Mattos-Graner Renata O, Napimoga Marcelo H, Fukushima Kasuo, Duncan Margaret J, Smith Daniel J
Department of Microbiology and Immunology, Piracicaba School of Dentistry, University of Campinas, São Paulo, Brazil.
J Clin Microbiol. 2004 Oct;42(10):4586-92. doi: 10.1128/JCM.42.10.4586-4592.2004.
Streptococcus mutans is the main pathogenic agent of dental caries. Glucosyltransferases (Gtfs) produced by these bacteria are important virulence factors because they catalyze the extracellular synthesis of glucans that are necessary for bacterial accumulation in the dental biofilm. The diversity of GtfB and GtfC isozymes was analyzed in 44 genotypes of S. mutans that showed a range of abilities to form biofilms in vitro. Several approaches were used to characterize these isozymes, including restriction fragment length polymorphism analysis of the gtfB and gtfC genes, zymographic analysis of the identified GtfB and GtfC genotypes, and quantitation of isozyme production in immunoblot experiments with specific monoclonal antibodies. A high diversity of gtf genes, patterns of enzymatic activity, and isozyme production was identified among the isolates tested. GtfC and, to a lesser extent, GtfB were produced in significantly higher amounts by strains that had high biofilm-forming ability than by strains with low biofilm-forming ability. Biofilm formation was independent of the GtfB and GtfC genotype. Atypical strains that showed an apparent single Gtf isozyme of intermediate size between GtfB and GtfC were also identified. The results indicate that various expression levels of GtfB and GtfC isozymes are associated with the ability of distinct S. mutans genotypes to grow as biofilms, strengthening the results of previous genetic and biochemical studies performed with laboratory strains. These studies also emphasize the need to identify factors that control gtf gene expression.
变形链球菌是龋齿的主要致病因子。这些细菌产生的葡糖基转移酶(Gtfs)是重要的毒力因子,因为它们催化葡聚糖的胞外合成,而葡聚糖是细菌在牙菌斑中聚集所必需的。在44种变形链球菌基因型中分析了GtfB和GtfC同工酶的多样性,这些基因型在体外形成生物膜的能力范围不同。采用了几种方法来表征这些同工酶,包括对gtfB和gtfC基因进行限制性片段长度多态性分析、对鉴定出的GtfB和GtfC基因型进行酶谱分析以及在使用特异性单克隆抗体的免疫印迹实验中对同工酶产生进行定量。在所测试的分离株中鉴定出gtf基因、酶活性模式和同工酶产生的高度多样性。生物膜形成能力高的菌株产生的GtfC以及在较小程度上产生的GtfB的量明显高于生物膜形成能力低的菌株。生物膜形成与GtfB和GtfC基因型无关。还鉴定出了非典型菌株,这些菌株显示出在GtfB和GtfC之间明显具有中等大小的单一Gtf同工酶。结果表明,GtfB和GtfC同工酶的不同表达水平与不同变形链球菌基因型形成生物膜的能力相关,这加强了先前对实验室菌株进行的遗传和生化研究的结果。这些研究还强调了识别控制gtf基因表达的因素的必要性。