Wide host range and strong lytic activity of Staphylococcus aureus lytic phage Stau2

Appl Environ Microbiol. 2011 Feb;77(3):756-61. doi: 10.1128/AEM.01848-10. Epub 2010 Dec 10.

Abstract

In searching for an alternative antibacterial agent against multidrug-resistant Staphylococcus aureus, we have isolated and characterized a lytic staphylophage, Stau2. It possesses a double-stranded DNA genome estimated to be about 134.5 kb and a morphology resembling that of members of the family Myoviridae. With an estimated latency period of 25 min and a burst size of 100 PFU/infected cell, propagation of Stau2 in liquid culture gave a lysate of ca. 6 × 10(10) PFU/ml. It was stable at pH 5 to 13 in normal saline at room temperature for at least 4 weeks and at -85°C for more than 2 years, while 1 × 10(9) out of 2 × 10(12) PFU/ml retained infectivity after 36 months at 4°C. Stau2 could lyse 80% of the S. aureus isolates (164/205) obtained from hospitals in Taiwan, with complete lysis of most of the isolates tested within 3 h; however, it was an S. aureus-specific phage because no lytic infection could be found in the coagulase-negative staphylococci tested. Its host range among S. aureus isolates was wider than that of polyvalent phage K (47%), which can also lyse many other staphylococcal species. Experiments with mice demonstrated that Stau2 could provide 100% protection from lethal infection when a multiplicity of infection of 10 was administered immediately after a challenge with S. aureus S23. Considering these results, Stau2 could be considered at least as a candidate for topical phage therapy or an additive in the food industry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / administration & dosage
  • Anti-Bacterial Agents / therapeutic use*
  • Bacteriolysis*
  • Host Specificity*
  • Humans
  • Lysogeny
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Myoviridae / genetics
  • Myoviridae / growth & development
  • Myoviridae / physiology
  • Myoviridae / ultrastructure
  • Staphylococcal Infections / microbiology
  • Staphylococcal Infections / therapy*
  • Staphylococcus Phages / genetics
  • Staphylococcus Phages / growth & development
  • Staphylococcus Phages / physiology*
  • Staphylococcus Phages / ultrastructure
  • Staphylococcus aureus / classification
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / pathogenicity
  • Staphylococcus aureus / virology*
  • Treatment Outcome

Substances

  • Anti-Bacterial Agents