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

机译:大肠杆菌O75:K1:H7血培养分离株表达的新型菌毛(与S / F1C相关的菌毛)的克隆和鉴定。

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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).
机译:大肠杆菌血液培养分离株BK658(O75:K1:H7)表达F1A和F1B菌毛以及与抗S纤维抗血清反应但未显示S特异性结合特性(即牛凝集)的第三种纤维类型红细胞)。为了表征这些菌毛,我们在大肠杆菌K-12中克隆了各自的遗传决定簇。所得重组克隆HB101(pMMP658-6)表达长度为1.2微米,直径约为7 nm的菌毛。该决定因子编码菌丝蛋白亚基,一种17千道尔顿的蛋白质,以及至少五种其他蛋白质,分别为87、31、23、14.3和13.8千道尔顿。通过限制性酶切分析和DNA-DNA杂交,可以证明克隆的菌株BK658的纤维决定簇与编码S纤维粘附素(sfa)和F1C菌毛(foc)的基因簇表现出高度的序列同源性。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,克隆的BK658菌毛,S菌毛和F1C菌毛具有交叉反应性表位以及每种纤维蛋白特异的抗原决定簇类型。没有检测到与F1C菌毛的抗原交叉反应。结果表明克隆的菌毛与S菌毛和F1C菌毛的遗传和血清学相关性。因此,这种新型的菌毛被初步称为S / F1C相关菌毛(Sfr)。

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