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首页> 外文期刊>Photodiagnosis and Photodynamic Therapy >Antifungal effect of photodynamic therapy mediated by curcumin on Candida albicans biofilms in vitro
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Antifungal effect of photodynamic therapy mediated by curcumin on Candida albicans biofilms in vitro

机译:姜黄素介导的光动力疗法对白色念珠菌生物膜的抗真菌作用

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摘要

Background: : Canida albicans can cause opportunistic infections ranging from superficial mucous membrane lesions to life-threatening disease. The aim of this study is to investigate the antifungal effect of photodynamic therapy (PDT) mediated by curcumin (CUR) on C. albicans biofilms in vitro.Methods: : One standard strain ATCC 90028 and two clinical isolates from HIV (CCA1) and oral lichen planus (CCA2) patients' oral cavities were used in this study. Biofilms were photosensitized with 60 mu M CUR and irradiated by light emitting diode (LED) under the wavelength of 455 nm and energy densities of 2.64, 5.28, 7.92, 10.56, 13.2 J/cm(2). Then the antifungal effects of CUR-PDT were evaluated by XTT reduction assay and confocal light scanning microscopy (CLSM) observations. The effects of CUR-PDT on the expression levels of hyphaspecific and biofilm-related genes including EFG1, UME6, HGC1 and ECE1 were assessed by quantitative Realtime PCR (qRT-PCR) method.Results: : The inhibition rates after CUR-PDT in three biofilms(ATCC 90028, CCA1, CCA2)were 90.87%, 66.44% and 86.74% respectively (p < 0.05). Relative gene expression levels of EFG1, UME6, HGC1 and ECE1 were all downregulated after CUR-PDT, with fold-decrease of 6.865, 3.382, 2.167 and 6.887 in ATCC 90028, 2.466, 2.146, 1.627 and 3.102 in CCA1, and 5.406, 2.347, 2.073and 3.711 in CCA2 (p < 0.05).Conclusions: : Curcumin-mediated PDT could effectively inactivateCandida albicans biofilms in vitro. Expression of genes involved in biofilms formation were downregulated after CUR-PDT.
机译:背景:白色念珠菌可引起机会性感染,从表层粘膜病变到危及生命的疾病。这项研究的目的是研究姜黄素(CUR)介导的光动力疗法(PDT)对白色念珠菌生物膜的抗真菌作用。方法::一株标准ATCC 90028菌株和两株HIV(CCA1)和口服的临床分离株本研究使用扁平苔藓(CCA2)患者的口腔。生物膜用60μM CUR光敏,并在455 nm的波长和2.64、5.28、7.92、10.56、13.2 J / cm(2)的能量密度下用发光二极管(LED)照射。然后通过XTT还原测定和共聚焦光扫描显微镜(CLSM)观察评估CUR-PDT的抗真菌作用。通过定量实时荧光定量PCR(qRT-PCR)方法评估了CUR-PDT对细菌特异性和生物膜相关基因(包括EFG1,UME6,HGC1和ECE1)表达水平的影响。结果:CUR-PDT对三种基因的抑制率生物膜(ATCC 90028,CCA1,CCA2)分别为90.87%,66.44%和86.74%(p <0.05)。 EFG1,UME6,HGC1和ECE1的相对基因表达水平在CUR-PDT之后均被下调,ATCC 90028中的2.865、3.382、2.167和6.887,CCA1中的2.102、1.627和3.102和5.406、2.347的折叠降低结论:姜黄素介导的PDT可以有效地灭活白色念珠菌生物膜。 CUR-PDT后下调了参与生物膜形成的基因的表达。

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