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参与肠致病性大肠杆菌弥漫性黏附的一种黏附素(AIDA-I)的克隆与表达

Cloning and expression of an adhesin (AIDA-I) involved in diffuse adherence of enteropathogenic Escherichia coli.

作者信息

Benz I, Schmidt M A

机构信息

Zentrum für Molekulare Biologie Heidelberg, Universität Heidelberg, Federal Republic of Germany.

出版信息

Infect Immun. 1989 May;57(5):1506-11. doi: 10.1128/iai.57.5.1506-1511.1989.

Abstract

The adherence of enteropathogenic Escherichia coli (EPEC) to the small bowel mucosa is an important step in the pathogenesis of diarrheal diseases. It has been shown that many EPEC strains adhere to HEp-2 and especially HeLa cells in characteristic patterns termed localized adherence (LA) and diffuse adherence (DA). A plasmid-derived DNA fragment encoding a factor specific for LA hybridized only to EPEC strains expressing LA, which demonstrated that LA and DA are mediated by two genetically distinct adhesins. EPEC strain 2787 (O127:H27), isolated from a case of infantile diarrhea, exhibited three major properties: (i) it showed DA to HeLa cells, (ii) it carried two large (ca. 100-kilobase [kb]) plasmids and one small plasmid of about 3 kb, and (iii) no fimbriae could be detected by electron microscopy in organisms grown on agar plates or in liquid cultures. Whole isolated plasmid DNA was partially digested with EcoRI and cloned into the vector pBR322. One recombinant clone (pIB6) was found to exhibit the same DA pattern on HeLa cells as did the parent strain. This clone contained an 11-kb DNA fragment derived from the largest of the three plasmids, as shown by Southern hybridization. By deletion analysis, a 6.0-kb DNA fragment was shown to be sufficient for expression of the DA phenotype. This insert encoded the production of a 100,000-dalton protein mediating adhesion to HeLa cells.

摘要

肠道致病性大肠杆菌(EPEC)对小肠黏膜的黏附是腹泻病发病机制中的重要一步。已表明许多EPEC菌株以称为局部黏附(LA)和弥漫性黏附(DA)的特征模式黏附于HEp-2细胞,尤其是HeLa细胞。编码LA特异性因子的质粒衍生DNA片段仅与表达LA的EPEC菌株杂交,这表明LA和DA由两种遗传上不同的黏附素介导。从一例婴儿腹泻病例中分离出的EPEC菌株2787(O127:H27)表现出三个主要特性:(i)它对HeLa细胞表现出DA;(ii)它携带两个大的(约100千碱基[kb])质粒和一个约3 kb的小质粒;(iii)在琼脂平板或液体培养物中生长的生物体中,通过电子显微镜未检测到菌毛。将分离的完整质粒DNA用EcoRI部分消化并克隆到载体pBR322中。发现一个重组克隆(pIB6)在HeLa细胞上表现出与亲本菌株相同的DA模式。如Southern杂交所示,该克隆包含一个源自三个质粒中最大质粒的11 kb DNA片段。通过缺失分析,显示一个6.0 kb DNA片段足以表达DA表型。该插入片段编码产生一种介导对HeLa细胞黏附的100,000道尔顿蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da7d/313306/8477e516af44/iai00065-0168-a.jpg

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