Department of Electrical Engineering, Pennsylvania State University, University Park, PA 16802, United States of America.
Department of Biomedical Engineering, Pennsylvania State University, University Park, PA 16802, United States of America.
Nanotechnology. 2024 Nov 4;36(4):042001. doi: 10.1088/1361-6528/ad892b.
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.
猴痘病毒(Mpox)对全球健康构成威胁,需要快速、简单和准确的检测方法来进行有效管理,这强调了对分散式即时检测(POC)诊断解决方案的日益增长的需求。簇状规律间隔短回文重复序列(CRISPR)最初因其有效的核酸检测能力而闻名,它本身就是一种有吸引力的诊断策略。CRISPR 具有出色的灵敏度、单碱基特异性和可编程性。在这里,我们回顾了基于 CRISPR 的 POC 设备和用于 Mpox 检测的测试策略的最新进展。我们探讨了基因测序在设计用于 CRISPR 反应的 crRNA 以及理解 Mpox 传播和突变方面的关键作用。此外,我们展示了 CRISPR-Cas12 策略与预扩增和无扩增方法的整合。我们的研究还侧重于 Cas12 蛋白的重要作用以及 Cas12 与重组酶聚合酶扩增(RPA)结合用于 Mpox 检测的有效性。我们设想了未来的前景和挑战,将基于 CRISPR-Cas12 的 POC 设备定位为下一代分子生物传感技术的领跑者。