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产肠毒素大肠杆菌新的假定定植因子CS20的鉴定与特性分析

Identification and characterization of CS20, a new putative colonization factor of enterotoxigenic Escherichia coli.

作者信息

Valvatne H, Sommerfelt H, Gaastra W, Bhan M K, Grewal H M

机构信息

Centre for Internation Health, University of Bergen, Norway. Havard.

出版信息

Infect Immun. 1996 Jul;64(7):2635-42. doi: 10.1128/iai.64.7.2635-2642.1996.

Abstract

An enterotoxigenic Escherichia coli (ETEC) strain producing a previously undescribed putative colonization factor was isolated from a child with diarrhea in India. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of bacterial heat extracts revealed a polypeptide band of 20.8 kDa when the bacteria were grown at 37 degrees C which was absent after growth at 22 degrees C. A specific rabbit antiserum raised against the purified 20.8-kDa protein bound specifically to the fimbriae, as shown by immunoelectron microscopy, and inhibited bacterial adhesion to tissue-cultured Caco-2 cells. Transformation with a recombinant plasmid harboring the cfaD gene, which encodes a positive regulator for several ETEC fimbriae, induced hyperexpression of the 20.8-kDa fimbrial subunit and a substantial increase in the proportion of bacterial cells that were fimbriated. The N-terminal amino acid sequence of the polypeptide showed 65 and 60% identity to the PCFO20 and 987P fimbriae of human and porcine ETEC, respectively. We propose the term CS20 for this new putative colonization factor of human ETEC.

摘要

从印度一名腹泻儿童中分离出一株产此前未描述的假定定植因子的产肠毒素大肠杆菌(ETEC)菌株。细菌热提取物的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳显示,当细菌在37℃下生长时出现一条20.8 kDa的多肽带,而在22℃下生长后该条带消失。如免疫电子显微镜所示,用针对纯化的20.8 kDa蛋白制备的特异性兔抗血清与菌毛特异性结合,并抑制细菌对组织培养的Caco-2细胞的黏附。用携带cfaD基因(该基因编码几种ETEC菌毛的正调控因子)的重组质粒进行转化,诱导20.8 kDa菌毛亚基的过度表达以及带菌毛细菌细胞比例的大幅增加。该多肽的N端氨基酸序列与人源和猪源ETEC的PCFO20和987P菌毛分别具有65%和60%的同一性。我们将这种新的人源ETEC假定定植因子命名为CS20。

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