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Updated: Jan 9, 2026

An In Vitro Bladder Model of Catheter-Associated Urinary Tract Infection
Published on: June 24, 2025
Metabolic cross-talk promotes persistence of Enterococcus in a model of polymicrobial catheter-associated urinary
Zongsen Zou1, Jerome S Pinkner1, Chloe L P Obernuefemann1
1Department of Molecular Microbiology and Center for Women's Infectious Disease Research, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Abstract:
Catheter-associated urinary tract infections (CAUTI) account for 70%~80% of urinary tract infections (UTI) and can lead to adverse outcomes. Most CAUTIs are polymicrobial with resilient communities maintaining a consistent composition of species over time, despite antibiotic treatment and catheter replacement. However, the mechanisms promoting persistence are poorly understood. Here we examine how a chemical interaction between Gram-positive Enterococcus faecalis and Gram-negative Klebsiella pneumoniae can explain their high rate of co-occurrence on long-term indwelling urinary catheters. Sequence analyses of longitudinal isolates from several human patients co-infected with E. faecalis and K. pneumoniae revealed that despite frequent replacement, catheters became re-colonized with the same or a nearly identical consortium of strains throughout the study collection period. Using artificial urine medium (AUM), monoculture revealed that the K. pneumoniae isolates grew robustly and formed biofilm, while the E. faecalis isolates grew poorly and did not form biofilm. However, co-culture of paired isolates resulted in enhanced E. faecalis growth and biofilm, which could be reproduced by supplementing E. faecalis with cell-free K. pneumoniae conditioned AUM supernatant (KpAUMSup). Analyses using comparative transcriptomics, mutant strains and chemical inhibitors with cell culture and murine CAUTI models revealed that: i) KpAUMSup, but not AUM, stimulated expression of the E. faecalis Fsr quorum-sensing system; ii) Fsr was required for E. faecalis to respond to KpAUMSup; iii) E. faecalis cultured in KpAUMSup was more efficient in initiating CAUTI; and iv) Disruption of Fsr inhibited initiation of CAUTI. This interspecies signaling may help explain the high rate of co-colonization of these CAUTI pathogens and highlights new therapeutic strategies to treat polymicrobial CAUTI.
Insights
Catheter-associated urinary tract infections (CAUTI) involve persistent polymicrobial communities. Researchers found that *Klebsiella pneumoniae* signals *Enterococcus faecalis* to enhance its growth and biofilm formation, aiding CAUTI persistence.
Area of Science:
- Microbiology
- Infectious Diseases
- Medical Science
Background:
- Catheter-associated urinary tract infections (CAUTI) are a major cause of hospital-acquired infections.
- Most CAUTIs are polymicrobial, with persistent communities that resist treatment.
- Mechanisms driving polymicrobial CAUTI persistence remain poorly understood.
Purpose of the Study:
- To investigate the chemical interactions between *Enterococcus faecalis* and *Klebsiella pneumoniae* contributing to CAUTI.
- To elucidate the signaling pathways involved in the co-colonization of urinary catheters by these pathogens.
- To identify potential therapeutic targets for treating polymicrobial CAUTI.
Main Methods:
- Longitudinal sequence analysis of clinical isolates from co-infected patients.
- In vitro studies using artificial urine medium (AUM) for monoculture and co-culture experiments.
- Comparative transcriptomics, mutant strain analysis, and chemical inhibitors.
- Cell culture and murine CAUTI models to assess infection initiation and persistence.
Main Results:
- Co-culture with *K. pneumoniae* significantly enhanced *E. faecalis* growth and biofilm formation.
- *K. pneumoniae* conditioned supernatant stimulated the *E. faecalis* Fsr quorum-sensing system.
- Fsr activation was essential for *E. faecalis* to respond to *K. pneumoniae* signals and initiate CAUTI.
- Disruption of Fsr inhibited CAUTI initiation by *E. faecalis*.
Conclusions:
- An interspecies chemical signaling pathway exists between *E. faecalis* and *K. pneumoniae*.
- This signaling mechanism promotes polymicrobial CAUTI persistence by enhancing pathogen growth and biofilm.
- Targeting the Fsr system represents a promising therapeutic strategy for polymicrobial CAUTI.
Related Concept Videos
Urinary Tract Infection II: Pathophysiology
Development of Antibiotic Resistance

