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Increased resistance to cationic antimicrobial peptide LL-37 in methicillin-resistant strains of Staphylococcus aureus

  • Kazuhisa Ouhara
  • , Hitoshi Komatsuzawa
  • , Toshihisa Kawai
  • , Hiromi Nishi
  • , Tamaki Fujiwara
  • , Yoshihiro Fujiue
  • , Masao Kuwabara
  • , Koji Sayama
  • , Koji Hashimoto
  • , Motoyuki Sugai

Research output: Contribution to journal › Article › peer-review

Abstract

Objectives: The susceptibility of clinical isolates of Staphylococcus aureus, including methicillin-resistant S. aureus (MRSA), to host-derived cationic antimicrobial peptides was investigated. Methods: We examined the susceptibility of 190 clinical strains of methicillin-susceptible S. aureus (MSSA) and 304 strains of MRSA to two different classes of cationic antimicrobial peptides: LL-37 and human β-defensin-3 (hBD3). Out of the total 494 clinical strains, a random selection of 54 S. aureus strains was examined to establish the relationship between the net charge, or zeta potential, of each strain and its susceptibility to hBD3 or LL-37. To further confirm bacterial susceptibility to either hBD3 or LL-37, we concurrently measured: (i) percentage survival after in vitro bacterial exposure and (ii) MBCs for both MRSA and MSSA strains. Results: Of the 54 randomly selected S. aureus strains, those MRSA strains resistant to LL-37 showed significantly higher zeta potentials than those susceptible to LL-37 (P < 0.05). In contrast, there was no difference in bacterial zeta potentials for MRSA strains that showed either resistance or susceptibility to hBD3. In addition, resistance to LL-37, but not to hBD3, as determined by either percentage survival or MBC, was significantly elevated in highly methicillin-resistant strains of S. aureus when compared with MSSA strains (P < 0.01). Conclusions: Clinical strains of MRSA, but not MSSA, that demonstrated an increased net charge also showed elevated resistance to LL-37, but not to hBD3.

Original languageEnglish
Pages (from-to)1266-1269
Number of pages4
JournalJournal of Antimicrobial Chemotherapy
Volume61
Issue number6
DOIs
StatePublished - Jun 2008
Externally publishedYes

ASJC Scopus Subject Areas

  • Pharmacology
  • Microbiology (medical)
  • Infectious Diseases
  • Pharmacology (medical)

Keywords

  • Antibiotic susceptibility
  • Cathelicidin family peptide
  • Clinical isolates
  • Human β-defensin
  • Innate immunity

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