清脆的
计算生物学
计算机科学
跟踪(心理语言学)
病毒学
生物
大流行
寄主(生物学)
翻译(生物学)
2019年冠状病毒病(COVID-19)
基因组
DNA
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
灵敏度(控制系统)
基因
极限(数学)
检出限
病毒
作者
Huang Zhen,Yajuan Dong,Yang Yang,Xuchun Han,Fuxiang Wang,Christopher J. Lyon,Shuai Ding,Yun Peng,Ganggang Zhang,Christina Hu,Huan Huang,Liu, Yang,Guoping Zhao,Xiao-Yong Fan,Shuihua Lu,Tony Hu,Jin Wang
标识
DOI:10.1038/s41467-025-65193-1
摘要
The ongoing monkeypox virus outbreak highlights the need for rapid and accurate diagnostics to enhance epidemic control. CRISPR-based assays hold promise, but clinical translation is hindered by high complexity and low throughput. Here, we describe a thermally regulated asynchronous CRISPR-enhanced (TRACE) assay that rapidly and sensitively detects multiple DNA targets in a streamlined, one-pot format. TRACE exhibits a 2.5 copies/test limit of detection - 40 times lower than a canonical one-pot CRISPR. When applied to clinical samples, it achieves 99.5% accuracy across diverse sample types, and can detect MPXV within 11 minutes. Point-of-care TRACE assays meet ASSURED criteria and deliver comparable performance to qPCR, with a fivefold reduced report time, in outpatient settings. Moreover, TRACE enables simultaneous detection of pathogen and host genes at comparable sensitivity to address a critical limitation of current CRISPR assays, which lack internal controls. TRACE thus enables rapid, on-site surveillance to facilitate bench-to-bedside translation of CRISPR diagnostics.
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