Thurnheer T, van der Ploeg J R, Giertsen E, Guggenheim B
Institute for Oral Biology, Section for Oral Microbiology and General Immunology, University of Zürich, Zürich, Switzerland.
Caries Res. 2006;40(2):163-71. doi: 10.1159/000091065.
The aim of this study was to examine the influence of glucosyltransferase-gene-negative (gtf-) Streptococcus mutans strains unable to synthesize water-insoluble or soluble glucan on the structure and macromolecular diffusion properties of in vitro grown mixed oral biofilms. Biofilms modeling supragingival plaque consisted of Actinomyces naeslundii OMZ 745, Candida albicans OMZ 110, Fusobacterium nucleatum KP-F2, Streptococcus oralis SK 248, Veillonella dispar ATCC 17748T and one of the S. mutans strains UA159, OMZ 966, OMZ 937 or OMZ 977. Biofilms were grown anaerobically on sintered hydroxyapatite disks for 64.5 h at 37 degrees C. To perform confocal laser scanning microscopy analyses, microorganisms were stained with Syto 13 and extracellular polysaccharides (EPS) with Calcofluor. Macromolecular diffusion properties were measured following timed biofilm exposure to Texas-Red-labeled 70-kDa dextran. Results showed that replacing wild-type S. mutans by a gtfC- mutant led to an increase in the volume fraction occupied by cells from 29 to 48% and a decrease of the EPS volume fraction from 51 to 33%. No such changes were observed when the S. mutans wild-type strain was replaced by a gtfB- or gtfD- mutant. The diffusion coefficient of 70-kDa dextran in biofilms containing the gtfC- S. mutans was 16-fold higher than in biofilms with the wild-type strain indicating a strong macromolecular sieving effect of GTF C-generated glucans. Our data demonstrate the influence of EPS on the structure and macromolecular diffusion properties of an oral biofilm model and uncover our still limited knowledge of the function of EPS in biofilms and plaque.
本研究的目的是检测无法合成水不溶性或可溶性葡聚糖的葡糖基转移酶基因阴性(gtf-)变形链球菌菌株对体外生长的混合口腔生物膜结构和大分子扩散特性的影响。模拟龈上菌斑的生物膜由内氏放线菌OMZ 745、白色念珠菌OMZ 110、具核梭杆菌KP-F2、口腔链球菌SK 248、差异韦荣球菌ATCC 17748T以及变形链球菌菌株UA159、OMZ 966、OMZ 937或OMZ 977中的一种组成。生物膜在烧结羟基磷灰石圆盘上于37℃厌氧培养64.5小时。为了进行共聚焦激光扫描显微镜分析,用Syto 13对微生物进行染色,并用荧光增白剂对细胞外多糖(EPS)进行染色。在生物膜定时暴露于Texas-Red标记的70-kDa葡聚糖后测量大分子扩散特性。结果表明,用gtfC突变体取代野生型变形链球菌导致细胞所占体积分数从29%增加到48%,EPS体积分数从51%降低到33%。当用gtfB或gtfD突变体取代变形链球菌野生型菌株时,未观察到此类变化。在含有gtfC变形链球菌的生物膜中,70-kDa葡聚糖的扩散系数比含有野生型菌株的生物膜高16倍,这表明GTF C产生的葡聚糖具有很强的大分子筛分作用。我们的数据证明了EPS对口腔生物膜模型结构和大分子扩散特性的影响,并揭示了我们对EPS在生物膜和菌斑中功能的了解仍然有限。