Genetic Analysis and Detection of fliC H1 and fliC H12 Genes Coding for Serologically Closely Related Flagellar Antigens in Human and Animal Pathogenic Escherichia coli.

The E. coli flagellar types H1 and H12 show a high serological cross-reactivity and molecular serotyping appears an advantageous method to establish a clear discrimination between these flagellar types. Analysis of ffiC(H1) and fliC(H12) gene sequences showed that they were 97.5% identical at the nucleotide level. Because of this high degree of homology we developed a two-step real-time PCR detection procedure for reliable discrimination of H1 and H12 flagellar types in E co/i. In the first step, a real-time PCR assay for common detection of both fliC(H1) and fliC(H12) genes is used, followed in a second step by real-time PCR assays for specific detection of fliC(H1) and fliC(H12), respectively. The real-time PCR for common detection of fliC(H1) and flicC(H12) demonstrated 100% sensitivity and specificity as it reacted with all tested E. coil H1 and H12 strains and not with any of the reference strains encoding all the other 51 flagellar antigens. The fliC(H1) and flic(H1)(2) gene specific assays detected all F call H1 and all E coli H12 strains, respectively (100% sensitivity). However, both assays showed cross-reactions with some flagellar type reference strains different from H1 and H12. The real-time PCR assays developed in this study can be used in combination for the detection and identification of E. coli H1 and H12 strains isolated from different sources.