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Updated: Sep 12, 2025

Super-resolution Imaging of Proteus mirabilis Biofilm by Expansion Microscopy
Published on: July 18, 2025
Decoding Proteus mirabilis biofilms: expression of selected virulence genes and association with antibiotic
Malshani Chathuranika Nissanka1, Ayomi Dilhari2, Jagath Anuradha Munasinghe3
1Department of Microbiology, Faculty of Medical Sciences, University of Sri Jayewardenepura, Nugegoda, Sri Lanka.
Background:
Proteus mirabilis is a uropathogens with a strong ability to form resilient crystalline biofilms, particularly on urinary catheters, contributing to its persistence and antibiotic resistance. As biofilm-driven virulence is key in complicated urinary tract infections, understanding its virulence genes and resistance mechanisms is crucial for improving treatment strategies. We investigated the presence, and expression of key virulence genes (ureC, mrpA, speA, and rsbA) in biofilm-forming P. mirabilis strains sourced from both urine (n = 26) and non-urine specimens, such as pus, wounds, and blood isolates (n = 26) and analyzed their association with antimicrobial resistance profiles. The presence and expression of P.mirabilis's virulence genes were detected using conventional PCR and Quantitative real-time PCR assays (qPCR), respectively. Antibiotic susceptibility test (AST) was conducted using the Kirby-Bauer method, adhering to Clinical and Laboratory Standards Institute (CLSI) guidelines. Statistical analysis was performed using the R language.
Results:
Virulence genes (ureC, mrpA, speA, and rsbA) exhibited high prevalence (> 92% in urine, > 84% in non-urine isolates) with no significant differences (Cochran's Q test; p = 0.801). Multidrug resistance (MDR) and extensively drug-resistant (XDR) were detected in 100% and 57.69% of urine isolates, and 96.15% and 65.38% of non-urine isolates, respectively. Gene combinations are strongly linked to higher resistance rates. mrpA exhibited the highest expression in urine-derived strains, followed by rsbA, and ureC, with speA having the lowest. Post-hoc analysis revealed a significant variation in the rsbA expression compared to speA (p = 0.029) and ureC (p = 0.007). speA showed the highest expression in non-urine isolates, followed by rsbA, ureC, and mrpA, with significant differences among all gene pairs (Conover's all-pairs test; p > 0.05) except rsbA vs. speA. XDR status showed no significant effect or interaction on gene expression in urine and non-urine isolates (p = 0.290; p > 0.05).
Conclusion:
The virulence genes ureC, mrpA, speA, and rsbA are consistently found in P. mirabilis strains from both urine and non-urine specimens; however, their expression varies significantly, likely due to host or environmental factors. The presence of high multidrug-resistant (MDR) and extensively drug-resistant (XDR) P. mirabilis strains, potentially driven by the combination of these virulence genes, suggests an increase in virulence.
Insights
Proteus mirabilis harbors key virulence genes (ureC, mrpA, speA, rsbA) in both urine and non-urine isolates, with varying expression linked to multidrug resistance (MDR) and extensively drug-resistant (XDR) strains, suggesting increased virulence.
Area of Science:
- Microbiology
- Infectious Diseases
- Genetics
Background:
- Proteus mirabilis is a significant uropathogen known for forming resilient crystalline biofilms on urinary catheters.
- Biofilm formation by P. mirabilis contributes to persistent infections and antibiotic resistance, particularly in complicated urinary tract infections.
- Understanding the virulence genes and resistance mechanisms of P. mirabilis is crucial for developing effective treatment strategies.
Purpose of the Study:
- To investigate the prevalence and expression of key P. mirabilis virulence genes (ureC, mrpA, speA, rsbA) in isolates from urine and non-urine sources.
- To analyze the association between the presence and expression of these virulence genes and antimicrobial resistance profiles.
- To determine the impact of multidrug resistance (MDR) and extensively drug-resistant (XDR) status on gene expression.
Main Methods:
- Conventional and quantitative real-time PCR (qPCR) were used to detect the presence and expression of virulence genes.
- Antibiotic susceptibility testing (AST) was performed using the Kirby-Bauer method according to CLSI guidelines.
- Statistical analysis was conducted using the R language to assess gene prevalence, expression, and associations.
Main Results:
- Virulence genes showed high prevalence (>84%) in both urine and non-urine isolates, with no significant differences.
- 100% of urine isolates and 96.15% of non-urine isolates exhibited multidrug resistance (MDR).
- Extensively drug-resistant (XDR) strains were prevalent (57.69% in urine, 65.38% in non-urine). Gene combinations correlated with higher resistance rates.
- Expression levels varied: mrpA highest in urine isolates, speA highest in non-urine isolates.
- XDR status did not significantly affect gene expression.
Conclusions:
- The virulence genes ureC, mrpA, speA, and rsbA are ubiquitously present in P. mirabilis, but their expression patterns differ between urine and non-urine isolates.
- Significant variations in gene expression suggest influence from host or environmental factors.
- The high prevalence of MDR and XDR strains, potentially driven by these virulence gene combinations, indicates an elevated virulence potential of P. mirabilis.
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