Ramage Gordon, Milligan Steven, Lappin David F, Sherry Leighann, Sweeney Petrina, Williams Craig, Bagg Jeremy, Culshaw Shauna
Infection and Immunity Research Group, Glasgow Dental School, School of Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow Glasgow, UK.
Front Microbiol. 2012 Jun 18;3:220. doi: 10.3389/fmicb.2012.00220. eCollection 2012.
Candida albicans forms oral biofilms that cause disease and are difficult to treat with conventional antifungal agents. Tea tree oil (TTO) is a natural compound with reported antimicrobial and immunomodulatory activities. The aims of the study were to evaluate the antifungal efficacy of TTO and key derivatives against C. albicans biofilms, to assess the toxicological effects of TTO on a clinically relevant oral cell line, and to investigate its impact on inflammation. TTO and its derivatives were examined against 100 clinical strains of C. albicans. Planktonic minimum inhibitory concentrations (MICs) were determined using the CLSI M-27A broth microdilution method. Sessile MICs were determined using an XTT reduction assay. Inhibition, time-kill, and mode of action studies were performed. OKF6-TERT2 epithelial cells were used for cytotoxicity and cytokine expression assays. Planktonic C. albicans isolates were susceptible to TTO, terpinen-4-ol (T-4-ol), and α-terpineol, with an MIC(50) of 0.5, 0.25, and 0.25%, respectively. These three compounds also displayed potent activity against the 69 biofilm-forming strains, of which T-4-ol and α-terpineol displayed rapid kill kinetics. For all three compounds, 1 × MIC(50) effectively inhibited biofilm growth when C. albicans were treated at 0, 1, and 2 h post adhesion. By scanning electron microscopy analysis and PI uptake, TTO and derivative components were shown to be cell membrane active. TTO and T-4-ol were cytotoxic at 1 × MIC(50), whereas at 0.5 × MIC(50) T-4-ol displayed no significant toxicity. Transcript and protein analysis showed a reduction of IL-8 when treated with TTO and T-4-ol. These data provide further in vitro evidence that TTO and its derivative components, specifically T-4-ol, exhibit strong antimicrobial properties against fungal biofilms. T-4-ol has safety advantages over the complete essential oil and may be suitable for prophylaxis and treatment of established oropharyngeal candidosis. A clinical trial of T-4-ol is worthy of consideration.
白色念珠菌可形成口腔生物膜,引发疾病,且难以用传统抗真菌药物进行治疗。茶树油(TTO)是一种天然化合物,具有抗菌和免疫调节活性的报道。本研究的目的是评估TTO及其关键衍生物对白色念珠菌生物膜的抗真菌效果,评估TTO对临床相关口腔细胞系的毒理学效应,并研究其对炎症的影响。对100株白色念珠菌临床菌株检测了TTO及其衍生物。采用CLSI M-27A肉汤微量稀释法测定浮游菌的最低抑菌浓度(MIC)。采用XTT还原法测定固着菌的MIC。进行了抑制、时间杀菌和作用方式研究。使用OKF6-TERT2上皮细胞进行细胞毒性和细胞因子表达检测。浮游的白色念珠菌分离株对TTO、萜品-4-醇(T-4-ol)和α-萜品醇敏感,MIC(50)分别为0.5%、0.25%和0.25%。这三种化合物对69株生物膜形成菌株也显示出强效活性,其中T-4-ol和α-萜品醇显示出快速杀菌动力学。对于所有三种化合物,当白色念珠菌在黏附后0、1和2小时进行处理时,1×MIC(50)可有效抑制生物膜生长。通过扫描电子显微镜分析和碘化丙啶摄取显示,TTO及其衍生物成分具有细胞膜活性。TTO和T-4-ol在1×MIC(50)时具有细胞毒性,而在0.5×MIC(50)时T-4-ol未显示出明显毒性。转录和蛋白质分析表明,用TTO和T-4-ol处理后白细胞介素-8减少。这些数据提供了进一步的体外证据,表明TTO及其衍生物成分,特别是T-4-ol,对真菌生物膜具有强大的抗菌特性。T-4-ol相对于完整精油具有安全优势,可能适用于预防和治疗已确诊的口咽念珠菌病。T-4-ol的临床试验值得考虑。