The antimicrobial peptide Dermaseptin S4 inhibits HIV-1 infectivity in vitro

被引:123
作者
Lorin, C
Saidi, H
Belaid, A
Zairi, A
Baleux, F
Hocini, H
Bélec, L
Hani, K
Tangy, F
机构
[1] Inst Pasteur, CNRS, URA 1930, Unite Virus Lents, F-75015 Paris, France
[2] Inst Biomed Cordeliers, INSERM, U430, F-75006 Paris, France
[3] Fac Med, Biochem Lab, Sousse, Tunisia
[4] Inst Pasteur, Unite Chim Organ, F-75724 Paris, France
关键词
Dermaseptin S4; microbicide; herpes simplex virus type 1;
D O I
10.1016/j.virol.2005.02.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Most of HIV-1 infections are acquired through sexual contact. In the absence of a preventive vaccine, the development of topical microbicides that can block infection at the mucosal tissues is needed. Dermaseptin S4 (DS4) is an antimicrobial peptide derived from amphibian skin, which displays a broad spectrum of activity against bacteria, yeast, filamentous fungi, and herpes simplex virus type 1. We show here that DS4 inhibits cell-free and cell-associated HIV-1 infection of P4-CCR5 indicator cells and human primary T lymphocytes. The peptide is effective against R5 and X4 primary isolates and laboratory-adapted strains of HIV-1. Its activity is directed against HIV-1 particles by disrupting the virion integrity. Increasing the number of DS4-positive charges reduced cytotoxicity without affecting the antiviral activity. The modified DS4 inhibited HIV-1 capture by dendritic cells and subsequent transmission to CD4(+) T cells, as well as HIV-1 binding on HEC-1 endometrial cells and transcytosis through a tight epithelial monolayer. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:264 / 275
页数:12
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