首页> 美国卫生研究院文献>Journal of Bacteriology >Comparative analysis of flagellin sequences from Escherichia coli strains possessing serologically distinct flagellar filaments with a shared complex surface pattern.
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Comparative analysis of flagellin sequences from Escherichia coli strains possessing serologically distinct flagellar filaments with a shared complex surface pattern.

机译:大肠杆菌菌株鞭毛蛋白序列的比较分析该菌株具有血清学上不同的鞭毛丝具有共享的复杂表面图案。

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摘要

Escherichia coli morphotype E flagellar filaments have a characteristic surface pattern of short-pitch loops when examined by electron microscopy. Seven of the 50 known E. coli H (flagellar antigen) serotypes (H1, H7, H12, H23, H45, H49, and H51) produce morphotype E filaments. Polymerase chain reaction was used to amplify flagellin structural (fliC) genes from E. coli strains producing morphotype E flagellar filaments and from strains with flagellar filaments representing other morphotypes. A single DNA fragment was obtained from each strain, and the size of the amplified DNA correlated with the molecular mass of the corresponding flagellin protein. This finding and hybridization data suggest that these bacteria are monophasic. fliC genes from three E. coli serotypes (H1, H7, and H12) possessing morphotype E flagellar filaments were sequenced in order to assess the contribution of conserved flagellin primary sequence to the characteristic filament architecture. The H1 and H12 fliC sequences were identical in length (1,788 bp), while the H7 fliC sequence was shorter (1,755 bp). The deduced molecular masses of the FliC proteins were 60,857 Da (H1), 59,722 Da (H7), and 60,978 Da (H12). The H1, H7, and H12 flagellins demonstrated 98 to 99% identity over the amino-terminal region (190 amino acid residues) and 89% (H7) to 99% (H1 and H12) identity in the carboxy-terminal region (100 amino acid residues). The complete primary amino acid sequences for H1 and H12 flagellins differed by only 10 amino acids, accounting for previously reported serological cross-reactions. However, the central region of H7 flagellin had only 38% identity with H1 and H12 flagellins.The characteristic morphology of morphotype E flagellar filaments is therefore not dependent on a highly conserved primary sequence within the exposed central region. Comparison of morphotype E E. coli flagellins with those from E. coli K-12, Serratia marcescens, and several Salmonella serovars supported the established concept of highly conserved terminal regions flanking a variable central region.
机译:当通过电子显微镜检查时,大肠杆菌形态E型鞭毛细丝具有短节距环的特征性表面图案。在50种已知的大肠杆菌H(鞭毛抗原)血清型中,有7种(H1,H7,H12,H23,H45,H49和H51)产生E型形态的细丝。聚合酶链反应用于从产生形态E型鞭毛细丝的大肠杆菌菌株和具有代表其他形态型的鞭毛细丝的菌株扩增鞭毛蛋白结构(fliC)基因。从每个菌株获得单个DNA片段,并且扩增的DNA的大小与相应鞭毛蛋白的分子量相关。这一发现和杂交数据表明这些细菌是单相的。对来自三种具有E型鞭毛细丝的大肠杆菌血清型(H1,H7和H12)的fliC基因进行了测序,以评估保守的鞭毛蛋白一级序列对特征性细丝结构的贡献。 H1和H12 fliC序列的长度相同(1,788 bp),而H7 fliC序列较短(1,755 bp)。 FliC蛋白的推导分子量为60,857 Da(H1),59,722 Da(H7)和60,978 Da(H12)。 H1,H7和H12鞭毛蛋白在氨基末端区域(190个氨基酸残基)表现出98至99%的同一性,在羧基末端区域(100个氨基酸中)表现出89%(H7)至99%(H1和H12)的同一性酸残基)。 H1和H12鞭毛蛋白的完整一级氨基酸序列仅相差10个氨基酸,这是先前报道的血清学交叉反应的原因。然而,H7鞭毛蛋白的中心区域与H1和H12鞭毛蛋白的同源性仅为38%,因此形态E型鞭毛细丝的特征形态不依赖于暴露中心区域内高度保守的一级序列。大肠杆菌鞭毛蛋白的形态型与大肠杆菌K-12,粘质沙雷氏菌和几种沙门氏菌的形态比较,支持了侧翼可变的中央区域高度保守的末端区域的概念。

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