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Updated: Jan 20, 2026

Super-resolution Imaging of Proteus mirabilis Biofilm by Expansion Microscopy
Published on: July 18, 2025
Genomic and Ecogenomic Characterization of Proteus mirabilis Bacteriophages
Diana R Alves1,2,3, Jonathan Nzakizwanayo1,4, Cinzia Dedi1
1School of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton, United Kingdom.
Abstract:
Proteus mirabilis often complicates the care of catheterized patients through the formation of crystalline biofilms which block urine flow. Bacteriophage therapy has been highlighted as a promising approach to control this problem, but relatively few phages infecting P. mirabilis have been characterized. Here we characterize five phages capable of infecting P. mirabilis, including those shown to reduce biofilm formation, and provide insights regarding the wider ecological and evolutionary relationships of these phages. Transmission electron microscopy (TEM) imaging of phages vB_PmiP_RS1pmA, vB_PmiP_RS1pmB, vB_PmiP_RS3pmA, and vB_PmiP_RS8pmA showed that all share morphologies characteristic of the Podoviridae family. The genome sequences of vB_PmiP_RS1pmA, vB_PmiP_RS1pmB, and vB_PmiP_RS3pmA showed these are species of the same phage differing only by point mutations, and are closely related to vB_PmiP_RS8pmA. Podophages characterized in this study were also found to share similarity in genome architecture and composition to other previously described P. mirabilis podophages (PM16 and PM75). In contrast, vB_PimP_RS51pmB showed morphology characteristic of the Myoviridae family, with no notable similarity to other phage genomes examined. Ecogenomic profiling of all phages revealed no association with human urinary tract viromes, but sequences similar to vB_PimP_RS51pmB were found within human gut, and human oral microbiomes. Investigation of wider host-phage evolutionary relationships through tetranucleotide profiling of phage genomes and bacterial chromosomes, indicated vB_PimP_RS51pmB has a relatively recent association with Morganella morganii and other non-Proteus members of the Morganellaceae family. Subsequent host range assays confirmed vB_PimP_RS51pmB can infect M. morganii.
Insights
Bacteriophage therapy shows promise for controlling Proteus mirabilis biofilms in catheterized patients. This study characterized five phages, revealing new insights into their biology and evolution for potential therapeutic applications.
Area of Science:
- Microbiology
- Virology
- Biofilm research
Background:
- Proteus mirabilis forms crystalline biofilms, complicating care for catheterized patients.
- Bacteriophage therapy is a potential solution, but few P. mirabilis phages are characterized.
Purpose of the Study:
- Characterize five novel phages infecting P. mirabilis.
- Investigate their potential for biofilm reduction.
- Explore their ecological and evolutionary relationships.
Main Methods:
- Transmission electron microscopy (TEM) for morphology.
- Genome sequencing for genetic analysis.
- Ecogenomic profiling and tetranucleotide analysis for evolutionary insights.
- Host range assays.
Main Results:
- Four phages (vB_PmiP_RS1pmA, vB_PmiP_RS1pmB, vB_PmiP_RS3pmA, vB_PmiP_RS8pmA) exhibited Podoviridae morphology and related genomes.
- One phage (vB_PimP_RS51pmB) showed Myoviridae morphology with a distinct genome.
- Phages were not associated with urinary tract viromes.
- vB_PimP_RS51pmB sequences found in gut/oral microbiomes, with evolutionary links to Morganellaceae.
Conclusions:
- Characterized phages offer potential for P. mirabilis biofilm control.
- vB_PimP_RS51pmB demonstrates broader host range, infecting M. morganii.
- Phylogenetic analysis reveals phage-host evolutionary dynamics.
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