DNA nanoscaffold-based SARS-CoV-2 detection for COVID-19 diagnosis

被引:72
作者
Jiao, Jin [1 ]
Duan, Chengjie [1 ]
Xue, Lan [1 ]
Liu, Yunfei [1 ]
Sun, Weihao [2 ]
Xiang, Yang [1 ]
机构
[1] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
[2] Nanjing Med Univ, Dept Geriatr Gastroenterol, Affiliated Hosp 1, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA self-Assembly; DNA nanoscaffold; Isothermal amplification; RNA detection; SARS-CoV-2; ROLLING CIRCLE AMPLIFICATION;
D O I
10.1016/j.bios.2020.112479
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
COVID-19 pandemic outbreak is the most astounding scene ever experienced in the 21st century. It has been determined to be caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). With the global pandemic, the lack of efficient rapid and accurate molecular diagnostic testing tools has hindered the public opportunely response to the emerging viral threat. Herein, a DNA nanoscaffold hybrid chain reaction (DNHCR)-based nucleic acid assay strategy is reported for rapid detection of SARS-CoV-2 RNA. In this method, the DNA nanoscaffolds have been first constructed by the self-assembly of long DNA strands and self-quenching probes (H1). Then, the SARS-CoV-2 RNA will initiate the hybridization of H1 and free H2 DNA probes along the nanoscaffold, and an illuminated DNA nanostring is instantly obtained. By taking advantages of the localization design of the H1 probes and the temperature tolerance of the isothermal amplification, the proposed DNHCR method can detect target at short responding time (within 10 min) and mild condition (15 degrees C-35 degrees C). Moreover, the reliability of DNHCR method in serum and saliva samples have also been validated. Therefore, DNHCR-based method is expected to provide a simple and faster alternative to the traditional SARS-CoV-2 qRT-PCR assay.
引用
收藏
页数:7
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