ArticleMedical microbiology and immunology2025
Fighting biofilm: bacteriophages eliminate biofilm formed by multidrug-resistant Enterobacter hormaechei on urological catheters.
Article in Medical microbiology and immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Giving Antibiotics a Second Chance: Evolutionary Trade-Offs and Phage-Driven Restoration of Antibiotic Susceptibility.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026Review
- Protecting Newborns from Multidrug-Resistant Infections: The Emerging Role of Bacteriophages.Viruses · 2026Review
- A comprehensive analysis of the kinetics of infection of lytic bacteriophages specific to the ESKAPE and critical pathogens.World journal of microbiology & biotechnology · 2026Review
- When bacteriophages encounter macrophages during their journey through the human body.Frontiers in cellular and infection microbiology · 2026Review
- Current Insights into Antibiotic Resistance in UropathogenicAntibiotics (Basel, Switzerland) · 2025Review
- Phage to ESKAPE: Personalizing Therapy for MDR Infections-A Comprehensive Clinical Review.Pathogens (Basel, Switzerland) · 2025Review
- Bacteriophage-Based Approach Against Biofilm Infections Associated with Medical Devices: A Narrative Review of ESKAPE Pathogens.International journal of molecular sciences · 2025Review
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The Enterobacter cloacae complex (ECC) is a prevalent nosocomial pathogen associated with various human infections, which currently comprises several species, including Enterobacter cloacae and Enterobacter hormaechei. Strains capable of producing biofilm on various biotic and abiotic surfaces pose a particular threat. Therefore, we focused on three E. hormaechei strains in whose genomes the presence of the biofilm-related genes: fimA, csgA, csgD, and sdiA was confirmed. Kinetic of biofilm formation by these strains on urological catheters depended on the catheter material (silicon or latex), temperature (24 °C or 37 °C) and incubation time. The ability of phages to disrupt biofilm formation was assessed and found to be the most effective when phages were applied at an early stages of this process. Moreover, destruction of existing biofilm by bacteriophages and/or silver or copper nanoparticles was strain-dependent. Incubation with Enterobacter-specific bacteriophages enabled, in some cases, almost complete eradication of three-day biofilms attached to urological catheters. In genomes of two Enterobacter-specific bacteriophages the presence of regions encoding proteins with lytic activity were identified (6 regions in Entb_43 phage and 4 regions in Entb_45 phage genomes, respectively). These results highlight the threat of biofilm-related infections, but also indicate the multifaceted anti-biofilm activity of bacteriophages, which should be considered for useful in clinical practice.
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