Bae Yoon Seol, Rhee Min Suk
Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea.
Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea,
Cell Physiol Biochem. 2019;53(2):285-300. doi: 10.33594/000000139.
BACKGROUND/AIMS: Although naturally-derived antifungals have been investigated for their ability to inactivate Candida albicans, which is a major cause of candidiasis, they have shown a less than 3 log reduction in C. albicans or required treatment times of longer than 3 h. Thus, the naturally-derived antifungals used in previous studies could not substantially eradicate C. albicans within a short period of time.
To improve the fungicidal effects of naturallyderived antifungals against C. albicans within short time periods, we developed composites showing antifungal synergism using caprylic acid (CA), carvacrol (CAR) and thymol (THM) for 1-10 min at 22/37°C. Using flow cytometry, we examined the mode of action for the synergism of these compounds on membrane integrity and efflux pump activity.
Whereas the maximum reduction by individual treatments was 0.6 log CFU/ml, CA + CAR/THM (all 1.5 mM) eliminated all pathogens (> 6.8 log reduction) after 1 min at 37°C and after 10 min at 22°C. The flow cytometry results showed that exposure to CA damaged the membranes in 15.7-36.5% of cells and inhibited efflux pumps in 15.4-31.3% of cells. Treatments with CAR/THM slightly affected cell membranes (in 1.8-6.9% of cells) but damaged efflux pumps in 14.4-29.6% of cells. However, the combined treatments clearly disrupted membranes (> 83.1% of cells) and pumps (> 95.0% of cells). The mechanism of this synergism may involve membrane damage by CA, which facilitates the entry of antifungals into the cytoplasm, and the inhibition of efflux pumps by CA, CAR or THM, causing their accumulation within cells and, leading to cell death.
Antifungal composites (CA + CAR/THM) showing synergism (i.e., an additional 6 log reduction) within minutes at room/body temperature can be used to treat candidiasis and improve the microbiological safety of facilities contaminated with fungi as a novel alternative to synthetic antifungals.
背景/目的:尽管天然来源的抗真菌剂已被研究其灭活白色念珠菌的能力,白色念珠菌是念珠菌病的主要病因,但它们对白色念珠菌的杀灭率低于3个对数,或所需治疗时间超过3小时。因此,先前研究中使用的天然来源抗真菌剂无法在短时间内大量根除白色念珠菌。
为了在短时间内提高天然来源抗真菌剂对白色念珠菌的杀菌效果,我们开发了复合制剂,其使用辛酸(CA)、香芹酚(CAR)和百里香酚(THM)在22/37°C下作用1 - 10分钟,表现出抗真菌协同作用。使用流式细胞术,我们研究了这些化合物协同作用对膜完整性和外排泵活性的作用模式。
单独处理的最大杀灭率为0.6 log CFU/ml,而CA + CAR/THM(均为1.5 mM)在37°C下作用1分钟和在22°C下作用10分钟后可消除所有病原体(杀灭率> 6.8个对数)。流式细胞术结果显示,暴露于CA会使15.7 - 36.5%的细胞的膜受损,使15.4 - 31.3%的细胞的外排泵受到抑制。用CAR/THM处理对细胞膜的影响较小(1.8 - 6.9%的细胞),但会使14.4 - 29.6%的细胞的外排泵受损。然而,联合处理明显破坏了细胞膜(> 83.1%的细胞)和外排泵(> 95.0%的细胞)。这种协同作用的机制可能涉及CA对膜的损伤,这有助于抗真菌剂进入细胞质,以及CA、CAR或THM对外排泵的抑制,导致它们在细胞内积累,从而导致细胞死亡。
在室/体温下数分钟内表现出协同作用(即额外降低6个对数)的抗真菌复合制剂(CA + CAR/THM)可用于治疗念珠菌病,并作为合成抗真菌剂的新型替代品提高被真菌污染设施的微生物安全性。