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用于快速即时检测琅琊亨尼帕病毒的辣根过氧化物酶整合型CRISPR-Cas12a生物传感器

HRP-integrated CRISPR-Cas12a biosensor for rapid point-of-care detection of Langya henipavirus.

作者信息

Wu Xuan, Xiang Rong, Yang Danting, He Xiaoyao, Zhu Lu, Sun Fangfang, Li Hanqing, Pi Ningning, Li Yi

机构信息

Key Laboratory of Environmental Chemistry and Ecotoxicology of Organic Pollutants of Chongqing, Ecological and Environment Monitoring Center of Chongqing, 252 Qishan Road, Chongqing 401132, China.

Hospital/School of Stomatology, Zunyi Medical University, 143 Dalian Road, Zunyi, Guizhou 563006, China.

出版信息

iScience. 2024 Nov 23;27(12):111466. doi: 10.1016/j.isci.2024.111466. eCollection 2024 Dec 20.

Abstract

Global pandemic has emphasized the needs for advanced pathogen diagnosis in dealing with newly emerged infectious threats, including the Langya henipavirus (LayV). LayV, as an emerging zoonotic pathogen, has potential to cause pandemic, but lacks of rapid diagnostic tools, particularly at point-of-care level. Here, we leveraged the merits of CRISPR-Cas12a biosensing and established a highly sensitive LayV detection method. By integrating CRISPR-Cas12a with RPA, 10 copies/μL ultra-sensitive LayV RNA detection has been achieved at room temperature within 30 min. More importantly, this study developed a special horseradish peroxidase (HRP)-single-stranded DNA (ssDNA) reporter enabling CRISPR-Cas12a to detect LayV RNA without pre-amplification, achieving a sensitivity of 1,200 copies/μL detectable by the naked eye. These explorations can serve as accelerator for CRISPR-Cas biosensing toward rapid response for newly emerged biological threats, and also provide a method to realize simple, precise, and amplicon-free point-of-care pathogen screening for resource limited or underdevelopment regions.

摘要

全球大流行凸显了在应对新出现的传染病威胁(包括琅琊亨尼帕病毒(LayV))时对先进病原体诊断的需求。LayV作为一种新出现的人畜共患病原体,有可能引发大流行,但缺乏快速诊断工具,尤其是在即时检测层面。在此,我们利用CRISPR-Cas12a生物传感的优点,建立了一种高灵敏度的LayV检测方法。通过将CRISPR-Cas12a与RPA相结合,在室温下30分钟内实现了10拷贝/μL的超灵敏LayV RNA检测。更重要的是,本研究开发了一种特殊的辣根过氧化物酶(HRP)-单链DNA(ssDNA)报告分子,使CRISPR-Cas12a能够在无需预扩增的情况下检测LayV RNA,实现了肉眼可检测的1200拷贝/μL的灵敏度。这些探索可作为CRISPR-Cas生物传感应对新出现的生物威胁快速响应的加速器,也为资源有限或欠发达地区实现简单、精确且无扩增的即时病原体筛查提供了一种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e33c/11697611/3e8436388d49/fx1.jpg

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