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Dietary Carbohydrates Modulate Candida albicans Biofilm Development on the Denture Surface

机译:饮食中的碳水化合物调节义齿表面白色念珠菌生物膜的发育

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摘要

The purpose of this study was to investigate whether dietary carbohydrates can modulate the development of Candida albicans biofilms on the denture material surface. Poly (methyl methacrylate) acrylic resin discs were fabricated and had their surface roughness measured. Biofilms of C. albicans ATCC 90028 were developed on saliva-coated specimens in culture medium without (control) or with carbohydrate supplementation by starch, starch+sucrose, glucose, or sucrose for 72 h. The cell count, metabolic activity, biovolume, average thickness, and roughness coefficient were evaluated at the adhesion phase (1.5 h) and after 24, 48, and 72 h. The secretion of proteinases and phospholipases, cell surface energy, and production of extra/intracellular polysaccharides were analyzed after 72 h of biofilm development. Data were analyzed by one- and two-way ANOVA followed by Tukey’s test at 5% significance level. In the early stages of colonization (adhesion and 24 h), the glucose group showed the highest cell counts and metabolic activity among the groups (p<0.05). After maturation (48 and 72 h), biofilms exposed to glucose, sucrose, or starch+sucrose showed higher cell counts and metabolic activity than the control and starch groups (p<0.001). Compared to the control group, biofilms developed on starch or starch+sucrose had more proteinase activity (p<0.001), whereas biofilms developed on glucose or sucrose had more phospholipase activity (p<0.05). Exposure to starch+sucrose increased the production of extracellular and intracellular polysaccharides (p<0.05). Biofilms developed on starch or without carbohydrate supplementation presented cells with more hydrophobic behavior compared to the other groups. Confocal images showed hyphae forms on biofilms exposed to starch or starch+sucrose. Within the conditions studied, it can be concluded that dietary carbohydrates can modulate biofilm development on the denture surface by affecting virulence factors and structural features.
机译:这项研究的目的是调查饮食中的碳水化合物是否可以调节义齿材料表面白色念珠菌生物膜的发育。制造聚(甲基丙烯酸甲酯)丙烯酸树脂盘并测量其表面粗糙度。白色念珠菌ATCC 90028的生物膜在无(对照)培养基或不含淀粉,淀粉+蔗糖,葡萄糖或蔗糖的碳水化合物的培养基中在唾液包被的标本上显影72小时。在粘附期(1.5 h)以及24、48和72 h后评估细胞计数,代谢活性,生物量,平均厚度和粗糙度系数。在生物膜形成72小时后,分析了蛋白酶和磷脂酶的分泌,细胞表面能以及细胞外/细胞内多糖的产生。通过单向和双向方差分析对数据进行分析,然后进行Tukey检验(显着性水平为5%)。在定植的早期(黏附和24 h),葡萄糖组显示出最高的细胞计数和代谢活性(p <0.05)。成熟后(48和72小时),暴露于葡萄糖,蔗糖或淀粉+蔗糖的生物膜显示出比对照组和淀粉组更高的细胞计数和代谢活性(p <0.001)。与对照组相比,在淀粉或淀粉+蔗糖上形成的生物膜具有更高的蛋白酶活性(p <0.001),而在葡萄糖或蔗糖上形成的生物膜具有更高的磷脂酶活性(p <0.05)。暴露于淀粉+蔗糖会增加细胞外和细胞内多糖的产生(p <0.05)。与其他组相比,在淀粉上或未添加碳水化合物的情况下形成的生物膜使细胞具有更多的疏水性。共聚焦图像显示在暴露于淀粉或淀粉+蔗糖的生物膜上形成菌丝。在研究的条件下,可以得出结论,饮食中的碳水化合物可以通过影响毒力因子和结构特征来调节义齿表面生物膜的发育。

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