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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.
Abstract:
Candida albicans, the most common opportunistic pathogenic fungus, is also the main pathogenic organism for oral candidiasis. This condition is particularly prevalent among the elderly, children, and individuals undergoing radiotherapy or suffering from HIV. The lack of new antifungal drugs, and drug resistance coupled with the side effects of current antifungal agents have increased the challenges of clinical antifungal therapies. Polyenes, including amphotericin B and nystatin, are clinical fungicidal drugs, however, their side effects and low solubility have limited their clinical applications. Here, we identified that moxidectin, a novel approved antiparasitic agent, could synergize with both amphotericin B and nystatin to inhibit the growth and biofilm formation of Candida albicans including 60 clinical isolates. The transcriptome and RT-PCR analysis indicated that moxidectin activated the biosynthesis pathway of ergosterol, the direct target of polyenes, further being verified by the loss of the synergistic activities with polyenes against ergosterol pathway mutants, including Δ/Δerg3, Δ/Δerg11 and Δ/Δerg3 Δ/Δerg11. Moxidectin was then confirmed to elevate the ergosterol biosynthesis levels of C. albicans and enhance the binding between cells and polyenes. In a mouse oral candidiasis model, moxidectin combined with low dosages of polyenes to significantly reduce the infection area, colonization of C. albicans and the inflammatory degree of tongue mucosa. Our study originally demonstrated that moxidectin could activate the ergosterol biosynthesis then elevate the ergosterol contents to enhance the antifungal effects of polyenes against C. albicans and its infections. Moxidectin can serve as the candidate potentiator of polyenes for further clinical practice. KEY POINTS: • Moxidectin synergized with polyenes against Candida albicans. • Moxidectin activated the ergosterol biosynthesis of Candida albicans. • Moxidectin combined with polyenes to effectively combat oral candidiasis in mice.
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.
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