Back to Search Start Over

Antifungal Activity of Resveratrol Derivatives against Candida Species

Authors :
Guillaume Delanoue
Nicolas Papon
Marc Clastre
Laurence Guérin
Jérôme Guillard
Vincent Courdavault
Benjamin Houillé
Cécile Enguehard-Gueiffier
Leslie Boudesocque
Arnaud Lanoue
Nathalie Giglioli-Guivarc’h
Jean-Philippe Bouchara
Sébastien Besseau
Eric Bourdeaud
Groupe d'Étude des Interactions Hôte-Pathogène (GEIHP)
Université d'Angers (UA)
UR Infectiologie animale et Santé publique (UR IASP)
Institut National de la Recherche Agronomique (INRA)
Institut de Chimie des Milieux et Matériaux de Poitiers (IC2MP)
Université de Poitiers-Centre National de la Recherche Scientifique (CNRS)
Biomolécules et biotechnologies végétales (BBV EA 2106)
Université de Tours
Nutrition, croissance et cancer (U 1069) (N2C)
Université de Tours-Institut National de la Santé et de la Recherche Médicale (INSERM)
Unité de VINs, Innovations, Itinéraires, TERroirs et Acteurs
Institut Français de la Vigne et du Vin (IFV)
Groupe d'Etude des Interactions Hôte-Parasite (GEIHP)
This work was supported by the Région Centre grants ACTISARM 201100068678 and VITITERROIR 201300083172. The authors wish to thank A. Mançois and F. Fourmont (Lycée Viticole d’Amboise, France) for providing the grape canes. We acknowledge A. J. Simkin for critical reading of the manuscript.
Source :
Journal of Natural Products, Journal of Natural Products, American Chemical Society, 2014, 77 (7), pp.1658-1662. ⟨10.1021/np5002576⟩, Journal of Natural Products, American Chemical Society, 2014, 77 ( 7), pp.1658-1662 ⟨10.1021/np5002576⟩, Journal of Natural Products, American Chemical Society, 2014, 77 (7), pp.A-E. ⟨10.1021/np5002576⟩
Publication Year :
2014
Publisher :
HAL CCSD, 2014.

Abstract

International audience; trans-Resveratrol (1a) is a phytoalexin produced by plants in response to infections by pathogens. Its potential activity against clinically relevant opportunistic fungal pathogens has previously been poorly investigated. Evaluated herein are the candidacidal activities of oligomers (2a, 3−5) of 1a purified from Vitis vinifera grape canes and several analogues (1b−1j) of 1a obtained through semisynthesis using methylation and acetylation. Moreover, trans-ε-viniferin (2a), a dimer of 1a, was also subjected to methylation (2b) and acetylation (2c) under nonselective conditions. Neither the natural oligomers of 1a (2a, 3−5) nor the derivatives of 2a were active against Candida albicans SC5314. However, the dimethoxy resveratrol derivatives 1d and 1e exhibited antifungal activity against C. albicans with minimum inhibitory concentration (MIC) values of 29−37 μg/mL and against 11 other Candida species. Compound 1e inhibited the yeast-to-hyphae morphogenetic transition of C. albicans at 14 μg/mL. trans Resveratrol (1a) is a natural stilbenoid produced by several plants in response to pathogenic infections. Although present in a restricted number of plant families, 1a forms the backbone of a wide range of stilbene biosynthetic products, leading to a spectrum of monomeric and oligomeric compounds with diverse biological activities.1,2 Stilbenes were first described for their fungicidal action against plant fungal diseases by Langcake and Pryce.3 Later, antimicrobial activities of stilbenes were reported against various phytopathogens, with 1a occurring as a major phytoalexin of the family Vitaceae.4,5 Resveratrol fully inhibits conidial germination of the gray mold agent Botrytis cinerea6 and reduces roughly 75% sporangial germination of the causal agent of grapevine downy mildew, Plasmopara viticola.7 Pterostilbene, the 3,5-dimethoxyresveratrol (1e), and trans ε-viniferin (2a) have been found to be 5- fold more active than 1a, indicating the potential of resveratrol derivatives as a source of effective antifungal agents.8,9 In the field of human health, several investigations have been conducted on 1a due to its multiple pharmacological activities including cardioprotective, antiaging, anticarcinogenic, antiinflammatory, estrogenic/antiestrogenic

Details

Language :
English
ISSN :
01633864 and 15206025
Database :
OpenAIRE
Journal :
Journal of Natural Products, Journal of Natural Products, American Chemical Society, 2014, 77 (7), pp.1658-1662. ⟨10.1021/np5002576⟩, Journal of Natural Products, American Chemical Society, 2014, 77 ( 7), pp.1658-1662 ⟨10.1021/np5002576⟩, Journal of Natural Products, American Chemical Society, 2014, 77 (7), pp.A-E. ⟨10.1021/np5002576⟩
Accession number :
edsair.doi.dedup.....dddbaf06f8693f52b44a5c6ab6d4717c