ORAL BIOFILMS: DIFFERENTIAL DISPLAY AND GENETIC EXCHANGE
口腔生物膜:差异显示和遗传交换
基本信息
- 批准号:6175909
- 负责人:
- 金额:$ 20.32万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1999
- 资助国家:美国
- 起止时间:1999-09-01 至 2004-06-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Adult periodontitis is a biota shift disease caused by an ecological transition of the dental plaque, and consequent chronic inflammation. Understanding the physiology of dental plaque and its complex ecology, to the point where it can be controlled, is therefore central to the prevention and treatment of periodontal disease. Dental plaque is an ecologically complex biofilm with over 350 microbial taxa represented; however the organization of the biofilm is not random. Oral streptococci, including Streptococcus gordonii, are among the first bacteria to colonize the pellicle coated tooth surface, creating a template for the subsequent attachment of other bacterial species, ultimately including periodontal pathogens. The initial binding of the tooth surface by pioneer species, such as S. gordonii, is therefore pivotal in the establishment of ecological communities associated both with gingival health and disease. The central hypothesis of this proposal is that within the dental plaque biofilm, bacteria are sentient and contribute to its maintenance, physiology, and development through receipt, transmission and response to chemical and physical signals. The goals of the proposed study are therefore to develop and use an optimized differential display approach, and scanning laser confocal microscopy, to: 1) identify the critical communications between bacteria that regulate growth and microcolony formation in a model biofilm, 2) identify bacterial responses to environmental cues, which include signals derived from other bacterial species as well as the host, and 3) determine the effect of biofilm formation on an additional form of intercellular communication, genetic exchange. The practical benefit of this study is that it may lead to new strategies for subverting or regulating key interactions in oral biofilm formation, and therefore to new therapies for controlling its establishment, rendering it sensitive to antibiotics, and facilitating its removal.
成人牙周炎是由牙菌斑的生态转变和随之而来的慢性炎症引起的生物群转移疾病。 因此,了解牙菌斑的生理学及其复杂的生态学,以达到可以控制的程度,是预防和治疗牙周病的核心。 牙菌斑是一种生态复杂的生物膜,代表了超过350种微生物分类群;然而,生物膜的组织不是随机的。 口腔链球菌,包括戈登链球菌,是第一批在覆盖薄膜的牙齿表面定居的细菌,为随后附着的其他细菌物种(最终包括牙周病原体)创造了模板。 先锋物种如S.因此,戈登氏菌在建立与牙龈健康和疾病相关的生态群落中是关键的。 该提议的中心假设是,在牙菌斑生物膜内,细菌是有感知的,并且通过接收、传递和对化学和物理信号的响应来促进其维持、生理和发育。因此,拟议研究的目标是开发和使用优化的差异显示方法和扫描激光共聚焦显微镜,以:1)鉴定在模型生物膜中调节生长和小菌落形成的细菌之间的关键通信,2)鉴定细菌对环境线索的响应,所述环境线索包括来源于其它细菌物种以及宿主的信号,和3)确定生物膜形成对细胞间通讯的另一种形式,遗传交换的影响。 这项研究的实际好处是,它可能会导致新的策略来颠覆或调节口腔生物膜形成中的关键相互作用,因此,新的治疗方法来控制其建立,使其对抗生素敏感,并促进其去除。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Michael S Gilmore其他文献
Michael S Gilmore的其他文献
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{{ truncateString('Michael S Gilmore', 18)}}的其他基金
The Role of Enterococcus Unique Hypothetical EF1909 in Intrinsic β-lactam Resistance
肠球菌独特的假设 EF1909 在内在 β-内酰胺耐药性中的作用
- 批准号:
10569041 - 财政年份:2022
- 资助金额:
$ 20.32万 - 项目类别:
The Role of Enterococcus Unique Hypothetical EF1909 in Intrinsic β-lactam Resistance
肠球菌独特的假设 EF1909 在内在 β-内酰胺耐药性中的作用
- 批准号:
10464409 - 财政年份:2022
- 资助金额:
$ 20.32万 - 项目类别:
New understanding of LTA as a determinant of daptomycin susceptibility in VRE E. faecium
对 LTA 作为 VRE 屎肠球菌达托霉素敏感性决定因素的新认识
- 批准号:
9926227 - 财政年份:2019
- 资助金额:
$ 20.32万 - 项目类别:
New understanding of LTA as a determinant of daptomycin susceptibility in VRE E. faecium
对 LTA 作为 VRE 屎肠球菌达托霉素敏感性决定因素的新认识
- 批准号:
9810471 - 财政年份:2019
- 资助金额:
$ 20.32万 - 项目类别:
Subproject 3 New Approaches to Treatment and Prevention of Antibiotic Resistant Infection
子项目3 治疗和预防抗生素耐药感染的新方法
- 批准号:
9151288 - 财政年份:2016
- 资助金额:
$ 20.32万 - 项目类别:
Molecular Basis for Ocular Surface Tropism in Conjunctivitis
结膜炎眼表向性的分子基础
- 批准号:
9264533 - 财政年份:2014
- 资助金额:
$ 20.32万 - 项目类别:
Molecular Basis for Ocular Surface Tropism in Conjunctivitis
结膜炎眼表向性的分子基础
- 批准号:
8670576 - 财政年份:2014
- 资助金额:
$ 20.32万 - 项目类别:
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