Evaluation of Phage Therapy for Pulmonary Infection of Mouse by Liquid Aerosol-Exposure Pseudomonas aeruginosa

Yajun Zhang1, Biao Meng2,3, Xiao Wei2

  • 1Department of Gastroenterology, The Sixth Medical Center of PLA General Hospital, Beijing, People's Republic of China.

Abstract

Insights

A novel bacteriophage, vB_PaeP_PA01EW, effectively treated Pseudomonas aeruginosa pneumonia in mice. This phage therapy reduced inflammation and bacterial load, offering a promising alternative to antibiotics for multidrug-resistant infections.

Area of Science:

  • Microbiology
  • Virology
  • Infectious Diseases

Background:

  • Pseudomonas aeruginosa is a significant cause of hospital-acquired infections.
  • Multidrug resistance in P. aeruginosa complicates antibiotic treatment, increasing patient morbidity and mortality.
  • Bacteriophages offer a specific lytic mechanism as an alternative to conventional antibiotics.

Purpose of the Study:

  • To isolate and characterize a bacteriophage targeting Pseudomonas aeruginosa.
  • To evaluate the efficacy of phage therapy in a murine model of P. aeruginosa pneumonia.

Main Methods:

  • Isolation and characterization of phage vB_PaeP_PA01EW, including electron microscopy and whole-genome sequencing.
  • Establishment of a mice pneumonia model via aerosolized P. aeruginosa.
  • Assessment of phage therapy efficacy through histological analysis and bacterial burden quantification.

Main Results:

  • Phage vB_PaeP_PA01EW, identified as a Luz24likevirus (family Podoviridae), demonstrated therapeutic effects in mice.
  • Phage therapy significantly alleviated lung inflammation, including edema and inflammatory cell infiltration.
  • Treatment with vB_PaeP_PA01EW led to reduced bronchial epithelial cell proliferation and a significant decrease in bacterial burden.

Conclusions:

  • The study supports the clinical application of bacteriophages for treating P. aeruginosa infections.
  • Bacteriophage therapy presents a viable alternative for managing multidrug-resistant bacterial pathogens.
  • Findings provide a basis for phage therapy applications against other pathogenic bacteria.

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