Pyruvate oxidase determines ecological fitness of oral streptococci

丙酮酸氧化酶决定口腔链球菌的生态适应性

• 批准号: 9001970
• 负责人: Jens Kreth
• 金额: $ 38.5万
• 依托单位: OREGON HEALTH & SCIENCE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-03-06 至 2019-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9001970
• 关键词: Animals; Area; Biological; Biometry; Biophotonics; Carbohydrates; Caries prevention; Cell Aggregation; Cells; Clinical; Clinical Research; Communicable Diseases; Communities; DNA; Data; Dental; Dental caries; Development; Disease; Ecology; Engineering; Ensure; Environment; Environmental Risk Factor; Event; Exhibits; Gene Expression; Genes; Genetic Transcription; Genomics; Goals; Growth; Health; Hydrogen Peroxide; Image; Investigation; Knowledge; Learning; Link; Mediating; Microbial Biofilms; Microbiology; Modeling; Molecular Analysis; Molecular Profiling; Monitor; Mouth Diseases; Mus; National Institute of Dental and Craniofacial Research; Oral; Oral health; Play; Prevalence; Process; Production; Proteins; Pyruvate Oxidase; Regulation; Regulator Genes; Research; Role; Streptococcus; Streptococcus gordonii; Streptococcus mutans; System; Testing; Time; Tooth Cell; base; disorder prevention; extracellular; fitness; improved; in vitro Model; in vivo; innovation; insight; interest; member; mouse model; mutant; novel; novel strategies; oral biofilm; oral commensal; oral infection; oral streptococci; overexpression; prevent; programs; response; tool

DESCRIPTION (provided by applicant): Streptococcus sanguinis and Streptococcus gordonii are considered health beneficial early colonizers of the oral biofilm. Their initial attachment influences subsequent biofilm development and species composition. The clinical relevant antagonism between commensals S. sanguinis and S. gordonii with cariogenic Streptococcus mutans provides the unique possibility to develop alternative strategies in oral disease prevention. Increasing S. sanguinis and S. gordonii competitiveness over cariogenic species like S. mutans could manipulate oral biofilm development towards a healthy composition. We recently identified pyruvate oxidase (SpxB) dependent hydrogen peroxide production by S. sanguinis and S. gordonii as major competitive factor in interspecies interactions with S. mutans. Furthermore, hydrogen peroxide induces the release of extracellular DNA required for biofilm formation. To better understand the role of hydrogen peroxide in these processes, we propose to: 1) elucidate the differences in the regulatory mechanisms of H2O2 production and self-compatibility by H2O2 producers, 2) elucidate the functional relationship between SpxB dependent H2O2 production, eDNA release and biofilm formation and 3) and probe ecological significance of SpxB in vivo at the host-bacterial interface in a novel murine model. This research provides an innovative approach to study the role of pyruvate oxidase dependent hydrogen peroxide production employing genomic, global transcription, protein interaction, and biostatistics data. The results of this research will provide an enhanced understanding of how environmental factors and the biofilm mode of growth in a multispecies setting influence the major competitive factor of oral commensals. Importantly, these studies directly link molecular analysis to biological significance. The goal is to use the gained information to increase oral commensal competitiveness, e.g. increasing hydrogen peroxide production under competitive conditions. This understanding should provide important new insight into the development of new strategies to prevent oral diseases.

描述（由申请人提供）：sanguinis链球菌和Gordonii链球菌被认为是口腔生物膜的健康有益的早期殖民者。它们的最初依恋会影响随后的生物膜发育和物种组成。共生链球菌和戈尔多尼与致癌链球菌突变之间的临床相关拮抗作用为预防口腔疾病的替代策略提供了独特的可能性。 增加了S. sanguinis和S. gordonii对诸如S. mutans之类的致癌物种的竞争力，可以操纵口服生物膜发育，从而朝着健康的组成方向发展。 我们最近确定丙酮酸氧化酶（SPXB）依赖性氢过氧化链球菌和戈多尼链球菌是与葡萄糖链球菌间相互作用的主要竞争因素。此外，过氧化氢诱导生物膜形成所需的细胞外DNA的释放。为了更好地理解过氧化氢在这些过程中的作用，我们提出：1）阐明H2O2生产的调节机制差异和H2O2生产者的自我兼容性的差异，2）阐明SPXB依赖H2O2的H2O2产生，EDNA释放和Biofilm promoge Intractiant obolote Intiv of Spxb In In In In In In In In In In In In In In In In In In In In In In In In In In In In In In In In In的功能关系。鼠模型。 这项研究提供了一种创新的方法来研究丙酮酸氧化酶依赖性氢过氧化氢的作用，该氢使用基因组，全球转录，蛋白质相互作用和生物统计学数据。这项研究的结果将增强人们对多物种设定中环境因素和生物膜增长方式如何影响口服共生的主要竞争因素。 重要的是，这些研究将分子分析与生物学意义联系起来。目的是利用所获得的信息来提高口头共生竞争力，例如在竞争条件下增加过氧化氢的产生。这种理解应该为预防口腔疾病的新策略的发展提供重要的新见解。