Identification and Characterization of vB_PreP_EPr2, a Lytic Bacteriophage of Pan-Drug Resistant Providencia rettgeri

Jaime L Mencke1,2, Yunxiu He1, Andrey A Filippov1

  • 1Wound Infections Department, Bacterial Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA.

Viruses
|April 23, 2022
PubMed

Insights

Researchers identified a bacteriophage (phage) named EPr2 effective against pan-drug resistant (PDR) Providencia rettgeri. This phage therapy offers a potential alternative treatment for PDR P. rettgeri infections, addressing rising antibiotic resistance concerns.

Area of Science:

  • Microbiology
  • Genetics
  • Infectious Diseases

Background:

  • Providencia rettgeri is an emerging opportunistic pathogen with increasing antibiotic resistance.
  • Pan-drug resistant (PDR) P. rettgeri infections pose a significant clinical challenge.
  • Bacteriophage therapy is gaining renewed interest as an alternative treatment strategy.

Purpose of the Study:

  • To identify and characterize a bacteriophage with lytic activity against PDR P. rettgeri.
  • To evaluate the therapeutic potential of the identified phage against a multi-drug resistant clinical isolate.

Main Methods:

  • Isolation and characterization of bacteriophage vB_PreP_EPr2 (EPr2) from an environmental sample.
  • Genomic analysis of EPr2, classifying it within the Autographiviridae family, Studiervirinae subfamily, and Kayfunavirus genus.
  • Phenotypic characterization including optimal multiplicity of infection (MOI) and burst size determination.
  • Assessment of EPr2's host range against clinical P. rettgeri strains.

Main Results:

  • Phage EPr2 demonstrated lytic activity against a PDR P. rettgeri clinical isolate (MRSN 845308).
  • EPr2 has a genome size of 41,261 base pairs and specific phenotypic characteristics (optimal MOI of 1, burst size of 12.3 ± 3.4 PFU/bacterium).
  • EPr2 exhibits a narrow host range against tested clinical P. rettgeri strains.

Conclusions:

  • Phage EPr2 is a promising lytic phage with potential for treating PDR P. rettgeri infections.
  • Despite a narrow host range, EPr2 represents a viable candidate for phage therapy development.
  • Further research into EPr2 and similar phages is warranted to combat antibiotic-resistant Gram-negative pathogens.