CRISPR-based strategies for sample-to-answer monkeypox detection: current status and emerging opportunities

被引:2
作者
Ahamed, Md Ahasan [1 ]
Politza, Anthony J. [2 ]
Liu, Tianyi [1 ]
Khalid, Muhammad Asad Ullah [1 ]
Zhang, Huanshu [1 ]
Guan, Weihua [1 ,2 ]
机构
[1] Penn State Univ, Dept Elect Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Biomed Engn, University Pk, PA 16802 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
monkeypox; nucleic acid; CRISPR; Cas12; RPA; point-of-care; TIME PCR ASSAYS; VIRUS DETECTION; DIFFERENTIATION; DIAGNOSTICS; SMALLPOX; VARIOLA;
D O I
10.1088/1361-6528/ad892b
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The global health threat posed by the Monkeypox virus (Mpox) requires swift, simple, and accurate detection methods for effective management, emphasizing the growing necessity for decentralized point-of-care (POC) diagnostic solutions. The clustered regularly interspaced short palindromic repeats (CRISPR), initially known for its effective nucleic acid detection abilities, presents itself as an attractive diagnostic strategy. CRISPR offers exceptional sensitivity, single-base specificity, and programmability. Here, we reviewed the latest developments in CRISPR-based POC devices and testing strategies for Mpox detection. We explored the crucial role of genetic sequencing in designing crRNA for CRISPR reaction and understanding Mpox transmission and mutations. Additionally, we showed the integration of CRISPR-Cas12 strategy with pre-amplification and amplification-free methods. Our study also focused on the significant role of Cas12 proteins and the effectiveness of Cas12 coupled with recombinase polymerase amplification (RPA) for Mpox detection. We envision the future prospects and challenges, positioning CRISPR-Cas12-based POC devices as a frontrunner in the next generation of molecular biosensing technologies.
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页数:21
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