首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >ENTEROPATHOGENIC ESCHERICHIA COLI CONTAINS A PUTATIVE TYPE III SECRETION SYSTEM NECESSARY FOR THE EXPORT OF PROTEINS INVOLVED IN ATTACHING AND EFFACING LESION FORMATION
【24h】

ENTEROPATHOGENIC ESCHERICHIA COLI CONTAINS A PUTATIVE TYPE III SECRETION SYSTEM NECESSARY FOR THE EXPORT OF PROTEINS INVOLVED IN ATTACHING AND EFFACING LESION FORMATION

机译:肠致病性大肠埃希氏菌含有一种第三型分泌系统,对于附着和形成小节形成的蛋白质来说是必需的

获取原文
获取原文并翻译 | 示例
       

摘要

Enteropathogenic Escherichia coli (EPEC) causes a characteristic histopathology in intestinal epithelial cells called the attaching and effacing lesion. Although the histopathological lesion is well described the bacterial factors responsible for it are poorly characterized. We have identified four EPEC chromosomal genes whose predicted protein sequences are similar to components of a recently described secretory pathway (type III) responsible for exporting proteins lacking a typical signal sequence. We have designated the genes sepA, sepB, sepC, and sepD (sep, for secretion off. coli proteins), The predicted Sep polypeptides are similar to the Lcr (low calcium response) and Ysc (yersinia secretion) proteins of Yersinia species and the Mxi (membrane expression of invasion plasmid antigens) and Spa (surface presentation of antigens) regions of Shigella flexneri. Culture supernatants of EPEC strain E2348/69 contain several polypeptides ranging in size from 110 kDa to 19 kDa, Proteins of comparable size were recognized by human convalescent serum from a volunteer experimentally infected with strain E2348/69. A sepB mutant of EPEC secreted only the 110-kDa polypeptide and was defective in the formation of attaching and effacing lesions and protein-tyrosine phosphorylation in tissue culture cells. These phenotypes mere restored upon complementation with a plasmid carrying an intact sepB gene. These data suggest that the EPEC Sep proteins are components of a type III secretory apparatus necessary for the export of virulence determinants. [References: 40]
机译:肠致病性大肠杆菌(EPEC)在肠道上皮细胞中引起一种特征性的组织病理学,称为附着和消失的病变。尽管组织病理学病变已被很好地描述,但造成该病害的细菌因子的特征却很差。我们已经确定了四个EPEC染色体基因,它们的预测蛋白序列与最近描述的分泌途径(III型)的成分相似,该分泌通路负责输出缺乏典型信号序列的蛋白。我们指定了基因sepA,sepB,sepC和sepD(sep,用于分泌大肠杆菌蛋白)。预测的Sep多肽与耶尔森菌属的Lcr(低钙反应)和Ysc(耶尔森氏菌分泌)蛋白相似,弗氏志贺氏菌的Mxi(侵袭质粒抗原的膜表达)和Spa(抗原的表面呈递)区域。 EPEC菌株E2348 / 69的培养上清液含有大小在110 kDa至19 kDa范围内的几种多肽。人的恢复期血清可从实验上感染了E2348 / 69菌株的志愿者身上发现大小相当的蛋白质。 EPEC的sepB突变体仅分泌110-kDa多肽,在组织培养细胞中附着和消失的损伤形成以及蛋白酪氨酸磷酸化方面存在缺陷。这些表型仅在与携带完整sepB基因的质粒互补后即可恢复。这些数据表明,EPEC Sep蛋白是输出毒性决定簇所必需的III型分泌设备的组成部分。 [参考:40]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号