CRISPR-Cas12-based field-deployable system for rapid detection of synthetic DNA sequence of the monkeypox virus genome

被引:46
作者
Chen, Qun [1 ,2 ]
Gul, Ijaz [1 ,2 ]
Liu, Changyue [1 ,2 ]
Lei, Zhengyang [1 ,2 ]
Li, Xingyu
Raheem, Muhammad A. [1 ,2 ,3 ]
He, Qian [1 ,2 ]
Zhang Haihui [1 ,2 ]
Leeansyah, Edwin [1 ,2 ]
Zhang, Can Y. [1 ,2 ]
Pandey, Vijay [1 ,2 ]
Du, Ke [4 ]
Qin, Peiwu [1 ,2 ]
机构
[1] Tsinghua Univ, Tsinghua Shenzhen Int Grad Sch, Inst Biopharmaceut & Hlth Engn, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Tsinghua Berkeley Shenzhen Inst, Tsinghua Shenzhen Int Grad Sch, Shenzhen, Peoples R China
[3] Cent South Univ, Dept Hepatobiliary & Pancreat Surg 2, Xiangya Hosp 3, Changsha, Hunan, Peoples R China
[4] Univ Calif Riverside, Dept Chem & Environm Engn, Riverside, CA 92521 USA
基金
中国国家自然科学基金;
关键词
CRISPR-Cas12a; detection; monkeypox endemic; monkeypox virus; recombinase polymerase amplification; VARIOLA; ASSAY;
D O I
10.1002/jmv.28385
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The global outbreak of the monkeypox virus (MPXV) highlights the need for rapid and cost-effective MPXV detection tools to effectively monitor and control the monkeypox disease. Herein, we demonstrated a portable CRISPR-Cas-based system for naked-eye detection of MPXV. The system harnesses the high selectivity of CRISPR-Cas12 and the isothermal nucleic acid amplification potential of recombinase polymerase amplification. It can detect both the current circulating MPXV clade and the original clades. We reached a limit of detection (LoD) of 22.4aM (13.5copies/mu l) using a microtiter plate reader, while the visual LoD of the system is 75aM (45copies/mu l) in a two-step assay, which is further reduced to 25aM (15copies/mu l) in a one-pot system. We compared our results with quantitative polymerase chain reaction and obtained satisfactory consistency. For clinical application, we demonstrated a sensitive and precise visual detection method with attomolar sensitivity and a sample-to-answer time of 35min.
引用
收藏
页数:11
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