Department of Biosciences and Oral Diagnosis, Institute of Science and Technology, São Paulo State University/UNESP, São José dos Campos, SP, Brazil.
Department of Biology, Laboratory of Microbial Ecology and Biotechnology Pici, Ceará Federal University, Fortaleza, CE, Brazil.
Photodiagnosis Photodyn Ther. 2022 Jun;38:102837. doi: 10.1016/j.pdpdt.2022.102837. Epub 2022 Mar 30.
Chitosan (CS) is a natural polymer extracted from the exoskeleton of crustaceans. Due to its cationic structure, CS has been studied as a possible enhancer of antimicrobial photodynamic therapy (aPDT). The objective was to evaluate the association of CS with methylene blue (MB)-mediated aPDT on Candida albicans, investigating its effects on planktonic growth, biofilms, and cells persistent to fluconazole. The ability of CS to interfere with MB absorption by Candida cells was also evaluated. For the assays, planktonic cells of C. albicans were cultivated for 24 h, and the biofilms were formed for 48 h. For the induction of persister cells, C. albicans was cultivated with high concentration of fluconazole for 48 h. Treatments were performed with MB, CS or MB+CS, followed by irradiation with LED (660 nm ). As results, aPDT with MB (300 µm) reduced the planktonic cells by 1.6 log10 CFU, while the MB+CS association led to a reduction of 4.8 log10 CFU. For aPDT in biofilms, there was a microbial reduction of 2.9 log10 CFU for the treatment with MB (600 µm) and 5.3 log10 CFU for MB+CS. In relation to persister cells, the fungal reductions were 0.4 log10 CFU for MB and 1.5 log10 CFU for MB+CS. In the absorption assays, the penetration of MB into Candida cells was increased in the presence of CS. It was concluded that CS enhanced the antimicrobial activity of aPDT in planktonic growth, biofilms, and persister cells of C. albicans, probably by facilitating the penetration of MB into fungal cells.
壳聚糖(CS)是一种从甲壳类动物的外骨骼中提取的天然聚合物。由于其阳离子结构,CS 已被研究作为一种可能的增强型抗菌光动力疗法(aPDT)的增强剂。本研究的目的是评估 CS 与亚甲蓝(MB)介导的 aPDT 联合应用对白色念珠菌的作用,研究其对浮游生长、生物膜和耐氟康唑的细胞的影响。还评估了 CS 对 MB 被念珠菌细胞吸收的干扰能力。对于实验,培养白色念珠菌浮游细胞 24 小时,形成生物膜 48 小时。为了诱导持久细胞,白色念珠菌在高浓度氟康唑中培养 48 小时。用 MB、CS 或 MB+CS 进行处理,然后用 LED(660nm)照射。结果显示,MB(300μm)的 aPDT 使浮游细胞减少了 1.6log10CFU,而 MB+CS 联合处理则使 CFU 减少了 4.8log10。对于生物膜中的 aPDT,MB(600μm)处理使微生物减少了 2.9log10CFU,MB+CS 处理使微生物减少了 5.3log10CFU。关于持久细胞,MB 的真菌减少量为 0.4log10CFU,MB+CS 的真菌减少量为 1.5log10CFU。在吸收实验中,CS 的存在增加了 MB 进入念珠菌细胞的渗透。综上所述,CS 增强了 MB 对浮游生长、生物膜和白色念珠菌持久细胞的 aPDT 的抗菌活性,可能是通过促进 MB 进入真菌细胞。