E. coli catheter-associated urinary tract infections are associated with distinctive virulence and biofilm gene determinants
Year: 2022
Type: article
Study design: Observational Study
Abstract: Urinary catheterization facilitates urinary tract colonization by E. coli and increases infection risk. Here, we aimed to identify strain-specific characteristics associated with the transition from colonization to infection in catheterized patients. In a single-site study population, we compared E. coli isolates from patients with catheter-associated asymptomatic bacteriuria (CAASB) to those with catheter-associated urinary tract infection (CAUTI). CAUTI isolates were dominated by a phylotype B2 subclade containing the multidrug-resistant ST131 lineage relative to CAASB isolates, which were phylogenetically more diverse. A distinctive combination of virulence-associated genes was present in the CAUTI-associated B2 subclade. Catheter-associated biofilm formation was widespread among isolates and did not distinguish CAUTI from CAASB strains. Preincubation with CAASB strains could inhibit catheter colonization by multiple ST131 CAUTI isolates. Comparative genomic analysis identified a group of variable genes associated with high catheter biofilm formation present in both CAUTI and CAASB strains. Among these, ferric citrate transport (Fec) system genes were experimentally associated with enhanced catheter biofilm formation using reporter and fecA deletion strains. These results are consistent with a variable role for catheter biofilm formation in promoting CAUTI by ST131-like strains or resisting CAUTI by lower-risk strains that engage in niche exclusion.
Source: JCI Insight
Authors: Zongsen Zou, Robert F. Potter, William H. McCoy, John A. Wildenthal, George L. Katumba, Peter J. Mucha, Gautam Dantas, Jeffrey P. Henderson
Institutions: Washington University in St. Louis, Dartmouth College
Language: English
Subfield: Epidemiology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $4,100
Funders: National Institutes of Health, Centers for Disease Control and Prevention, National Institute of Allergy and Infectious Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Center for Advancing Translational Sciences
Awards: Metabolomic Mechanisms of Nutritional Immunity in the Urinary Tract, G1285564249, G2058035923, G2704428435, G2824222223, WASHINGTON UNIVERSITY AND BJC EPI-CENTER FOR PREVENTION OF HEALTHCARE ASSOCIATED, G5471500696, Mechanistic Investigations of Sebaceous Skin Microbial Community Remodeling in Acne Remission, G9000037442, G9000112248, G9000335215, Washington University Institute of Clinical and Translational Sciences (KL2), Structural, mechanistic, & evolutionary characterization of tetracycline destructases
OpenAlex ID: W4311285795
