Department of Agricultural and Environmental Sciences, Tennessee State University, Nashville, TN 37209, USA.
Department of Human Sciences, Tennessee State University, Nashville, TN 37209, USA.
Sensors (Basel). 2022 Jan 9;22(2):475. doi: 10.3390/s22020475.
is one of the major foodborne pathogens responsible for many cases of illnesses, hospitalizations and deaths worldwide. Although different methods are available to timely detect in foods, surface plasmon resonance (SPR) has the benefit of real-time detection with a high sensitivity and specificity. The purpose of this study was to develop an SPR method in conjunction with magnetic nanoparticles (MNPs) for the rapid detection of Typhimurium. The assay utilizes a pair of well-characterized, flagellin-specific monoclonal antibodies; one is immobilized on the sensor surface and the other is coupled to the MNPs. Samples of romaine lettuce contaminated with Typhimurium were washed with deionized water, and bacterial cells were captured on a filter membrane by vacuum filtration. SPR assays were compared in three different formats-direct assay, sequential two-step sandwich assay, and preincubation one-step sandwich assay. The interaction of flagellin and MNPs with the antibody-immobilized sensor surface were analyzed. SPR signals from a sequential two-step sandwich assay and preincubation one-step sandwich assay were 7.5 times and 14.0 times higher than the direct assay. The detection limits of the assay were 4.7 log cfu/mL in the buffer and 5.2 log cfu/g in romaine lettuce samples.
是一种主要的食源性病原体,可导致全球许多疾病、住院和死亡病例。尽管有许多方法可用于及时检测食品中的 ,但表面等离子体共振(SPR)具有实时检测、高灵敏度和特异性的优势。本研究旨在开发一种 SPR 方法,结合磁性纳米颗粒(MNPs),用于快速检测 鼠伤寒沙门氏菌。该检测方法利用一对经过充分表征的鞭毛特异性单克隆抗体;一种固定在传感器表面,另一种与 MNPs 偶联。用去离子水清洗受 鼠伤寒沙门氏菌污染的罗曼生菜样品,并用真空过滤将细菌细胞捕获在滤膜上。在三种不同的格式(直接检测、两步顺序夹心检测和预孵育一步夹心检测)中比较了 SPR 检测。分析了鞭毛蛋白与 MNPs 与抗体固定传感器表面的相互作用。两步顺序夹心检测和预孵育一步夹心检测的 SPR 信号分别比直接检测高 7.5 倍和 14.0 倍。该检测方法在缓冲液中的检测限为 4.7 log cfu/mL,在罗曼生菜样品中的检测限为 5.2 log cfu/g。