Genetic diversity of intimin genes of attaching and effacing Escherichia coli strains

被引:219
作者
Zhang, WL
Köhler, B
Oswald, E
Beutin, L
Karch, H
Morabito, S
Caprioli, A
Suerbaum, S
Schmidt, H
机构
[1] Univ Munster, Inst Hyg, D-48149 Munster, Germany
[2] Univ Wurzburg, Inst Hyg & Mikrobiol, D-97080 Wurzburg, Germany
[3] Robert Koch Inst, Div Emerging Bacterial Pathogens, D-13353 Berlin, Germany
[4] Ecole Natl Vet Toulouse, INRA, Microbiol Mol UMR960, F-31000 Toulouse, France
[5] Ist Super Sanita, Lab Med Vet, I-00161 Rome, Italy
关键词
D O I
10.1128/JCM.40.12.4486-4492.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In this study, we determined the sequences of four intimin variant genes detected in attaching and effacing Escherichia coli isolates of human origin. Three of them were novel and were designated eae-eta (eta), eae-iota (iota), and eae-kappa (kappa). The fourth was identical to the recently described eae-xi (zeta), isolated from a bovine E. coli 084AM isolate. We compared these sequences with those of published intimin-alpha, intimin-beta, intimin-gamma1, intimin-gamma2, intimin-epsilon, and intimin-theta alleles. Sequence analysis of these 10 intimin alleles confirmed extensive genetic diversity within the intimin gene family in E. coli. The genetic diversity was more prominent in the 3' region (starting at bp 2112), which encodes the binding domain of intimin. Phylogenetic analyses revealed four groups of closely related intimin genes: alpha and xi; beta and kappa; gamma1 and gamma2/theta; and epsilon and eta. Calculation of homoplasy ratios of sequences of the 5' region of eae (positions 1 to 2111) revealed evidence for intragenic recombination. Split decomposition analysis also indicates that recombination events have played a role in the evolutionary history of eae. In conclusion, we recommend an eae nomenclature system based on the Greek alphabet and provide an updated PCR scheme for amplification and typing of E. coli eae.
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页码:4486 / 4492
页数:7
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