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Provedor de dados:  ArchiMer
País:  France
Título:  Oyster hemocytes express a proline-rich peptide displaying synergistic antimicrobial activity with a defensin
Autores:  Gueguen, Yannick
Romestand, Bernard
Fievet, Julie
Schmitt, Paulina
Destoumieux Garzon, Delphine
Franck, Vandenbulcke
Philippe, Bulet
Bachere, Evelyne
Data:  2009-02
Ano:  2009
Palavras-chave:  Antimicrobial peptide
Mollusk
Synergy
Invertebrate
Innate immunity
Pacific oyster
Resumo:  A cDNA sequence that encodes a 61-amino acid polypeptide precursor with homologies to proline-rich antimicrobial peptides (AMPs) was identified in the oyster Crassostrea gigas. After release of a hydrophobic signal peptide. the resulting 37-amino acid peptide, Cg-Prp, is composed of an acidic region and a cationic proline-rich region. To evaluate the biological properties of Cg-Prp, multiple proline-rich peptides corresponding to putative processing of the full-length Cg-Prp were synthesized. A limited antimicrobial activity was observed for two of them, which also showed strong synergistic antimicrobial activity with Cg-Def, a defensin from C gigas. To our knowledge, this is the first evidence of synergy between a defensin and another AMP in an invertebrate. By in situ hybridization, the expression of Cg-prp was found to be restricted to hemocytes and induced following bacterial challenge. Cg-prp transcripts were also detected in hemocytes infiltrating mantle, where Cg-Def is expressed. Additionally, by immunocytochemistry, we showed that Cg-Prp or one of its variants is present in some hemocytes together with defensins. In conclusion, we described here the first proline-rich AMP from mollusk. From our study, it is likely to provide a first line of defense against bacterial invasion by acting through synergy with defensins. (C) 2008 Elsevier Ltd. All rights reserved.
Tipo:  Text
Idioma:  Inglês
Identificador:  http://archimer.ifremer.fr/doc/2009/publication-6232.pdf

DOI:10.1016/j.molimm.2008.07.021
Editor:  Elsevier
Relação:  http://archimer.ifremer.fr/doc/00000/6232/
Formato:  application/pdf
Fonte:  Molecular Immunology (0161-5890) (Elsevier), 2009-02 , Vol. 46 , N. 4 , P. 516-522
Direitos:  2009 Elsevier
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