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Updated: Jun 5, 2026

Cystic Fibrosis Aggregate Biofilm Model to Study Infection-relevant Gene Expression
Published on: April 18, 2025
Biofilm disruption and gene expression alteration by phages against multidrug-resistant Pseudomonas aeruginosa
Amna Aftab Mian1, Abid Hussain2, Saba Saba3
1University Institute of Medical Lab Technology, The University of Lahore, Defense Road Campus, Lahore, Pakistan.
Abstract:
Pseudomonas aeruginosa is a major opportunistic pathogen responsible for severe human infections and is increasingly associated with multidrug resistance and limited treatment options. In this study, we isolated and characterized bacteriophages targeting drug-resistant P. aeruginosa strains and evaluated their capacity to disrupt biofilms and modulate biofilm-associated gene expression. Phages recovered from sewage showed broad lytic activity against P. aeruginosa and were classified morphologically into the families Podoviridae and Myoviridae. Two phages, A2 and A4, exhibited the highest lytic activity against the resistant strains examined. Both phages significantly degraded preformed biofilms, with phage A4 showing comparatively stronger antibiofilm activity. In addition, phage exposure altered the expression of several biofilm-associated genes, including pelA, htpB, bifA, psl, fimW, and wspA. A notable finding was the reversal of bifA expression from downregulation at 12 h to upregulation at 24 h following treatment with phage A4. Collectively, these results demonstrate that phages A2 and A4 possess strong lytic and antibiofilm activities and are capable of modulating biofilm-associated transcriptional responses in drug-resistant P. aeruginosa. The findings support the potential application of bacteriophages as alternative therapeutic agents against drug-resistant biofilm-associated infections.
Insights
Bacteriophages targeting drug-resistant Pseudomonas aeruginosa strains were isolated and characterized. These phages effectively disrupted biofilms and modulated gene expression, showing potential as alternative therapies for resistant infections.
Area of Science:
- Microbiology
- Molecular Biology
- Infectious Diseases
Background:
- Pseudomonas aeruginosa is a significant opportunistic pathogen causing severe infections.
- Multidrug resistance in P. aeruginosa limits treatment options.
- Biofilm formation contributes to persistent and difficult-to-treat infections.
Purpose of the Study:
- To isolate and characterize bacteriophages effective against drug-resistant P. aeruginosa.
- To evaluate the antibiofilm capacity of isolated phages.
- To investigate the impact of phage treatment on biofilm-associated gene expression.
Main Methods:
- Isolation and morphological classification of bacteriophages from sewage.
- Determination of lytic activity against multidrug-resistant P. aeruginosa strains.
- Assessment of phage-mediated biofilm degradation and gene expression analysis.
Main Results:
- Two bacteriophages, A2 and A4, demonstrated broad lytic activity and significant biofilm degradation.
- Phage A4 exhibited superior antibiofilm activity.
- Phage treatment modulated the expression of key biofilm-associated genes, including bifA, pelA, and psl.
Conclusions:
- Bacteriophages A2 and A4 possess potent lytic and antibiofilm properties against drug-resistant P. aeruginosa.
- Phage therapy can alter transcriptional responses in P. aeruginosa biofilms.
- These findings support bacteriophages as a promising alternative therapeutic strategy for multidrug-resistant P. aeruginosa infections.
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