Ultrasensitive and Specific Clustered Regularly Interspaced Short Palindromic Repeats Empowered a Plasmonic Fiber Tip System for Amplification-Free Monkeypox Virus Detection and Genotyping
清脆的
基因分型
聚合酶链反应
生物
病毒学
计算生物学
遗传学
基因
基因型
作者
Yuzhi Chen,Zhi Chen,Tianzhong Li,Minli Qiu,Jinghan Zhang,Yan Wang,Wu Yuan,Ho‐Pui Ho,Omar A. Al‐Hartomy,S. Wageh,Abdullah G. Al‐Sehemi,Xiujuan Shi,Jing‐Feng Li,Zhongjian Xie,Xuejin Li,Han Zhang
出处
期刊:ACS Nano [American Chemical Society] 日期:2023-06-29卷期号:17 (13): 12903-12914被引量:24
The urgent necessity for highly sensitive diagnostic tools has been accentuated by the ongoing mpox (monkeypox) virus pandemic due to the complexity in identifying asymptomatic and presymptomatic carriers. Traditional polymerase chain reaction-based tests, despite their effectiveness, are hampered by limited specificity, expensive and bulky equipment, labor-intensive operations, and time-consuming procedures. In this study, we present a clustered regularly interspaced short palindromic repeats (CRISPR)/Cas12a-based diagnostic platform with a surface plasmon resonance-based fiber tip (CRISPR-SPR-FT) biosensor. The compact CRISPR-SPR-FT biosensor, with a 125 μm diameter, offers high stability and portability, enabling exceptional specificity for mpox diagnosis and precise identification of samples with a fatal mutation site (L108F) in the F8L gene. The CRISPR-SPR-FT system can analyze viral double-stranded DNA from mpox virus without amplification in under 1.5 h with a limit of detection below 5 aM in plasmids and about 59.5 copies/μL when in pseudovirus-spiked blood samples. Our CRISPR-SPR-FT biosensor thus offers fast, sensitive, portable, and accurate target nucleic acid sequence detection.