多路复用
环介导等温扩增
病毒学
放大器
假阳性悖论
计算生物学
核酸扩增试验
检出限
分子信标
生物
甲型流感病毒
病毒
化学
聚合酶链反应
沙眼衣原体
DNA
计算机科学
基因
生物信息学
遗传学
色谱法
寡核苷酸
机器学习
作者
Xingyu Ye,Haiwei Zhou,Xiang Guo,Donglai Liu,Zhonglei Li,Junwei Sun,Juntong Huang,Tao Liu,Pengshu Zhao,Huiqin Xu,Kai Li,Hanming Wang,Jihua Wang,Li Wang,Weili Zhao,Qian Liu,Sihong Xu,Yan Feng
标识
DOI:10.1016/j.bios.2022.114169
摘要
Isothermal amplification methods are a promising trend in virus detection because of their superiority in rapidity and sensitivity. However, the generation of false positives and limited multiplexity are major bottlenecks that must be addressed. In this study, we developed a multiplex Argonaute (Ago)-based nucleic acid detection system (MULAN) that integrates rapid isothermal amplification with the multiplex inclusiveness of a single Ago for simultaneous detection of multiple targets such as SARS-CoV-2 and influenza viruses. Owing to its high specificity, MULAN can distinguish targets at a single-base resolution for mutant genotyping. Moreover, MULAN also supports portable and visible devices with a limit of detection of five copies per reaction. Validated by SARS-CoV-2 pseudoviruses and clinical samples of influenza viruses, MULAN showed 100% agreement with quantitative reverse-transcription PCR. These results demonstrated that MULAN has great potential to facilitate reliable, easy, and quick point-of-care diagnosis for promoting the control of infectious diseases.
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