Whole-genome sequencing (WGS) enables precise analysis of the genetic characteristics of bacteria. In this study, we used WGS to analyze 13 clinical uropathogenic Escherichia coli (UPEC) strains, isolated from urine samples of patients with urinary tract infections (UTIs). Bioinformatic methods were used to investigate the phylogenetic background, the presence of virulence-associated genes (VAG), antibiotic resistance genes (ARG), and biofilm synthesis genes, as well as to assess the role of mobile genetic elements in horizontal gene transfer (HGT). The majority of the UPEC strains studied were asigned to phylogenetic group B2, which is known for its high pathogenic potential. The strains from phylogenetic group A exhibited a weaker virulence profile but a broader resistance spectrum. Multidrug resistance (MDR) was detected in 69% of strains, with DL07 and DL17 standing out due to the presence of plasmid-encoded and rare ARGs conferring resistance to macrolides and amphenicols. Analysis of biofilm synthesis genes revealed that most strains carried chromosomally encoded genes for cellulose, curli fimbriae, and colanic acid, with exception of strains DL09, DL14, and DL90, which lacked colanic acid biosynthesis genes. The results obtained confirm a high degree of genetic diversity among all 13 UPEC strains studied and point to complex evolutionary adaptation mechanisms, including horizontal gene transfer, variations in biofilm formation potential, virulence, and antibiotic resistance profiles.
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