TY - JOUR
T1 - Biological Characterization and in Vivo Assessment of the Activity of a New Synthetic Macrocyclic Antifungal Compound
AU - Deodato, Davide
AU - Maccari, Giorgio
AU - De Luca, Filomena
AU - Sanfilippo, Stefania
AU - Casian, Alexandru
AU - Martini, Riccardo
AU - D'Arezzo, Silvia
AU - Bonchi, Carlo
AU - Bugli, Francesca
AU - Posteraro, Brunella
AU - Vandeputte, Patrick
AU - Sanglard, Dominique
AU - Docquier, Jean-Denis
AU - Sanguinetti, Maurizio
AU - Visca, Paolo
AU - Botta, Maurizio
PY - 2016
Y1 - 2016
N2 - We recently identified a novel family of macrocyclic amidinoureas showing potent antifungal activity against Candida spp. In this study, we demonstrate the fungicidal effect of these compounds as well as their killing activity in a dose-dependent manner. Transcriptional analysis data indicate that our molecules induce a significant change in the transcriptome involving ABC transporters genes. Notably, experiments against Candida albicans mutants lacking those genes showed resistance to the compound, suggesting the involvement of ABC transporters in the uptake or intracellular accumulation of the molecule. To probe the mode of action, we performed fluorescence microscopy experiments on fungal cells treated with an ad-hoc synthesized fluorescent derivative. Fluorescence microscopy images confirm the ability of the compound to cross the membrane and show a consistent accumulation within the cytoplasm. Finally, we provide data supporting the in vivo efficacy in a systemic infection murine model setup with a drug-resistant strain of Candida albicans.
AB - We recently identified a novel family of macrocyclic amidinoureas showing potent antifungal activity against Candida spp. In this study, we demonstrate the fungicidal effect of these compounds as well as their killing activity in a dose-dependent manner. Transcriptional analysis data indicate that our molecules induce a significant change in the transcriptome involving ABC transporters genes. Notably, experiments against Candida albicans mutants lacking those genes showed resistance to the compound, suggesting the involvement of ABC transporters in the uptake or intracellular accumulation of the molecule. To probe the mode of action, we performed fluorescence microscopy experiments on fungal cells treated with an ad-hoc synthesized fluorescent derivative. Fluorescence microscopy images confirm the ability of the compound to cross the membrane and show a consistent accumulation within the cytoplasm. Finally, we provide data supporting the in vivo efficacy in a systemic infection murine model setup with a drug-resistant strain of Candida albicans.
KW - Candida albicans
KW - Candida albicans
UR - http://hdl.handle.net/10807/73657
U2 - 10.1021/acs.jmedchem.6b00018
DO - 10.1021/acs.jmedchem.6b00018
M3 - Article
SN - 0022-2623
SP - N/A-N/A
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
ER -