A novel virulent Litunavirus phage possesses therapeutic value against multidrug resistant Pseudomonas aeruginosa

Varintip Lerdsittikul1, Metawee Thongdee2, Somjit Chaiwattanarungruengpaisan2

  • 1Veterinary Diagnostic Center, Faculty of Veterinary Science, Mahidol University, Nakhon Pathom, Thailand.

Scientific Reports
|December 8, 2022
PubMed

Insights

A novel Pseudomonas phage, VL1, effectively lyses multidrug-resistant Pseudomonas aeruginosa strains. This virulent phage shows promise for phage therapy, reducing bacterial load and biofilms, and increasing survival rates in animal models.

Area of Science:

  • Microbiology
  • Virology
  • Bacteriology

Background:

  • Pseudomonas aeruginosa is a significant nosocomial pathogen causing severe infections.
  • The rise of multidrug-resistant (MDR) P. aeruginosa necessitates alternative treatments like phage therapy.
  • Phages offer a targeted approach to combatting bacterial infections.

Purpose of the Study:

  • To isolate and characterize a novel Pseudomonas phage for potential therapeutic applications.
  • To evaluate the efficacy of the isolated phage against MDR P. aeruginosa strains.
  • To assess the phage's safety and specificity for therapeutic use.

Main Methods:

  • Isolation of Pseudomonas phage vB_PaeS_VL1 (VL1) from urban sewage.
  • Phylogenetic analysis to determine phage classification.
  • Lysis assays against MDR P. aeruginosa strains and other bacteria.
  • In vitro experiments to assess bacterial load and biofilm reduction.
  • In vivo efficacy testing using Galleria mellonella infection models.

Main Results:

  • VL1 was identified as a novel species within the Litunavirus genus, confirmed as a virulent phage.
  • VL1 lysed 56% of tested MDR P. aeruginosa strains, showing high specificity.
  • Significant reduction in bacterial load (approx. 6 log) and pre-formed biofilms (75%) was observed.
  • VL1 treatment increased survival rates in infected Galleria mellonella larvae.

Conclusions:

  • Phage VL1 exhibits potent lytic activity against MDR P. aeruginosa.
  • Its genetic and biological properties suggest it is a strong candidate for phage therapy.
  • VL1 demonstrates specificity and efficacy in reducing bacterial burden and enhancing host survival.