多路复用
计算生物学
核酸检测
核酸
分子诊断学
传染病(医学专业)
周转时间
病毒学
爆发
核糖核酸
病菌
诊断试验
化学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
多重聚合酶链反应
检测点注意事项
甲型流感病毒
大流行性流感
广谱
2019年冠状病毒病(COVID-19)
纳米技术
病毒
作者
Hajime Shinoda,Asami Makino,Mami Yoshimura,Noriko Minagawa,Tatsuya Iida,Masahiro Nakano,Takeshi Noda,Masashi Toyoda,Rikiya Watanabe
标识
DOI:10.1021/acs.analchem.5c06305
摘要
The COVID-19 pandemic and recurring outbreaks of infectious diseases underscore the urgent demand for multiplex diagnostics capable of rapid and accurate pathogen identification. Although multiplex nucleic acid amplification tests (NAATs) are widely used for diagnosing diverse infectious diseases, their inherent amplification bias and long turnaround times highlight the demand for faster and reliable alternatives. Here, we present multicolor SATORI (mSATORI), an amplification-free single-molecule genetic test that leverages the complementary activities of CRISPR-Cas13a and Cas13b to achieve simultaneous detection of dual RNA targets. mSATORI identified Influenza A and SARS-CoV-2 RNAs within ∼10 min, with analytical limits of detection (LoD) of 86 aM and 52 aM, respectively. Validation using clinical specimens demonstrated robust diagnostic performance, achieving femtomolar limits of detection (550 aM for Influenza A and 640 aM for SARS-CoV-2), along with sensitivities exceeding 80% and specificities of 100%. Collectively, these results establish mSATORI as a platform for next-generation molecular diagnostics, with broad implications for clinical implementation, outbreak preparedness, and global infectious disease surveillance.
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