P-1158. Molecular Characterization of Extraintestinal Pathogenic Escherichia coli (ExPEC) from the Emerging Infections Program (EIP)─United States, 2023

Abstract Background Extraintestinal pathogenic E. coli (ExPEC) is a major contributor to healthcare-associated infections (HAIs) and a leading cause of urinary tract infections (UTIs) and sepsis in the United States. Despite its substantial burden, comprehensive molecular epidemiological data on ExPEC in the United States remain limited. Methods In 2023, the Emerging Infections Program piloted active laboratory- and population-based surveillance for invasive ExPEC (iEC) across nine U.S. sites (CA, CO, GA, MD, MN, NM, NY, OR, TN) from June to August and for urinary ExPEC (uEC) at three sites (CA, GA, NY) in August. Cases were defined as the first isolation of E. coli from a sterile site (iEC) or urine (uEC) from a surveillance-area resident in a 30-day period. All iEC and a random sample of uEC isolates were sent to the CDC for molecular subtyping via whole-genome sequencing (WGS) analysis including multi-locus sequence typing, in silico serotyping, and antibiotic resistance gene profiling. Results The collection included 846 iEC and 939 uEC isolates. The sequence type (ST) 131 pandemic clone was the most prevalent lineage, comprising 19.0% and 15.4% of iEC and uEC isolates, respectively. In silico serotyping identified O25b as the dominant serotype, representing 16.2% and 12.2% of iEC and uEC isolates, respectively. All isolates harbored at least one beta-lactamase gene, three isolates harbored a carbapenemase gene (KPC-3 and OXA-244), and 11% harbored at least one extended-spectrum beta-lactamase gene. Additionally, approximately one-third of isolates harbored genetic determinants associated with multidrug resistance (defined as resistance to ≥3 antimicrobial classes). Conclusion These findings enhance our understanding of ExPEC molecular epidemiology, highlighting the dominance of ST131 and O25b, along with widespread beta-lactamase and multidrug resistance. These baseline data are crucial considerations for vaccine development and antimicrobial stewardship to mitigate ExPEC’s public health impact. Disclosures All Authors: No reported disclosures

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Journal
Open Forum Infectious Diseases
Published
2026-01-01
DOI
https://doi.org/10.1093/ofid/ofaf695.1351
Primary Topic
Escherichia coli research studies
Type
article
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article

P-1158. Molecular Characterization of Extraintestinal Pathogenic Escherichia coli (ExPEC) from the Emerging Infections Program (EIP)─United States, 2023

Joshua Brandenburg, Christopher A. Elkins, Susannah L. McKay, Amy S. Gargis et al.
Open Forum Infectious Diseases
Escherichia coli research studies
article

P-1158. Molecular Characterization of Extraintestinal Pathogenic Escherichia coli (ExPEC) from the Emerging Infections Program (EIP)─United States, 2023

Joshua Brandenburg, Christopher A. Elkins, Susannah L. McKay, Amy S. Gargis, Alyssa G. Kent, Heather N. Grome, Alice Y. Guh, Uzma Ansari, Ruben Raymond, Latasha Curtis
article en

Abstract

Abstract Background Extraintestinal pathogenic E. coli (ExPEC) is a major contributor to healthcare-associated infections (HAIs) and a leading cause of urinary tract infections (UTIs) and sepsis in the United States. Despite its substantial burden, comprehensive molecular epidemiological data on ExPEC in the United States remain limited. Methods In 2023, the Emerging Infections Program piloted active laboratory- and population-based surveillance for invasive ExPEC (iEC) across nine U.S. sites (CA, CO, GA, MD, MN, NM, NY, OR, TN) from June to August and for urinary ExPEC (uEC) at three sites (CA, GA, NY) in August. Cases were defined as the first isolation of E. coli from a sterile site (iEC) or urine (uEC) from a surveillance-area resident in a 30-day period. All iEC and a random sample of uEC isolates were sent to the CDC for molecular subtyping via whole-genome sequencing (WGS) analysis including multi-locus sequence typing, in silico serotyping, and antibiotic resistance gene profiling. Results The collection included 846 iEC and 939 uEC isolates. The sequence type (ST) 131 pandemic clone was the most prevalent lineage, comprising 19.0% and 15.4% of iEC and uEC isolates, respectively. In silico serotyping identified O25b as the dominant serotype, representing 16.2% and 12.2% of iEC and uEC isolates, respectively. All isolates harbored at least one beta-lactamase gene, three isolates harbored a carbapenemase gene (KPC-3 and OXA-244), and 11% harbored at least one extended-spectrum beta-lactamase gene. Additionally, approximately one-third of isolates harbored genetic determinants associated with multidrug resistance (defined as resistance to ≥3 antimicrobial classes). Conclusion These findings enhance our understanding of ExPEC molecular epidemiology, highlighting the dominance of ST131 and O25b, along with widespread beta-lactamase and multidrug resistance. These baseline data are crucial considerations for vaccine development and antimicrobial stewardship to mitigate ExPEC’s public health impact. Disclosures All Authors: No reported disclosures

Open Forum Infectious DiseasesVol. 13(Supplement_1)
Tân Tạo University (VN), CDC Foundation (US), Universidad de la Ciénega (MX)
Good health and well-being
Openalex Percentile: Top 91%
Escherichia coli research studies
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