Baldy-Chudzik K, Stosik M
Department of Microbiology and Genetics, Institute of Biotechnology and Environmental Science, University of Zielona Góra, 65-561 Zielona Góra, Poland.
Folia Microbiol (Praha). 2007;52(3):261-72. doi: 10.1007/BF02931308.
Relations between the diversity of the fliC gene conditioning flagellum protein in E. coli and the source of the strain origin are presented. The fliC genes have been identified and characterized in commensal E. coli derived from 10 healthy animal species living in Zoo Safari Park (Poland). The fliC gene was found in 150 strains by the PCR method. The amplifiedfliC products revealed single bands within the range 1.26-2.16 kbp. Forty restriction patterns (classed by restriction analysis with the use of RsaI (PCR-RFLP RsaI; R-types) were determined. The neighbor-joining method was employed to illustrate the distribution of the kinds of R-types. There are 3-8 various R-types of a diversified frequency of occurrence in strains. Application of PCR-RFLP RsaI permitted the identification of alleles of fliC genes characteristic for E. coli and the estimation of their diversity among the animal species. The transmission ways of E. coli fliC+ between organisms of different species were determined and confirmed the role of transmission and horizontal gene transfer in the generation of the allelic diversity of fliC gene in natural E. coli populations.
本文介绍了大肠杆菌中决定鞭毛蛋白的fliC基因多样性与菌株来源之间的关系。已对来自波兰动物园野生动物园中10种健康动物的共生大肠杆菌中的fliC基因进行了鉴定和表征。通过PCR方法在150株菌株中发现了fliC基因。扩增的fliC产物在1.26 - 2.16 kbp范围内显示出单一条带。确定了40种限制性模式(通过使用RsaI进行限制性分析分类,即PCR-RFLP RsaI;R型)。采用邻接法来说明R型种类的分布。菌株中存在3 - 8种不同频率出现的各种R型。PCR-RFLP RsaI的应用允许鉴定大肠杆菌特有的fliC基因等位基因,并估计它们在动物物种中的多样性。确定了不同物种生物体之间大肠杆菌fliC+的传播方式,并证实了传播和水平基因转移在自然大肠杆菌群体中fliC基因等位基因多样性产生中的作用。