Antimicrobial peptides are proposed to act as the first line of mucosal host defense by exerting broadspectrum microbicidal activity against pathogenic microbes. Pleurocidin, a new 25-residue linear antimicrobial peptide, was recently isolated from the skin secretions of winter flounder (Pleuronectes americanus). The present study identifies the cDNA and gene encoding pleurocidin. The pleurocidin gene comprises four exons. Its upstream region demonstrates consensus binding sequences for transcription factors found in host defense genes in mammals, including sequences identical to the NF-IL6 and alpha and gamma interferon response elements. Pleurocidin is predicted to exist as a 68-residue prepropeptide that undergoes proteolytic cleavage of its amino-terminal signal and carboxy-terminal anionic propiece to form the active, mature peptide. Transmission electron microscopy localized pleurocidin to the mucin granules of skin and intestinal goblet cells. Significant synergy was shown to occur between pleurocidin and D-cycloserine targeting Mycobacterium smegmatis. Pleurocidin was functionally active at physiologic concentrations of magnesium and calcium; however, high concentrations of these divalent cations ablated pleurocidin's activity against a standard test strain, Escherichia coli D31. Pleurocidin was tested against bacterial and fungal clinical isolates and showed broad-spectrum antimicrobial activity. Together, these data support the hypothesis that pleurocidin participates in innate mucosal immunity, and it may prove to be a beneficial therapeutic agent.Increasing evidence suggests that endogenous peptides with antimicrobial properties play an important role in host defense. These peptides possess marked microbicidal activity and have been isolated from a variety of cells of myeloid lineage and mucosal surfaces in most species tested thus far (4,5,8,12). The recent focus has been on mucus-derived peptides and their roles in innate host defense at organism-environment interfaces, such as the integument and the respiratory and digestive epithelia. The multitude of peptides discovered at mucosal surfaces include human -defensin 1 (HBD-1) in urogenital tissues (43) and bronchoalveolar lavage fluid (39), HBD-2 at sites of inflammation (24, 39), cryptdins from the Paneth cells (18), tracheal antimicrobial peptide (TAP) and lingual antimicrobial peptide (LAP) from cows (10, 33), and magainin and PGLa from frogs (46). Each peptide class confers a broad spectrum of antimicrobial activity and cationic charge at physiologic pH. Many peptides show high interspecies cDNA and protein sequence homology, frequently across evolutionarily diverse phyla.We recently discovered pleurocidin, a novel 25-residue linear antimicrobial peptide in the skin mucous secretions of the winter flounder, Pleuronectes americanus (6). The sequence of the mature molecule, GWGSFFKKAAHVGKHVGKAAL THYL, shows sequence homology with the dermaseptin (tree frog) and ceratotoxin (medfly) classes of antimicrobial peptides. Pleurocidin is a highly basic...