Owen R J, Fayos A, Hernandez J, Lastovica A
National Collection of Type Cultures, Central Public Health Laboratory, London, UK.
Mol Cell Probes. 1993 Dec;7(6):471-80. doi: 10.1006/mcpr.1993.1070.
Genotypes were analysed within 29 geographically diverse strains of Campylobacter jejuni mainly from human enteritis cases and four strains representing C. coli, C. lari and C. helveticus. A 1723 bp DNA fragment, amplified by the polymerase chain reaction (PCR) from the flagellin (fla) genes, was used to probe genomic Southern blots for restriction site variation at homologous loci. Internal Hin fl restriction fragment length polymorphisms (RFLP) of the fla gene PCR amplification product were also used to characterize isolates. Copy number and polymorphisms in and around the fla genes were detected, and strains were grouped into 10 genotypes on the basis of fla restriction site similarities. Campylobacter jejuni had a fla gene copy number of two and the majority (64%) of strains in the species had common internal fla gene sequences as indicated by Hin fl restriction analysis. A greater degree of diversity was detected around the fla loci in Hae III and Bgl II genomic Southern blots. The results showed that analysis of fla genes provided a novel and fundamental approach to grouping strains and offered a basis for defining a predominant clonal evolutionary line within C. jejuni.
对主要来自人类肠炎病例的29株地理分布多样的空肠弯曲菌菌株以及代表大肠弯曲菌、海鸥弯曲菌和瑞士弯曲菌的4株菌株进行了基因型分析。通过聚合酶链反应(PCR)从鞭毛蛋白(fla)基因扩增得到的1723 bp DNA片段,用于探测基因组Southern杂交印迹,以检测同源位点的限制性酶切位点变异。fla基因PCR扩增产物的内部Hin fl限制性片段长度多态性(RFLP)也用于菌株的鉴定。检测了fla基因及其周围的拷贝数和多态性,并根据fla限制性酶切位点的相似性将菌株分为10个基因型。空肠弯曲菌的fla基因拷贝数为两个,该物种中大多数(64%)菌株具有共同的fla基因内部序列,Hin fl限制性分析表明了这一点。在Hae III和Bgl II基因组Southern杂交印迹中,在fla位点周围检测到了更高程度的多样性。结果表明,fla基因分析为菌株分组提供了一种新颖且基本的方法,并为定义空肠弯曲菌内的主要克隆进化系提供了基础。