Feng Jiayu, Wu Ze, Zhu Wenhui, Jin Fei, Zhao Minghai, Zhong Wenjie, Dai Chen, He Yongjian, Yan Lizhi, Wu Shengquan, Wang Yuhang, Rui Yongyu, Zheng Lei, Fu Qiangqiang
Department of Laboratory Medicine, Guangdong Provincial Key Laboratory of Precision Medical Diagnostics, Guangdong Engineering and Technology Research Center for Rapid Diagnostic Biosensors, Guangdong Provincial Key Laboratory of Single-cell and Extracellular Vesicles, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, PR China.
Department of Kidney Transplantation, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, PR China.
Biosens Bioelectron. 2025 Nov 15;288:117839. doi: 10.1016/j.bios.2025.117839. Epub 2025 Jul 29.
Mycoplasma pneumoniae (M. pneumoniae), a major human respiratory pathogen, necessitates the development of rapid point-of-care testing (POCT) platforms for clinical management. However, current two-step workflows suffer from operational complexity and aerosol contamination risks. This limitation stems from CRISPR-Cas12 mediated template degradation in single-reaction systems, which compromises amplification efficiency and detection sensitivity. Here, we combined RPA and CRISPR Cas12b by leveraging the difference in their optimal temperatures to construct a novel TRACER (Thermo-activated RPA Amplification for CRISPR-Cas12b Efficient Recognition) technology. Through precise temperature modulation, TRACER sequentially executes isothermal amplification and CRISPR-mediated detection while preventing premature template cleavage, thereby maintaining optimal reaction efficiency. The platform demonstrates exceptional analytical sensitivity with a detection limit of 1 copy/μL, representing a 100-fold improvement over conventional one-pot RPA-CRISPR-Cas12a systems. Clinical validation using 195 specimens revealed diagnostic performance metrics of 99.2 % sensitivity (119/120), 100.0 % specificity (75/75), and 99.5 % accuracy (194/195). This innovative combination of single-tube reaction, field-deployable instrumentation, and cost-effectiveness establishes TRACER as an ideal POCT solution for M. pneumoniae detection in diverse clinical settings.
肺炎支原体(M. pneumoniae)是一种主要的人类呼吸道病原体,需要开发用于临床管理的快速即时检测(POCT)平台。然而,目前的两步工作流程存在操作复杂性和气溶胶污染风险。这一局限性源于单反应系统中CRISPR-Cas12介导的模板降解,这会影响扩增效率和检测灵敏度。在这里,我们利用RPA和CRISPR Cas12b的最佳温度差异,将它们结合起来构建了一种新型的TRACER(用于CRISPR-Cas12b高效识别的热激活RPA扩增)技术。通过精确的温度调节,TRACER依次进行等温扩增和CRISPR介导的检测,同时防止模板过早切割,从而保持最佳反应效率。该平台表现出卓越的分析灵敏度,检测限为1拷贝/μL,比传统的一锅式RPA-CRISPR-Cas12a系统提高了100倍。使用195份标本进行的临床验证显示,诊断性能指标为灵敏度99.2%(119/120),特异性100.0%(75/75),准确性99.5%(194/195)。这种单管反应、可现场部署的仪器和成本效益的创新组合,使TRACER成为在各种临床环境中检测肺炎支原体的理想POCT解决方案。