Related Experiment Video
Updated: Jul 26, 2026

Establishment and Characterization of UTI and CAUTI in a Mouse Model
Published on: June 23, 2015
Characterization of the Entner-Douderoff Pathway in Pseudomonas aeruginosa Catheter-associated Urinary Tract
Nour El Husseini1, Solomon A Mekonnen1, Cherisse L Hall1
1Cell Biology and Molecular Genetics, University of Maryland at College Park, MD 20742.
Abstract:
Pseudomonas aeruginosa is an opportunistic nosocomial pathogen responsible for catheter-associated urinary tract infections (CAUTI). In a murine model of P. aeruginosa CAUTI, we previously demonstrated that urea within urine suppresses quorum sensing and induces the Entner-Douderoff (E-D) pathway. The E-D pathway consists of the genes zwf, pgl, edd, and eda. Zwf and Pgl convert glucose-6-phosphate into 6-phosphogluconate. Edd hydrolyzes 6-phosphogluconate to 2-keto-3-deoxy-6-phosphogluconate (KDPG). Finally, Eda cleaves KDPG to glyceraldehyde-3-phosphate and pyruvate, which enters the citric acid cycle. Here, we generated in-frame E-D mutants in strain PA14 and assessed their growth phenotypes on chemically defined media. These E-D mutants have a growth defect when grown on glucose or gluconate as sole carbon source which are similar to results previously reported for PAO1 mutants lacking E-D genes. RNA-sequencing following short exposure to urine revealed minimal gene regulation differences compared to the wild type. In a murine CAUTI model, virulence testing of E-D mutants revealed that two mutants lacking zwf and pgl showed minor fitness defects. Infection with the ∆pgl strain exhibited a 20% increase in host survival, and the ∆zwf strain displayed decreased colonization of the catheter and kidneys. Consequently, our findings suggest that the E-D pathway in P. aeruginosa is dispensable in this model of CAUTI.
Insights
The Entner-Douderoff (E-D) pathway in Pseudomonas aeruginosa is dispensable for catheter-associated urinary tract infections (CAUTI). Mutants lacking E-D genes showed minimal impact on virulence in a murine CAUTI model.
Area of Science:
- Microbiology
- Pathogenesis
- Bacterial Metabolism
Background:
- Pseudomonas aeruginosa is a key cause of nosocomial infections, particularly catheter-associated urinary tract infections (CAUTI).
- Urea in urine was previously shown to suppress quorum sensing and induce the Entner-Douderoff (E-D) pathway in P. aeruginosa.
- The E-D pathway involves genes zwf, pgl, edd, and eda, crucial for glucose metabolism via 6-phosphogluconate and KDPG intermediates.
Conclusions:
- The Entner-Douderoff (E-D) pathway is dispensable for Pseudomonas aeruginosa virulence in the established murine model of CAUTI.
- Specific E-D pathway genes (zwf, pgl) contribute minimally to P. aeruginosa fitness during CAUTI.
- These findings challenge the essentiality of the E-D pathway for P. aeruginosa pathogenesis in this specific infection context.
Related Concept Videos
Urinary Tract Infection I: Introduction
Urinary Tract Infection II: Pathophysiology
Other Glycolytic Pathways
Gene Regulation in Microbial Communities: Quorum Sensing

