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用于金黄色葡萄球菌检测的CRISPR/Cas12a双模式生物传感器:通过无酶等温扩增技术

CRISPR/Cas12a dual-mode biosensor for Staphylococcus aureus detection via enzyme-free isothermal amplification.

作者信息

Gao Hongmin, Zhang Hehua, Qi Xue, Miao Meng, Que Longbin, Gu Xin, Chang Dong, Pan Hongzhi

机构信息

School of Health Science and Engineering, University of Shanghai for Science and Technology, Shanghai, 200093, People's Republic of China; Collaborative Research Center, Shanghai University of Medicine and Health Sciences, Shanghai, 201318, People's Republic of China.

Collaborative Research Center, Shanghai University of Medicine and Health Sciences, Shanghai, 201318, People's Republic of China.

出版信息

Talanta. 2025 Jan 1;282:127013. doi: 10.1016/j.talanta.2024.127013. Epub 2024 Oct 10.

Abstract

Accurate and reliable detection of Staphylococcus aureus (S. aureus) is essential for preventing infections, particularly in healthcare and food safety contexts. This work presents a novel dual-mode biosensor that integrates the CRISPR/Cas12a system with an enzyme-free isothermal amplification method for detecting S. aureus. Hybridization chain reaction (HCR) and catalytic hairpin assembly (CHA) amplify the aptamer-triggered response, significantly enhancing sensitivity. CRISPR/Cas12a's nuclease activity is utilized in two modes: cis cleavage generates a fluorescence signal, while trans cleavage produces an electrochemical signal, enabling dual-mode detection. The biosensor demonstrates outstanding performance, with a limit of detection (LOD) as low as 5.7 CFU mL in electrochemical mode and 133.7 CFU mL in fluorescence mode, showcasing excellent accuracy, stability, and sensitivity. It has been successfully applied to detecting actual samples, confirming its practical applicability. This innovative approach offers a powerful tool for the swift and precise identification of S. aureus and paves the way for developing next-generation dual-mode biosensors for various analytes. Future research will aim to simplify the detection process further, making it more accessible for use in resource-limited settings.

摘要

准确可靠地检测金黄色葡萄球菌对于预防感染至关重要,尤其是在医疗保健和食品安全领域。这项工作提出了一种新型双模式生物传感器,该传感器将CRISPR/Cas12a系统与一种无酶等温扩增方法相结合,用于检测金黄色葡萄球菌。杂交链式反应(HCR)和催化发夹组装(CHA)放大了适配体触发的反应,显著提高了灵敏度。CRISPR/Cas12a的核酸酶活性以两种模式使用:顺式切割产生荧光信号,而反式切割产生电化学信号,实现双模式检测。该生物传感器表现出出色的性能,在电化学模式下检测限低至5.7 CFU/mL,在荧光模式下为133.7 CFU/mL,展示了出色的准确性、稳定性和灵敏度。它已成功应用于实际样品的检测,证实了其实际适用性。这种创新方法为快速准确地鉴定金黄色葡萄球菌提供了一个强大的工具,并为开发用于各种分析物的下一代双模式生物传感器铺平了道路。未来的研究将旨在进一步简化检测过程,使其在资源有限的环境中更易于使用。

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