Biofilms formed by the human fungal pathogen Candida albicans are naturally resistant to many of the antifungal agents commonly used in the clinic. We screened a library containing 1600 clinically tested drug compounds to identify compounds that inhibit C. albicans biofilm formation. The compounds that emerged from the initial screen were validated in a secondary screen and then tested for (1) their abilities to disrupt mature biofilms and (2) for synergistic interactions with representatives of the three antifungal agents most commonly prescribed to treat Candida infections, fluconazole, amphotericin B, and caspofungin. Twenty compounds had antibiofilm activity in at least one of the secondary assays and several affected biofilms but, at the same concentration, had little or no effect on planktonic (suspension) growth of C. albicans. Two calcium channel blockers, a selective serotonin reuptake inhibitor, and an azole-based proton pump inhibitor were among the hits, suggesting that members of these three classes of drugs or their derivatives may be useful for treating C. albicans biofilm infections.
A Selective Serotonin Reuptake Inhibitor, a Proton Pump Inhibitor, and Two Calcium Channel Blockers Inhibit Candida albicans Biofilms.
选择性血清素再摄取抑制剂、质子泵抑制剂和两种钙通道阻滞剂可抑制白色念珠菌生物膜的形成
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作者:Nobile Clarissa J, Ennis Craig L, Hartooni Nairi, Johnson Alexander D, Lohse Matthew B
| 期刊: | Microorganisms | 影响因子: | 4.200 |
| 时间: | 2020 | 起止号: | 2020 May 18; 8(5):756 |
| doi: | 10.3390/microorganisms8050756 | 研究方向: | 微生物学 |
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