Characterization of Virulent T4-Like Acinetobacter baumannii Bacteriophages DLP1 and DLP2

Viruses. 2023 Mar 13;15(3):739. doi: 10.3390/v15030739.

Abstract

The world is currently facing a global health crisis due to the rapid increase in antimicrobial-resistant bacterial infections. One of the most concerning pathogens is Acinetobacter baumannii, which is listed as a Priority 1 pathogen by the World Health Organization. This Gram-negative bacterium has many intrinsic antibiotic resistance mechanisms and the ability to quickly acquire new resistance determinants from its environment. A limited number of effective antibiotics against this pathogen complicates the treatment of A. baumannii infections. A potential treatment option that is rapidly gaining interest is "phage therapy", or the clinical application of bacteriophages to selectively kill bacteria. The myoviruses DLP1 and DLP2 (vB_AbaM-DLP_1 and vB_AbaM-DLP_2, respectively) were isolated from sewage samples using a capsule minus variant of A. baumannii strain AB5075. Host range analysis of these phages against 107 A. baumannii strains shows a limited host range, infecting 15 and 21 for phages DLP1 and DLP2, respectively. Phage DLP1 has a large burst size of 239 PFU/cell, a latency period of 20 min, and virulence index of 0.93. In contrast, DLP2 has a smaller burst size of 24 PFU/cell, a latency period of 20 min, and virulence index of 0.86. Both phages show potential for use as therapeutics to combat A. baumannii infections.

Keywords: Acinetobacter baumannii; Acinetobacter phage; T4-like phage; antimicrobial resistance; bacteriophage; lytic phage; phage; phage therapy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acinetobacter baumannii*
  • Anti-Bacterial Agents
  • Bacteriophages* / genetics
  • Host Specificity

Substances

  • Anti-Bacterial Agents

Grants and funding

This study was partially supported by the National Research Council (NRC) Canada’s Ideation Small Team Project (National Program Office) (DLP and WC), the Natural Sciences and Engineering Research Council of Canada Discovery grant (238414-2018)(JD), and the Department of Veterans Affairs awards I01BX001725 and IK6BX004470 (PNR).