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Eucalyptal D Enhances the Antifungal Effect of Fluconazole on Fluconazole-Resistant Candida albicans by Competitively Inhibiting Efflux Pump

机译:桉树术通过竞争性地抑制出水泵,增强了氟康唑对氟康唑抗性念珠菌抗念珠菌的抗真菌效应

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摘要

The frequent emergence of azole-resistant strains has increasingly led azoles to fail in treating candidiasis. Combination with other drugs is a good option to effectively reduce or retard its incidence of resistance. Natural products are a promising synergist source to assist azoles in treating resistant candidiasis. Eucalyptal D (ED), a formyl-phloroglucinol meroterpenoid, is one of the natural synergists, which could significantly enhance the anticandidal activity of fluconazole (FLC) in treating FLC resistant C. albicans. The checkerboard microdilution assay showed their synergistic effect. The agar disk diffusion test illustrated the key role of ED in synergy. The rhodamine 6G (R6G) efflux assay reflected ED could reduce drug efflux, but quantitative reverse transcription PCR analysis revealed the upregulation of CDR1 and CDR2 genes in ED treating group. Efflux pump-deficient strains were hyper-susceptible to ED, thus ED was speculated to be the substrate of efflux pump Cdr1p and Cdr2p to competitively inhibit the excretion of FLC or R6G, which mainly contributed to its synergistic effect.
机译:抗唑抗性菌株的频繁出现越来越多地LED唑由于治疗念珠菌病而失败。与其他药物的组合是有效减少或延迟其抗性发生率的良好选择。天然产品是一个有前途的协同源,可以帮助唑类治疗耐念珠菌病。桉树D(ED)是一种甲醛 - 甘油蛋白莫丙醇萜类萜类萜类化合物,是天然增效剂之一,可以显着增强氟康唑(FLC)治疗FLC抗性C.醛糖型的反黑化活性。棋盘微漏测定结果显示了它们的协同效果。 AGAR磁盘扩散测试说明了ED在协同作用中的关键作用。 Rhodamine 6G(R6G)流出测定的反射ED可以减少药物流出,但定量逆转录PCR分析显示CDR1和CDR2基因在ED治疗组中的上调。外排泵缺陷型菌株是超敏感性到ED,ED因而推测为外排泵Cdr1p和Cdr2p的的基板竞争性抑制FLC或R6G,主要促成了其协同作用的排泄。

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