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An optical biosensor for detection of pathogen biomarkers from Shiga toxin-producing Escherichia coli in ground beef samples

机译:用于检测来自Shiga毒素的病原体生物标志物的光学生物传感器在碎牛肉样品中产生滋生毒素的大肠杆菌

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Shiga toxin-producing Escherichia coli (STEC) poses a serious threat to human health through the consumption of contaminated food products, particularly beef and produce. Early detection in the food chain, and discrimination from other non-pathogenic Escherichia coli (E. coli), is critical to preventing human outbreaks, and meeting current agricultural screening standards. These pathogens often present in low concentrations in contaminated samples, making discriminatory detection difficult without the use of costly, time-consuming methods (e.g. culture). Using multiple signal transduction schemes (including novel optical methods designed for amphiphiles), specific recognition antibodies, and a waveguide-based optical biosensor developed at Los Alamos National Laboratory, we have developed ultrasensitive detection methods for lipopolysaccharides (LPS), and protein biomarkers (Shiga toxin) of STEC in complex samples (e.g. beef lysates). Waveguides functionalized with phospholipid bilayers were used to pull down amphiphilic LPS, using methods (membrane insertion) developed by our team. The assay format exploits the amphiphilic biochemistry of lipoglycans, and allows for rapid, sensitive detection with a single fluorescent reporter. We have used a combination of biophysical methods (atomic force and fluorescence microscopy) to characterize the interaction of amphiphiles with lipid bilayers, to efficiently design these assays. Sandwich immunoassays were used for detection of protein toxins. Biomarkers were spiked into homogenated ground beef samples to determine performance and limit of detection. Future work will focus on the development of discriminatory antibodies for STEC serotypes, and using quantum dots as the fluorescence reporter to enable multiplex screening of biomarkers.
机译:Shiga Toxin生产大肠杆菌(StEC)通过消耗污染的食品,特别是牛肉和生产来对人类健康构成严重威胁。食物链的早期检测,以及其他非致病大肠杆菌(大肠杆菌)的歧视对于预防人类爆发至关重要,并满足当前的农业筛查标准。这些病原体通常存在于污染样品中的低浓度下,使得在不使用昂贵耗时,耗时的方法(例如培养)的情况下使辨别性检测困难。使用多个信号转导方案(包括用于两亲物的新型光学方法),特定识别抗体,以及在LOS Alamos国家实验室开发的基于波导的光学生物传感器,我们对脂多糖(LPS)和蛋白质生物标志物(Shiga)开发了超敏检测方法。复杂样品中STEC的毒素(例如牛裂解物)。用磷脂双层官能化的波导用于拉下两亲性LPS,使用我们团队开发的方法(膜插入)。测定形式利用脂质化合物的两亲生物化学,并允许用单个荧光报告器进行快速,敏感的检测。我们使用了生物物理方法(原子力和荧光显微镜)的组合来表征两亲与脂双层的两亲物相互作用,以有效地设计这些测定。夹层免疫测定用于检测蛋白质毒素。将生物标志物掺入均匀的磨碎牛肉样品中以确定检测的性能和限制。未来的工作将重点关注STEC血清型的鉴别抗体,并使用量子点作为荧光报告,以实现生物标志物的多重筛选。

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