Infectious Disease Research Center, Birjand University of Medical Sciences, Birjand 9717853577, Iran.
Department of Medical Mycology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran 14115111, Iran.
Medicina (Kaunas). 2023 Apr 10;59(4):743. doi: 10.3390/medicina59040743.
: Vulvovaginal candidiasis (VVC) is a mucous membrane infection, with an increased rate of antifungal resistance of species. In this study, the in vitro efficacy of farnesol alone or in combination with traditional antifungals was assessed against resistant strains recovered from women with VVC. : Eighty isolates were identified by multiplex polymerase chain reaction (PCR), and the antifungal susceptibility to amphotericin B (AMB), fluconazole (FLU), itraconazole (ITZ), voriconazole (VOR), clotrimazole (CTZ), and farnesol was tested by the standard microdilution method. The combinations of farnesol with each antifungal were calculated based on the fractional inhibitory concentration index (FICI). was the predominant species (48.75%) isolated from vaginal discharges, followed by (43.75%), (3.75%), a mixed infection of and (2.5%) and and (1%). and isolates had lower susceptibility to FLU (31.4% and 23.0%, respectively) and CTZ (37.1% and 33.3%, respectively). Importantly, there was "synergism" between farnesol-FLU and farnesol-ITZ against and (FICI = 0.5 and 0.35, respectively), reverting the original azole-resistant profile. : These findings indicate that farnesol can revert the resistance profile of azole by enhancing the activity of FLU and ITZ in resistant isolates, which is a clinically promising result.
外阴阴道假丝酵母菌病(VVC)是一种黏膜感染,其 物种的抗真菌耐药率增加。在这项研究中,评估了法尼醇单独或与传统抗真菌药联合应用对来自 VVC 女性的耐药 株的体外疗效。
通过多重聚合酶链反应(PCR)鉴定了 80 株分离株,并用标准微量稀释法测试了两性霉素 B(AMB)、氟康唑(FLU)、伊曲康唑(ITZ)、伏立康唑(VOR)、克霉唑(CTZ)和法尼醇对这些分离株的抗真菌敏感性。根据部分抑菌浓度指数(FICI)计算了法尼醇与每种抗真菌药的组合。从阴道分泌物中分离出的主要菌种是 (48.75%),其次是 (43.75%)、 (3.75%)、 和 的混合感染(2.5%)以及 和 的混合感染(1%)。 和 分离株对 FLU(分别为 31.4%和 23.0%)和 CTZ(分别为 37.1%和 33.3%)的敏感性较低。重要的是,法尼醇-FLU 和法尼醇-ITZ 对 和 (FICI = 0.5 和 0.35)表现出“协同作用”,逆转了最初的唑类耐药谱。
这些发现表明,法尼醇可以通过增强 FLU 和 ITZ 在耐药 分离株中的活性来逆转唑类的耐药谱,这是一个有临床前景的结果。