Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.5/13716
Título: Blad-containing oligomer fungicidal activity on human pathogenic yeasts. From the outside to the inside of the target cell
Autor: Pinheiro, Ana M.
Carreira, Alexandra
Rollo, Filipe
Fernandes, Rui
Ferreira, Ricardo Boavida
Monteiro, Sara A.
Palavras-chave: Candida albicans
antifungal
natural product
pathogenic yeast
protein-based
Data: 2016
Editora: Maria Tereza dos Santos Correia (ed.)
Citação: Pinheiro AM, Carreira A, Rollo F, Fernandes R, Ferreira RB and Monteiro SA (2016) Blad-Containing Oligomer Fungicidal Activity on Human Pathogenic Yeasts. From the Outside to the Inside of the Target Cell. Front. Microbiol. 7:1803.
Resumo: Blad polypeptide comprises residues 109–281 of Lupinus albus b-conglutin precursor. It occurs naturally as a major subunit of an edible, 210 kDa oligomer which accumulates to high levels, exclusively in the cotyledons of Lupinus seedlings between the 4th and 14th day after the onset of germination. Blad-containing oligomer (BCO) exhibits a potent and broad spectrum fungicide activity toward plant pathogens and is now on sale in the US under the tradename FractureTM. In this work we demonstrate its antifungal activity toward human pathogens and provide some insights on its mode of action. BCO bioactivity was evaluated in eight yeast species and compared to that of amphotericin B (AMB). BCO behaved similarly to AMB in what concerns both cellular inhibition and cellular death. As a lectin, BCO binds strongly to chitin. In addition, BCO is known to possess ‘exochitinase’ and ‘endochitosanase’ activities. However, no clear disruption was visualized at the cell wall after exposure to a lethal BCO concentration, except in cell buds. Immunofluorescent and immunogold labeling clearly indicate that BCO enters the cell, and membrane destabilization was also demonstrated. The absence of haemolytic activity, its biological origin, and its extraordinary antifungal activity are the major outcomes of this work, and provide a solid background for a future application as a new antifungal therapeutic drug. Furthermore, its predictable multisite mode of action suggests a low risk of inducing resistance mechanisms, which are now a major problem with other currently available antifungal drugs.
Peer review: yes
URI: http://hdl.handle.net/10400.5/13716
DOI: 10.3389/fmicb.2016.01803
Aparece nas colecções:ISA - Artigos em Revistas Internacionais

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