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The effect of fluconazole in combination with rifampin in vitro on Candida albicans biofilms

机译:氟康唑联合利福平对白色念珠菌生物膜的影响

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Production of Candida albicans biofilms is one resistance mechanism of fluconazole in C. albicans and accordingly biofilm-related infections pose a great challenge to antifungal therapy. In this study, each of the three antibacterial agents of azithromycin, fosfomycin and rifampin, which could destroy bacteria biofilms, was respectively tested in combination with fluconazole to verify whether they had synergistic effects on C. albicans biofilms. The nature of drug interaction was interpreted by calculating fractional inhibitory concentration index (FICI) and percentages of growth difference (ΔE) from the results of checkerboard assay. In order to evaluate the potential of the three antibiotics on fluconazole penetrating the biofilms, a penetrating experiment was explored. In addition, fluorescein diacetate staining method was adopted to observe metabolic activity of the sessile cell. It was revealed that rifampin could work synergistically with fluconazole against the biofilms, while only negligible antifungal effects were observed for the other drug combinations. A potent synergistic interaction in vitro between fluconazole and rifampin against the biofilms by a fluconazole-resistant strain was demonstrated by a FICI value of 0.035 and synergistic high-interaction percentages of 1256% as interpreted by the ΔE model. Results of the penetrating experiment indicated that fluconazole combined with rifampin markedly enhanced inhibitory zone of an indicative organism. Fluorescence micrographs showed that the addition of rifampin rendered the cellular metabolism largely reduced. To sum up, rifampin could sensibilize fluconazole' antifungal effect on C. albicans biofilms and the synergistic mechanism needs further investigating.
机译:白色念珠菌生物膜的产生是氟康唑在白色念珠菌中的一种耐药机制,因此与生物膜相关的感染对抗真菌治疗提出了巨大挑战。在这项研究中,阿奇霉素,磷霉素和利福平这三种可能破坏细菌生物膜的抗菌剂分别与氟康唑组合进行了试验,以验证它们是否对白色念珠菌生物膜具有协同作用。药物相互作用的性质是通过根据棋盘格分析的结果计算分数抑制浓度指数(FICI)和生长差异百分比(ΔE)来解释的。为了评估三种抗生素对氟康唑穿透生物膜的潜力,我们进行了穿透实验。另外,采用荧光素二乙酸盐染色法观察无柄细胞的代谢活性。揭示了利福平可以与氟康唑协同作用对抗生物膜,而其他药物组合仅观察到微不足道的抗真菌作用。氟康唑耐药菌株在氟康唑和利福平之间对抗生物膜的有效协同作用由FICI值为0.035,协同高相互作用百分率为1256%,如ΔE模型所示。渗透实验的结果表明,氟康唑与利福平的结合显着增强了指示生物的抑制区。荧光显微照片显示,利福平的添加使细胞代谢大大降低。综上所述,利福平可以增强氟康唑对白色念珠菌生物膜的抗真菌作用,其协同作用机理尚需进一步研究。

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