presentation] G蛋白質第37位へのN型糖鎖の効率的な付加は狂犬病ウイルス街上毒の病原性を低下させる2013

    • Author(s)
      山田健太郎、野口賀津子、西園晃
    • Organizer
      第156回日本獣医学会学術集会
    • Place of Presentation
      岐阜市
    • Related Report
      2013 Final Research Report
  • [Presentation] 狂犬病ウイルス街上毒においてG蛋白質第37位へのN型糖鎖の効率的な付加は末梢感染後の病原性を低下させる2013

    • Author(s)
      山田健太郎、野口賀津子、西園晃
    • Organizer
      第61回日本ウイルス学会学術集会
    • Place of Presentation
      神戸市
    • Related Report
      2013 Final Research Report
  • [Presentation] G蛋白質第37位へのN型糖鎖の効率的な付加は狂犬病ウイルス街上毒の病原性を低下させる2013

    • Author(s)
      山田健太郎、野口賀津子、西園晃
    • Organizer
      日本獣医学会
    • Place of Presentation
      岐阜市
    • Related Report
      2013 Annual Research Report
  • [Presentation] 狂犬病ウイルス街上毒においてG蛋白質第37位へのN型糖鎖の効率的な付加は末梢感染後の病原性を低下させる2013

    • Author(s)
      山田健太郎、野口賀津子、西園晃
    • Organizer
      日本ウイルス学会
    • Place of Presentation
      神戸市
    • Related Report
      2013 Annual Research Report

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Published: 2013-05-31   Modified: 2019-07-29  

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