State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & West China School of Stomatology, Sichuan University, Chengdu, 610041, China.
Department of Pediatric Dentistry, West China Hospital of Stomatology, Sichuan University, Chengdu, 610041, China.
Appl Microbiol Biotechnol. 2024 Nov 11;108(1):509. doi: 10.1007/s00253-024-13343-8.
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.
白色念珠菌是最常见的机会致病性真菌,也是口腔念珠菌病的主要病原体。这种情况在老年人、儿童和接受放疗或感染 HIV 的人群中尤为普遍。缺乏新的抗真菌药物以及药物耐药性加上现有抗真菌药物的副作用,增加了临床抗真菌治疗的挑战。多烯类药物,包括两性霉素 B 和制霉菌素,是临床杀真菌药物,但其副作用和低溶解度限制了它们的临床应用。在这里,我们发现莫昔克丁,一种新批准的抗寄生虫药物,可以与两性霉素 B 和制霉菌素协同抑制白色念珠菌的生长和生物膜形成,包括 60 株临床分离株。转录组和 RT-PCR 分析表明,莫昔克丁激活了多烯类药物的直接靶点麦角固醇的生物合成途径,进一步通过与多烯类药物对麦角固醇途径突变体的协同活性丧失得到验证,包括 Δ/Δerg3、Δ/Δerg11 和 Δ/Δerg3 Δ/Δerg11。然后证实莫昔克丁可提高白色念珠菌的麦角固醇生物合成水平并增强细胞与多烯类药物的结合。在小鼠口腔念珠菌病模型中,莫昔克丁与低剂量的多烯类药物联合使用可显著减少感染面积、白色念珠菌定植和舌黏膜的炎症程度。我们的研究最初表明,莫昔克丁可以激活麦角固醇的生物合成,然后提高麦角固醇含量,增强多烯类药物对白色念珠菌及其感染的抗真菌作用。莫昔克丁可作为多烯类药物的候选增效剂,用于进一步的临床实践。关键点: • 莫昔克丁与多烯类药物协同作用抗白色念珠菌。 • 莫昔克丁激活白色念珠菌的麦角固醇生物合成。 • 莫昔克丁与多烯类药物联合有效治疗小鼠口腔念珠菌病。