The abuse of
antibiotics has resulted in the emergence of multi-
drug-resistant bacteria. Staphylococcus aureus is a frequent cause of
infections, and
antibiotic-resistant S. aureus has become a serious problem.
Antimicrobial peptides play an important role in innate immunity and are attracting increasing attention as alternative
antibiotics. In a previous study,
pleurocidin, derived from winter flounder, was identified as a 25-amino
acid antimicrobial peptide with no cytotoxicity toward mammalian cells and low hemolytic activity. In the present study,
pleurocidin was observed to exhibit antimicrobial activity against gram-positive and gram-negative bacteria, especially against
drug resistant S. aureus.
Pleurocidin retained its antibacterial activity against
drug resistant S. aureus in the presence of a physiological
salt concentration. Membrane depolarization assays and
propidium iodide uptake indicated that
pleurocidin kills bacteria by damaging the integrity of the bacterial membrane.
DNA binding assays revealed that
pleurocidin binds to
DNA. Thus,
pleurocidin targets not only the bacterial membrane, but also their
DNA. S. aureus biofilms have become a serious problem because of increased resistance to
antibiotics. Therefore, we investigated the effect of
pleurocidin on biofilm inhibition and eradication using
crystal violet staining and microscopic observation.
Pleurocidin inhibited and eradicated biofilms at low concentrations. Taken together, the results suggested that
pleurocidin is a promising candidate therapeutic agent to treat
drug-resistant bacteria and biofilm-related
infections.