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一株大肠杆菌O75:K1:H7血培养分离株所表达的新型菌毛(S/F1C相关菌毛)的克隆与特性分析

Cloning and characterization of a new type of fimbria (S/F1C-related fimbria) expressed by an Escherichia coli O75:K1:H7 blood culture isolate.

作者信息

Pawelzik M, Heesemann J, Hacker J, Opferkuch W

机构信息

Medical Microbiology and Immunology, Ruhr-Universität Bochum, Federal Republic of Germany.

出版信息

Infect Immun. 1988 Nov;56(11):2918-24. doi: 10.1128/iai.56.11.2918-2924.1988.

Abstract

The Escherichia coli blood culture isolate BK658 (O75:K1:H7) expresses F1A and F1B fimbriae as well as a third fimbrial type which reacts with anti-S-fimbrial antiserum but fails to show S-specific binding properties (i.e., agglutination of bovine erythrocytes). To characterize these fimbriae, we cloned the respective genetic determinant in E. coli K-12. The resulting recombinant clone HB101(pMMP658-6) expresses fimbriae of 1.2-micron length and a diameter of approximately 7 nm. The determinant codes for the fimbrillin subunit, a protein of 17 kilodaltons in size, and for at least five other proteins of 87, 31, 23, 14.3, and 13.8 kilodaltons. By restriction analysis and by DNA-DNA hybridization, it could be shown that the cloned fimbrial determinant of strain BK658 exhibits a high degree of sequence homology to the gene clusters coding for S fimbrial adhesins (sfa) and F1C fimbriae (foc). By using the Western blot (immunoblot) technique and a quantitative enzyme-linked immunosorbent assay, it could be further demonstrated that the cloned fimbriae of BK658, S fimbriae, and F1C fimbriae share cross-reactive epitopes as well as antigenic determinants specific for each fimbrial type. No antigenic cross-reactivity with F1C fimbriae could be detected. The results indicate a genetical and serological relatedness of the cloned fimbriae to S fimbriae and F1C fimbriae. Therefore, this new type of fimbriae is preliminarily termed S/F1C-related fimbriae (Sfr).

摘要

从血液培养中分离出的大肠杆菌BK658(O75:K1:H7)表达F1A和F1B菌毛以及第三种菌毛类型,该菌毛与抗S菌毛抗血清发生反应,但未表现出S特异性结合特性(即牛红细胞凝集)。为了对这些菌毛进行表征,我们在大肠杆菌K-12中克隆了相应的遗传决定簇。所得重组克隆HB101(pMMP658-6)表达长度为1.2微米、直径约为7纳米的菌毛。该决定簇编码菌毛蛋白亚基,一种大小为17千道尔顿的蛋白质,以及至少另外五种大小分别为87、31、23、14.3和13.8千道尔顿的蛋白质。通过限制性分析和DNA-DNA杂交,可以证明菌株BK658克隆的菌毛决定簇与编码S菌毛黏附素(sfa)和F1C菌毛(foc)的基因簇具有高度的序列同源性。通过使用蛋白质印迹(免疫印迹)技术和定量酶联免疫吸附测定,可以进一步证明BK658克隆的菌毛、S菌毛和F1C菌毛具有交叉反应性表位以及每种菌毛类型特有的抗原决定簇。未检测到与F1C菌毛的抗原交叉反应性。结果表明克隆的菌毛与S菌毛和F1C菌毛在遗传和血清学上具有相关性。因此,这种新型菌毛被初步称为S/F1C相关菌毛(Sfr)。

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