Chromosomal DNAs of enterohemorrhagic, uropathogenic, and laboratory attenuated Escherichia coli strains differ in the rpoS-mutS region. Many uropathogens lack a deletion and an insertion characteristic of enterohemorrhagic strains. At the same chromosomal position, they harbor a 2.1-kb insertion of unknown origin with a base composition suggestive of horizontal gene transfer. Unlike virulence determinants associated with urinary tract infection and/or neonatal meningitis (pap or prs, sfa, kps, and hly), the 2.1-kb insertion is shared by all group B2 strains of the E. coli Reference Collection.Genomic sequencing offers unprecedented opportunities for the identification of genetic polymorphisms related to bacterial evolution and virulence. The complete nucleotide sequence of Escherichia coli MG1655 (4), a representative laboratory-attenuated E. coli K-12 strain, provides a foundation for studies of the evolution and virulence of E. coli strains associated with diverse pathologies. The expanding list of E. coli virotypes includes diverse diarrheagenic organisms (labeled enterotoxigenic, enteropathogenic, enterohemorrhagic, enteroaggregative, enteroinvasive, and diffusely adherent) (28) as well as isolates associated with extraintestinal diseases, including neonatal meningitis (7) and urinary tract infections (UTIs) (including bacteriuria, cystitis, and pyelonephritis) (11). By complementing phenotypic analysis and multilocus enzyme electrophoresis, sequence comparisons are now providing profound insights into the pathogenesis and evolution of E. coli (5, 12, 19, 23-25, 28, 29, 37, 39-42). These and other studies (13,15) reveal that the chromosomal DNA sequences of modern organisms reflect both their clonal origins and horizontal gene transfer.A uropathogen-associated, rpoS-proximal DNA polymorphism in E. coli. Recently, LeClerc et al. (21) reported that, in comparison to E. coli MG1655, E. coli O157:H7, related enterohemorrhagic E. coli strains, and Shigella dysenteriae lack 6