Isolation, characterization and molecular cloning of new temporins from the skin of the North African ranid Pelophylax saharica

Peptides. 2008 Sep;29(9):1526-33. doi: 10.1016/j.peptides.2008.05.008. Epub 2008 May 18.

Abstract

Temporins are small antimicrobial peptides isolated from North American and Eurasian ranid frogs that are particularly active against Gram-positive bacteria. To date, no temporins have been characterized from North African frog species. We isolated three novel members of the temporin family, named temporin-1Sa (FLSGIVGMLGKLF(amide)), -1Sb (FLPIVTNLLSGLL(amide)), and -1Sc (FLSHIAGFLSNLF(amide)), from the skin of the Sahara frog Pelophylax (Rana) saharica originating from Tunisia. These temporins were identified by a combined mass spectrometry/molecular cloning approach. Temporin-1Sa was found to be highly active against Gram-positive and Gram-negative bacteria, yeasts and fungi (MIC=2-30 microM). To our knowledge, this is the first 13-residue member of the temporin family with a net charge of +2 that shows such broad-spectrum activity with particularly high potency on the clinically relevant Gram-negative strains, Escherichia coli (MIC=10 microM) and Pseudomonas aeruginosa (MIC=31 microM). Moreover, temporin-1Sa displays significant antiparasitic activity (IC50 approximately 20 microM) against the promastigote and amastigote stages of Leishmania infantum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Antifungal Agents / pharmacology
  • Antimicrobial Cationic Peptides / isolation & purification
  • Antimicrobial Cationic Peptides / pharmacology
  • Antiprotozoal Agents / pharmacology
  • Base Sequence
  • Chromatography, High Pressure Liquid
  • Cloning, Molecular
  • Erythrocytes / drug effects
  • Hemolytic Agents / pharmacology
  • Humans
  • Leishmania infantum / drug effects
  • Molecular Sequence Data
  • Proteins / chemistry
  • Proteins / isolation & purification*
  • Ranidae*

Substances

  • Anti-Bacterial Agents
  • Antifungal Agents
  • Antimicrobial Cationic Peptides
  • Antiprotozoal Agents
  • Hemolytic Agents
  • Proteins
  • temporin

Associated data

  • GENBANK/AM748899
  • GENBANK/AM748900
  • GENBANK/AM748901