Suppr超能文献

用于耐甲氧西林的快速单管RPA-CRISPR/Cas12检测平台

Rapid One-Tube RPA-CRISPR/Cas12 Detection Platform for Methicillin-Resistant .

作者信息

Li Yanan, Shi Zhonglin, Hu Anzhong, Cui Junsheng, Yang Ke, Liu Yong, Deng Guoqing, Zhu Cancan, Zhu Ling

机构信息

Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei 230031, China.

Science Island Branch of Graduate School, University of Science and Technology of China, Hefei 230026, China.

出版信息

Diagnostics (Basel). 2022 Mar 28;12(4):829. doi: 10.3390/diagnostics12040829.

Abstract

Methicillin-resistant (MRSA) is a severe health threat causing high-level morbidity and mortality in health care environments and in community settings. Though existing diagnostic methods, including PCR and culture-based methods, are routinely used in clinical practice, they are not appropriate for rapid point-of-care testing (POCT). Recently, since the development of the CRISPR/Cas technology, new possibilities for rapid point-of-care detection have emerged. In this study, we developed a rapid, accurate, and contamination-free platform for MRSA detection by integrating recombinase polymerase amplification (RPA) with the Cas12 system into one tube. Using this approach, visual MRSA detection could be achieved in 20 min. Based on the one-tube RPA-CRISPR/Cas12a platform, the assay results are visualized by lateral flow test strips (LFS) and fluorescent-based methods, including real-time and end-point fluorescence. This platform allows specific MRSA detection with a sensitivity of 10 copies for the fluorescence method and a range of 10-100 copies for the LFS. The results of 23 samples from clinical MRSA isolates showed that the coincidence rate was 100% and 95.7% of the fluorescence method and LFS, respectively, compared to qPCR. In conclusion, the one-tube RPA-CRISPR/Cas12a platform is an effective method for MRSA detection with significant potential in future practical POCT applications.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)是一种严重的健康威胁,在医疗环境和社区环境中都会导致高发病率和死亡率。尽管包括聚合酶链式反应(PCR)和基于培养的方法在内的现有诊断方法在临床实践中经常使用,但它们并不适用于快速即时检测(POCT)。最近,自CRISPR/Cas技术发展以来,快速即时检测出现了新的可能性。在本研究中,我们通过将重组酶聚合酶扩增(RPA)与Cas12系统整合到一个试管中,开发了一种用于MRSA检测的快速、准确且无污染的平台。使用这种方法,20分钟内即可实现MRSA的可视化检测。基于单管RPA-CRISPR/Cas12a平台,检测结果通过侧向流动试纸条(LFS)和基于荧光的方法(包括实时荧光和终点荧光)进行可视化。该平台能够特异性检测MRSA,荧光法的灵敏度为10个拷贝,LFS的灵敏度范围为10 - 100个拷贝。来自临床MRSA分离株的23个样本结果显示,与定量PCR相比,荧光法和LFS的符合率分别为100%和95.7%。总之,单管RPA-CRISPR/Cas12a平台是一种有效的MRSA检测方法,在未来实际POCT应用中具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/068f/9028452/9c3d339c0f7c/diagnostics-12-00829-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验