Biosensor‐based multiple cross displacement amplification platform for visual and rapid identification of hepatitis C virus

病毒学 丙型肝炎病毒 检出限 病毒 生物 环介导等温扩增 分子生物学 化学 色谱法 DNA 遗传学
作者
Xu Chen,Shilei Dong,Yuanfang Shi,Zengguang Wu,Xue Wu,Xiaoyan Zeng,Xinggui Yang,Qi Zhao,Zhenghua Xiao,Qingxue Zhou
出处
期刊:Journal of Medical Virology [Wiley]
卷期号:96 (3): e29481-e29481 被引量:4
标识
DOI:10.1002/jmv.29481
摘要

Hepatitis C remains a global health problem, especially in poverty-stricken areas. A rapid and sensitive point-of-care (POC) diagnostic tool is critical for the early detection and timely treatment of hepatitis C virus (HCV) infection. Here, for the first time, we reported a novel molecular diagnostic assay, termed reverse transcription multiple cross displacement amplification integrated with a gold-nanoparticle-based lateral flow biosensor (RT-MCDA-AuNPs-LFB), which was developed for rapid, sensitive, specific, and visual identification of HCV. HCV-RT-MCDA induced rapid isothermal amplification through a specific primer set targeting the 5'untranslated region gene from the major HCV genotypes 1b, 2a, 3b, 6a, and 3a that are prevalent in China. The optimal reaction temperature and time for RT-MCDA-AuNPs-LFB were 68°C and 25 min, respectively. The limit of detection of the assay was 10 copies per test, and the specificity was 100% for the experimental strains. The whole detection procedure, including crude nucleic acid isolation (~5 min), RT-MCDA (68°C, 25 min), and visual AuNPs-LFB result confirmation (less than 2 min), was performed within 35 min. The preliminary results indicated that the HCV-RT-MCDA-AuNPs-LFB assay could be a valuable tool for sensitive, specific, visual, cost-saving, and rapid detection of HCV and has potential as a POC diagnostic platform for field screening and early clinical detection of HCV infection.
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