P3MA: A Promising Mycobacteriophage Infecting Mycobacterium abscessus

Antonio Broncano-Lavado1, John Jairo Aguilera-Correa2,3, Françoise Roquet-Banères2

  • 1Clinical Microbiology Department, IIS-Fundación Jiménez Díaz, Autonomous University of Madrid, 28040 Madrid, Spain.

PubMed
Abstract

Insights

Mycobacteriophage P3MA effectively inhibits Mycobacterium abscessus growth in planktonic, biofilm, and granuloma models. This bacteriophage shows potential for phage therapy, particularly when combined with imipenem for lung infections.

Area of Science:

  • Microbiology
  • Bacteriophage Therapy
  • Infectious Diseases

Background:

  • Mycobacterium abscessus is an opportunistic pathogen causing difficult-to-treat infections, often requiring prolonged treatment with high recurrence rates.
  • Current treatment limitations necessitate the exploration of novel therapeutic strategies, such as bacteriophage therapy.

Purpose of the Study:

  • To characterize mycobacteriophage P3MA and evaluate its efficacy against Mycobacterium abscessus.
  • To assess the potential of P3MA as a therapeutic agent, alone and in combination with antibiotics.

Main Methods:

  • Phylogenetic analysis, electron microscopy, growth curve analysis, and biofilm assays were employed.
  • Checkerboard assays and granuloma-like medium studies were conducted to evaluate P3MA's efficacy and interactions with antibiotics.

Main Results:

  • P3MA demonstrated significant inhibition of Mycobacterium abscessus growth in planktonic and biofilm states, and within a granuloma-like model.
  • P3MA showed synergistic effects with imipenem, antagonistic effects with clarithromycin, and indifference with amikacin.

Conclusions:

  • Mycobacteriophage P3MA is a promising candidate for phage therapy against Mycobacterium abscessus infections.
  • Genetic engineering of P3MA, in combination with imipenem, could offer a novel treatment strategy for lung infections caused by this pathogen.