Bioagent Characterization by Iterative Extension
通过迭代扩展进行生物剂表征
基本信息
- 批准号:7051529
- 负责人:
- 金额:$ 33.6万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2006
- 资助国家:美国
- 起止时间:2006-02-01 至 2008-01-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): Project Summary - A new syndrome-based diagnostic system for rapid detection and identification of category B and C priority pathogens is proposed. Phase 1 will focus on V. cholerae genes and genes from similar pathogens. The technique relies upon a helicase-driven iterative primer extension reaction (HDIE) that uses isothermal, multiplexed target amplification to produce short, labeled, single-stranded DNA products with sequences representative of the sample DNA. These reaction products are ideal for hybridization to short probes immobilized on microarrays, thus providing gene identification of any pathogen in the sample. Phase II will expand the technique to a wide variety of category B and C priority pathogens. Successful completion of the research will result in a syndrome-based diagnostic system that can identify one or more pathogens in a sample among a large number of candidates. The technique will be isothermal and require minimum equipment for the initial reactions, making it useful to first responders in a biowarfare attack or an outbreak.
HDIE relies on the fact that there are a large number of regions in any gene that are missing one of the four DNA bases over a span of 12 to 40 bases. HDIE primers are designed to be complementary to a section of the target DNA immediately adjacent to the 3' end of one of these void regions. Once the primer is annealed to the target DNA, the extension reaction proceeds from the 3' end of the primer using the region lacking either A, T, G, or C as the template. When the first occurrence of the missing base is encountered the extension reaction is terminated by incorporation of a complementing dideoxynucleotide. DNA helicases separate the extension reaction products from the template molecules, allowing iterative non-exponential target amplification. The HDIE products can be hybridized to microarray probes and detected using conventional fluorescence methods. The fact that the reaction is terminated after a very short extension, along with fact that amplification is linear rather than exponential, allows hundreds of primers to be present in a single reaction tube.
Although the HDIE approach is designed to overcome difficulties specific to parallel pathogen diagnosis, it can be extended to many applications that tap into the lucrative molecular diagnostics market, including foodborne pathogen detection, agricultural and veterinary testing, water testing, and clinical testing. In 2005, the global market for molecular diagnostics is expected to be $6.5 billion, or about 3.3% of the total diagnostics market and approximately 14% of the in vitro diagnostic market. The molecular diagnostics market is forecast to increase to $12 billion by 2010 and $35 billion by 2015.
Relevance - The proposed research directly addresses the need for a syndrome-based assay that can rapidly identify' the pathogen or pathogens responsible for disease in case of a biowarfare attack or a major outbreak.
描述(由申请人提供):项目摘要-提出了一种新的基于症状的诊断系统,用于快速检测和识别B和C类优先病原体。第一阶段将集中在霍乱弧菌基因和类似病原体的基因。该技术依赖于解旋酶驱动的迭代引物延伸反应(HDIE),该反应使用等温、多重靶扩增来产生具有代表样品DNA的序列的短的、标记的单链DNA产物。这些反应产物非常适合与固定在微阵列上的短探针杂交,从而提供样品中任何病原体的基因鉴定。第二阶段将把该技术扩展到各种各样的B和C类优先病原体。研究的成功完成将产生一个基于症状的诊断系统,可以在大量候选人中识别样本中的一种或多种病原体。该技术将是等温的,需要最少的设备进行初始反应,使其在生物战攻击或爆发中对第一反应者有用。
HDIE依赖于这样一个事实,即在任何基因中,都有大量区域在12到40个碱基的范围内缺失了四个DNA碱基中的一个。HDIE引物被设计成与紧邻这些空隙区之一的3'端的靶DNA部分互补。一旦引物与靶DNA退火,延伸反应就从引物的3'端开始,使用缺乏A、T、G或C的区域作为模板。当第一次出现缺失的碱基时,通过掺入互补的双脱氧核苷酸终止延伸反应。DNA解旋酶将延伸反应产物与模板分子分离,允许迭代非指数靶扩增。HDIE产物可以与微阵列探针杂交并使用常规荧光方法检测。反应在非常短的延伸后终止的事实,沿着扩增是线性的而不是指数的事实,允许数百个引物存在于单个反应管中。
虽然HDIE方法旨在克服并行病原体诊断的特定困难,但它可以扩展到许多应用,这些应用可以进入利润丰厚的分子诊断市场,包括食源性病原体检测,农业和兽医测试,水测试和临床测试。2005年,全球分子诊断市场预计为65亿美元,约占诊断市场总额的3.3%,约占体外诊断市场的14%。分子诊断市场预计到2010年将增加到120亿美元,到2015年将增加到350亿美元。
相关性-拟议的研究直接解决了对基于综合征的检测的需求,该检测可以在生物战袭击或重大疫情爆发的情况下快速识别出导致疾病的病原体。
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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RICHARD Ashley HURT其他文献
RICHARD Ashley HURT的其他文献
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{{ truncateString('RICHARD Ashley HURT', 18)}}的其他基金
Ultra-Sensitive Molecular Diagnostic for Borrelia Species
伯氏疏螺旋体物种的超灵敏分子诊断
- 批准号:
7481939 - 财政年份:2008
- 资助金额:
$ 33.6万 - 项目类别:
Bioagent Characterization by Iterative Extension
通过迭代扩展进行生物剂表征
- 批准号:
7172261 - 财政年份:2006
- 资助金额:
$ 33.6万 - 项目类别:
Specific Diagnostic for Members of Genus Mycobacterium
分枝杆菌属成员的特异性诊断
- 批准号:
6933252 - 财政年份:2005
- 资助金额:
$ 33.6万 - 项目类别:
SNP Detection with Unlabeled, Unamplified Target DNA
使用未标记、未扩增的目标 DNA 进行 SNP 检测
- 批准号:
6753502 - 财政年份:2002
- 资助金额:
$ 33.6万 - 项目类别:
SNP Detection with Unlabeled, Unamplified Target DNA
使用未标记、未扩增的目标 DNA 进行 SNP 检测
- 批准号:
6643759 - 财政年份:2002
- 资助金额:
$ 33.6万 - 项目类别: