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Palmarumycin P3 Reverses Mrr1-Mediated Azole Resistance by Blocking the Efflux Pump Mdr1.

Minghui SongMing ZhangJinghui LuFei XieJintong SongXiaoyi LuanXuben HouHongxiang LouWenqiang Chang
Published in: Antimicrobial agents and chemotherapy (2022)
Palmarumycin P3 (PP3) reduces fluconazole-induced MDR1 transcription to reverse azole resistance in clinical Candida strains. Here, we demonstrated that PP3 restores the susceptibility to several antifungal drugs for Candida albicans strains with gain-of-function mutations in the transcription factor Mrr1. In addition, PP3 inhibits the efflux of Mdr1 substrates by C. albicans strains harboring hyperactive MRR1 alleles. Molecular docking revealed that PP3 is a potential Mdr1 blocker that binds to the substrate binding pocket of Mdr1.
Keyphrases
  • candida albicans
  • multidrug resistant
  • molecular docking
  • biofilm formation
  • transcription factor
  • escherichia coli
  • dna binding
  • staphylococcus aureus
  • oxidative stress
  • angiotensin converting enzyme