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.
Biosens Bioelectron. 2016 Nov 15;85:734-739. doi: 10.1016/j.bios.2016.05.057. Epub 2016 May 20.
A pattern of signal amplification lateral flow immunoassay (LFIA) for pathogen detection, which used fluorescein isothiocyanate (FITC) labeled antigen and antibody for dual FITC-LFIA was developed. Escherichia coli O157:H7 (E.coli O157:H7) was selected as the model analyte. In the signal amplification LFIA method, FITC was mixed with sample culture medium, with the presence of E.coli O157:H7 in the samples, the bacteria could emit a yellow-green fluorescence after incubation, creating a fluorescent antigen probe. This antigen probe was added to LFIA, which already contained E.coli O157:H7 monoclonal antibodies-FITC (McAb-E.coli O157:H7-FITC) dispersed in the conjugate pad. Another E.coli O157:H7 McAb was the test line, and goat anti-mouse IgG antibody was the control line in nitrocellulose (NC) membrane. The visual limit of detection (LOD) of the strip for qualitative detection was 10(5) CFU/mL while the LOD for semi-quantitative detection could down to 10(4) CFU/mL by using scanning reader. Signal amplification LFIA was perfectly applied to the detection of food samples with E.coli O157:H7. The LOD was substantially improved to 1 CFU/mL of the original bacterial content after pre-incubation of the bread, milk and jelly samples in broth for 10, 8 and 8h respectively. The results of this method was more sensitive by 10-fold than the conventional colloidal gold (CG) based strips and comparable to the traditional ELISA. This simple, low-cost and easy to be popularized method served as a significant step towards the development of monitoring food-borne pathogens in food-safety testing.
一种用于病原体检测的信号放大侧向流动免疫分析(LFIA)模式,该方法使用荧光素异硫氰酸酯(FITC)标记的抗原和抗体进行双 FITC-LFIA。选择大肠杆菌 O157:H7(E.coli O157:H7)作为模型分析物。在信号放大 LFIA 方法中,FITC 与样品培养基混合,样品中存在大肠杆菌 O157:H7 时,细菌孵育后会发出黄绿色荧光,形成荧光抗原探针。将该抗原探针加入 LFIA 中,其中已经分散了大肠杆菌 O157:H7 单克隆抗体-FITC(McAb-E.coli O157:H7-FITC)在结合垫中。另一种大肠杆菌 O157:H7 McAb 是测试线,硝酸纤维素(NC)膜中的山羊抗小鼠 IgG 抗体是控制线。用于定性检测的条带的目视检测限(LOD)为 10(5)CFU/mL,而通过使用扫描读取器,半定量检测的 LOD 可低至 10(4)CFU/mL。信号放大 LFIA 非常适用于检测含有大肠杆菌 O157:H7 的食品样品。通过在肉汤中分别预孵育面包、牛奶和果冻样品 10、8 和 8 小时,将原始细菌含量的 LOD 提高到 1 CFU/mL,大大提高了 LOD。与传统 ELISA 相比,该方法的灵敏度提高了 10 倍,比传统的胶体金(CG)基条带更灵敏。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的重要一步。