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Investigation of liver infection mechanisms of malaria parasites

Research Project

Project/Area Number 18390128
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Parasitology (including Sanitary zoology)
Research InstitutionMie University

Principal Investigator

YUDA Masao  Mie University, Graduate School of Medicine, Professor (90293779)

Co-Investigator(Kenkyū-buntansha) IWANAGA Shiro  Tottori University, Graduate School of Medicine, Lecturer (20314510)
Project Period (FY) 2006 – 2007
Project Status Completed (Fiscal Year 2007)
Budget Amount *help
¥16,510,000 (Direct Cost: ¥14,800,000、Indirect Cost: ¥1,710,000)
Fiscal Year 2007: ¥7,410,000 (Direct Cost: ¥5,700,000、Indirect Cost: ¥1,710,000)
Fiscal Year 2006: ¥9,100,000 (Direct Cost: ¥9,100,000)
KeywordsMalaria / sporozoite / 肝臓 / 侵入 / 感染
Research Abstract

Malarial sporozoites, the liver-invasive forms, are injected into the skin by a mosquito bite. We found that cell traversal is important for sporozoites migrate to the circulation through the host dermis. This ability prevents sporozoite destruction by phagocytes and arrest by nonphagocytic cells in the host dermis. Then they are effectively targeted to hepatocytes and proliferate in them. So far, however, sporozoite molecules that mediate the specific infection of the liver remain unknown. We found that two proteins, Pbs36p and Pbs36, belonging to the plasmodium 6-cys domain protein family, and another novel protein, designated Pbs41, carry out this function. These molecules are specifically produced in liver-infective sporozoites. Target disruption of the respective genes nearly abolished sporozoite infectivity in the mammalian host. Invasion assays revealed that the mutant parasites could not commit to infection, even when they encounter with hepatocytes, resulting in continuous traversal of hepatocytes. These results suggest that these proteins are necessary for sporozoites to recognize hepatocytes and commit to infection. This finding might lead to novel anti-malarial strategies that prevent sporozoite infection of the hepatocyte.

Report

(3 results)
  • 2007 Annual Research Report   Final Research Report Summary
  • 2006 Annual Research Report
  • Research Products

    (8 results)

All 2008 2006

All Journal Article (6 results) (of which Peer Reviewed: 2 results) Presentation (2 results)

  • [Journal Article] Host cell traversal is important for progression of the malaria parasite through the dermis to the liver2008

    • Author(s)
      Amino R, Giovannini D, Thiberge S, Gueirard P, Boisson B, Dubremetz JF, Prevost MC, Ishino T, Yuda M, and Menard R.
    • Journal Title

      Cell Host Microbe 3

      Pages: 88-96

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
    • Peer Reviewed
  • [Journal Article] Host cell traversal is important for progression of the malaria Parasite through the dermis to the liver2008

    • Author(s)
      Amino, R. Giovannini, D. Thiberge, S. Gueirard, P. Boisson, B. Dubremetz, IF. Prevost, MC. Ishino, T. Yuda, M. Menard, R
    • Journal Title

      Cell Host Microbe 3

      Pages: 86-96

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Journal Article] Host cell traversal is important for progession of the malaria parasite through the dermis to the liver2008

    • Author(s)
      Amino R, Giovannini D, Thiberge S, Gueirard P, Boisson B, Dubremetz JF, Prevost MC, Ishino T, Yuda M, and Menard R.
    • Journal Title

      Cell Host Microbe 3

      Pages: 88-96

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] CelTOS,a novel malarial protein that mediates transmission to mosquito and vertebrate hosts.2006

    • Author(s)
      Tohru Kariu, Tomoko Ishino, Kazuhiko Yano, Yasuo Chinzei, Masao Yuda
    • Journal Title

      Molecular Microbiol 59

      Pages: 1369-1379

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Identification and characterization of a collagen-induced platelet aggregation inhibitor, triplatin, from salivary glands of the assassin bug, Triatoma infestans2006

    • Author(s)
      Akihiro Morita, Haruhiko Isawa, Yuki Orito, Shiroh Iwanaga, Yasuc Chinzei, Masao Yuda
    • Journal Title

      FEBS J. 273

      Pages: 2955-2962

    • Related Report
      2006 Annual Research Report
  • [Journal Article] A calcium-dependent protein kinase regulates Plasmodium ookinete access to the midgut epithelial cell2006

    • Author(s)
      Tomoko Ishino, Yuki Orito, Yasuo Chinzei, Masao Yuda
    • Journal Title

      Molecular Microbiol. 59

      Pages: 1175-1184

    • Related Report
      2006 Annual Research Report
  • [Presentation] Identification of a master transcription facter that controls gene expression of the mosquito-invasive stage of malaria prasites2008

    • Author(s)
      Masao Yuda
    • Organizer
      Molecular approach to malaria 2008
    • Place of Presentation
      オーストラリア
    • Year and Date
      2008-02-03
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] Identification of a master transcription facter that controls gene expression of the mosquito-invasive stage of malaria prasites Molecular approach to Malaria2008

    • Author(s)
      Masao, Yuda
    • Place of Presentation
      Lorne Australia
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary

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Published: 2006-04-01   Modified: 2016-04-21  

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