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Comparative genomic and phenotypic analysis of Escherichia coli ST1193 and ST131 from urinary and bloodstream infections: insights into resistance, virulence, and divergent strategies

Zeng Q, Wang S, Xiao S, Liu H, Gu F, Han L, Jiang X

BMC infectious diseases, 2025

24 participants · 3 citations

Abstract

BACKGROUND: The global dissemination of multidrug-resistant (MDR) Escherichia coli (E. coli) clones, particularly the pandemic ST131 and the emerging ST1193, poses a serious public health threat. While ST131 is well-studied, the factors enabling ST1193’s rapid dissemination across both urinary and bloodstream infection niches remain unclear. METHODS: We compared 48 urinary (UPEC) and bloodstream (BPEC) E. coli isolates of ST1193 (n = 24) and ST131 (n = 24) from Shanghai, using integrated phenotypic-genotypic analysis, including antimicrobial susceptibility, whole-genome sequencing (WGS), hemolysin assays, Galleria mellonella larval infection model. RESULTS: Both lineages exhibited high rates of multidrug resistance with strongly genotype-phenotype concordance. Key contrasts emerged: ST1193-BPEC showed significantly higher resistance to trimethoprim/sulfamethoxazole than ST131-BPEC (p < 0.05), while ST131 overall demonstrated greater resistance to cefotaxime/cefazolin and a higher ESBL prevalence (ST131 83.33% vs. ST1193 50.00%, p < 0.05). All ST1193 isolates were resistant to fluoroquinolones but remained susceptible to carbapenems and ceftazidime-avibactam. Genomic analysis revealed striking conservation in ST1193, with near-uniform presence of fimH64 (23/24), K1 capsule (100%), and O75:H5 serotype (91.7%), along with unique virulence genes (vat, neuABCD, hcp2, kpsT, espL1). In contrast, ST131 displayed heterogeneity in fimH alleles (predominantly fimH30), K5 capsule…

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