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基于鞭毛蛋白基因对肖维氏梭菌、溶血梭菌、诺维氏梭菌A和B型以及败血梭菌进行系统发育分析和PCR检测

Phylogenetic analysis and PCR detection of Clostridium chauvoei, Clostridium haemolyticum, Clostridium novyi types A and B, and Clostridium septicum based on the flagellin gene.

作者信息

Sasaki Yoshimasa, Kojima Akemi, Aoki Hiroshi, Ogikubo Yasuaki, Takikawa Noriyasu, Tamura Yutaka

机构信息

National Veterinary Assay Laboratory, Ministry of Agriculture, Forestry and Fisheries, 1-15-1 Tokura, Kokubunji, Tokyo, Japan.

出版信息

Vet Microbiol. 2002 May 1;86(3):257-67. doi: 10.1016/s0378-1135(02)00002-0.

Abstract

The flagellin genes (fliC) of Clostridium chauvoei, Clostridium haemolyticum, Clostridium novyi types A and B, and Clostridium septicum were analysed by PCR amplification and DNA sequencing. The five Clostridium species have at least two copies of the flagellin gene (fliC) arranged in tandem on the chromosome. The deduced N- and C-terminal aminoacid sequences of the flagellin proteins (FliCs) of these clostridia are well conserved but their central region aminoacid sequences are not. Phylogenic analysis based on the N-terminal aminoacid sequence of the FliC protein revealed that these clostridia, which belong to Clostridium 16S rDNA phylogenic cluster I (), are more closely related to Bacillus subtilis than to Clostridium difficile, which belongs to the cluster XI. Moreover, a multiplex polymerase reaction (PCR) system based on the fliC sequence was developed to rapidly identify C. chauvoei, C. haemolyticum, C. novyi types A and B, and C. septicum. PCR of each Clostridium amplified a species-specific band. The multiplex PCR system may be useful for rapid identification of pathogenic clostridia.

摘要

通过聚合酶链反应(PCR)扩增和DNA测序,对产气荚膜梭菌、溶血梭菌、诺维氏梭菌A和B型以及败血梭菌的鞭毛蛋白基因(fliC)进行了分析。这五种梭菌在染色体上至少有两个串联排列的鞭毛蛋白基因(fliC)拷贝。这些梭菌鞭毛蛋白(FliCs)推导的N端和C端氨基酸序列高度保守,但它们的中央区域氨基酸序列并不保守。基于FliC蛋白N端氨基酸序列的系统发育分析表明,这些属于梭菌16S rDNA系统发育簇I的梭菌与枯草芽孢杆菌的亲缘关系比与属于簇XI的艰难梭菌更近。此外,基于fliC序列开发了一种多重聚合酶反应(PCR)系统,用于快速鉴定产气荚膜梭菌、溶血梭菌、诺维氏梭菌A和B型以及败血梭菌。每种梭菌的PCR扩增出一条物种特异性条带。该多重PCR系统可能有助于快速鉴定致病性梭菌。

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