Li Tianzhong, Chen Yuzhi, Chen Zhi, Hao Yuan, Liang Minyi, Liu Yingxia, Ou Guanyong, Zhang Huanian, Tang Yuxuan, Hao Yabing, Wageh Swelm, Al-Hartomy Omar A, Kalam Abul, Zhang Bin, Shi Xin, Li Xuejin, Zhang Han
College of Physics and Optoelectronic Engineering, Institute of Translational Medicine, Department of Otolaryngology, Shenzhen Second People's Hospital, First Affiliated Hospital of Shenzhen University, Health Science Center, Shenzhen University, Shenzhen 518060, China.
Shenzhen Key Laboratory of Sensor Technology, Shenzhen 518060, China.
Research (Wash D C). 2023 Jul 28;6:0205. doi: 10.34133/research.0205. eCollection 2023.
Infectious diseases severely threaten public health and global biosafety. In addition to transmission through the air, pathogenic microorganisms have also been detected in environmental liquid samples, such as sewage water. Conventional biochemical detection methodologies are time-consuming and cost-ineffective, and their detection limits hinder early diagnosis. In the present study, ultrafine plasmonic fiber probes with a diameter of 125 μm are fabricated for clustered regularly interspaced short palindromic repeats/CRISPR-associated protein (CRISPR/Cas)-12a-mediated sensing of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Single-stranded DNA exposed on the fiber surface is trans-cleaved by the Cas12a enzyme to release gold nanoparticles that are immobilized onto the fiber surface, causing a sharp reduction in the surface plasmon resonance (SPR) wavelength. The proposed fiber probe is virus-specific with the limit of detection of ~2,300 copies/ml, and genomic copy numbers can be reflected as shifts in wavelengths. A total of 21 sewage water samples have been examined, and the data obtained are consistent with those of quantitative polymerase chain reaction (qPCR). In addition, the Omicron variant and its mutation sites have been fast detected using S gene-specific Cas12a. This study provides an accurate and convenient approach for the real-time surveillance of microbial contamination in sewage water.
传染病严重威胁着公众健康和全球生物安全。除了通过空气传播外,在环境液体样本(如污水)中也检测到了致病微生物。传统的生化检测方法耗时且成本效益低,其检测限阻碍了早期诊断。在本研究中,制备了直径为125μm的超细等离子体光纤探针,用于基于成簇规律间隔短回文重复序列/CRISPR相关蛋白(CRISPR/Cas)-12a介导的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)传感。暴露在光纤表面的单链DNA被Cas12a酶反式切割,释放出固定在光纤表面的金纳米颗粒,导致表面等离子体共振(SPR)波长急剧降低。所提出的光纤探针具有病毒特异性,检测限约为2300拷贝/毫升,基因组拷贝数可通过波长变化反映出来。共检测了21份污水样本,获得的数据与定量聚合酶链反应(qPCR)的数据一致。此外,使用S基因特异性Cas12a快速检测了奥密克戎变体及其突变位点。本研究为污水中微生物污染的实时监测提供了一种准确、便捷的方法。