检出限
病毒
核酸
病毒学
甲型流感病毒
连锁反应
寡核苷酸
聚合酶链反应
分析物
DNA–DNA杂交
病菌
DNA
生物
猝灭(荧光)
化学
分子生物学
荧光
微生物学
基因
色谱法
生物化学
光化学
物理
量子力学
作者
Mingxuan Sun,Rongtao Zhao,Yang Li,Wen Kong,Yi Yang,Xudong Guo,Wanying Liu,Hongbin Song,Zhihong Zhang,Rongzhang Hao
标识
DOI:10.16476/j.pibb.2018.0083
摘要
Rapid point-of-care (POC) detection of influenza A virus is critical for timely and effective flu prevention and control. In this study, we developed a hybridization chain reaction (HCR)-based assay, through coupling HCR reaction with fluorescence quenching by graphene oxide (GO), for the rapid detection of influenza A virus. The target is detected as it triggers HCR, which results in the extension of short DNA chains, protecting the 6-carboxy-fluorescein amidite (FAM) group from GO quenching. The results demonstrate that it could specifically recognize target nucleic acid fragment of influenza A virus from other pathogen, and even from single-base mismatched oligonucleotides. A good linear correlation between fluorescence intensity and the target concentrations ranging from 10 to 40 nmol/L was achieved, with a detection limit of 5 nmol/L. Its detection performance was verified on nasopharyngeal swab samples, which is the first clinical application of HCR-based influenza assay. This HCR-based method shows many advantages including the enzyme-free amplification of nucleic acids, simple reaction system and convenient protocols, suggesting its availability for POC detection
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