Reverse Line Blot Daignostic Test for Agents of Sepsis

败血症因子的反向线印迹诊断测试

• 批准号: 7083622
• 负责人: Andrew E. Levin
• 金额: $ 46.36万
• 依托单位: IMMUNETICS, INC.
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-07-01 至 2008-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7083622
• 关键词: bacterial disease; blood disorder diagnosis; blood tests; clinical research; cooperative study; diagnosis design /evaluation; diagnosis quality /standard; human subject; microorganism classification; mycosis; nucleic acid hybridization; nucleic acid probes; polymerase chain reaction; rapid diagnosis; septicemia

DESCRIPTION (provided by applicant): Sepsis claims up to 120,000 lives per year in the U.S., is a leading cause of death in hospitalized patients, and is estimated to cost $17 billion annually in healthcare. Yet, at present there is no straightforward diagnostic test available. Blood cultures are in routine use, yet typically require 24-48 hours for results and are negative in a substantial percentage of cases. Identification of the causative organism(s) is critical to effective diagnosis and treatment. Matching the antimicrobial to the infectious agent significantly enhances the probability of successful treatment and outcome. In particular, multiplexed detection methods which would enable simultaneous probing for a range of organisms may potentially substitute for culture. The aim of this project is development of a Reverse Line Blot assay for multiple bacterial and fungal agents of sepsis. In the Reverse Line Blot (RLE) approach, separate probes are attached to a membrane in discrete bands. Extracted bacterial DNA is then incubated with the membrane permitting complementary sequences to hybridize with the corresponding probes. The advantages of this method are that (1) typing of organisms can be accomplished via a matrix of probes, with hybridization occurring independently to each probe; (2) the source sample can be amplified by PCR prior to hybridization; (3) the matrix is macroscopic, easily analyzed without expensive instrumentation, and is suitable for analysis of tens to hundreds of probe hybridizations. Applicants intend to further improve this methodology by converting it to a flow-through membrane format, in order to significantly reduce hybridization times. In the proposed approach, bacterial DNA will be extracted directly from a blood sample to eliminate the delay associated with blood culture, and subject to PCR amplification using universal degenerate primers for a region of the chaperonin 60 gene (Cpn60 or HSP60) widely conserved among prokaryotic species. Cpn60 has been shown to contain species-specific sequences useful as probes for identification of bacterial species. The final product will be a diagnostic test kit for identification of bacterial and fungal agents of sepsis, comprising the flow-through hybridization unit, a Reverse Line Blot membrane containing Cpn60-derived probes to multiple pathogens, and primers necessary for PCR amplification of the Cpn60 sequence in pathogens present in blood samples.

描述（由申请人提供）：败血症在美国每年夺去多达120,000人的生命，是住院患者死亡的主要原因，估计每年在医疗保健方面花费170亿美元。然而，目前还没有直接的诊断测试。血培养是常规使用，但通常需要24-48小时才能得到结果，并且在相当大比例的病例中呈阴性。鉴定致病生物对有效的诊断和治疗至关重要。将抗菌药物与感染原相匹配，可显著提高治疗成功的可能性和结果。特别是，能够同时探测一系列生物体的多路检测方法可能潜在地替代培养。