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Cell Membrane Integrity of Candida Albicans after Different Protocols of Microwave Irradiation

机译:不同微波辐射方案后白色念珠菌的细胞膜完整性

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Purpose: To evaluate the ability of low time microwaveexposureto inactivate and damage cell membrane integrity of C. albicans. Materials and Methods: Two 200ml C. albicans suspensions were obtained. Sterile dentures were placed in a beaker containing Experimental (ES) or Control suspensions (CS). ES was microwaved at 650 W for 1, 2, 3, 4 or 5 min. Suspensions were optically counted using Methylene blue dye as indicative of membrane-damaged cells; spread on Agar Sabouraud dextrose (ASD) for viability assay; or spectrophotometrically measured at 550nm. Cell-free solutions were submitted to content analyses of protein (Bradford and Pyrogallol red methods); Ca++ (Cresolphthalein Complexone method); DNA (spectrophotometer measurements at 260nm) and K+ (selective electrode technique). Data were analyzed by Student-t test and linear regression (α=0.05). In addition, flowcytometry analysis of Candida cells in suspensionwas performed using propidium iodide. Results: All ES cells demonstrated cell membrane damage at 3, 4 and 5 min,viable cells were nonexistent at 3, 4 and 5 min ES ASD plates and optical density of ES and CS was not significantly differentfor all exposition times. ES cells released highcontents of protein, K+, Ca++ and DNA after 2 min exposition when compared to that of the CSs. Similar results were observed with flow cytometry analysiswith regard to the periodsof microwave exposure. Conclusions: Microwave irradiation inactivated C. albicansafter 3min and damaged cell membrane integrity after 2 min exposition.
机译:目的:评估低时间微波暴露灭活和破坏白色念珠菌细胞膜完整性的能力。材料和方法:获得两个200ml白色念珠菌悬浮液。将无菌假牙放入装有实验(ES)或对照悬液(CS)的烧杯中。 ES在650 W微波处理1、2、3、4或5分钟。使用亚甲基蓝染料对悬浮液进行光学计数,以指示细胞受损的细胞。铺在琼脂沙氏葡萄糖(ASD)上进行活力测定;或用分光光度法在550nm处测量。将无细胞溶液提交蛋白质含量分析(Bradford和Pyrogallol红法); Ca ++(Cresolphthalein Complexone方法); DNA(分光光度计在260nm处测量)和K +(选择性电极技术)。通过Student-t检验和线性回归分析数据(α= 0.05)。另外,使用碘化丙啶进行悬浮液中念珠菌细胞的流式细胞术分析。结果:所有ES细胞在3、4和5分钟时均显示出细胞膜损伤,ES,ASD板在3、4和5分钟时不存在活细胞,并且ES和CS的光密度在所有暴露时间内均无显着差异。与CSs相比,ES细胞在暴露2分钟后释放出高含量的蛋白质,K +,Ca ++和DNA。流式细胞仪分析在微波暴露时间方面观察到相似的结果。结论:微波照射3分钟后灭活了白色念珠菌,暴露2分钟后破坏了细胞膜的完整性。

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