Department of Dentistry I, School of Dentistry, Federal University of Maranhão, São Luis, Maranhão, Brazil.
PLoS One. 2013 May 30;8(5):e64645. doi: 10.1371/journal.pone.0064645. Print 2013.
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.
本研究旨在探讨饮食碳水化合物是否能调节白色念珠菌生物膜在义齿材料表面的形成。制作聚甲基丙烯酸甲酯丙烯酸树脂圆盘,并测量其表面粗糙度。在不含(对照)或含碳水化合物(淀粉、淀粉+蔗糖、葡萄糖或蔗糖)补充剂的培养基中,在唾液涂层标本上开发白色念珠菌 ATCC 90028 的生物膜,培养 72 小时。在黏附阶段(1.5 小时)和 24、48 和 72 小时后,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 小时后分析蛋白水解酶和磷脂酶的分泌、细胞表面能量和胞外/胞内多糖的产生。数据采用单因素和双因素方差分析,然后采用 Tukey 检验,显著性水平为 5%。在定植的早期阶段(黏附和 24 小时),葡萄糖组的细胞计数和代谢活性均高于其他组(p<0.05)。成熟后(48 和 72 小时),暴露于葡萄糖、蔗糖或淀粉+蔗糖的生物膜的细胞计数和代谢活性高于对照和淀粉组(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水解酶活性(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+蔗糖增加了胞外和胞内多糖的产生(p<0.05)。与其他组相比,在淀粉或无碳水化合物补充的情况下形成的生物膜的细胞表现出更疏水的行为。共聚焦图像显示暴露于淀粉或淀粉+蔗糖的生物膜上有菌丝体形式。在研究条件下,可以得出结论,饮食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的生物膜形成。