Peptides with differential cytolytic activity from skin secretions of the lemur leaf frog Hylomantis lemur (Hylidae: Phyllomedusinae)

被引:64
作者
Conlon, J. Michael [1 ]
Woodhams, Douglas C.
Raza, Haider
Coquet, Laurent
Leprince, Jerome
Jouenne, Thierry
Vaudry, Hubert
Rollins-Smith, Louise A.
机构
[1] United Arab Emirates Univ, Fac Med & Hlth Sci, Dept Biochem, Al Ain 17666, U Arab Emirates
[2] Vanderbilt Univ, Med Ctr, Dept Microbiol & Immunol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN 37232 USA
[4] Univ Rouen, CNRS, European Inst Peptide Res, F-76821 Mont St Aignan, France
[5] Univ Rouen, CNRS, UMR 6522, F-76821 Mont St Aignan, France
[6] Univ Rouen, CNRS, INSERM, U 413, F-76821 Mont St Aignan, France
关键词
amphibian; antimicrobial; cytolysis; hepatoma; chytrid;
D O I
10.1016/j.toxicon.2007.04.017
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Two peptides with differential cytolytic activity against bacteria, a fungus pathogenic to amphibians, and mammalian cells were isolated from norepinephrine-stimulated skin secretions of the Lemur leaf frog Hylomantis lemur Boulenger, 1882. Dermaseptin-L1 (GLWSKIKEAAKAAGKAALNAVTGLVNQGDQPS) was active against the Gram-negative bacterium Escherichia coli (MIC = 8 mu M) but inactive against the Gram-positive bacterium Staphylococcus aureus. This peptide inhibited growth of zoospores of the chytrid fungus Batrachochytrium dendrobatidis at concentrations above 25 mu M but did not completely inhibit growth at 100 mu M. Phylloseptin-L1 (LLGMIPLAISAISALSKL.NH2) was active against S. aureus (MIC = 8 mu M) but was inactive against E coli. This peptide also inhibited growth of R dendrobatidis zoospores at concentrations above 25 mu M with complete inhibition at 100 mu M. Dermaseptin-L1 showed selective cytolytic activity against HepG2 human hepatoma-derived cells (LC50 = 45 mu M) compared with human erythrocytes (LC50 = 200 M) whereas phylloseptin-L1 was approximately equipotent against both HepG2 cells (LC50 = 35 M) and erythrocytes (LC50 = 40 mu M). (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:498 / 506
页数:9
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