Moxidectin elevates Candida albicans ergosterol levels to synergize with polyenes against oral candidiasis

Xingchen Ye1,2, Yaqi Liu1,2, Ding Chen1

  • 1State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & West China School of Stomatology, Sichuan University, Chengdu, 610041, China.

Insights

Moxidectin synergizes with polyenes to combat Candida albicans oral infections by boosting ergosterol production. This combination therapy shows promise for treating candidiasis in mice, offering a potential new strategy against drug-resistant fungal infections.

Area of Science:

  • Mycology and Infectious Diseases
  • Pharmacology and Drug Discovery

Background:

  • Candida albicans is a major cause of opportunistic oral candidiasis, particularly in vulnerable populations.
  • Existing antifungal therapies like polyenes face challenges due to drug resistance, side effects, and limited solubility.
  • There is a critical need for novel therapeutic strategies to overcome these limitations in treating fungal infections.

Purpose of the Study:

  • To investigate the synergistic potential of moxidectin, an antiparasitic agent, with polyene antifungals against Candida albicans.
  • To elucidate the mechanism underlying the observed synergy between moxidectin and polyenes.
  • To evaluate the efficacy of the moxidectin-polyene combination in a preclinical model of oral candidiasis.

Main Methods:

  • In vitro testing of moxidectin and polyene (amphotericin B, nystatin) synergy against Candida albicans clinical isolates.
  • Transcriptome and RT-PCR analysis to identify the molecular mechanisms of synergy, focusing on ergosterol biosynthesis.
  • In vivo efficacy study using a mouse model of oral candidiasis to assess the therapeutic effect of the combination.

Main Results:

  • Moxidectin demonstrated significant synergy with amphotericin B and nystatin, inhibiting Candida albicans growth and biofilm formation.
  • Moxidectin was found to activate the ergosterol biosynthesis pathway in Candida albicans, enhancing polyene drug efficacy.
  • The combination therapy significantly reduced oral candidiasis severity, fungal load, and inflammation in a mouse model.

Conclusions:

  • Moxidectin acts as a potentiator for polyene antifungals by enhancing ergosterol biosynthesis in Candida albicans.
  • The combination of moxidectin and polyenes offers a promising therapeutic approach for managing oral candidiasis.
  • Moxidectin represents a potential candidate for clinical use as an adjuvant therapy to improve antifungal treatments.