Differential effects of alpha-helical and beta-hairpin antimicrobial peptides against Acanthamoeba castellanii


Autoria(s): SACRAMENTO, R. S.; MARTINS, R. M.; MIRANDA, A.; DOBROFF, A. S. S.; DAFFRE, S.; FORONDA, A. S.; FREITAS, D. De; SCHENKMAN, S.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

In this work we evaluated the ability of different types of antimicrobial peptides to promote permeabilization and growth inhibition of Acanthamoeba castellanii trophozoites, which cause eye keratitis. We used cationic alpha-helical peptides P5 and a beta-hairpin amphipathic molecule (gomesin), of the spider Acanthoscurria gomesiana haemocytes. A. castellanii permeabilization was obtained after 1 h incubation with micromolar concentrations of both types of peptides. While permeabilization induced by gomesin increased with longer incubations, P5 permeabilization did not increase with time and occurred at doses that are more toxic for SIRC cells, P5, however, at doses below the critical dose used to kill rabbit corneal cells was quite effective in promoting growth inhibition. Similarly, P5 was more effective when serine protease inhibitor was added simultaneously to the permeabilization assay. High performance chromatography followed by mass spectrometry analysis confirmed that, in contrast to gomesin, P5 is hydrolysed by A. castellanii culture supernatants. We conclude that the use of antimicrobial peptides to treat A. castellanii infections requires the search of more specific peptides that are resistant to proteolysis.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico Tecnologico (CNPq), Brazil

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Identificador

PARASITOLOGY, v.136, n.8, p.813-821, 2009

0031-1820

http://producao.usp.br/handle/BDPI/28539

10.1017/S0031182009006283

http://dx.doi.org/10.1017/S0031182009006283

Idioma(s)

eng

Publicador

CAMBRIDGE UNIV PRESS

Relação

Parasitology

Direitos

restrictedAccess

Copyright CAMBRIDGE UNIV PRESS

Palavras-Chave #Acanthamoeba castellanii #antimicrobial peptides #amphipathic peptides permeabilization #protease #SPIDER ACANTHOSCURRIA-GOMESIANA #OCULAR SURFACE #KERATITIS #EXPRESSION #CHLORHEXIDINE #INFLAMMATION #POLYPHAGA #TRIALYSIN #PROTEASES #MAGAININS #Parasitology
Tipo

article

original article

publishedVersion