Chen Borui, Sun Yi, Zhang Jinyan, Chen Ruijun, Zhong Xiurong, Wu Xiaomo, Zheng Libao, Zhao Jingjun
Department of Dermatology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Dermatology Hospital of Fuzhou, Fuzhou, China.
Front Microbiol. 2019 Jun 7;10:1228. doi: 10.3389/fmicb.2019.01228. eCollection 2019.
Dermatophytes are the most common cause of onychomycosis, counting for 90% fungal nail infection. Although dermatophyte pathogens are normally susceptible to antifungal agents, onychomycosis often results in refractory chronic disease, and the formation of biofilms frequently underlines the inadequate responses and resistance to standard antifungal treatment. Numerous and antimicrobial photodynamic therapy (aPDT) studies have shown biofilm eradication or substantial reduction, however, such investigation has not yet been expanded to the biofilms of dermatophytes involved in onychomycosis. To shed a light on the potential application of aPDT in the clinic management of onychomycosis, in particular with the manifestation of dermatophytoma, we investigated photodynamic effects on the viabilities and the drug susceptibilities of the biofilm of dermatophytes . Here, methylene blue at the concentration of 8, 16, and 32 μg/ml applied as photosensitizing agent and LED (635 ± 10 nm, 60 J/cm) as light source were employed against six strains of , ten strains of and three strains of isolated from clinical specimens. Our results indicated highly efficient photodynamic inhibition, exhibiting CFU (colony forming unit) reduction up to 4.6 log, 4.3 log, and 4.7 log against the biofilms formed by , and , respectively. Subjected biofilms displayed considerable decreases in SMICs (sessile minimum inhibitory concentrations) to multiple antifungal agents when compared with untreated groups, indicating the biofilms of dermatophytes became more susceptible to conventional antifungal drugs after aPDT. Additionally, the obliteration of biofilm after aPDT could be observed as shattered and ruptured structures being evident in SEM (Scanning Electron Microscopy) images. These findings suggest that aPDT is an attractive alternative treatment holding great promise for combating recalcitrant onychomycosis associated with the biofilm formation.
皮肤癣菌是甲癣最常见的病因,占真菌性指甲感染的90%。尽管皮肤癣菌病原体通常对抗真菌药物敏感,但甲癣常导致难治性慢性病,生物膜的形成常常是对标准抗真菌治疗反应不足和产生耐药性的原因。许多抗菌光动力疗法(aPDT)研究表明生物膜可被根除或显著减少,然而,此类研究尚未扩展到涉及甲癣的皮肤癣菌生物膜。为了阐明aPDT在甲癣临床管理中的潜在应用,特别是针对皮肤癣菌瘤的表现,我们研究了光动力对皮肤癣菌生物膜活力和药敏性的影响。在此,以浓度为8、16和32μg/ml的亚甲蓝作为光敏剂,以发光二极管(635±10nm,60J/cm)作为光源,对从临床标本中分离出的6株红色毛癣菌、10株须癣毛癣菌和3株絮状表皮癣菌进行实验。我们的结果表明光动力抑制效率很高,对红色毛癣菌、须癣毛癣菌和絮状表皮癣菌形成的生物膜,其菌落形成单位(CFU)分别减少高达4.6对数、4.3对数和4.7对数。与未处理组相比,经处理的生物膜对多种抗真菌药物的静态最小抑菌浓度(SMIC)显著降低,表明皮肤癣菌生物膜在aPDT后对传统抗真菌药物更敏感。此外,在扫描电子显微镜(SEM)图像中可以观察到aPDT后生物膜被破坏,结构破碎、破裂。这些发现表明光动力疗法是一种有吸引力的替代治疗方法,在对抗与生物膜形成相关的顽固性甲癣方面具有很大前景。