Doke Sonali Kashinath, Raut Jayant Shankar, Dhawale Shashikant, Karuppayil Sankunny Mohan
School of Pharmacy, SRTM University.
J Gen Appl Microbiol. 2014;60(5):163-8. doi: 10.2323/jgam.60.163.
Infections associated with the biofilms of Candida albicans are a challenge to antifungal treatment. Combinatorial therapy involving plant molecules with antifungal drugs would be an effective complementary approach against drug-resistant Candida biofilms. The aim of this study was to evaluate the efficacy of three bioactive terpenoids (carvacrol, eugenol and thymol) in combination with fluconazole against planktonic cells, biofilm development and mature biofilms of C. albicans. Activities of the selected molecules were tested using a microplate-based methodology, while their combinations with fluconazole were performed in a checkerboard format. Biofilms were quantitated by XTT-metabolic assay and confirmed by microscopic observations. Combinations of carvacrol and eugenol with fluconazole were found synergistic against planktonic growth of C. albicans, while that of thymol with fluconazole did not have any interaction. Biofilm development and mature biofilms were highly resistant to fluconazole, but susceptible to three terpenoids. Sensitization of cells by sub-inhibitory concentrations of carvacrol and eugenol resulted in prevention of biofilm formation at low fluconazole concentrations, i.e. 0.032 and 0.002 mg ml(-1), respectively. Addition of thymol could not potentiate activity of fluconazole against biofilm formation by C. albicans. Fractional inhibitory concentration indices (FICI) for carvacrol-fluconazole and eugenol-fluconazole combinations for biofilm formation were 0.311 and 0.25, respectively. The FICI value of 1.003 indicated a status of indifference for the combination of thymol and fluconazole against biofilm formation. Eugenol and thymol combinations with fluconazole did not have useful interaction against mature biofilms of C. albicans, but the presence of 0.5 mg ml(-1) of carvacrol caused inhibition of mature biofilms at a significantly low concentration (i.e. 0.032 mg ml(-1)) of fluconazole. The study indicated that carvacrol and eugenol combinations with fluconazole would be a potential alternative strategy for prevention and control of biofilm-associated C. albicans infections.
白色念珠菌生物膜相关感染对抗真菌治疗构成挑战。将植物分子与抗真菌药物联合使用的联合疗法将是对抗耐药性白色念珠菌生物膜的一种有效补充方法。本研究的目的是评估三种生物活性萜类化合物(香芹酚、丁香酚和百里酚)与氟康唑联合使用对白色念珠菌浮游细胞、生物膜形成和成熟生物膜的疗效。使用基于微孔板的方法测试所选分子的活性,同时以棋盘格式进行它们与氟康唑的联合实验。通过XTT代谢测定法定量生物膜,并通过显微镜观察进行确认。发现香芹酚和丁香酚与氟康唑的组合对白色念珠菌的浮游生长具有协同作用,而百里酚与氟康唑的组合没有任何相互作用。生物膜形成和成熟生物膜对氟康唑高度耐药,但对三种萜类化合物敏感。亚抑制浓度的香芹酚和丁香酚对细胞的致敏作用导致在低氟康唑浓度下(分别为0.032和0.002 mg/ml)预防生物膜形成。添加百里酚不能增强氟康唑对白色念珠菌生物膜形成的活性。香芹酚 - 氟康唑和丁香酚 - 氟康唑组合对生物膜形成的分数抑制浓度指数(FICI)分别为0.311和0.25。FICI值为1.003表明百里酚和氟康唑组合对生物膜形成无明显相互作用。丁香酚和百里酚与氟康唑的组合对白色念珠菌成熟生物膜没有有效的相互作用,但存在0.5 mg/ml的香芹酚会在显著低浓度(即0.032 mg/ml)的氟康唑下抑制成熟生物膜。该研究表明,香芹酚和丁香酚与氟康唑的组合将是预防和控制生物膜相关白色念珠菌感染的潜在替代策略。