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Antiplasmodial and antileishmanial activities of phylloseptin-1, an antimicrobial peptide from the skin secretion of Phyllomedusa azurea (Amphibia).

Abstract
The development of drug resistance by infectious agents represents a major hindrance for controlling parasitic diseases and has stimulated the search for new compounds. We have previously shown that phylloseptin-1 (PS-1), a cationic peptide from the skin secretion of Phyllomedusa azurea, exhibited potent antimicrobial activity. Now we evaluate the effect of PS-1 on Leishmania amazonensis and Plasmodium falciparum. Concentrations as low as 0.5 microg/mL of PS-1 exhibited antileishmanial activity comparable to that of antimoniate of N-metilglucamine, while the antiplasmodial effect of PS-1 was evident at the concentration of 16 microg/mL, and reached an activity comparable to that of artesunate, at the concentration of 64 microg/mL. The high antiparasitic activity of PS-1, together with the unrelatedness of its chemical structure to any present antimicrobial drug, which prevents the development of cross-resistance, together with its non-toxicity to mammalian cells make this peptide a promising candidate for the treatment of malaria and leishmaniasis.
AuthorsSelma A S Kückelhaus, José Roberto S A Leite, Maria Imaculada Muniz-Junqueira, Raimunda Nonata Sampaio, Carlos Bloch Jr, C Eduardo Tosta
JournalExperimental parasitology (Exp Parasitol) Vol. 123 Issue 1 Pg. 11-6 (Sep 2009) ISSN: 1090-2449 [Electronic] United States
PMID19460376 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antimicrobial Cationic Peptides
  • Antiprotozoal Agents
  • phylloseptin-1, Phyllomedusa
Topics
  • Animals
  • Antimicrobial Cationic Peptides (pharmacology, toxicity)
  • Antiprotozoal Agents (pharmacology, toxicity)
  • Anura
  • Dose-Response Relationship, Drug
  • Erythrocytes (parasitology)
  • Female
  • Humans
  • Leishmania mexicana (drug effects, growth & development)
  • Macrophages, Peritoneal (drug effects)
  • Mice
  • Plasmodium falciparum (drug effects, growth & development)
  • Skin (metabolism)

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