Contribution of glucan‐binding protein A to firm and stable biofilm formation by Streptococcus mutans

生物膜 格罗尔 微生物学 突变体 葡萄糖基转移酶 变形链球菌 葡聚糖 拉伤 生物 免疫电镜 葡萄糖基转移酶 严格的回应 基因表达 基因 化学 细菌 生物化学 大肠杆菌 遗传学 抗体 解剖
作者
Yuki Matsumi,Kazuyo Fujita,Yasuo Takashima,Kanako Yanagida,Yuko Morikawa,Michiyo Matsumoto‐Nakano
出处
期刊:Molecular Oral Microbiology [Wiley]
卷期号:30 (3): 217-226 被引量:24
标识
DOI:10.1111/omi.12085
摘要

Glucan-binding proteins (Gbps) of Streptococcus mutans, a major pathogen of dental caries, mediate the binding of glucans synthesized from sucrose by the action of glucosyltransferases (GTFs) encoded by gtfB, gtfC, and gtfD. Several stress proteins, including DnaK and GroEL encoded by dnaK and groEL, are related to environmental stress tolerance. The contribution of Gbp expression to biofilm formation was analyzed by focusing on the expression levels of genes encoding GTFs and stress proteins. Biofilm-forming assays were performed using GbpA-, GbpB-, and GbpC-deficient mutant strains and the parental strain MT8148. The expression levels of gtfB, gtfC, gtfD, dnaK, and groEL were evaluated by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Furthermore, the structure of biofilms formed by these Gbp-deficient mutant strains was observed using confocal laser scanning microscopy (CLSM). Biofilm-forming assay findings demonstrated that the amount formed by the GbpA-deficient mutant strain (AD1) was nearly the same as that by the parental strain, while the GbpB- and GbpC-deficient mutant strains produced lower amounts than MT8148. Furthermore, RT-qPCR assay results showed that the expressions of gtfB, dnaK, and groEL in AD1 were elevated compared with MT8148. CLSM also revealed that the structure of biofilm formed by AD1 was prominently different compared with that formed by the parental strain. These results suggest that a defect in GbpA influences the expression of genes controlling biofilm formation, indicating its importance as a protein for firm and stable biofilm formation.
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