Kim Jason S, Taitt Chris R, Ligler Frances S, Anderson George P
Naval Research Laboratory, Center for Bio/Molecular Science and Engineering, 4555 Overlook Ave. SW, Washington, DC, USA.
Sens Instrum Food Qual Saf. 2010 May 4;4(2):73-81. doi: 10.1007/s11694-010-9097-x.
Foodstuffs have traditionally been challenging matrices for conducting immunoassays. Proteins, carbohydrates, and other macromolecules present in food matrices may interfere with both immunoassays and PCR-based tests, and removal of particulate matter may also prove challenging prior to analyses. This has been found true when testing for bacterial contamination of foods using the standard polystyrene microspheres utilized with Luminex flow cytometers. Luminex MagPlex microspheres are encoded with the same dyes as standard xMAP microspheres, but have superparamagnetic properties to aid in preparation of samples in complex matrices. In this work, we present results demonstrating use of MagPlex for sample preparation and identification of bacteria and a toxin spiked into a variety of food samples. Fluorescence-coded MagPlex microsphere sets coated with antibodies for Salmonella, Campylobacter, Escherichia coli, Listeria, and staphylococcal enterotoxin B (SEB) were used to capture these bacteria and toxin from spiked foodstuffs and then evaluated by the Luminex system in a multiplex format; spiked foods included apple juice, green pepper, tomato, ground beef, alfalfa sprouts, milk, lettuce, spinach, and chicken washes. Although MagPlex microspheres facilitated recovery of the microspheres and targets from the complex matrices, assay sensitivity was sometimes inhibited by up to one to three orders of magnitude; for example the detection limits E. coli spiked into apple juice or milk increased 100-fold, from 1000 to 100,000 cfu/mL. Thus, while the magnetic and fluorescent properties of the Luminex MagPlex microspheres allow for rapid, multiplexed testing for bacterial contamination in typically problematic food matrices, our data demonstrate that achieving desired limits of detection is still a challenge.
传统上,食品一直是进行免疫测定具有挑战性的基质。食品基质中存在的蛋白质、碳水化合物和其他大分子可能会干扰免疫测定和基于聚合酶链反应(PCR)的检测,并且在分析之前去除颗粒物也可能具有挑战性。当使用Luminex流式细胞仪配套的标准聚苯乙烯微球检测食品中的细菌污染时,情况确实如此。Luminex MagPlex微球与标准xMAP微球使用相同的染料进行编码,但具有超顺磁性特性,有助于在复杂基质中制备样品。在这项工作中,我们展示了使用MagPlex进行样品制备以及鉴定掺入各种食品样品中的细菌和毒素的结果。用针对沙门氏菌、弯曲杆菌、大肠杆菌、李斯特菌和葡萄球菌肠毒素B(SEB)的抗体包被的荧光编码MagPlex微球集,用于从加标食品中捕获这些细菌和毒素,然后通过Luminex系统以多重形式进行评估;加标食品包括苹果汁、青椒、番茄、碎牛肉、苜蓿芽、牛奶、生菜、菠菜和鸡肉清洗液。尽管MagPlex微球有助于从复杂基质中回收微球和靶标,但检测灵敏度有时会受到高达一到三个数量级的抑制;例如,掺入苹果汁或牛奶中的大肠杆菌检测限从1000 cfu/mL增加到100,000 cfu/mL,提高了100倍。因此,虽然Luminex MagPlex微球的磁性和荧光特性允许在通常有问题的食品基质中快速进行多重细菌污染检测,但我们的数据表明,实现所需的检测限仍然是一个挑战。