Zhang Yunsong, Zhu Yingbo, Chen Jia, Wang Yucheng, Sherwood Margaret E, Murray Clinton K, Vrahas Mark S, Hooper David C, Hamblin Michael R, Dai Tianhong
a Department of Plastic Surgery and Cosmetic , The Second People's Hospital of Guangdong Province , Guangzhou , China.
b Wellman Center for Photomedicine, Massachusetts General Hospital , Boston , MA , USA.
Virulence. 2016 Jul 3;7(5):536-45. doi: 10.1080/21505594.2016.1155015. Epub 2016 Feb 24.
Fungal infections are a common cause of morbidity, mortality and cost in critical care populations. The increasing emergence of antimicrobial resistance necessitates the development of new therapeutic approaches for fungal infections. In the present study, we investigated the effectiveness of an innovative approach, antimicrobial blue light (aBL), for inactivation of Candida albicans in vitro and in infected mouse burns. A bioluminescent strain of C. albicans was used. The susceptibilities to aBL (415 nm) were compared between C. albicans and human keratinocytes. The potential development of aBL resistance by C. albicans was investigated via 10 serial passages of C. albicans on aBL exposure. For the animal study, a mouse model of thermal burn infected with the bioluminescent C. albicans strain was used. aBL was delivered to mouse burns approximately 12 h after fungal inoculation. Bioluminescence imaging was performed to monitor in real time the extent of infection in mice. The results obtained from the studies demonstrated that C. albicans was approximately 42-fold more susceptible to aBL than human keratinocytes. Serial passaging of C. albicans on aBL exposure implied a tendency of reduced aBL susceptibility of C. albicans with increasing numbers of passages; however, no statistically significant difference was observed in the post-aBL survival rate of C. albicans between the first and the last passage (P>0.05). A single exposure of 432 J/cm(2) aBL reduced the fungal burden in infected mouse burns by 1.75-log10 (P=0.015). Taken together, our findings suggest aBL is a potential therapeutic for C. albicans infections.
真菌感染是重症监护人群发病、死亡和成本的常见原因。抗菌药物耐药性的不断出现使得开发针对真菌感染的新治疗方法成为必要。在本研究中,我们调查了一种创新方法——抗菌蓝光(aBL)在体外和感染的小鼠烧伤模型中对白色念珠菌的灭活效果。使用了白色念珠菌的生物发光菌株。比较了白色念珠菌和人角质形成细胞对aBL(415nm)的敏感性。通过在aBL照射下对白色念珠菌进行10次连续传代,研究了白色念珠菌对aBL耐药性的潜在发展情况。对于动物研究,使用了感染生物发光白色念珠菌菌株的小鼠热烧伤模型。在真菌接种后约12小时将aBL照射到小鼠烧伤部位。进行生物发光成像以实时监测小鼠的感染程度。研究结果表明,白色念珠菌对aBL的敏感性是人角质形成细胞的约42倍。白色念珠菌在aBL照射下连续传代表明,随着传代次数增加,白色念珠菌对aBL的敏感性有降低的趋势;然而,在第一次和最后一次传代之间,白色念珠菌在aBL照射后的存活率没有观察到统计学上的显著差异(P>0.05)。单次432J/cm²的aBL照射使感染小鼠烧伤中的真菌负荷降低了1.75个对数单位(P=0.015)。综上所述,我们的研究结果表明aBL是治疗白色念珠菌感染的一种潜在疗法。