Mechanisms underlying spatial interaction in the oral microbiota
口腔微生物群空间相互作用的潜在机制
基本信息
- 批准号:9816352
- 负责人:
- 金额:$ 42.85万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-07-08 至 2024-06-30
- 项目状态:已结题
- 来源:
- 关键词:AdherenceAdhesionsAerobicAnaerobic BacteriaBacteriaBacterial AdhesinsBindingBiochemicalBiological AssayCoculture TechniquesCommunitiesCorynebacteriumDataDevelopmentDiseaseErinaceidaeFeedsGenesGoalsGrowthHaemophilus parainfluenzaeHealthHemophilusHumanHydrogen PeroxideImageImpairmentIn VitroIndividualIntegration Host FactorsInterventionKnowledgeLibrariesMeasurementMediatingMetabolicMethodsMicrobial BiofilmsMicroscopyMolecularMouth DiseasesMutagenesisOpportunistic InfectionsOrganismOxidative StressPatternProbioticsProductionReproducibilityResearchSalivarySalivary ProteinsSamplingScanningShapesStreptococcusStreptococcus cristatusStreptococcus mitisStructureSuggestionSurfaceTechnologyTestingTranscriptbasebiological adaptation to stressdental biofilmdesignexperimental studyfeedinggene productimaging probein vivoinnovationmicrobiomemutantoral microbial communityoral plaqueoral streptococcipreservationpreventprophylacticreceptortranscriptometranscriptome sequencing
项目摘要
ABSTRACT
Human oral plaque is a polymicrobial community whose composition varies during health and disease.
Recent advances in technology have yielded new information on the identity and abundance of
constituent species during these conditions yet do not allow predictions of direct interactions between
specific organisms. The biogeography of reproducible structures within supragingival plaque has been
characterized through advanced microscopy methods suggesting key organisms that may help arrange
plaque structure. Species-species co-proximity within these ordered structures is suggestive of
metabolite mediated interactions between them. Our global hypothesis is that adjacent species in healthy
plaque biofilms have specific metabolic and physical interactions that shape both the physical and
compositional structure of this community. To identify mechanistic interactions between adjacent
species, we must determine which species exist together in vivo. Preliminary data indicates that the
highly abundant Corynebacterium matruchotii and Haemophilus parainfluenzae bacterial species exist
directly adjacent to several Streptococcus spp. suggesting they must be able to tolerate pH and oxidative
stress produced by oral streptococci. Direct imaging further suggests that some species bind directly to
each other or mutually to a host intermediate such as salivary protein. The physical means of attachment
for C. matruchotii and H. parainfluenzae to Streptococcus spp. are unknown. This proposal will
determine which Streptococcus species interact with C. matruchotii and H. parainfluenzae via
microscopy (Aim 1). It will also determine if C. matruchotii and H. parainfluenzae participate in cross-
feeding interactions with streptococcal produced metabolites and will identify mechanisms that either
bacterium uses to tolerate pH and oxidative stress through transcriptome analyses, mutant library
assays, and quantitative metabolite measurements (Aim 2). Lastly, our proposal will determine physical
factors produced by bacteria that are responsible for co-adhesion between different species. These will
be identified by direct and random mutagenesis of C. matruchotii and H. parainfluenzae and tested in
combination with known interacting Streptococcus species. The goal of this proposal is to identify
interacting species in healthy supragingival plaque and characterize mechanistic interactions between
them, revealing how they may contribute to plaque structure and composition. Our rationale is that we
will identify mechanisms that promote interactions between highly abundant organisms in healthy plaque
and identify candidate species and their associated interactions for use in probiotic or prophylactic
interventions to manage oral plaque communities to prevent opportunistic infection.
摘要
人类口腔菌斑是一个多微生物群落,其组成在健康和疾病期间变化。
最近的技术进步已经产生了新的信息,
在这些条件下的组成物种还不允许预测之间的直接相互作用
特定的有机体。龈上菌斑内可再现结构的血管造影术已被
通过先进的显微镜方法进行表征,表明可能有助于排列的关键生物体
斑块结构在这些有序结构中的种-种共存暗示着
代谢物介导的相互作用。我们的全球假设是,健康的邻近物种
菌斑生物膜具有特定的代谢和物理相互作用,
这个社区的组成结构。为了识别相邻的
物种,我们必须确定哪些物种共同存在于体内。初步数据显示,
存在高度丰富的马鲁霍棒状杆菌和副流感嗜血杆菌细菌物种
与几种链球菌属直接相邻。这表明它们必须能够耐受pH和氧化
口腔链球菌产生的压力。直接成像进一步表明,一些物种直接结合到
彼此或相互与宿主中间体如唾液蛋白结合。依恋的物理手段
梭matruchotii和H.副流感菌与链球菌属是未知的。这项建议会
确定哪些链球菌与C. matruchotii和H.副流感病毒
显微镜(目的1)。它还将确定C. matruchotii和H.副流感病毒参与交叉
与链球菌产生的代谢物的摄食相互作用,并将确定机制,
通过转录组分析,突变体库,细菌用于耐受pH和氧化应激
分析和定量代谢物测量(目标2)。最后,我们的建议将确定物理
由细菌产生的因子,负责不同物种之间的共粘附。这些将
通过C. matruchotii和H.副流感病毒,
与已知相互作用的链球菌属物种组合。本提案的目的是确定
健康龈上菌斑中的相互作用物种,并表征
他们,揭示他们如何可能有助于斑块的结构和组成。我们的理由是,
将确定促进健康斑块中高度丰富的生物体之间相互作用的机制
并鉴定候选物种及其相关的相互作用,用于益生菌或预防性
采取干预措施管理口腔菌斑群落,以预防机会性感染。
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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Matthew Ramsey其他文献
Matthew Ramsey的其他文献
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{{ truncateString('Matthew Ramsey', 18)}}的其他基金
Mechanisms underlying spatial interaction in the oral microbiota
口腔微生物群空间相互作用的潜在机制
- 批准号:
10180938 - 财政年份:2019
- 资助金额:
$ 42.85万 - 项目类别:
Mechanisms underlying spatial interaction in the oral microbiota
口腔微生物群空间相互作用的潜在机制
- 批准号:
10653199 - 财政年份:2019
- 资助金额:
$ 42.85万 - 项目类别:
Mechanisms underlying spatial interaction in the oral microbiota
口腔微生物群空间相互作用的潜在机制
- 批准号:
10215687 - 财政年份:2019
- 资助金额:
$ 42.85万 - 项目类别:
Mechanisms underlying spatial interaction in the oral microbiota
口腔微生物群空间相互作用的潜在机制
- 批准号:
9974507 - 财政年份:2019
- 资助金额:
$ 42.85万 - 项目类别:
Mechanisms underlying spatial interaction in the oral microbiota
口腔微生物群空间相互作用的潜在机制
- 批准号:
10408065 - 财政年份:2019
- 资助金额:
$ 42.85万 - 项目类别:
Polymicrobial dynamics in transfer of vancomycin resistance to MRSA
万古霉素耐药性向 MRSA 转移的多微生物动力学
- 批准号:
8721616 - 财政年份:2012
- 资助金额:
$ 42.85万 - 项目类别:
Polymicrobial dynamics in transfer of vancomycin resistance to MRSA
万古霉素耐药性向 MRSA 转移的多微生物动力学
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8519048 - 财政年份:2012
- 资助金额:
$ 42.85万 - 项目类别:
Polymicrobial dynamics in transfer of vancomycin resistance to MRSA
万古霉素耐药性向 MRSA 转移的多微生物动力学
- 批准号:
8655516 - 财政年份:2012
- 资助金额:
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Polymicrobial dynamics in transfer of vancomycin resistance to MRSA
万古霉素耐药性向 MRSA 转移的多微生物动力学
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口腔细菌的相互作用如何增强对先天免疫的抵抗力
- 批准号:
7847475 - 财政年份:2009
- 资助金额:
$ 42.85万 - 项目类别:
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