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, Cecília Rocha da Silva1,2, João Batista de Andrade Neto1,2, Francisca Bruna Stefany Aires do Nascimento1,2, Fátima Daiana Dias Barroso1,2, Lisandra Juvêncio da Silva1,2, Vitória Pessoa de Farias Cabral1,2
, Amanda Dias Barbosa1,2
, Jacilene Silva3, Emmanuel Silva Marinho3
, Manoel Odorico de Moraes4, Maria Erivanda França Rios2, Bruno Coêlho Cavalcanti2, Iri Sandro Pampolha Lima5 and Hélio Vitoriano Nobre Júnior2
This study evaluated the effect of etomidate against biofilms of Candida spp. and analysed through molecular docking the interaction of this drug with ALS3, an important protein for fungal adhesion. Three fluconazole-resistant fungi were used: Candida albicans, Candida parapsilosis and Candida tropicalis. Growing biofilms were exposed to etomidate at 31.25–500 µg ml−1. Then, an ALS3 adhesive protein from C. albicans was analysed through a molecular mapping technique, composed of a sequence of algorithms to perform molecular mapping simulation based on classic force field theory. Etomidate showed antifungal activity against growing biofilms of resistant C. albicans, C. parapsilosis and C. tropicalis at all concentrations used in the study. The etomidate coupling analysis revealed three interactions with the residues of interest compared to hepta-threonine, which remained at the ALS3 site. In addition, etomidate decreased the expression of mannoproteins on the surface of C. albicans. These results revealed that etomidate inhibited the growth of biofilms.
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