Combination of Antifungal Drugs and Protease Inhibitors Prevent Candida albicans Biofilm Formation and Disrupt Mature Biofilms

Biofilms formed by the fungal pathogen are resistant to many of the antifungal agents commonly used in the clinic. Previous reports suggest that protease inhibitors, specifically inhibitors of aspartyl proteases, could be effective antibiofilm agents. We screened three protease inhibitor libraries,...

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Published inFrontiers in microbiology Vol. 11; p. 1027
Main Authors Lohse, Matthew B, Gulati, Megha, Craik, Charles S, Johnson, Alexander D, Nobile, Clarissa J
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 25.05.2020
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Summary:Biofilms formed by the fungal pathogen are resistant to many of the antifungal agents commonly used in the clinic. Previous reports suggest that protease inhibitors, specifically inhibitors of aspartyl proteases, could be effective antibiofilm agents. We screened three protease inhibitor libraries, containing a total of 80 compounds for the abilities to prevent biofilm formation and to disrupt mature biofilms. The compounds were screened individually and in the presence of subinhibitory concentrations of the most commonly prescribed antifungal agents for infections: fluconazole, amphotericin B, or caspofungin. Although few of the compounds affected biofilms on their own, seven aspartyl protease inhibitors inhibited biofilm formation when combined with amphotericin B or caspofungin. Furthermore, nine aspartyl protease inhibitors disrupted mature biofilms when combined with caspofungin. These results suggest that the combination of standard antifungal agents together with specific protease inhibitors may be useful in the prevention and treatment of biofilm infections.
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Present address: Megha Gulati, Molecular Cell – Cell Press, Cambridge, MA, United States
Edited by: Juliana Campos Junqueira, São Paulo State University, Brazil
This article was submitted to Infectious Diseases, a section of the journal Frontiers in Microbiology
Reviewed by: Rohitashw Kumar, University at Buffalo, United States; Isabel M. Miranda, University of Porto, Portugal
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2020.01027