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首页> 外文期刊>Journal of Clinical Microbiology >Molecular Characterization of fliD Gene Encoding Flagellar Cap and Its Expression among Clostridium difficileIsolates from Different Serogroups
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Molecular Characterization of fliD Gene Encoding Flagellar Cap and Its Expression among Clostridium difficileIsolates from Different Serogroups

机译:fliD基因编码鞭毛帽的分子表征及其在不同血清群的艰难梭菌中的表达

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The fliD gene encoding the flagellar cap protein (FliD) of Clostridium difficile was studied in 46 isolates belonging to serogroups A, B, C, D, F, G, H, I, K, X, and S3, including 30 flagellated strains and 16 nonflagellated strains. In all but three isolates, amplification by PCR and reverse transcription-PCR demonstrated that the fliD gene is present and transcribed in both flagellated and nonflagellated strains. PCR-restriction fragment length polymorphism (RFLP) analysis of amplifiedfliD gene products revealed interstrain homogeneity, with one of two major patterns (a and b) found in all but one of the strains, which had pattern c. A polyclonal monospecific antiserum raised to the recombinant FliD protein reacted in immunoblots with crude flagellar preparations from 28 of 30 flagellated strains but did not recognize FliD from nonflagellated strains. The fliDgenes from five strains representative of the three different RFLP groups were sequenced, and sequencing revealed 100% identity between the strains with the same pattern and 88% identity among strains with different patterns. Our results show that even though FliD is a structure exposed to the outer environment, the flagellar cap protein is very well conserved, and this high degree of conservation suggests that it has a very specific function in attachment to cell or mucus receptors.
机译:在艰难梭菌血清群A,B,C,D,F,G,H的46个分离株中研究了编码艰难梭菌的鞭毛帽蛋白(FliD)的 fliD 基因。 I,K,X和S3,包括30个带鞭毛的菌株和16个非带鞭毛的菌株。除三个分离株外,通过PCR和逆转录PCR进行的扩增表明, fliD 基因在鞭毛和非鞭毛菌株中均存在并转录。扩增的 fliD 基因产物的PCR限制性片段长度多态性(RFLP)分析显示出菌株间的同质性,除一个菌株外,在所有菌株中均发现了两种主要模式(a和b)之一。产生于重组FliD蛋白的多克隆单特异性抗血清在免疫印迹中与来自30个带鞭毛菌株的粗鞭毛制品反应,但不识别来自非带鞭毛菌株的FliD。对来自代表三个不同RFLP组的五个菌株的 fliD 基因进行了测序,测序结果显示,相同模式的菌株之间具有100%的同一性,不同模式的菌株之间具有88%的同一性。我们的结果表明,即使FliD是暴露于外部环境的结构,鞭毛帽蛋白也非常保守,而且这种高度的保守性表明它在附着于细胞或粘液受体上具有非常特殊的功能。

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