Papers

Peer-reviewed Open access
2007

Efficient elimination of multidrug-resistant Staphylococcus aureus by cloned lysin derived from bacteriophage φMR11

Journal of Infectious Diseases
  • Mohammad Rashel
  • Jumpei Uchiyama
  • Takako Ujihara
  • Yoshio Uehara
  • Shu Kuramoto
  • Shigeyoshi Sugihara
  • Ken Ichi Yagyu
  • Asako Muraoka
  • Motoyuki Sugai
  • Keiichi Hiramatsu
  • Koichi Honke
  • Shigenobu Matsuzaki
  • Display all

Volume
196
Number
8
First page
1237
Last page
1247
Language
Publishing type
Research paper (scientific journal)
DOI
10.1086/521305
Publisher
The University of Chicago Press

We report the successful purification of a cloned lysin encoded by the novel Staphylococcus aureus bacteriophage φMR11. The lysin, designated MV-L, rapidly and completely lysed cells of a number of S. aureus strains tested, including methicillin-resistant S. aureus (MRSA) and vancomycin-resistant S. aureus and a subset of vancomycin-intermediate S. aureus (VISA) in growing conditions. MV-L-mediated killing is specific to S. aureus and not to other species, except for S. simulans. MV-L exerted its staphylocidal effect synergistically with glycopeptide antibiotics against VISA. MV-L efficiently eliminated MRSA that had been artificially inoculated into the nares of mice. The intraperitoneal administration of MV-L also protected mice against MRSA septic death, without any harmful effects. Although MV-L evoked detectable levels of a humoral response in mice, the antibodies did not abolish the bacteriolytic activity. These results indicate that MV-L might be useful as a powerful therapeutic agent against multidrug-resistant S. aureus infections. © 2007 by the Infectious Diseases Society of America. All rights reserved.

Link information
DOI
https://doi.org/10.1086/521305
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/17955443
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000249595700017&DestApp=WOS_CPL
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=35348839572&origin=inward Open access
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=35348839572&origin=inward
ID information
  • DOI : 10.1086/521305
  • ISSN : 0022-1899
  • ORCID - Put Code : 49158209
  • Pubmed ID : 17955443
  • SCOPUS ID : 35348839572
  • Web of Science ID : WOS:000249595700017

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