MOE Joint International Research Laboratory of Animal Health and Food Safety, Key Laboratory of Animal Bacteriology, Ministry of Agriculture, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
School of Food Science & Biological Engineering, Engineering Research Center of Bio-process, MOE, Hefei University of Technology, Hefei, 230009, China.
Mikrochim Acta. 2020 Mar 4;187(4):198. doi: 10.1007/s00604-020-4170-6.
A method for rapid and accurate determination of avian pathogenic Escherichia coli serotype O78 (APEC O78) by the gold nanoparticle-labeled lateral flow strip method, entitled molecule capturer analysis system (MCAS), is described. Target virulence-associated gene of APEC O78 is adopted as the analyte. After pre-amplification with the designed functional primer set, numerous new-formed amplicons are simultaneously labeled with fluorescein isothiocyanate (FITC) and digoxin. AuNPs with a diameter of 18 nm and the characteristic plasmonic peak at 526 nm are utilized for labeling. These two labels of FITC and digoxin are further captured and measured with the AuNP-labeled lateral flow strip, and the AuNPs are retained on the test line through the immunoreaction for signal output. Under optimized conditions, this MCAS protocol can determine the target APEC O78 with excellent determination limit of 4.3 cfu mL based on the optical density of AuNPs on the test line of lateral flow strips. The working range is 2.52 × 10 to 1.63 × 10 cfu mL. Spiked serum samples are rapid and accurately measured, and the results are highly correlated with those of the real-time PCR. With this MCAS protocol, rapid and on-site determination of APEC O78 can be realized without expensive instruments or professional personnel. This MCAS protocol can be easily applied to other analytes by just replacing the traditional primer set with functionalization primer set. Graphical abstract Schematic illustration of molecule capturer analysis system for rapid and accurate determination of avian pathogenic Escherichia coli serotype O78.
一种利用金纳米粒子标记的侧向流动条带方法(称为分子捕获分析系统,MCAS)快速准确测定禽致病性大肠杆菌血清型 O78(APEC O78)的方法。以 APEC O78 的靶毒力相关基因为分析物。经过设计的功能引物对的预扩增,大量新形成的扩增子同时用荧光素异硫氰酸酯(FITC)和地高辛标记。使用直径为 18nm 且特征等离子体峰在 526nm 的 AuNPs 进行标记。FITC 和地高辛这两种标记物进一步通过 AuNP 标记的侧向流动条带进行捕获和测量,AuNPs 通过免疫反应保留在测试线上以进行信号输出。在优化条件下,该 MCAS 方案可以根据侧向流动条带测试线上的 AuNP 光密度以出色的测定限 4.3cfu/mL 来确定目标 APEC O78。工作范围为 2.52×10 至 1.63×10 cfu/mL。对添加的血清样本进行快速准确的测量,并且结果与实时 PCR 高度相关。通过这种 MCAS 方案,可以在没有昂贵仪器或专业人员的情况下实现 APEC O78 的快速现场测定。通过用功能化引物对替换传统引物对,该 MCAS 方案可以轻松应用于其他分析物。