Molecular epidemiology of cytolethal distending toxin-producing Escherichia coli

产细胞致死膨胀毒素大肠杆菌的分子流行病学

基本信息

  • 批准号:
    15406019
  • 负责人:
  • 金额:
    $ 7.23万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 财政年份:
    2003
  • 资助国家:
    日本
  • 起止时间:
    2003 至 2004
  • 项目状态:
    已结题

项目摘要

We have shown that cdtB gene was specifically identified among enteropathogenic E.coli(EPEC). Some of the strains are associated in causing bloody diarrhea among children and exhibited higher production of CDT. The cdtB positive strain mostly belongs to O86a and O127a serogroups. Pulsed-field gel electrophoresis profiles showed that the EPEC strains harboring ctdB were genetically diverse.In this study, 1607 stool specimens were screened for the cdtB harboring enteric pathogens. In the probe hybridization assay, 6 samples (0.4%) were positive and the PCR assay confirmed 5 strains. Form the cdtB probe or PCR positive samples only E.coli strains were isolated and confirmed by serology. Four out of six strains were identified as serogroup O142. Characterization of these strains for different virulence genes specific for diarrheagenic E.coli showed that six strains were enteropathogenic E.coli(EPEC), as they harbored eae as well as bfp genes. We have reported the same trend in our early reports.Expect for two, all the strains harbored cdtA and cdtC genes. These two strains were negative for cdtB by PCR and did not express the CDT in the tissue culture assay. Based on the variation in the sequence of amino acids, the Cdt is classified into CdtI, CdtII and CdtIII. Currently, we are analyzing all our strains to detect the Cdt alleles.Clinical and bacteriological studies have revealed that production of colicin by E.coli having a part of intestinal microbiocenasis is related to the clinical manifestation of inflammatory disease of the gastrointestinal tract. Colicin expression was determined in many enteric pathogens especially among enteropathogenic E.coli(EPEC) and enterohemorrhagic E.coli(EHEC). Colicin expression was confirmed with 3 out of 18 strains (16.7%). There is no correlation between serogroups and colicin expression.
我们已经证明cdtB基因在肠致病性大肠杆菌(EPEC)中被特异性地鉴定。一些菌株与引起儿童血性腹泻有关,并表现出较高的CDT产量。cdtB阳性菌株主要属于O86a和O127a血清群。脉冲场凝胶电泳图谱显示携带ctdB的EPEC菌株具有遗传多样性。探针杂交法检测阳性6例(0.4%),PCR法检测阳性5例。从cdtB探针或PCR阳性样品中,仅分离大肠杆菌菌株并通过血清学确认。6个菌株中有4个被鉴定为血清群O142。对这些菌株的不同致病性大肠杆菌特异性毒力基因的表征表明,6种菌株为肠致病性大肠杆菌(EPEC),因为它们携带eae和bfp基因。我们在早期的报道中也报道了同样的趋势,除了两个菌株外,所有菌株都携带cdtA和cdtC基因。这两个菌株通过PCR对cdtB是阴性的,并且在组织培养测定中不表达CDT。根据氨基酸序列的变化,Cdt分为CdtI、CdtII和CdtIII。目前,我们正在分析所有菌株以检测Cdt等位基因。临床和细菌学研究表明,具有部分肠道微生物菌群的大肠杆菌产生大肠杆菌素与胃肠道炎性疾病的临床表现有关。在许多肠道病原体中确定了大肠杆菌素表达,特别是在肠致病性大肠杆菌(EPEC)和肠出血性大肠杆菌(EHEC)中。大肠杆菌素的表达被证实与18株(16.7%)的3。血清群与大肠杆菌素表达之间没有相关性。

项目成果

期刊论文数量(23)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
4.腸管出血性大腸菌
4.肠出血性大肠杆菌
Virulence characterization and molecular epidemiology of enteroaggregative Escherichia coli isolates from hospitalized diarrheal patients in Kolkata, India
印度加尔各答住院腹泻患者肠聚集性大肠杆菌分离株的毒力特征和分子流行病学
Association of cytolethal distending toxin locus cdtB with enteropathogenic Escherichia coli isolated from patients with acute diarrhea in Calcutta, India
  • DOI:
    10.1128/jcm.41.11.5277-5281.2003
  • 发表时间:
    2003-11-01
  • 期刊:
  • 影响因子:
    9.4
  • 作者:
    Pandey, M;Khan, A;Ramamurthy, T
  • 通讯作者:
    Ramamurthy, T
Characterization of Shiga toxin-producing Escherichia coli (STEC) isolated from seafood and beef
从海鲜和牛肉中分离出的产志贺毒素大肠杆菌 (STEC) 的特性
  • DOI:
  • 发表时间:
    2004
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Kodama;S.;Yamamoto;A.;Iio;R.;Sakamoto;K;Hayakawa;K.;et al.;Kumar H.S.et al.
  • 通讯作者:
    Kumar H.S.et al.
Association of cytolethal distending toxin locus cdtB with entrooathogenic Escherichia coli isolated from acute diarrheal natients in Calcutta India
细胞致死膨胀毒素位点 cdtB 与印度加尔各答急性腹泻患者分离的致病性大肠杆菌的关联
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YAMASAKI Shinji其他文献

YAMASAKI Shinji的其他文献

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{{ truncateString('YAMASAKI Shinji', 18)}}的其他基金

Comparative analysis of prevalence and antimicrobial resistance of Campylobacters among Thailand, China and Japan
泰国、中国、日本弯曲杆菌流行率及耐药性比较分析
  • 批准号:
    21406013
  • 财政年份:
    2009
  • 资助金额:
    $ 7.23万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Genetic analysis of horizontal gene transfer of cyto lethal distending toxin(cdt) gene in Shigella spp. and Escherichia coli
志贺氏菌细胞致死膨胀毒素(cdt)基因水平基因转移的遗传分析。
  • 批准号:
    21590487
  • 财政年份:
    2009
  • 资助金额:
    $ 7.23万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Development of a simple and rapid PCR-RFLP for molecular epidemiologic analysis of enterohemorrhagic Escherichia coli
开发简单快速的PCR-RFLP用于肠出血性大肠杆菌的分子流行病学分析
  • 批准号:
    19590455
  • 财政年份:
    2007
  • 资助金额:
    $ 7.23万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Prevalence and comparative molecular epidemiologic analysis of enteric bacteria in south Asia and Africa
南亚和非洲肠道细菌的患病率和比较分子流行病学分析
  • 批准号:
    19406015
  • 财政年份:
    2007
  • 资助金额:
    $ 7.23万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Multi-drug resistance strains in Bengal region and analysis of their resistance genes as compared with those in Japan
孟加拉地区多重耐药菌株及其耐药基因与日本比较分析
  • 批准号:
    17406012
  • 财政年份:
    2005
  • 资助金额:
    $ 7.23万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
RESEARCH ON TRANSITION AND DIFFUSION OF ROOF-TILE TECHNOLOGY IN ANCIENT EAST ASIA
古代东亚屋瓦技术的变迁与传播研究
  • 批准号:
    17202022
  • 财政年份:
    2005
  • 资助金额:
    $ 7.23万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
A Study of Medieval Rooftiles
中世纪屋顶瓦的研究
  • 批准号:
    08610412
  • 财政年份:
    1996
  • 资助金额:
    $ 7.23万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
A Study of Nara Period Roof Tiles made by the same Mold in Palaces, Buddhist Temples and Provincial Center
宫殿、佛寺、省中心奈良时代同模瓦的研究
  • 批准号:
    05610339
  • 财政年份:
    1993
  • 资助金额:
    $ 7.23万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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Early prediction and evaluation cohort of bronchopulmonary dysplasia (EPEC-BPD) study
支气管肺发育不良的早期预测和评估队列(EPEC-BPD)研究
  • 批准号:
    21K07863
  • 财政年份:
    2021
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    $ 7.23万
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Host-cell mitochondrial alterations play a central role in EPEC pathogenesis
宿主细胞线粒体改变在 EPEC 发病机制中发挥核心作用
  • 批准号:
    10405052
  • 财政年份:
    2019
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    $ 7.23万
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Host-cell mitochondrial alterations play a central role in EPEC pathogenesis
宿主细胞线粒体改变在 EPEC 发病机制中发挥核心作用
  • 批准号:
    9815790
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    2019
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Host-cell mitochondrial alterations play a central role in EPEC pathogenesis
宿主细胞线粒体改变在 EPEC 发病机制中发挥核心作用
  • 批准号:
    10640083
  • 财政年份:
    2019
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  • 项目类别:
Prevalence, antimicrobial susceptibility and characterization of typical and atypical EPEC in Thailand and Kenya
泰国和肯尼亚典型和非典型 EPEC 的患病率、抗菌药物敏感性和特征
  • 批准号:
    17H04651
  • 财政年份:
    2017
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    $ 7.23万
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Host-pathogen interaction in a novel in vivo model of enteropathogenic Escherichia coli (EPEC) infection
肠道病原性大肠杆菌 (EPEC) 感染的新型体内模型中宿主与病原体的相互作用
  • 批准号:
    396639086
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    2017
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    $ 7.23万
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    Research Grants
Identification of novel molecular components at the cell periphery: Taking advantage of EPEC pedestals
细胞外围新型分子成分的鉴定:利用 EPEC 基座
  • 批准号:
    355316-2013
  • 财政年份:
    2017
  • 资助金额:
    $ 7.23万
  • 项目类别:
    Discovery Grants Program - Individual
Modulation of EPEC susceptibility and severity by the microbiome
微生物组对 EPEC 易感性和严重程度的调节
  • 批准号:
    9481667
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    2017
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    $ 7.23万
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Identification of novel molecular components at the cell periphery: Taking advantage of EPEC pedestals
细胞外围新型分子成分的鉴定:利用 EPEC 基座
  • 批准号:
    355316-2013
  • 财政年份:
    2016
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    $ 7.23万
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    Discovery Grants Program - Individual
Identification of novel molecular components at the cell periphery: Taking advantage of EPEC pedestals
细胞外围新型分子成分的鉴定:利用 EPEC 基座
  • 批准号:
    355316-2013
  • 财政年份:
    2015
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    $ 7.23万
  • 项目类别:
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