Bacteriophage Therapy Against Biofilm-Forming MDR Pseudomonas aeruginosa: Insights into Efficacy and Mechanisms

Authors

  • Kandhan Pooncholai Author
  • Suresh Dhanaraj* Author
  • Rajyoganandh S. Vijayaraman Author
  • Ashok Kumar K Author
  • Somanathan Thirunavukkarasu Author

DOI:

https://doi.org/10.64149/J.Carcinog.24.9s.19-27

Keywords:

Biofilm, Bacteriophages, Phage Therapy, Multi Drug Resistance (MDR), Bacteriophage – biofilm interaction

Abstract

Bacteria possess an outer layer known as a biofilm, which contributes to their resistance. Genetic mutations in pathogenic microbiota posed significant challenges to human health. The treatment of harmful bacteria has become increasingly difficult, leading pharmaceutical companies to withdraw from developing drugs targeting bacterial resistance. Consequently, there are limited alternative approaches available for treating bacterial infections, with phage therapy emerging as one of the more accessible options in certain countries, such as Russia, Georgia, and Poland, as well as in some states within the United States. Phages act as a bactericidal agent, targeting certain bacteria. There are various types of phages, each with distinct properties that influence the microbial environment. Beneficial phages have important roles in Phage therapy and are the focus of our study, which specifically examines the interactions between biofilm-forming bacteria and Pseudomonas bacteriophages. The study primarily focuses on the predominant multidrug-resistant strain, Pseudomonas aeruginosa, and its interactions with both strong and weak bacteriophage activities, which play a significant role in healthcare systems.  This research may benefit populations by offering an alternative treatment strategy for diseases caused by biofilm – producing Pseudomonas aeruginosa.

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Published

2025-10-08

How to Cite

Bacteriophage Therapy Against Biofilm-Forming MDR Pseudomonas aeruginosa: Insights into Efficacy and Mechanisms. (2025). Journal of Carcinogenesis, 24(9s), 19-27. https://doi.org/10.64149/J.Carcinog.24.9s.19-27

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