Suppr超能文献

内源性多酚的吸附可减轻果汁和新鲜农产品对大肠杆菌O157:H7免疫PCR检测的抑制作用。

Adsorption of endogenous polyphenols relieves the inhibition by fruit juices and fresh produce of immuno-PCR detection of Escherichia coli O157:H7.

作者信息

Ogunjimi A A, Choudary P V

机构信息

Antibody Engineering Laboratory, University of California, Davis 95616-8584, USA.

出版信息

FEMS Immunol Med Microbiol. 1999 Mar;23(3):213-20. doi: 10.1111/j.1574-695X.1999.tb01241.x.

Abstract

The immuno-polymerase chain reaction (PCR) approaches facilitate rapid (8 h) detection of Escherichia coli O157:H7 in contaminated dairy products and ground beef samples with detection sensitivities approaching 1 colony forming unit (cfu) g-1 ml-1. However, no PCR products were obtained when the method was applied to identify E. coli O157:H7 in tainted apple juice. Enzyme-linked immuno-assay (ELISA) results suggested non-specific binding of endogenous polyphenols (ubiquitous in plant products) to antibodies present on the surface of the immunobeads, making the latter unavailable for capturing the target bacteria Treatment of the test sample, prior to IMS, with a synthetic fining agent, polyvinylpyrrolidone, restored the full function and sensitivity of the immuno-PCR. The study demonstrates the suitability of the improved method as a generic strategy for rapid screening of fruit juices and plant produce for E. coli O157:H7.

摘要

免疫聚合酶链反应(PCR)方法有助于在8小时内快速检测受污染乳制品和绞碎牛肉样品中的大肠杆菌O157:H7,检测灵敏度接近1个菌落形成单位(cfu)g-1 ml-1。然而,当该方法用于鉴定受污染苹果汁中的大肠杆菌O157:H7时,未获得PCR产物。酶联免疫吸附测定(ELISA)结果表明,内源性多酚(在植物产品中普遍存在)与免疫磁珠表面的抗体发生非特异性结合,导致后者无法捕获目标细菌。在免疫磁珠分离法(IMS)之前,用合成澄清剂聚乙烯吡咯烷酮处理测试样品,可恢复免疫PCR的全部功能和灵敏度。该研究证明了改进后的方法作为快速筛查果汁和植物产品中大肠杆菌O157:H7的通用策略的适用性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验