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.

BMC Microbiology
|August 6, 2025
PubMed
Abstract

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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