Song Chunmei, Li Jianwu, Liu Jinxin, Liu Qing
School of Medical Instrument and Food Engineering, University of Shanghai for Science and Technology, Shanghai 200093, China.
School of Medical Instrument and Food Engineering, University of Shanghai for Science and Technology, Shanghai 200093, China.
Talanta. 2016 Aug 15;156-157:42-47. doi: 10.1016/j.talanta.2016.04.054. Epub 2016 Apr 29.
A simple, one-step, rapid method to detect Escherichia coli O157: H7 (E. coli O157: H7) using a label-free immunofluorescence strip sensor is presented. Fluorescein isothiocyanate (FITC) was added to the sample culture medium to prepare the fluorescent probe for the label-free strip sensor. With the presence of E. coli O157: H7 in the samples, the bacteria could emit a yellow-green fluorescence after incubation and maintain good affinity to the monoclonal antibodies (McAb) against E. coli O157: H7. The direct-type immunofluorescence strip sensor was based on the binding between fluorescent bacteria and the unlabeled McAb immobilized at the test line in nitrocellulose membrane (NC membrane) reaction zone. The visual limit of detection (LOD) of the strip for qualitative detection was 10(6)cells/mL while the LOD for semi-quantitative detection could go down to 10(5)cells/mL by using scanning reader. The LOD was substantially improved to 1cells/mL of the original bacterial content after pre-incubation of the bread, milk and jelly samples in broth for 10, 10 and 8h respectively, which was competitive to some current rapid E. coli O157: H7 detection methods. Besides the obvious advantages, including reduced detection time and operation procedures, the results of this method meet the various detection requirements for E. coli O157: H7 and are comparable to the traditional enzyme-linked immunosorbent assay (ELISA) and double antibody sandwich gold-labeled strips. This is the first report of semi-quantitative immunofluorescence strip for directly detecting foodborne pathogen using only one unlabeled antibody. All detections could be achieved in less than 5min. In addition, this simple, low-cost and easy to be popularized method served as a significant step towards the development of monitoring foodborne pathogens in food-safety testing.
本文介绍了一种使用无标记免疫荧光试纸传感器检测大肠杆菌O157:H7(E. coli O157:H7)的简单、一步式快速方法。将异硫氰酸荧光素(FITC)添加到样品培养基中,以制备用于无标记试纸传感器的荧光探针。样品中存在大肠杆菌O157:H7时,细菌在孵育后可发出黄绿色荧光,并与抗大肠杆菌O157:H7的单克隆抗体(McAb)保持良好的亲和力。直接型免疫荧光试纸传感器基于荧光细菌与固定在硝酸纤维素膜(NC膜)反应区检测线上的未标记McAb之间的结合。试纸用于定性检测的视觉检测限(LOD)为10(6)个细胞/mL,而使用扫描读数器进行半定量检测的LOD可降至10(5)个细胞/mL。面包、牛奶和果冻样品分别在肉汤中预孵育10、10和8小时后,原始细菌含量的LOD大幅提高至1个细胞/mL,这与目前一些快速检测大肠杆菌O157:H7的方法具有竞争力。除了检测时间和操作步骤减少等明显优势外,该方法的结果满足了对大肠杆菌O157:H7的各种检测要求,与传统的酶联免疫吸附测定(ELISA)和双抗体夹心金标试纸相当。这是首次报道仅使用一种未标记抗体直接检测食源性病原体的半定量免疫荧光试纸。所有检测均可在不到5分钟内完成。此外,这种简单、低成本且易于推广的方法是食品安全检测中监测食源性病原体发展的重要一步。