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Super-resolution Imaging of Proteus mirabilis Biofilm by Expansion Microscopy
Published on: July 18, 2025
Insights into novel diagnostic assay development, antimicrobial resistance, and pathogenicity in Proteus mirabilis
Zhiqiu Yin1, Xiaman Chen1, Juncong Xiao2,3,4
1Department of Clinical Laboratory, Key Laboratory of Biological Targeting Diagnosis, Therapy and Rehabilitation of Guangdong Higher Education Institutes, The Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Abstract:
Proteus mirabilis, a significant pathogen associated with human urinary tract infections (UTIs), demonstrates escalating multidrug resistance (MDR) that complicates clinical management. Accurate identification and in-depth genomic analysis are essential for monitoring and controlling this pathogen. This study aimed to identify the species-specific gene repertoire, antimicrobial resistance (AMR), and virulence genetic profiles through pan-genome analysis to develop novel detection methods and better understand emerging public health threats. The genus Proteus exhibits an open pan-genome, with P. mirabilis harboring a distinct species-specific gene repertoire. Two species-specific core genes, PMI3020 and PMI3598, were identified as molecular targets. We developed conventional PCR and TaqMan probe-based real-time PCR assays, which demonstrated high specificity when tested against P. mirabilis and non-P. mirabilis isolates. The TaqMan probe-based real-time PCR demonstrated a sensitivity of 3.43 × 10² CFU/mL using serial dilutions of P. mirabilis DNA. Comparative genomic analysis revealed significant differences in AMR and pathogenicity-related gene repertoires between P. mirabilis and other Proteus spp. The higher prevalence of AMR phenotypes in P. mirabilis correlated with its greater abundance of AMR genes. Emerging AMR genes acquired through horizontal gene transfer (HGT) have increased MDR risks, particularly to carbapenems and cephalosporins. Additionally, P. mirabilis genomes contain more virulence genes mainly related to adherence and iron acquisition. Our findings establish pan-genome analysis as an effective tool for identifying specific genetic markers to detect pathogens accurately and provide a comprehensive genomic framework illuminating AMR dynamics and virulence in P. mirabilis, thereby providing a valuable foundation for future public health risk assessments.IMPORTANCEP. mirabilis is a major uropathogen with increasing AMR prevalence. The dissemination of AMR genes across healthcare and community settings poses critical challenges to infection control. This study conducted pan-genome analysis of Proteus to identify P. mirabilis-specific gene repertoire, of which species-specific core genes were used as molecular targets to develop highly sensitive PCR assays for accurate detection of this pathogen. Compared with other Proteus spp., P. mirabilis possesses a greater abundance of AMR genes, resulting in a higher prevalence of AMR phenotypes, including significant resistance to carbapenems and cephalosporins. This study establishes pan-genome analysis as an effective strategy for mining species-specific genetic markers, enabling the development of novel PCR assays for accurate pathogen detection. The comprehensive genomic framework enhances understanding of AMR dynamics and virulence mechanisms essential for public health risk assessment.
Insights
This study identifies specific genes in Proteus mirabilis, a multidrug-resistant (MDR) pathogen causing urinary tract infections (UTIs). Novel PCR assays were developed for accurate detection and to understand its increasing antimicrobial resistance (AMR).
Area of Science:
- Genomics and Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Proteus mirabilis is a significant cause of urinary tract infections (UTIs).
- Increasing multidrug resistance (MDR) in P. mirabilis complicates clinical treatment and infection control.
- Accurate identification and genomic understanding are crucial for managing this pathogen.
Purpose of the Study:
- To identify species-specific genes in P. mirabilis through pan-genome analysis.
- To develop novel detection methods based on identified genetic markers.
- To elucidate the antimicrobial resistance (AMR) and virulence profiles of P. mirabilis.
Main Methods:
- Pan-genome analysis of the Proteus genus to identify species-specific gene repertoires.
- Development of conventional PCR and TaqMan probe-based real-time PCR assays using PMI3020 and PMI3598 as targets.
- Comparative genomic analysis of AMR and virulence genes across Proteus species.
Main Results:
- Two species-specific core genes (PMI3020, PMI3598) were identified in P. mirabilis.
- Developed PCR assays demonstrated high specificity for P. mirabilis detection.
- Real-time PCR achieved a sensitivity of 3.43 × 10² CFU/mL.
- P. mirabilis possesses a greater abundance of AMR and virulence genes compared to other Proteus species, correlating with higher AMR prevalence and MDR risks (carbapenems, cephalosporins).
Conclusions:
- Pan-genome analysis is effective for identifying specific genetic markers for pathogen detection.
- Novel PCR assays enable accurate and sensitive detection of P. mirabilis.
- Genomic insights into AMR and virulence provide a foundation for public health risk assessment of P. mirabilis.
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