Cavalcanti Yuri Wanderley, Wilson Melanie, Lewis Michael, Williams David, Senna Plínio Mendes, Del-Bel-Cury Altair Antoninha, da Silva Wander José
Periodontology and Prosthodontics Department, Piracicaba Dental School, University of Campinas, Piracicaba, SP, Brazil; Department of Dentistry, School of Dentistry, State University of Paraíba (UEPB), Campina Grande, PB, Brazil.
Tissue Engineering and Reparative Dentistry, School of Dentistry, Cardiff University, Cardiff, Wales, UK.
Arch Oral Biol. 2016 Jun;66:129-40. doi: 10.1016/j.archoralbio.2016.02.016. Epub 2016 Feb 28.
Numerous environmental factors influence the pathogenesis of Candida biofilms and an understanding of these is necessary for appropriate clinical management.
To investigate the role of material type, pellicle and stage of biofilm development on the viability, bioactivity, virulence and structure of C. albicans biofilms.
The surface roughness (SR) and surface free energy (SFE) of acrylic and titanium discs was measured. Pellicles of saliva, or saliva supplemented with plasma, were formed on acrylic and titanium discs. Candida albicans biofilms were then generated for 1.5 h, 24h, 48 h and 72 h. The cell viability in biofilms was analysed by culture, whilst DNA concentration and the expression of Candida virulence genes (ALS1, ALS3 and HWP1) were evaluated using qPCR. Biofilm metabolic activity was determined using XTT reduction assay, and biofilm structure analysed by Scanning Electron Microscopy (SEM).
Whilst the SR of acrylic and titanium did not significantly differ, the saliva with plasma pellicle increased significantly the total SFE of both surface. The number of viable microorganisms and DNA concentration increased with biofilm development, not differing within materials and pellicles. Biofilms developed on saliva with plasma pellicle surfaces had significantly higher activity after 24h and this was accompanied with higher expression of virulence genes at all periods.
Induction of C. albicans virulence occurs with the presence of plasma proteins in pellicles, throughout biofilm growth. To mitigate such effects, reduction of increased plasmatic exudate, related to chronic inflammatory response, could aid the management of candidal biofilm-related infections.
众多环境因素影响念珠菌生物膜的发病机制,了解这些因素对于适当的临床管理至关重要。
研究材料类型、薄膜以及生物膜发育阶段对白色念珠菌生物膜的活力、生物活性、毒力和结构的作用。
测量丙烯酸树脂和钛盘的表面粗糙度(SR)和表面自由能(SFE)。在丙烯酸树脂和钛盘上形成唾液薄膜或补充血浆的唾液薄膜。然后分别培养白色念珠菌生物膜1.5小时、24小时、48小时和72小时。通过培养分析生物膜中的细胞活力,同时使用qPCR评估DNA浓度和念珠菌毒力基因(ALS1、ALS3和HWP1)的表达。使用XTT还原试验测定生物膜的代谢活性,并通过扫描电子显微镜(SEM)分析生物膜结构。
虽然丙烯酸树脂和钛的SR没有显著差异,但含有血浆薄膜的唾液显著增加了两种表面的总SFE。活微生物数量和DNA浓度随生物膜发育而增加,在不同材料和薄膜之间没有差异。在含有血浆薄膜表面的唾液上形成的生物膜在24小时后具有显著更高的活性,并且在所有时期都伴随着毒力基因的更高表达。
在整个生物膜生长过程中,薄膜中血浆蛋白的存在会诱导白色念珠菌的毒力。为减轻此类影响,减少与慢性炎症反应相关的血浆渗出增加可能有助于念珠菌生物膜相关感染的管理。