Key Laboratory of Dairy Science, Ministry of Education, Department of Food Science, Northeast Agricultural University, Harbin, China, 150030.
Key Laboratory of Dairy Science, Ministry of Education, Department of Food Science, Northeast Agricultural University, Harbin, China, 150030.
J Dairy Sci. 2018 May;101(5):3835-3843. doi: 10.3168/jds.2017-14265. Epub 2018 Mar 1.
Cronobacter sakazakii is an opportunistic foodborne pathogen that can infect newborns through powdered infant formula (PIF). In this study, we developed a novel enhanced lateral flow immunoassay (LFA) with enhanced sensitivity for detection of C. sakazakii in PIF by the naked eye. The proposed strategy for signal enhancement of the traditional LFA used concentrated gold nanoparticles (AuNP) as the enhancer to conjugate with capture antibodies, which could increase the immobilized capture antibodies concentration at the detection zone to improve capture efficiency. Besides, the detection signal was further amplified by accumulated AuNP as the C. sakazakii labeled with AuNP probes was captured by antibodies conjugated with enhancer at the test line. We also studied the effect of different concentrations of capture antibodies and concentrated AuNP on detection performance, and found that 2.2 mg/mL of capture antibodies and 0.06 nM concentrated AuNP were the optimal combination that could avoid a false-positive signal and maximally amplify the detection signal of the enhanced LFA. Using this strategy, the detection sensitivity of the enhanced LFA was 10 cfu/mL and improved 100-fold compared with traditional LFA. The strip was highly specific to C. sakazakii, and the time for detection of C. sakazakii in PIF was shortened by 3 h. In summary, the enhanced LFA developed by the addition of concentrated AuNP as the enhancer can be used as a sensitive, rapid, visual qualitative and point-of-care test method for detecting target analytes.
阪崎克罗诺杆菌是一种机会致病菌,可通过配方奶粉(PIF)感染新生儿。在本研究中,我们通过肉眼开发了一种新型的增强型侧向流动免疫分析(LFA),用于检测 PIF 中的阪崎克罗诺杆菌,具有更高的灵敏度。该传统 LFA 的信号增强策略使用浓缩金纳米颗粒(AuNP)作为增强剂与捕获抗体结合,从而可以增加检测区的固定捕获抗体浓度,以提高捕获效率。此外,通过累积的 AuNP 进一步放大了检测信号,因为与 AuNP 探针标记的 C. sakazakii 被与增强剂结合的抗体在测试线上捕获。我们还研究了不同浓度的捕获抗体和浓缩 AuNP 对检测性能的影响,发现 2.2 mg/mL 的捕获抗体和 0.06 nM 的浓缩 AuNP 是最佳组合,可以避免假阳性信号并最大程度地放大增强 LFA 的检测信号。使用该策略,增强型 LFA 的检测灵敏度为 10 cfu/mL,与传统 LFA 相比提高了 100 倍。该条带对 C. sakazakii 具有高度特异性,并且 PIF 中 C. sakazakii 的检测时间缩短了 3 小时。总之,通过添加浓缩 AuNP 作为增强剂,开发的增强型 LFA 可作为一种灵敏、快速、直观的定性和即时检测方法,用于检测目标分析物。