SLPW: A Virulent Bacteriophage Targeting Methicillin-Resistant Staphylococcus aureus In vitro and In vivo

Zhaofei Wang1, Panpan Zheng1, Wenhui Ji1

  • 1Shanghai Key Laboratory of Veterinary Biotechnology, Key Laboratory of Urban Agriculture (South), Ministry of Agriculture, School of Agriculture and Biology, Shanghai Jiao Tong University Shanghai, China.

Insights

A novel lytic phage, SLPW, effectively targets drug-resistant Staphylococcus aureus (S. aureus), including methicillin-resistant S. aureus (MRSA). This phage demonstrates therapeutic potential against MRSA infections in preclinical models.

Area of Science:

  • Microbiology
  • Virology
  • Infectious Diseases

Background:

  • Staphylococcus aureus (S. aureus) is a significant Gram-positive pathogen.
  • Antibiotic resistance, particularly methicillin-resistant S. aureus (MRSA), poses a major global health threat.
  • Novel therapeutic strategies are urgently needed to combat drug-resistant bacterial infections.

Purpose of the Study:

  • To isolate and characterize a lytic bacteriophage with activity against drug-resistant S. aureus.
  • To evaluate the therapeutic efficacy of the isolated phage against MRSA infections in vitro and in vivo.
  • To assess the stability and host range of the candidate phage.

Main Methods:

  • Isolation and characterization of a lytic phage (SLPW) from pig farm sewage.
  • Genomic analysis of the phage SLPW, including genome size and open reading frames.
  • Assessment of phage host range, efficiency of plating, and one-step growth kinetics.
  • Evaluation of phage stability under various environmental conditions (pH, temperature, chloroform, UV light).
  • In vitro and in vivo efficacy studies against MRSA strains, including mouse infection models.

Main Results:

  • Phage SLPW, belonging to the Podoviridae family, possesses a double-stranded DNA genome (17,861 bp).
  • SLPW exhibited a broad host range against S. aureus, with a short latency (10 min) and lytic (120 min) period.
  • The phage demonstrated stability across a range of temperatures and pH, and resistance to chloroform and UV light.
  • SLPW efficiently lysed MRSA strains in vitro and significantly reduced bacterial burden and inflammatory cytokines in vivo.
  • Intraperitoneal administration of SLPW successfully treated intra-abdominal MRSA infections in mice.

Conclusions:

  • Phage SLPW is a robust lytic bacteriophage with significant antibacterial activity against diverse S. aureus strains, including MRSA.
  • Its stability, broad host range, and demonstrated efficacy in preclinical models highlight its potential as a therapeutic agent.
  • Phage SLPW offers a promising alternative strategy for combating challenging MRSA infections.

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