IBB-Institute for Biotechnology and Bioengineering, Centre of Biological Engineering, University of Minho, Braga, Portugal.
Med Mycol. 2013 Feb;51(2):178-84. doi: 10.3109/13693786.2012.700492. Epub 2012 Jul 17.
The aim of this study was to compare biofilm formation by Candida glabrata and Candida albicans on acrylic, either individually or when combined (single and dual species) and then examine the antimicrobial effects of silver nanoparticles and nystatin on these biofilms. Candidal adhesion and biofilm assays were performed on acrylic surface in the presence of artificial saliva (AS) for 2 h and 48 h, respectively. Candida glabrata and C. albicans adherence was determined by the number of colony forming units (CFUs) recovered from the biofilms on CHROMagar(®) Candida. In addition, crystal violet (CV) staining was used as an indicator of biofilm biomass and to quantify biofilm formation ability. Pre-formed biofilms were treated either with silver nanoparticles or nystatin and the effect of these agents on the biofilms was evaluated after 24 h. Results showed that both species adhered to and formed biofilms on acrylic surfaces. A significantly (P < 0.05) higher number of CFUs was evident in C. glabrata biofilms compared with those formed by C. albicans. Comparing single and dual species biofilms, equivalent CFU numbers were evident for the individual species. Both silver nanoparticles and nystatin reduced biofilm biomass and the CFUs of single and dual species biofilms (P < 0.05). Silver nanoparticles had a significantly (P < 0.05) greater effect on reducing C. glabrata biofilm biomass compared with C. albicans. Similarly, nystatin was more effective in reducing the number of CFUs of dual species biofilms compared with those of single species (P < 0.05). In summary, C. glabrata and C. albicans can co-exist in biofilms without apparent antagonism, and both silver nanoparticles and nystatin exhibit inhibitory effects on biofilms of these species.
本研究旨在比较光滑念珠菌和白念珠菌在丙烯酸上的生物膜形成情况,分别单独或联合(单种和混合种)时,然后检查纳米银和制霉菌素对这些生物膜的抗菌作用。在人工唾液(AS)存在下,分别在丙烯酸表面进行 2 小时和 48 小时的念珠菌黏附及生物膜试验。通过从 CHROMagar® Candida 上回收的生物膜中的菌落形成单位(CFU)数量来确定光滑念珠菌和白念珠菌的黏附。此外,结晶紫(CV)染色用作生物膜生物量的指示剂,并用于定量生物膜形成能力。用纳米银或制霉菌素处理预先形成的生物膜,然后在 24 小时后评估这些药物对生物膜的作用。结果表明,两种菌均黏附并在丙烯酸表面形成生物膜。与白念珠菌形成的生物膜相比,光滑念珠菌生物膜的 CFU 数量明显更高(P<0.05)。比较单种和混合种生物膜,单个种的 CFU 数量相等。纳米银和制霉菌素均减少了生物膜生物量和单种及混合种生物膜的 CFU(P<0.05)。与白念珠菌相比,纳米银对减少光滑念珠菌生物膜生物量具有显著(P<0.05)的更大作用。同样,制霉菌素在减少混合种生物膜的 CFU 数量方面比单种生物膜更有效(P<0.05)。总之,光滑念珠菌和白念珠菌可以在无明显拮抗作用的情况下共存于生物膜中,纳米银和制霉菌素对这些菌的生物膜均具有抑制作用。