Topologically constrained DNA-mediated one-pot CRISPR assay for rapid detection of viral RNA with single nucleotide resolution.

IF 10.8 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL EBioMedicine Pub Date : 2025-02-01 Epub Date: 2025-01-24 DOI:10.1016/j.ebiom.2025.105564
Yanan Li, Ru Xu, Fenglei Quan, Yonghua Wu, Yige Wu, Yongyuan Zhang, Yan Liang, Zhenzhong Zhang, Hua Gao, Ruijie Deng, Kaixiang Zhang, Jinghong Li
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Abstract

Background: The widespread and evolution of RNA viruses, such as the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), highlights the importance of fast identification of virus subtypes, particularly in non-laboratory settings. Rapid and inexpensive at-home testing of viral nucleic acids with single-base resolution remains a challenge.

Methods: Topologically constrained DNA ring is engineered as substrates for the trans-cleavage of Cas13a to yield an accelerated post isothermal amplification. The capacity of CRISPR/Cas13a for discriminating single nucleotide variant (SNV) in viral genome is leveraged by designing synthetic mismatches and hairpin structure in CRISPR RNA (crRNA), enabling robust discrimination of different SARS-CoV-2 variants. Via optimisation of CasTDR3pot to be one-pot assay, CasTDR1pot can detect Omicron and its subvariants, with only a few copies in clinical samples in less than 30 min without pre-amplification.

Findings: The detection system boasts high sensitivity (0.1 aM), single-base specificity, and the advantage of a rapid "sample-to-answer" process, which takes only 30 min. In the detection of SARS-CoV-2 clinical samples and their variant strains, CasTDR1pot has achieved 100% accuracy. Furthermore, the design of a portable signal-reading device facilitates user-friendly result interpretation. For the detection needs of different RNA viruses, the system can be adapted simply by designing the corresponding crRNA.

Interpretation: Our study provides a rapid and accurate molecular diagnostic tool for point-of-care testing, epidemiological screening, and the detection of diseases associated with other RNA biomarkers with excellent single nucleotide differentiation, high sensitivity, and simplicity.

Funding: National Key Research and Development Program of China (No. 2023YFB3208302), National Natural Science Foundation of China (No. 22377110, 22034004, 82402749, 82073787, 22122409), National Key Research and Development Program of China (No. 2021YFA1200104), Henan Province Fund for Cultivating Advantageous Disciplines (No. 222301420019).

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拓扑约束dna介导的单锅CRISPR快速检测病毒RNA的单核苷酸分辨率。
背景:RNA病毒,如严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的广泛传播和进化,突出了快速识别病毒亚型的重要性,特别是在非实验室环境中。快速和廉价的病毒核酸单碱基分辨率的家庭测试仍然是一个挑战。方法:拓扑约束的DNA环作为Cas13a反式切割的底物,以产生加速的等温后扩增。CRISPR/Cas13a通过设计CRISPR RNA (crRNA)的合成错配和发夹结构,利用CRISPR/Cas13a识别病毒基因组中单核苷酸变体(SNV)的能力,实现对不同SARS-CoV-2变体的稳健区分。通过将CasTDR3pot优化为单锅法,无需预扩增,CasTDR1pot可以在不到30分钟的时间内检测到临床样品中仅有少量拷贝的Omicron及其亚变体。结果:检测系统灵敏度高(0.1 aM),单碱基特异性强,具有快速“从样品到答案”的优势,仅需30 min。在SARS-CoV-2临床样本及其变异菌株的检测中,CasTDR1pot达到100%的准确率。此外,便携式信号读取装置的设计便于用户友好的结果解释。针对不同RNA病毒的检测需求,只需设计相应的crRNA即可对该系统进行简单适配。解释:我们的研究提供了一种快速准确的分子诊断工具,用于即时检测、流行病学筛查,以及与其他RNA生物标志物相关的疾病检测,具有出色的单核苷酸分化、高灵敏度和简单性。资助项目:国家重点研发计划项目(No. 2023YFB3208302),国家自然科学基金项目(No. 22377110, 22034004, 82402749, 82073787, 22122409),国家重点研发计划项目(No. 2021YFA1200104),河南省优势学科培育基金项目(No. 222301420019)。
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来源期刊
EBioMedicine
EBioMedicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
17.70
自引率
0.90%
发文量
579
审稿时长
5 weeks
期刊介绍: eBioMedicine is a comprehensive biomedical research journal that covers a wide range of studies that are relevant to human health. Our focus is on original research that explores the fundamental factors influencing human health and disease, including the discovery of new therapeutic targets and treatments, the identification of biomarkers and diagnostic tools, and the investigation and modification of disease pathways and mechanisms. We welcome studies from any biomedical discipline that contribute to our understanding of disease and aim to improve human health.
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