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In vitro activity of dermaseptin S1 derivatives against genital pathogens
Author(s) -
SAVOIA DIANELLA,
DONALISIO MANUELA,
CIVRA ANDREA,
SALVADORI SEVERO,
GUERRINI REMO
Publication year - 2010
Publication title -
apmis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.909
H-Index - 88
eISSN - 1600-0463
pISSN - 0903-4641
DOI - 10.1111/j.1600-0463.2010.02637.x
Subject(s) - in vitro , microbiology and biotechnology , chemistry , biology , biochemistry
Savoia D, Donalisio M, Civra A, Salvadori S, Guerrini R. In vitro activity of dermaseptin S1 derivatives against genital pathogens. APMIS 2010; 118: 674–80. The aim of this study was to evaluate the biological activity of nine dermaseptin‐S1 (DRS‐S1) derivatives (synthesized by solid‐phase methods and purified) against different pathogens causing genital infections ( Trichomonas vaginalis , Herpes simplex virus, Papillomavirus). The in vitro activity on T. vaginalis was determined by counting the protozoon in a hemocytometer after vital staining with trypan blue; antiviral activity of the compounds was tested on monolayers of Vero cells for Herpes simplex virus‐1 (GFP) and on 293TT cells for human papillomavirus (HPV‐16) pseudovirions (GFP). The cytotoxicity of the derivatives was assessed by evaluating both the hemolytic activity and the effect on Vero and 293TT cells. The DRS‐S1 longer peptides demonstrated a superior activity on T. vaginalis but also a certain cytopathic effect . The compounds with 29 amino acids exhibited activity against the two viruses tested at concentrations not toxic to cells. The results obtained show that some of the synthetic peptides assessed have inhibitory activity against the pathogens tested, indicating a potential for the development of new molecules for use as topical microbicides to prevent the sexual transmission of microorganisms.