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Investigation of detection method for Vancomycin intermediated-resistant Staphylococcus aureus

Research Project

Project/Area Number 26461513
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Infectious disease medicine
Research InstitutionKitasato University

Principal Investigator

Hanaki Hideaki  北里大学, 北里生命科学研究所, 特任教授 (60286747)

Co-Investigator(Kenkyū-buntansha) 崔 龍洙  自治医科大学, 医学部, 教授 (50306932)
Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywordsバンコマイシン / VISA / ヘテロVISA / 検出 / 混合培養 / Vancomycin / VRSA / 耐性 / MALDI-TOFMS / hVISA / MRSA / ヘテロ耐性 / Staphylococcus aureus / 薬剤耐性 / hetero-VISA
Outline of Final Research Achievements

Antibiotic resistant cells emerge spontaneously at a certain frequency in the bacterial population that is termed as hetero-resistance. One of the most problematic antibiotic resistant bacteria in the clinical setting may be Staphylococcus aureus MRSA that exhibits resistance to structurally diverse multiple antibiotics including vancomycin. Among them, vancomycin intermediate resistant cells (VISA) appear in the population of vancomycin heteroresistant cells (hVISA). Therefore, detection of VISA cells in the hVISA population is difficult due to the fact that VISA appears at the frequency of 0.012% of hVISA. To detect VISA by the MIC method, over 10 times of cells are required compared with that of the conventional MIC determination. To overcome this difficulty, studies are on progress to detect VISA specific proteins by using MALDI-TOF-Mass spectroscopy.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (3 results)

All 2014

All Presentation (3 results) (of which Invited: 2 results)

  • [Presentation] VISAとその前駆体であるヘテロVISAを考える2014

    • Author(s)
      花木秀明
    • Organizer
      第62回日本化学療法学会西日本支部総会 第57回日本感染症学会中日本地方会学術集会 第84回日本感染症学会西日本地方会学術集会 合同学会
    • Place of Presentation
      岡山コンベンションセンター, 岡山県
    • Year and Date
      2014-10-24
    • Related Report
      2014 Research-status Report
    • Invited
  • [Presentation] MRSAの基礎2014

    • Author(s)
      花木秀明
    • Organizer
      第88回日本感染症学会学術集会 第62回日本化学療法学会総会 合同学会
    • Place of Presentation
      ヒルトン福岡シーホーク, 福岡県
    • Year and Date
      2014-06-20
    • Related Report
      2014 Research-status Report
    • Invited
  • [Presentation] A MODIFIED AGAR SCREENING METHOD FOR DETECTION OF HETEROGENEOUS VANCOMYCIN-INTERMEDIATE STAPHYLOCOCCUS AUREUS2014

    • Author(s)
      Longzhu Cui, Hidehito Matsui and Hideaki Hanaki
    • Organizer
      24th European Congress of Clinical Microbiology and Infectious Diseases
    • Place of Presentation
      Centre Convencions Internacional Barcelona, Barcelona, Spain
    • Year and Date
      2014-05-13
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2018-03-22  

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