High-performance Food Pathogen Detection Instrument
高性能食品病原体检测仪器
基本信息
- 批准号:6994886
- 负责人:
- 金额:$ 37.95万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2003
- 资助国家:美国
- 起止时间:2003-09-30 至 2007-08-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): The primary objective of this Phase II project is to develop an innovative benchtop instrument for use on-site at food processing facilities with high performance, ease-of-use, and a low per sample cost for rapid, specific, and sensitive detection of multiple pathogens including Escherichia coli O157:H7, Listeria monocytogenes, and Salmonella Typhimurium in ready-to-eat (RTE) foods, such as processed meat and poultry products and fresh fruits and vegetables. Our proposed technique provides the ability to quantify pathogenic bacteria down to less than 10 cells/mL in less than one hour with a minimum of false positives or negatives. The proposed instrument is fully integrated and includes a cartridge containing multiple capillary column-based bioseparator/bioreactors (for pathogen capture), and a liquid core waveguide (LCW) optical detector (for pathogen detection). It will not require pre-enrichment of target bacteria in growth medium and all steps of the assay will require minimal operator skill. Microbial contamination of food products by pathogenic bacteria is a major concern of our society. Contaminated food is estimated to cause 76 million illnesses, 325,000 serious illnesses resulting in hospitalization, and 5,000 deaths in the United States each year. The economic impact of foodborne illness has been estimated as high as $10 billion annually. The Center for Science in the Public Interest reported that fruits and vegetables are the leading culprits in confirmed cases of foodborne illness in the United States. Of particular concern is the presence of pathogens in imported produce. Because of the persistence of these pathogens on fresh produce, both FDA and USDA have supported research on developing standardized methods to determine the efficacy of proposed sanitizer strategies for inactivating these pathogens on fresh produce. A heat kill step is not feasible for such foods. An obvious companion need in the U.S. food safety program is a rapid, simple method, such as is proposed here, to determine the number of pathogens that persist after the sanitizing step has been administered.
描述(申请人提供):该第二阶段项目的主要目标是开发一种创新的台式仪器,用于食品加工设施的现场使用,具有高性能、易用和低每份样本成本,用于快速、特异和灵敏地检测即食食品中的多种病原体,包括大肠杆菌O157:H7、单核细胞增生性李斯特菌和鼠伤寒沙门氏菌。我们建议的技术提供了在不到一小时的时间内将病原菌量化到低于10个细胞/毫升的能力,并将假阳性或假阴性降至最低。拟议的仪器是完全集成的,包括一个装有多个毛细管柱生物分离器/生物反应器(用于病原体捕获)的色带,以及一个液芯波导(LCW)光学检测器(用于病原体检测)。它不需要在生长介质中预富集目标细菌,检测的所有步骤都需要最低限度的操作员技能。病原菌对食品的微生物污染是我们社会关注的主要问题。据估计,受污染的食物每年在美国导致7600万人患病,32.5万人患重病住院,5000人死亡。据估计,食源性疾病每年的经济影响高达100亿美元。公共利益科学中心报告称,水果和蔬菜是美国食源性疾病确诊病例的主要罪魁祸首。特别令人关注的是进口农产品中存在病原体。由于这些病原体在新鲜农产品上持续存在,FDA和美国农业部都支持开发标准化方法的研究,以确定拟议的消毒剂策略在新鲜农产品上灭活这些病原体的效果。对于这样的食物,热杀灭步骤是不可行的。在美国食品安全计划中,一个明显的配套需求是一种快速、简单的方法,如这里提出的,用于确定在实施消毒步骤后仍然存在的病原体数量。
项目成果
期刊论文数量(0)
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