E. coli O157:H7 Detection Using Surface Plasmon Resonance Based Biosensor

Esma ESER, Okan Öner EKİZ, H. İbrahim EKİZ
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Abstract

The detection of foodborne pathogenic bacteria remains a significant challenge, and the need for fast and sensitive detection methods is becoming increasingly important. Escherichia coli is a prevalent bacteria associated with foodborne illness, and this study aimed to evaluate the ability of a surface plasmon resonance (SPR) based biosensor to detect E. coli O157:H7 at low levels in pure culture and artificially contaminated bay leaves (Laurus nobilis) using different injection methods. To develop a biological sensing surface, the sensor surface was functionalized with 3-aminopropyltriethoxysilane (APTES), and polyclonal antibodies were immobilized on the surface for bacteria detection. Bacterial attachment to the antibodies resulted in a change in resonance angle. The biosensor was able to discriminate between cellular concentrations of 103 to 107 CFU/mL and showed potential in detecting different pathogens in various food samples. Before the SPR detection, the sample preparation step was optimized to ensure complex food matrices were suitable for SPR analysis. The results suggest that the SPR based biosensor is a promising tool for the rapid detection of foodborne pathogens in complex food matrices.
基于表面等离子体共振的生物传感器检测大肠杆菌O157:H7
食源性致病菌的检测仍然是一项重大挑战,对快速、灵敏的检测方法的需求正变得越来越重要。大肠杆菌是一种与食源性疾病相关的常见细菌,本研究旨在评价基于表面等离子体共振(SPR)的生物传感器在不同注射方法的纯培养和人工污染月桂叶(月桂叶)中检测低水平大肠杆菌O157:H7的能力。利用3-氨基丙基三乙氧基硅烷(APTES)对传感器表面进行功能化,并将多克隆抗体固定在传感器表面进行细菌检测。细菌附着在抗体上导致共振角的改变。该生物传感器能够区分103至107 CFU/mL的细胞浓度,并显示出检测各种食品样品中不同病原体的潜力。在SPR检测前,对样品制备步骤进行优化,以确保复杂的食品基质适合SPR分析。结果表明,基于SPR的生物传感器是快速检测复杂食品基质中食源性病原体的一种有前景的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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