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.

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.