Pseudomonas aeruginosa PAO 1 In Vitro Time-Kill Kinetics Using Single Phages and Phage Formulations-Modulating Death,

Ana Mafalda Pinto1,2, Alberta Faustino3, Lorenzo M Pastrana1

  • 1INL-International Iberian Nanotechnology Laboratory, Av. Mestre José Veiga, 4715-330 Braga, Portugal.

Insights

Bacteriophage therapy offers a promising alternative for treating multidrug-resistant Pseudomonas aeruginosa infections. Combining multiple phages effectively reduced bacterial resistance and virulence, though formulation strategies require careful consideration.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Biotechnology

Background:

  • Pseudomonas aeruginosa causes challenging healthcare-associated infections.
  • Antibiotic resistance in P. aeruginosa necessitates alternative treatments.
  • Bacteriophage therapy is a potential strategy against multidrug-resistant bacteria.

Purpose of the Study:

  • To characterize five bacteriophages with varying lytic spectra against clinical P. aeruginosa isolates.
  • To evaluate the efficacy of different phage formulations in treating P. aeruginosa PAO1.
  • To investigate the impact of phage treatment on bacterial resistance, motility, and virulence.

Main Methods:

  • Isolation and characterization of five bacteriophages (two Phikmvviruses, three Pbunaviruses).
  • Testing of different phage formulations against P. aeruginosa PAO1.
  • Assessment of time-kill kinetics, bacterial resistance frequency, motility (swimming and swarming), and virulence.

Main Results:

  • A formulation combining all five phages demonstrated the most effective bacterial killing.
  • Phage treatment significantly reduced bacterial swimming (73.7%) and swarming (79%) motility.
  • Phage-resistant variants showed diminished virulence but increased resistance to multiple phages.
  • Not all phage combinations enhanced bacterial killing due to receptor competition.

Conclusions:

  • Phage cocktail formulations require careful design to maximize efficacy and minimize resistance.
  • Consideration of phage-resistant bacteria emergence is crucial for developing effective phage therapy strategies.
  • Formulation selection should align with intended application duration (short-term vs. extended).