Differential Contribution of Hydrogen Metabolism to Proteus mirabilis Fitness during Single-Species and Polymicrobial Catheterized Urinary Tract Infection.
Aimee L BrauerBrian S LearmanChelsie E ArmbrusterPublished in: Pathogens (Basel, Switzerland) (2023)
Proteus mirabilis is a common uropathogen and a leading cause of catheter-associated urinary tract infections (CAUTIs), which are often polymicrobial. Through a genome-wide screen, we previously identified two [NiFe] hydrogenases as candidate fitness factors for P. mirabilis CAUTI: a Hyb-type Group 1c H 2 -uptake hydrogenase and a Hyf-type Group 4a H 2 -producing hydrogenase. In this study, we disrupted one gene of each system ( hyfE and hybC ) and also generated a double mutant to examine the contribution of flexible H 2 metabolism to P. mirabilis growth and fitness in vitro and during experimental CAUTI. Since P. mirabilis is typically present as part of a polymicrobial community in the urinary tract, we also examined the impact of two common co-colonization partners, Providencia stuartii and Enterococcus faecalis , on the expression and contribution of each hydrogenase to fitness. Our data demonstrate that neither system alone is critical for P. mirabilis growth in vitro or fitness during experimental CAUTI. However, perturbation of flexible H 2 metabolism in the ∆ hybC ∆ hyfE double mutant decreased P. mirabilis fitness in vitro and during infection. The Hyf system alone contributed to the generation of proton motive force and swarming motility, but only during anaerobic conditions. Unexpectedly, both systems contributed to benzyl viologen reduction in TYET medium, and disruption of either system increased expression of the other. We further demonstrate that polymicrobial interactions with P. stuartii and E. faecalis alter the expression of Hyb and Hyf in vitro as well as the contribution of each system to P. mirabilis fitness during CAUTI.
Keyphrases
- urinary tract infection
- body composition
- physical activity
- poor prognosis
- genome wide
- healthcare
- dna methylation
- urinary tract
- binding protein
- microbial community
- copy number
- machine learning
- hepatitis c virus
- wastewater treatment
- risk assessment
- pseudomonas aeruginosa
- artificial intelligence
- cystic fibrosis
- biofilm formation
- electronic health record
- human immunodeficiency virus
- resting state
- genetic diversity