Metallopeptidase inhibitors arrest vital biological processes in the fungal pathogen Scedosporium apiospermum


Autoria(s): SILVA, Bianca A.; SOUZA-GONCALVES, Ana Luiza; PINTO, Marcia R.; BARRETO-BERGTER, Eliana; SANTOS, Andre L. S.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

P>Scedosporium apiospermum is an emerging agent of opportunistic mycoses in humans. Previously, we showed that mycelia of S. apiospermum secreted metallopeptidases which were directly linked to the destruction of key host proteins. In this study, we analysed the effect of metallopeptidase inhibitors on S. apiospermum development. As germination of inhaled conidia is a crucial event in the infectious process of S. apiospermum, we studied the morphological transformation induced by the incubation of conidia in Sabouraud-dextrose medium at 37 degrees C. After 6 h, some conidia presented a small projection resembling a germ-tube. A significant increase, around sixfold, in the germ-tube length was found after 12 h, and hyphae were exclusively observed after 24 h. Three distinct metallopeptidase inhibitors were able to arrest the transformation of conidia into hyphae in different ways; for instance, 1,10-phenanthroline (PHEN) completely blocked this process at 10 mu mol l-1, while ethylenediamine tetraacetic acid (EDTA) and ethylene glycol-bis (beta-aminoethyl ether; EGTA) only partially inhibited the differentiation at up to 10 mmol l-1. EGTA did not promote any significant reduction in the conidial growth, while PHEN and EDTA, both at 10 mmol l-1, inhibited the proliferation around 100% and 65%, respectively. The secretion of polypeptides into the extracellular environment and the metallopeptidase activity secreted by mycelia were completely inhibited by PHEN. These findings suggest that metallo-type enzymes could be potential targets for future therapeutic interventions against S. apiospermum.

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ)

Fundacao de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ)

Fundacao Universitaria Jose Bonifacio (FUJB)

Fundacao Universitaria Jose Bonifacio (FUJB)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[05/02776-0]

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

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

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[05/56161-6]

Identificador

MYCOSES, v.54, n.2, p.105-112, 2011

0933-7407

http://producao.usp.br/handle/BDPI/28654

10.1111/j.1439-0507.2009.01767.x

http://dx.doi.org/10.1111/j.1439-0507.2009.01767.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

Relação

Mycoses

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #Scedosporium apiospermum #growth #differentiation #polypeptide secretion #metallopeptidase inhibitors #PSEUDALLESCHERIA-BOYDII #CANDIDA-ALBICANS #BIOCHEMICAL-CHARACTERIZATION #FONSECAEA-PEDROSOI #METAL-COMPLEXES #1,10-PHENANTHROLINE #PROTEINASES #PEPTIDORHAMNOMANNAN #METALLOPROTEASES #DIFFERENTIATION #Dermatology #Mycology
Tipo

article

original article

publishedVersion