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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.
Abstract:
Pseudomonas aeruginosa is responsible for nosocomial and chronic infections in healthcare settings. The major challenge in treating P. aeruginosa-related diseases is its remarkable capacity for antibiotic resistance development. Bacteriophage (phage) therapy is regarded as a possible alternative that has, for years, attracted attention for fighting multidrug-resistant infections. In this work, we characterized five phages showing different lytic spectrums towards clinical isolates. Two of these phages were isolated from the Russian Microgen Sextaphage formulation and belong to the Phikmvviruses, while three Pbunaviruses were isolated from sewage. Different phage formulations for the treatment of P. aeruginosa PAO1 resulted in diversified time-kill outcomes. The best result was obtained with a formulation with all phages, prompting a lower frequency of resistant variants and considerable alterations in cell motility, resulting in a loss of 73.7% in swimming motility and a 79% change in swarming motility. These alterations diminished the virulence of the phage-resisting phenotypes but promoted their growth since most became insensitive to a single or even all phages. However, not all combinations drove to enhanced cell killings due to the competition and loss of receptors. This study highlights that more caution is needed when developing cocktail formulations to maximize phage therapy efficacy. Selecting phages for formulations should consider the emergence of phage-resistant bacteria and whether the formulations are intended for short-term or extended antibacterial application.
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).
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