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Screening of novel vivax malaria transmission-blicking vaccine candidate molecule

Research Project

Project/Area Number 25305009
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypePartial Multi-year Fund
Section海外学術
Research Field Parasitology (including sanitary zoology)
Research InstitutionEhime University

Principal Investigator

TORII MOTOMI  愛媛大学, プロテオサイエンスセンター, 教授 (20164072)

Co-Investigator(Kenkyū-buntansha) Tachibana Mayumi  愛媛大学, プロテオサイエンスセンター, 助教 (00301325)
Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥17,550,000 (Direct Cost: ¥13,500,000、Indirect Cost: ¥4,050,000)
Fiscal Year 2015: ¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
Fiscal Year 2014: ¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
Fiscal Year 2013: ¥6,630,000 (Direct Cost: ¥5,100,000、Indirect Cost: ¥1,530,000)
Keywords寄生虫学 / マラリア / ワクチン / 三日熱マラリア / 伝播阻止ワクチン / 感染症 / 熱帯病 / 伝播阻止 / 三日熱マラリア原虫 / 伝搬阻止 / 寄生虫
Outline of Final Research Achievements

Malaria transmission-blocking vaccines (TBV) aim to interfere with the development of the malaria parasite in the mosquito vector, and thus prevent spread of transmission in a community. We aimed to discover novel Plasmodium vivax TBV candidates by using rodent malaria model and finally selected four target molecules; PvG#3, PvG#6, PvG#13 and PvG#16. We produced the recombinant proteins of these target molecules using wheat germ cell-free system. Rabbit antisera against these recombinant proteins were generated. In IFA, anti-PvG#3, -PvG#6, -PvG#13 and -PvG#16 antisera were reacted on the surface of P. vivax gametocytes. Membrane feeding transmission assays using P. vivax isolates obtained in Thailand demonstrated that anti-PvG#3, anti-PvG#6 and anti-PvG#16 antisera significantly reduced the number of oocysts developing in the mosquito midgut. In conclusion, our results indicate that PvG#3, PvG#6 and PvG#16 are potential transmission-blocking vaccine candidates of P. vivax.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Annual Research Report
  • 2013 Annual Research Report
  • Research Products

    (4 results)

All 2016 2015 2014 2013

All Presentation (4 results)

  • [Presentation] 新規伝播阻止ワクチン候補PyGM75の抗原決定領域の決定2016

    • Author(s)
      橘 真由美、鳥居本美、須藤 萌、坪井敬文
    • Organizer
      第85回日本寄生虫学会大会
    • Place of Presentation
      宮崎県宮崎市
    • Year and Date
      2016-03-19
    • Related Report
      2015 Annual Research Report
  • [Presentation] Screening for highly immunogenic region of PyGM75, a novel transmission-blocking vaccine candidate2015

    • Author(s)
      Tachibana M, Torii M, Sudo M, Tsuboi T, Ishino T.
    • Organizer
      64th Annual Meeting of American Society of Tropical Medicine and Hygiene
    • Place of Presentation
      Philadelphia, USA
    • Year and Date
      2015-10-25
    • Related Report
      2015 Annual Research Report
  • [Presentation] 三日熱マラリア伝搬阻止ワクチン候補抗原(Pvs25)の反復整列化とそのワクチン効果2014

    • Author(s)
      原國 哲也、山田 清太郎、宮田 健、山口 類、玉城 志博、坪井 敬文、Jetsumon Sattabongkot、橘 真由美、鳥居 本美、新川 武
    • Organizer
      第83回日本寄生虫学会
    • Place of Presentation
      松山市、愛媛
    • Related Report
      2013 Annual Research Report
  • [Presentation] Novel molecule that is supecifically expressed on male gametocyte and microgamete has potential role on exflageration.2013

    • Author(s)
      Tachibana M, Torii M, Sudo M, Yokouchi Y, Tsuboi T, Ishino T.
    • Organizer
      ASTMH 62nd Annual Meeting
    • Place of Presentation
      Washington DC, USA
    • Related Report
      2013 Annual Research Report

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Published: 2013-05-21   Modified: 2019-07-29  

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