Differential and quantitative analyses of mRNA expression of glucosyltransferases from Streptococcus mutans MT8148

被引:40
作者
Fujiwara, T
Hoshino, T
Ooshima, T
Hamada, S
机构
[1] Osaka Univ, Grad Sch Dent, Dept Pedodont, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Dent, Dept Oral Microbiol, Suita, Osaka 5650871, Japan
关键词
glucosyltransferase; Streptococcus mutans; real-time RT-PCR; gene expression;
D O I
10.1177/154405910208100205
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Streptococcus mutans produces three glucosyl-transferases, coded by gtfB, gtfC, and gtfD, whose cooperative action is essential for sucrose-dependent cellular adhesion. This cellular adhesion plays an important role in the formation of dental plaque and the initiation of dental caries. Since they bear genetic similarities and are large in size, differentiation of their gene expression has been difficult, and little is known about the dynamic process of gtf expression. Using a real-time reverse-transcription/polymerase chain-reaction, we determined the expression of each gtf. Under various conditions, the relative levels of transcription were gtfB > gtfD > gtfC. Sucrose enhanced gtfD expression, whereas it reduced that of gtfB and gtfC, suggesting the presence of independent promoters, Quantitative analyses demonstrated coincidence between the ratio of expression of each gtf and the ratio previously identified as optimal for sucrose-dependent adhesion in vitro, suggesting that S. mutans produces GTF at an optimal ratio to adhere to the tooth surface.
引用
收藏
页码:109 / 113
页数:5
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