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Study on synthesizing of intracellular polysaccharide by Streptococcus mutans in dentinal tubules.

Study on synthesizing of intracellular polysaccharide by Streptococcus mutans in dentinal tubules.
牙本质小管内变形链球菌合成胞内多糖的研究
批准号:
17591993
负责人:
OZAKI Kazumi
金额:
$2.24万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2005
资助国家:
日本
项目状态:
已结题
起止时间:
2005 至 2006

项目摘要

项目成果

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中文摘要
翻译
变形链球菌是致龋菌之一,由蔗糖合成水溶性葡聚糖(WSG)和水不溶性葡聚糖(WIG),粘附在牙齿上并增殖。在本研究中,S.本研究检测了变异株UA159及其缺失comC、comX和G4A突变株的初始粘附、葡聚糖合成和侵入牙本质小管的能力。所有突变株的水不溶性葡聚糖合成比例均低于野生型。所有突变株中粘附于牙本质切片的水溶性葡聚糖的比例也低于野生型。三种葡聚糖组分的总剂量在所有突变株中均降低。在脑心浸液中培养24天后,突变体牙本质小管的扩张率比野生型牙本质小管的扩张率高。野生型和突变型之间的生长没有可检测到的差异。在蔗糖存在下,突变体WSG和WIG的产量低于野生型。本研究表明,群体感应系统和PTS系统可能在变形链球菌葡聚糖合成、生物膜形成、胞内多糖的产生和牙本质小管的侵袭中起重要作用。
英文摘要
Streptococcus mutans that is one of the cariogenic bacterium is synthesized the water-soluble glucan (WSG) and the water-insoluble glucan (WIG) from sucrose, adheres on the tooth, and proliferates. In this study, S. mutans wild-type strain UA159 and its knockout mutants, which were defective in comC, comX and scrA mutant, were examined for their ability for initial adhesion, glucan synthesis and invasion into dentinal tubles. The proportions of water-insoluble glucan synthesis in all mutant strains were less than the wild type. The proportions of water-soluble glucan adhering to dentin slices in all mutant strains were also less than in the wild type. The total dose of three kinds of glucan composition decreased in all mutant strains. The expansion rates of dentinal tubules by comC and comX mutant increased more than by the wild type when cultured in brain heart infusion for 24 days. There were no detectable difference in growth between wild-type and scrA-mutant. In the presence of sucrose, the produce of WSG and WIG in scrA-mutant was less than in wild-type. This study demonstrated that the quorum-sensing system and PTS system may play a crucial role in glucan synthesis, biofilm formation, production of intracellular-polysaccharide and invasion to dentinal tubules of S.mutans.
期刊论文(30)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1111/j.1365-2249.2006.03064.x
发表时间: 2006-06-01
期刊: CLINICAL AND EXPERIMENTAL IMMUNOLOGY
影响因子: 4.6
作者: [Hosokawa, Y, Hosokawa, I, Matsuo, T]
通讯作者: Matsuo, T
Langerhans細胞における抗菌ペプチドの発現について
关于抗菌肽在朗格汉斯细胞中的表达
DOI: --
发表时间: 2005
期刊: 日本歯周病学会会誌 47秋季特別号
影响因子: --
作者: [Nakaoki Y, Sasakawa W, Noda M, Inoue S, Komatsu N, Sano H., Unemori M et al., Unemori M et al., Uemori M et al., Hosokawa Y. et al., Hosokawa Y. et al., 細川義隆ら, 細川義隆ら, 藤坂菊美ら, Hosokawa Y.et al., Hosokawa Y. et al., Hosokawa Y.et al., Hosokawa Y.et al., Fujisaka K.et al., Hosokawa Y. et al., Hosokawa Y. et al., 細川義孝ら, 細川義孝ら, 藤坂菊美ら, 細川育子ら]
通讯作者: 細川育子ら
DOI: 10.1111/j.1365-2249.2006.03233.x
发表时间: 2006-12-01
期刊: CLINICAL AND EXPERIMENTAL IMMUNOLOGY
影响因子: 4.6
作者: [Hosokawa, Y., Hosokawa, I., Matsuo, T.]
通讯作者: Matsuo, T.
Cytokines differentially regulate ICAM-land VCAM-1expression on human gingival fibroblasts
细胞因子差异调节人牙龈成纤维细胞上的 ICAM 和 VCAM-1 表达
DOI: --
发表时间: 2006
期刊: Clinical and Experimental Immunology 144・3
影响因子: --
作者: [Nakaoki Y, Sasakawa W, Noda M, Inoue S, Komatsu N, Sano H., Unemori M et al., Unemori M et al., Uemori M et al., Hosokawa Y. et al.]
通讯作者: Hosokawa Y. et al.
共 21 条
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      20K04066
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    Study of the effects of polyphenol-silver nanoparticles complex upon oral biofilm formation and antimicrobial activity
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