Anju S, Kumar Nishanth S, Krishnakumar B, Kumar B S Dileep
Environmental Technology, CSIR-National Institute for Interdisciplinary Science and Technology Thiruvananthapuram, India.
Agroprocessing and Natural Products Division, CSIR-National Institute for Interdisciplinary Science and Technology Thiruvananthapuram, India.
Front Cell Infect Microbiol. 2015 Aug 11;5:57. doi: 10.3389/fcimb.2015.00057. eCollection 2015.
Superficial mycoses caused by dermatophytic fungi such as Trichophyton rubrum represent the most common type of worldwide human infection affecting various keratinized tissues in our body such as the skin, hair, and nails, etc. The dermatophytic infection is a significant public health threat due to its persistent nature and high recurrence rates, and thus alternative treatments to cure this fungal infection are urgently required. The present study mainly focused on the synergistic activity of violacein with four azole drugs (ketoconazole, fluconazole, clotrimazole, and itraconazole) against T. rubrum. The synergistic antifungal activities of violacein and azoles were measured by checkerboard microdilution and time-kill assays. In our study, combinations of violacein and azoles predominantly recorded synergistic effect (FIC index < 0.5). Significant synergistic value was recorded by the combination of violacein and clotrimazole. Time-kill assay by the combination of MIC concentration of violacein and azoles recorded that the growth of the T. rubrum was significantly arrested after 4-12 h of treatment. The combination of violacein and azoles leads to the enhanced inhibition of mycelial growth and conidial germination. Moreover combination enhanced the rate of release of intracellular materials. Morphological changes by SEM analysis were also prominent with the combination. A normal human cell line [Foreskin (FS) normal fibroblast] was used to check the cytotoxicity of violacein. Interestingly violacein recorded no cytotoxicity up to 100 μg/ml. The in vitro synergistic effect of violacein and azoles against clinically relevant fungi, T. rubrum, is reported here for the first time. Finally, our findings support the potential use of the violacein as an antifungal agent especially against dermatophytic fungi T. rubrum.
由红色毛癣菌等皮肤癣菌引起的浅部真菌病是全球最常见的人类感染类型,会影响人体的各种角化组织,如皮肤、毛发和指甲等。皮肤癣菌感染因其持续性和高复发率对公共卫生构成重大威胁,因此迫切需要替代疗法来治愈这种真菌感染。本研究主要关注紫罗碱与四种唑类药物(酮康唑、氟康唑、克霉唑和伊曲康唑)对红色毛癣菌的协同活性。通过棋盘微量稀释法和时间杀菌试验测定了紫罗碱和唑类药物的协同抗真菌活性。在我们的研究中,紫罗碱与唑类药物的组合主要表现出协同作用(FIC指数<0.5)。紫罗碱与克霉唑的组合具有显著的协同价值。紫罗碱和唑类药物的MIC浓度组合进行的时间杀菌试验表明,处理4-12小时后,红色毛癣菌的生长显著受到抑制。紫罗碱与唑类药物的组合导致对菌丝生长和分生孢子萌发的抑制增强。此外,组合还提高了细胞内物质的释放速率。扫描电镜分析显示组合处理后的形态变化也很明显。使用正常人细胞系[包皮(FS)正常成纤维细胞]检测紫罗碱的细胞毒性。有趣的是,紫罗碱在浓度高达100μg/ml时未表现出细胞毒性。本文首次报道了紫罗碱和唑类药物对临床相关真菌红色毛癣菌的体外协同作用。最后,我们的研究结果支持紫罗碱作为抗真菌剂的潜在用途,尤其是针对皮肤癣菌红色毛癣菌。