Biofilm formation by Candida albicans is inhibited by 4,4-dichloro diphenyl diselenide (pCl-PhSe)2

Curr Drug Discov Technol. 2014;11(3):234-8. doi: 10.2174/1570163811666140924121758.

Abstract

Candida species are the fourth most common cause of nosocomial bloodstream infections. An increase in the frequency of infections which have become refractory to standard antifungal therapyhave been observed. Recently, the effect of different organochalcogenide compounds reducing both growth and germ tube formation by Candida albicans was demonstrated. This work studied the effect of the organochalcogenide compound (pCl-PhSe)2 on both growth and biofilm formation by Candida albicans. A decrease in C. albicans growth in the presence of crescent concentrations of (pCl- PhSe)2 was observed, in a cell density dependent manner. The inhibition of Candida growth by 10µM (pCl-PhSe)2 was ~60, 57, 47 and 24%, in cell densities of 10(3), 10(4), 10(5) and 10(6) cells/ml, respectively. The compound (pCl-PhSe)2 was able to inhibit biofilm formation by Candida albicans, when biofilm was performed using a cell density of 10(6) cells/ml. In addition, an increase in both ROS production (96%) and cell membrane permeability (1.107-fold) by 10 µM (pCl-PhSe)2 was observed in C. albicans.These results demonstrate that the organochalcogenide compound (pCl-PhSe)2 presents a great potential to inhibit both growth and biofilm formation by C. albicans.

MeSH terms

  • Antifungal Agents / chemistry
  • Antifungal Agents / pharmacology
  • Benzene Derivatives / chemistry
  • Benzene Derivatives / pharmacology*
  • Biofilms / drug effects*
  • Biofilms / growth & development*
  • Candida albicans / drug effects*
  • Candida albicans / growth & development*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Organoselenium Compounds / chemistry
  • Organoselenium Compounds / pharmacology*

Substances

  • Antifungal Agents
  • Benzene Derivatives
  • Organoselenium Compounds
  • diphenyldiselenide