Strain typing methods that compare electrophoresis banding patterns are commonly used but are difficult to standardize and poorly portable. Multilocus sequence typing (MLST) is a sequence-based alternative, but it is not practical for large-scale epidemiological studies. In the present study, the usefulness of fimH singlenucleotide polymorphisms (SNPs) for Escherichia coli typing was explored. fimH SNPs were determined for 345 E. coli clinical isolates (including 3 reference strains) and compared to PCR-based ECOR (E. coli reference collection) phylogrouping. The fimH gene could be amplified for 316 (92%) of the 345 isolates. fimH SNP analysis found 46 distinct terminal groups in the nucleotide sequence-based phylogenetic tree (fimH types). A subset of the E. coli isolates (162 clinical isolates and the 3 reference strains) were compared by fimH type, PCR phylogroup, and MLST. These isolates fell into 27 fimH types and 18 MLST clonal complexes (CCs) that contained 2 to 28 isolates per complex. The combination of PCR phylogroup and fimH type corresponded to a single CC for 113 (68%) isolates and 2 or 3 CCs for the other 52 (32%) isolates. We propose that the combination of PCR phylogrouping and fimH SNP analysis may be a useful method to type a large collection of clinical E. coli isolates for epidemiologic studies.Molecular strain typing methods have enhanced our understanding of the epidemiology of many infectious diseases by contributing to the characterization of new modes of transmission, vehicles, and risk factors for infections. Recently, a new understanding about the epidemiology of community-acquired urinary tract infections (UTI) emerged from the systematic strain typing analysis of uropathogenic Escherichia coli (UPEC). Community-acquired UTI typically occurs as an endemic infection. In 2001, Manges and colleagues identified clusters of UTI on 3 different college campuses in the United States caused by an E. coli clonal group that was designated CgA based on a characteristic enterobacterial repetitive intergenic consensus (ERIC)-PCR electrophoresis banding pattern (14). Additional strain typing by E. coli reference collection (ECOR) phylogenetic grouping, pulsed-field gel electrophoresis (PFGE), multilocus sequence typing (MLST), serotyping, and virulence profiling revealed that the CgA strains belonged to an identical or a very closely related lineage of E. coli (9,14,20). In 2009, in Rio de Janeiro, Brazil, CgA was also found to comprise the largest clonal group observed among women with community-acquired UTI (4).Although reference laboratory surveillance systems using PFGE, such as PulseNet, have been highly successful, the analysis of multiple electrophoresis banding patterns is subject to interlaboratory variability and is not amenable to simple standardization for portability and the creation of public databases. MLST was developed as an attractive sequence-based genotyping technique because it provides reproducibility, comparability, and transferability between laboratories. Although MLST seems...