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Analysis of species specificity in endoparasitoids

Research Project

Project/Area Number 09660047
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 植物保護
Research InstitutionNagoya University

Principal Investigator

TANAKA Toshiharu  Agricultural Sciences, Nagoya University Associate Professor, 農学部, 助教授 (30227152)

Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 1998: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1997: ¥1,500,000 (Direct Cost: ¥1,500,000)
Keywordshost specificity / endoparasitoid / stage specificity / Cotesia kariyai / Cotesia ruficrus / Pseudaletia separata / Pseudaletia separata / カリヤコマユバチ / イネヨトウコマユバチ / ポリドナウイルス
Research Abstract

Larval endoparasitoids have to regulate the host in the physiological condition to acquire the suitable state for the development of their eggs and larvae. Between two different parasitoids being able to attack the same host species (Pseudaletia separata), one parasitoid, Cotesia ruficrus is restricted to parasitize the young stadium of the host, while another parasitoid, Cotesia kariyai is able to parasitize successfully through all stadium. Reciprocal exchanging of the polydnavirus and the venom of each parasitoid produced the host regulation according to the characteristics of the polydnavirus. Each genomic DNA segments hybridized with the reciprocal genornic DNA segments of PDV.
Furthermore, we reported the cloning and characterization of Cotesia kariyai polydnavirus (CkPV) genes expressed in host Pseudaletia separata testes. We isolated clones encoding CkPV mRNAs from a cDNA library of host testes. We found two motif sequences of the RNase T_2 family in one of CkPV gene expressed in host testes. The CkPV RNase T_2 fragment was hybridized to more than one viral genome segments. By northern blot analysis using cloned CkPV RNase T_2 gene as a probe, we showed the 3.1 kbp and 2.3 kbp mRNAs were detected 4-12h after parasitization, which Was before the appearance of cells with abnormal chromatin in the host testes.

Report

(3 results)
  • 1998 Annual Research Report   Final Research Report Summary
  • 1997 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] 田中 利治: "ポリドナウイルス-幼虫寄生バチの共生者" 植物防疫. 52. 499-504 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Toshiharu Tanaka: "Polydnavirus-symbiont of larval endoparasitoid" Shokubutu-Boeki. 52(in Japanese). 499-504 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 田中 利治: "ポリドナウイルス一幼虫寄生バチの共生者" 植物防疫. 52. 499-504 (1998)

    • Related Report
      1998 Annual Research Report

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Published: 1997-04-01   Modified: 2016-04-21  

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