Functional Analysis and Antivirulence Properties of a New Depolymerase from a Myovirus That Infects Acinetobacter

Hugo Oliveira1, Ana Rita Costa1, Alice Ferreira1

  • 1CEB-Centre of Biological Engineering, University of Minho, Braga, Portugal.

Journal of Virology
|November 23, 2018
PubMed

Insights

A novel bacteriophage, B9, and its depolymerase enzyme show promise for combating antibiotic-resistant Acinetobacter baumannii infections. The depolymerase effectively degrades bacterial capsules, enhancing susceptibility to immune responses and avoiding resistance development.

Area of Science:

  • Microbiology
  • Bacteriophage Therapy
  • Antimicrobial Resistance

Background:

  • Acinetobacter baumannii is a significant cause of healthcare-associated infections.
  • Rapid development of antibiotic resistance, including to colistin, poses a major therapeutic challenge.
  • Bacteriophage therapy is being re-evaluated as an alternative strategy for difficult-to-treat bacterial infections.

Purpose of the Study:

  • To isolate and characterize a novel bacteriophage effective against Acinetobacter baumannii.
  • To investigate the therapeutic potential of a phage-encoded capsule depolymerase as an antimicrobial agent.
  • To evaluate the enzyme's efficacy and safety against specific Acinetobacter baumannii capsule types.

Main Methods:

  • Isolation and characterization of a novel myovirus, vB_AbaM_B9 (Phage B9).
  • Genomic analysis of Phage B9 and identification of its encoded proteins, including capsule depolymerase B9gp69.
  • Assessment of B9gp69 activity across various pH, ionic strength, and temperature conditions.
  • Evaluation of B9gp69's efficacy in degrading K45 and K30 capsule types and its effect on bacterial susceptibility to serum killing in vitro.
  • Toxicity assessment of B9gp69 in a human lung cell line model.

Main Results:

  • Phage B9 specifically infects and lyses Acinetobacter baumannii strains of K45 and K30 capsule types.
  • The phage-encoded capsule depolymerase, B9gp69, effectively digests exopolysaccharides from both capsule types.
  • B9gp69 remains active under diverse environmental conditions (pH 5-9, 0-500 mM ionic strength, 20-80°C).
  • B9gp69 is non-toxic to human lung cells and renders the K45 strain susceptible to serum killing in vitro.
  • No bacterial resistance to B9gp69 was observed, unlike with phage treatment.

Conclusions:

  • Capsular depolymerases, such as B9gp69, represent a promising alternative antimicrobial strategy against Acinetobacter baumannii.
  • The K45 capsule type is identified as a key virulence factor, and its removal by depolymerase aids host immune response.
  • Phage-encoded depolymerases offer a potentially manageable therapeutic agent with a low risk of resistance development.

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