Isolation and Characterization of a Phapecoctavirus Infecting Multidrug-Resistant Acinetobacter baumannii in A549

Phitchayapak Wintachai1,2, Komwit Surachat3,4, Ganyalak Chaimaha1

  • 1School of Science, Walailak University, Thasala, Nakhon Si Thammarat 80161, Thailand.

Viruses
|November 24, 2022
PubMed

Insights

A novel lytic bacteriophage, vB_AbaM_ABPW7, effectively targets multidrug-resistant Acinetobacter baumannii. This phage shows potential as a safe and effective antimicrobial agent against resistant bacterial infections.

Area of Science:

  • Microbiology
  • Bacteriophage Therapy
  • Antimicrobial Resistance

Background:

  • Multidrug-resistant Acinetobacter baumannii (MDR A. baumannii) is a significant global health threat within the ESKAPE pathogen group.
  • The escalating crisis of antimicrobial resistance necessitates exploration of alternative treatments, such as bacteriophage therapy.

Purpose of the Study:

  • To isolate and characterize a bacteriophage with specific activity against MDR A. baumannii.
  • To evaluate the therapeutic potential of the isolated phage, vB_AbaM_ABPW7 (vABPW7), including its lytic activity, stability, anti-biofilm properties, and safety in a cellular model.

Main Methods:

  • Isolation and characterization of bacteriophage vABPW7 targeting MDR A. baumannii.
  • Morphological and genomic analyses to determine phage classification (Myoviridae family, Caudovirales order, Phapecoctavirus genus).
  • Assessment of lytic activity, stability, biofilm inhibition, and cytotoxicity in A549 alveolar epithelial cells.

Main Results:

  • Phage vABPW7, a lytic bacteriophage from the Myoviridae family, exhibits a short latent period and large burst size.
  • vABPW7 demonstrates high stability and potent lytic activity against MDR A. baumannii, effectively reducing and removing biofilms.
  • In vitro studies showed vABPW7 significantly reduced planktonic MDR A. baumannii and bacterial adhesion to A549 cells without inducing cytotoxicity.

Conclusions:

  • Phage vABPW7 is a promising candidate for further development as a novel antimicrobial agent against multidrug-resistant Acinetobacter baumannii.
  • The phage's non-cytotoxic nature and efficacy against biofilms and planktonic bacteria highlight its potential in phage therapy applications.

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