In vitro and in vivo antimicrobial activity of two α-helical cathelicidin peptides and of their synthetic analogs

被引:80
作者
Benincasa, M
Skerlavaj, B
Gennaro, R
Pellegrini, A
Zanetti, M
机构
[1] Univ Udine, Dept Sci & Med Technol, I-33100 Udine, Italy
[2] Univ Trieste, Dept Biochem Biophys & Macromol Chem, I-34127 Trieste, Italy
[3] Univ Zurich, Inst Vet Physiol, Div Appl Physiol, CH-8057 Zurich, Switzerland
[4] CIB, Nat Lab, I-34012 Padriciano Trieste, Italy
关键词
cathelicidin peptide; alpha-helical antimicrobial peptide; synthetic analog; antimicrobial activity; clinical isolate; in vivo protection; infection;
D O I
10.1016/j.peptides.2003.07.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two alpha-helical antimicrobial peptides (BMAP-27 and -28) and four synthetic analogs were compared for in vitro and in vivo antimicrobial efficacy. All peptides proved active in vitro at micromolar concentrations against a range of clinical isolates, including antibiotic-resistant strains. BMAP-27 and two analogs were more effective towards Gram-negative, and BMAP-28 towards Gram-positive organisms. In addition, BMAP-28 provided some protection in vitro against human herpes simplex virus type 1 (HSV-1). The parent peptides and mBMAP-28 analog protected mice from lethal i.p. infections in an acute peritonitis model at peptide doses significantly lower than those toxic to the animals, suggesting a satisfactory therapeutic index. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:1723 / 1731
页数:9
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