Pan Lili, Yao Yuanyuan, Zheng Hailin, Yan Shuzhen, Chen Shuanglin
Jiangsu Province Key Laboratory for Microbes and Functional Genomics, College of Life Sciences, Nanjing Normal University, Nanjing 210023, China.
Jiangsu Province Key Laboratory of Molecular Biology of Dermatology and Venereal Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing 210042, China.
J Fungi (Basel). 2022 Aug 11;8(8):841. doi: 10.3390/jof8080841.
Biofilm-associated infections, the leading cause of invasive candidiasis, can cause high mortality rates in immunocompromised patients. Photodynamic antimicrobial chemotherapy (PACT) is a promising approach for controlling infections caused by biofilm-associated . This study shows the effect of Elsinochrome A (EA) against different stages of biofilms in vitro by XTT reduction assay and crystal violet staining. The mechanism of action of EA on biofilm was analyzed with flow cytometry, confocal laser microscopy, and the Real-Time Quantitative Reverse Transcription PCR (qRT-PCR). EA-mediated PACT significantly reduced the viability of , with an inhibition rate on biofilm of 89.38% under a concentration of 32 μg/mL EA. We found that EA could not only inhibit the adhesion of in the early stage of biofilm formation, but that it also had good effects on pre-formed mature biofilms with a clearance rate of 35.16%. It was observed that EA-mediated PACT promotes the production of a large amount of reactive oxygen species (ROS) in and down-regulates the intracellular expression of oxidative-stress-related genes, which further disrupted the permeability of cell membranes, leading to mitochondrial and nuclear damage. These results indicate that EA has good photodynamic antagonizing activity against the biofilm, and potential clinical value.
生物膜相关感染是侵袭性念珠菌病的主要原因,可导致免疫功能低下患者的高死亡率。光动力抗菌化学疗法(PACT)是控制生物膜相关感染的一种有前景的方法。本研究通过XTT还原试验和结晶紫染色显示了埃尔希诺色素A(EA)对体外生物膜不同阶段的影响。用流式细胞术、共聚焦激光显微镜和实时定量逆转录PCR(qRT-PCR)分析了EA对生物膜的作用机制。EA介导的PACT显著降低了(此处原文缺失相关菌名)的活力,在32μg/mL EA浓度下对生物膜的抑制率为89.38%。我们发现EA不仅可以在生物膜形成的早期抑制(此处原文缺失相关菌名)的黏附,而且对预先形成的成熟生物膜也有良好的效果,清除率为35.16%。观察到EA介导的PACT促进(此处原文缺失相关菌名)中大量活性氧(ROS)的产生,并下调细胞内氧化应激相关基因的表达,这进一步破坏了细胞膜的通透性,导致线粒体和细胞核损伤。这些结果表明EA对(此处原文缺失相关菌名)生物膜具有良好的光动力拮抗活性和潜在的临床价值。