MOLECULAR MECHANISM OF VIRULENT FACTOR PRODUCTION IN GRAM POSITIVE BACTERIA

革兰氏阳性菌毒力因子产生的分子机制

基本信息

  • 批准号:
    08407010
  • 负责人:
  • 金额:
    $ 23.36万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
  • 财政年份:
    1996
  • 资助国家:
    日本
  • 起止时间:
    1996 至 1999
  • 项目状态:
    已结题

项目摘要

Molecular mechanism of production of toxins and the other virulence factors in Gram positive bacteria has been investigated to develop novel infection control measures for Gram positive bacteria which produce variety of virulence factors to cause desease in human.1. The production of toxins and enzymes was regulated by the environmental factors.The production of toxins (α, β, γ, ε, θ, etc, in Clostridium perfringens, toxin A and B in C. difficile, soluble and surface virulent factors in Staphylococcus aureus) was regulated by the growth phase, density/population of bacteria (quoram sensing), carbon source and nutritional substrate, inter-cellular factors (like pheromon). Under the stressful condition for bacteria, ie ; heat, extream pH, in the presence of heavy metals, antibiotics, the bacteria induced the stress responsible genes including virulent genes.2. Specific receptors for sensing environmental factors.Each bacterium has a certain specific receptors for environmental factors, i … More .e., the most common one is the sensor component of two-component system. In C. perfringens, several systems have been identified, among which one for activation and the other for inhibition of production of toxin. In S. aureus, the receptors for zinc, alkaline, β-lactams were mostly identified.3. Information transmitting network in bacteria.Along with genomic analysis of C. perfringens, and that of Staphylococci, molecular basis of information transmitting system in bacteria has been made clear from receptor to effecter production as an sequential "molecular net work" with global regulatory system. This information is useful for the design of antibiotics in future.4. Regulation at the level of transcription, translation, post translation and secretion from cell.On basing upon those results, molecular net work of virulent factor production has been more clearly confirmed and the results will contribute to those who are looking for more specific effective anti-infection drugs and preventive measures. Less
研究革兰氏阳性菌产生毒素和其他毒力因子的分子机制,为革兰氏阳性菌的感染控制提供新的方法.产气荚膜梭菌产生α、β、γ、ε、θ等毒素,C.艰难梭菌、金黄色葡萄球菌中的可溶性和表面毒力因子)受生长期、细菌密度/群体(quoram传感)、碳源和营养底物、细胞间因子(如信息素)调节。细菌在高温、极端pH、重金属、抗生素等胁迫条件下,诱导了包括毒力基因在内的胁迫相关基因.感受环境因子的特异性受体。每一种细菌都有一定的感受环境因子的特异性受体, ...更多信息 例如,最常见的是双组分体系的传感器组分。In C.在产气荚膜杆菌中,已经鉴定了几种系统,其中一种用于激活,另一种用于抑制毒素的产生。In S.金黄色葡萄球菌主要为锌、碱性、β-内酰胺类药物的受体.沿着对C.通过对产气荚膜杆菌和葡萄球菌的研究,阐明了细菌信息传递系统从受体到效应子的分子基础是一个具有全局调控系统的有序的“分子网络”。这些信息对今后抗生素的设计具有参考价值.在转录水平、翻译水平、翻译后水平和细胞分泌水平上的调控,进一步明确了毒力因子产生的分子网络,为寻找更特异有效的抗感染药物和预防措施提供了依据。少

项目成果

期刊论文数量(49)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Shimizu, T., K. Ohtani, W. Ba-Thein, S. Inui, S. Nakamura, and H. Hayashi: "Characterization of a toxin-deficient Clostridium perfringens strain, KZ1340."Microbiol. Immunol.. 40. 141-145 (1996)
Shimizu, T.、K. Ohtani、W. Ba-Thein、S. Inui、S. Nakamura 和 H. Hayashi:“毒素缺陷产气荚膜梭菌菌株 KZ1340 的表征。”微生物学。
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    0
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Banu, Syera, Ohtani, K., Yaguchi, H., Sew, Tint, Cole, S. T., Hayashi, H. and Shimizu, T.: "Identification of novel VirR/VirS-regulated genes in Clostridium perfringens"Mol. Microbiol. 35. 1-12 (2000)
Banu,Syera,Ohtani,K.,Yaguchi,H.,Sew,Tint,Cole,S.T.,Hayashi,H. 和 Shimizu,T.:“产气荚膜梭菌中新型 VirR/VirS 调节基因的鉴定”Mol。
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    0
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Aoki,Y.,et al.: "Characterization of small colony variants of methicillin-resistant Staphylococcus aureus regrown in the presence of Arbekacin." J.Infect Chemother. 4. 107-111 (1999)
Aoki,Y.,et al.:“在阿贝卡星存在下重新生长的耐甲氧西林金黄色葡萄球菌小菌落变体的特征。”
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  • 影响因子:
    0
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  • 通讯作者:
Karazawa,T., et al: "Effect of arginine on toxin production by Clostridium difficile in definedmedium." Microbiol.Immunol. 41(8). 581-585 (1997)
Karazawa,T. 等人:“精氨酸对特定培养基中艰难梭菌产生毒素的影响”。
  • DOI:
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  • 影响因子:
    0
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  • 通讯作者:
K.Ohtani,M.Bando,T.Swe,S.Banu,M.Ooe,H.Hayashi,and T.Shimizu.: "Collagenase gene (colA) is located in the 3'-flanking region of the perfringolysin O (pfoA) locus in Clostridium perfringens." FEMS Microbiol..Lett.146. 155-160 (1997)
K.Ohtani、M.Bando、T.Swe、S.Banu、M.Ooe、H.Hayashi 和 T.Shimizu.:“胶原酶基因 (colA) 位于产气荚膜溶血素 O 的 3 侧翼区域(
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HAYASHI Hideo其他文献

HAYASHI Hideo的其他文献

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{{ truncateString('HAYASHI Hideo', 18)}}的其他基金

Acylhomoserine lactone synthase inhibitors mimicking the enzyme reaction intermediate
模拟酶反应中间体的酰基高丝氨酸内酯合酶抑制剂
  • 批准号:
    23658101
  • 财政年份:
    2011
  • 资助金额:
    $ 23.36万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Investigation of branching inhibitors secreted by non-host plants of arbuscular mycorrhizal fungi
丛枝菌根真菌非寄主植物分泌的分枝抑制剂的研究
  • 批准号:
    19580127
  • 财政年份:
    2007
  • 资助金额:
    $ 23.36万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Lipid composition and the synthesis system that responds to environmental change in Stapylococcus aureus.
金黄色葡萄球菌响应环境变化的脂质组成和合成系统。
  • 批准号:
    17590405
  • 财政年份:
    2005
  • 资助金额:
    $ 23.36万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Chemical signals controlling the arbuscular mycorrhiza symbiosis
控制丛枝菌根共生的化学信号
  • 批准号:
    15580097
  • 财政年份:
    2003
  • 资助金额:
    $ 23.36万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
RESEARCH ON THE EFFICIENCY OF CREATIVE FUNCTION OF ANALOGIES IN LEARNING SCIENCE
类比创造性功能在学习科学中的有效性研究
  • 批准号:
    11680199
  • 财政年份:
    1999
  • 资助金额:
    $ 23.36万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Studies on Okaramine-Production promoting Factor in Soyabean
大豆中豆渣胺促产因子的研究
  • 批准号:
    09660119
  • 财政年份:
    1997
  • 资助金额:
    $ 23.36万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Studies on Biosysnthesis of Insecticidal Indole Alkaloid Okaramines
杀虫吲哚生物碱奥卡胺的生物合成研究
  • 批准号:
    07660142
  • 财政年份:
    1995
  • 资助金额:
    $ 23.36万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Studies on biosynthesis of okaramines, insecticidal indole alkaloids.
豆蔻胺、杀虫吲哚生物碱的生物合成研究。
  • 批准号:
    05660122
  • 财政年份:
    1993
  • 资助金额:
    $ 23.36万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)
Pathogenic factors of cell adherent Escherichia coli
细胞贴壁大肠杆菌的致病因素
  • 批准号:
    62480156
  • 财政年份:
    1987
  • 资助金额:
    $ 23.36万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)

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Stress response mechanism regulated by the exonic promoter of Saccharomyces cerevisiae HKR1
酿酒酵母HKR1外显子启动子调控的应激反应机制
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表观遗传调控作为器官再生的新方法——从应激反应机制中学习
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    2021
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人体细胞新型应激反应机制的研究
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Stress response mechanism through temperature sensitivity of Importin alpha
通过 Importin alpha 温度敏感性的压力响应机制
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变形链球菌口腔生物膜形成的应激反应机制分析
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阐明导致抗衰老的线粒体应激反应机制并寻找诊断分子、功效
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