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人肠产毒性大肠杆菌中的一种新的菌毛假定定植因子PCFO20。

A new fimbrial putative colonization factor, PCFO20, in human enterotoxigenic Escherichia coli.

作者信息

Viboud G I, Binsztein N, Svennerholm A M

机构信息

Department of Medical Microbiology and Immunology, University of Göteborg, Sweden.

出版信息

Infect Immun. 1993 Dec;61(12):5190-7. doi: 10.1128/iai.61.12.5190-5197.1993.

Abstract

The ability to colonize the small intestine is essential for enterotoxigenic Escherichia coli (ETEC) to cause diarrhea. Several colonization factor antigens (CFAs) and putative colonization factors (PCFs) have been described for ETEC. However, there are still many ETEC strains isolated from patients with diarrhea which do not possess any of these antigens. To identify CFAs in ETEC lacking the above-mentioned antigens, we exploited the ability of ETEC to adhere to tissue-cultured cells from an enterocyte-like cell line, Caco-2. An ETEC strain producing heat-labile toxin and heat-stable toxin of serotype O20:K27:H- (ARG-2) that was isolated from a child with diarrhea in Argentina and bound to Caco-2 cells was studied in further detail. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analyses of this strain revealed a band of 25 kDa when bacteria were grown at 37 degrees C that was missing when the same strain was cultured at 20 degrees C. Furthermore, electron microscopy examination revealed the presence of fimbriae on the surfaces of cells of this strain when cells were grown at 37 degrees C but not at 20 degrees C. Rabbit antiserum raised against purified fimbriae reacted with the 25-kDa protein in immunoblotting and bound specifically to the fimbriae, as shown by immunoelectron microscopy. The presence of fimbriae, adhesion to Caco-2 cells, and the 25-kDa band seen in the SDS-PAGE were all simultaneously lost by single-insertion mutations. The N-terminal amino acid sequence of the protein subunit of the fimbriae showed no relation with those of the known colonization factors of ETEC. Furthermore, the fimbriae of the ARG-2 strain did not cross-react immunologically with any of the previously described adhesive factors in human ETEC when specific antisera against colonization factor antigens and putative colonization factors were used. Moreover, a specific antiserum raised against the fimbriae in ARG-2 did not react with ETEC carrying known colonization factors. We propose to name these new fimbriae PCFO20.

摘要

对产肠毒素大肠杆菌(ETEC)而言,定殖于小肠的能力对于其引发腹泻至关重要。已针对ETEC描述了几种定殖因子抗原(CFA)和假定定殖因子(PCF)。然而,仍有许多从腹泻患者中分离出的ETEC菌株不具备这些抗原中的任何一种。为了鉴定缺乏上述抗原的ETEC中的CFA,我们利用了ETEC粘附于来自肠上皮样细胞系Caco-2的组织培养细胞的能力。对一株从阿根廷一名腹泻儿童分离出的、产生不耐热毒素和耐热毒素且血清型为O20:K27:H-(ARG-2)并能与Caco-2细胞结合的ETEC菌株进行了更深入的研究。对该菌株进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分析发现,当细菌在37℃生长时出现一条25 kDa 的条带,而在20℃培养同一菌株时该条带缺失。此外,电子显微镜检查显示,当细胞在37℃生长时该菌株细胞表面存在菌毛,而在20℃生长时则没有。用针对纯化菌毛产生的兔抗血清在免疫印迹中与25 kDa蛋白发生反应,并如免疫电子显微镜所示特异性结合菌毛。单插入突变同时导致菌毛的存在、对Caco-2细胞的粘附以及SDS-PAGE中出现的25 kDa条带全部丧失。菌毛蛋白亚基的N端氨基酸序列与ETEC已知定殖因子的序列无关。此外,当使用针对定殖因子抗原和假定定殖因子的特异性抗血清时,ARG-2菌株的菌毛与人类ETEC中任何先前描述的粘附因子均无免疫交叉反应。此外,针对ARG-2中菌毛产生的特异性抗血清不与携带已知定殖因子的ETEC发生反应。我们提议将这些新菌毛命名为PCFO20。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf5/281300/fcab87caacee/iai00024-0262-a.jpg

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