Chao Anqi, Hu Qinqin, Yin Kun
School of Global Health, Chinese Center for Tropical Diseases Research, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Biosensors (Basel). 2025 Apr 5;15(4):230. doi: 10.3390/bios15040230.
CRISPR/Cas-based diagnostics offer unparalleled specificity, but their reliance on fluorescently labeled probes and complex nucleic acid extraction limits field applicability. To tackle this problem, we have developed a label-free, equipment-free platform integrating FTA card-based extraction, CRISPR/Cas12a, and pre-folded G-quadruplex (G4)-Thioflavin T (ThT) signal reporter. This system eliminates costly fluorescent labeling by leveraging G4-ThT structural binding for visible fluorescence output, while FTA cards streamline nucleic acid isolation without centrifugation. Achieving a limit of detection (LOD) to 10 CFU/mL for O157:H7 in spiked food samples, the platform demonstrated 100% concordance with qPCR and standard fluorescent probe-based CRISPR/Cas12a system. Its simplicity, minimal equipment (portable heating/imaging), and cost-effectiveness make it a revolutionary tool for detecting foodborne pathogens in resource-limited environments.
基于CRISPR/Cas的诊断方法具有无与伦比的特异性,但其对荧光标记探针的依赖以及复杂的核酸提取过程限制了其在现场的适用性。为了解决这个问题,我们开发了一个无标记、无需设备的平台,该平台整合了基于FTA卡的提取方法、CRISPR/Cas12a以及预折叠的G-四链体(G4)-硫黄素T(ThT)信号报告器。该系统通过利用G4-ThT结构结合实现可见荧光输出,从而消除了昂贵的荧光标记,而FTA卡无需离心即可简化核酸分离过程。该平台在加标食品样本中对O157:H7的检测限达到10 CFU/mL,与qPCR和基于标准荧光探针的CRISPR/Cas12a系统的一致性为100%。其简单性、最少的设备(便携式加热/成像)和成本效益使其成为在资源有限环境中检测食源性病原体的革命性工具。