STREPTOCOCCUS SANGUIS MICROBIAL GENOME PROJECT
血链球菌微生物基因组计划
基本信息
- 批准号:6379870
- 负责人:
- 金额:$ 28.55万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2000
- 资助国家:美国
- 起止时间:2000-07-01 至 2003-06-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (Adapted from the Investigator's Abstract): The investigators
propose to determine the nucleotide sequence of the genome of Streptococcus
sanguis. This member of the human indigenous oral microflora has long been
recognized as a key player in the bacterial colonization of the mouth. It
directly binds to oral surfaces and serves as a tether for the attachment of a
variety of other oral microorganisms which colonize the tooth surface, form
dental plaque, and contribute to the etiology of both caries and periodontal
disease. Furthermore, S. sanguis has been long recognized as a leading cause of
bacterial endocarditis, a disease of high morbidity which is fatal if
untreated. Moreover, S. sanguis and other viridans streptococci of the mouth
are emerging as life-threatening bloodstream pathogens in neutropenic patients.
And such infections are being compounded by the increasing frequency with which
penicillin resistance is being observed in this group of organisms. New
knowledge about this organism could be used in controlling oral microbial
colonization so as to minimize or eliminate plaque-related oral diseases. Since
the mouth is the source of S. sanguis isolates that cause endocarditis and
bacteremia, novel controlling strategies also would have an impact on systemic
infections. S. sanguis genomic data will provide new insights into this
organism's lifestyle and virulence properties that cannot be extrapolated from
analyzing the genomic data of even closely related species. The investigators
believe that the complete genomic structure of S. sanguis is certain to lead to
the discovery of new genes, insights into their regulation, and an appreciation
of their interactions at both the genotypic and phenotypic levels. This, in
turn, will provide researchers with new targets for vaccines and rationally
designed drugs.
描述(改编自研究者摘要):研究者
建议确定链球菌基因组的核苷酸序列
血。这种人类本土口腔微生物群落的成员长期以来一直是
被认为是口腔细菌定植的关键因素。它
直接结合到口腔表面,并作为连接
各种其它口腔微生物在牙齿表面定居,
牙菌斑,并有助于龋齿和牙周病的病因
疾病此外,S.长期以来,血吸虫病一直被认为是导致
细菌性心内膜炎是一种高发病率的疾病,如果
未经治疗。此外,S.血链球菌和其他口腔草绿色链球菌
正在作为威胁生命的血流病原体出现在血小板减少症患者中。
而这种感染正因越来越频繁的
在这组微生物中观察到青霉素耐药性。新
关于这种微生物知识可用于控制口腔微生物,
从而最小化或消除牙菌斑相关的口腔疾病。以来
口是S的来源。引起心内膜炎的血液分离株,
菌血症,新的控制策略也会对全身性
感染. S. sanguis基因组数据将为这一点提供新的见解
生物体的生活方式和毒力特性,不能从
分析甚至是密切相关物种的基因组数据。调查人员
认为S.血肯定会导致
新基因的发现,对它们的调节的见解,以及对
它们在基因型和表型水平上的相互作用。而这
反过来,将为研究人员提供新的疫苗靶点,
设计药物
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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{{ truncateString('FRANCIS L. MACRINA', 18)}}的其他基金
Cardiovascular Injury and Repair Research Facility
心血管损伤与修复研究设施
- 批准号:
7000233 - 财政年份:2009
- 资助金额:
$ 28.55万 - 项目类别:
Novel Plasmids for Porphyromonas Post-Genomic Research
用于卟啉单胞菌后基因组研究的新型质粒
- 批准号:
6820994 - 财政年份:2004
- 资助金额:
$ 28.55万 - 项目类别:
Novel Plasmids for Porphyromonas Post-Genomic Research
用于卟啉单胞菌后基因组研究的新型质粒
- 批准号:
7035892 - 财政年份:2004
- 资助金额:
$ 28.55万 - 项目类别:
Novel Plasmids for Porphyromonas Post-Genomic Research
用于卟啉单胞菌后基因组研究的新型质粒
- 批准号:
6915781 - 财政年份:2004
- 资助金额:
$ 28.55万 - 项目类别:
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