Development of a single-tube RPA/CRISPR-cas12a detection platform for monkeypox virus

被引:0
|
作者
Liu, Shan [1 ]
Yang, Yang [2 ]
Li, Xue [3 ,4 ]
Choi, Jeong-Woo [5 ]
Guo, Jinhong [6 ]
Luo, Hongzhi [7 ]
Li, Chenzhong [3 ,4 ,8 ]
机构
[1] Univ Elect Sci & Technol China, Sichuan Acad Med Sci & Sichuan Prov Peoples Hosp, Dept Med Genet, Sichuan Prov Key Lab Human Dis Gene Study, Chengdu 610072, Peoples R China
[2] Southern Univ Sci & Technol, Shenzhen Key Lab Pathogen & Immun, Shenzhen Clin Res Ctr Infect Dis, Shenzhen Peoples Hosp 3,Hosp 2, Shenzhen 518112, Guangdong, Peoples R China
[3] Tianfu Jincheng Lab, City Future Med, Chengdu 641400, Peoples R China
[4] Juxintang Chengdu Biotechnol Co Ltd, Chengdu 641400, Peoples R China
[5] Sogang Univ, Dept Chem & Biomol Engn, Seoul 04107, South Korea
[6] Shanghai Jiao Tong Univ, Sch Sensing Sci & Engn, Shanghai 200240, Peoples R China
[7] Sichuan Univ, Jintang Peoples Hosp 1, Dept Expt Med, West China Hosp,JinTang Hosp, Chengdu 610400, Peoples R China
[8] Chinese Univ Hong Kong, Sch Med, Biomed Engn, Shenzhen 518172, Peoples R China
来源
BIOSENSORS & BIOELECTRONICS | 2025年 / 278卷
基金
中国国家自然科学基金;
关键词
Monkeypox; Point-of-care testing; CRISPR-Cas12a; Recombinase polymerase amplification; Single-tube assay; VARIOLA;
D O I
10.1016/j.bios.2025.117221
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Monkeypox is a zoonotic disease caused by the monkeypox virus (MPXV), with outbreaks primarily occurring in West and Central Africa. The recent global MPXV outbreak underscores the urgent need for effective detection methods. Currently, qPCR is considered the gold standard for MPXV detection; however, it requires specialized personnel and costly equipment. This study introduces a CRISPR-Cas12a-based detection system targeting the MPXV A27L gene, achieving a detection limit as low as 10 aM. This system exhibits high specificity, with no cross-reactivity with other orthopoxviruses, and delivers results in under 40 min. To support point-of-care testing (POCT), we developed a lateral flow assay (LFA) strip for easy result visualization. The detection system was validated using six different clinical sample types, revealing that herpes fluid and saliva are the most suitable sources. The findings of this study align with qPCR results. Additionally, we lyophilized the RPA and CRISPR reagents to improve transport, storage, and field deployment. In conclusion, this study presents a reliable molecular diagnostic approach for early MPXV detection and point-of-care testing, contributing to epidemic prevention and control.
引用
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页数:10
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