Bruno John G, Sivils Jeffrey C, Phillips Taylor
Operational Technologies Corp., 4100 NW Loop 410, Suite 230, San Antonio, TX 78229.
J AOAC Int. 2017 Jul 1;100(4):895-899. doi: 10.5740/jaoacint.17-0163. Epub 2017 Jun 16.
DNA and RNA aptamers have been extensively investigated as potential competitors for antibodies for a variety of applications including food safety testing. Ultrasensitive fluorescence detection of foodborne pathogenic bacteria as low as 1-10 cells/mL has been achieved using aptamers coupled to quantum dots in clear pristine buffers for environmental sample detection. Quantum dots offer other advantages, including single UV or blue light source multiplex (multicolored) detection. However, quantum dots can exhibit decreased fluorescence in some food matrixes and even completely fail to fluoresce in some fatty matrixes, as documented in this report. Given the need to detect substances in complex food matrixes (and from data reported elsewhere), aptamer-magnetic bead pull-down methods followed by enzymatic/fluorometric- or PCR-based detection methods may be more robust methods for testing in foods or enrichment cultures. Other lessons learned, including the initial choice of aptamer targets to enhance assay specificity, are also discussed.
DNA和RNA适配体作为抗体的潜在竞争对手已被广泛研究,用于包括食品安全检测在内的各种应用。在清澈的原始缓冲液中,使用与量子点偶联的适配体实现了对低至1-10个细胞/mL的食源性病原体细菌的超灵敏荧光检测,用于环境样品检测。量子点还具有其他优势,包括单紫外或蓝光光源多重(多色)检测。然而,如本报告所述,量子点在某些食品基质中可能会出现荧光降低,甚至在某些脂肪基质中完全不发荧光。鉴于需要在复杂的食品基质中检测物质(以及其他地方报道的数据),适配体-磁珠下拉法随后采用基于酶促/荧光或PCR的检测方法,可能是用于食品或富集培养物检测的更可靠方法。还讨论了其他经验教训,包括增强检测特异性的适配体靶标的初始选择。