Enhanced Isothermal Amplification for Ultrafast Sensing of SARS-CoV-2 in Microdroplets

被引:21
|
作者
Zhou, Mengyun [1 ]
Fan, Chuan [1 ]
Wang, Lirong [1 ]
Xu, Tailin [1 ]
Zhang, Xueji [1 ]
机构
[1] Shenzhen Univ, Hlth Sci Ctr, Sch Biomed Engn, Guangdong Key Lab Biomed Measurements & Ultrasoun, Shenzhen 518060, Guangdong, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
RECOMBINASE POLYMERASE AMPLIFICATION; SENSITIVE DETECTION; ASSAY; POINT;
D O I
10.1021/acs.analchem.2c00008
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Rapid and high-throughput screening is critical to control the COVID-19 pandemic. Recombinase polymerase amplification (RPA) with highly accessible and sensitive nucleic acid amplification has been widely used for point-of-care infection diagnosis. Here, we report an integrated microdroplet array platform composed of an ultrasonic unit and minipillar array to enhance the RPA for ultrafast, high-sensitivity, and high-throughput detection of SARS-CoV-2. On such a platform, the independent microvolume reactions on individual minipillars greatly decrease the consumption of reagents. The microstreaming driven by ultrasound creates on-demand contactless microagitation in the microdroplets and promotes the interaction between RPA components, thus greatly accelerating the amplification. In the presence of microstreaming, the detection time is 6-12 min, which is 38.8-59.3% shorter than that of controls without microstreaming, and the end-point fluorescence intensity also increased 1.3-1.7 times. Furthermore, the microagitation-enhanced RPA also exhibits a lower detection limit (0.42 copy/mu L) for SARS-CoV-2 in comparison to the controls. This integrated microdroplet array detection platform is expected to meet the needs for high-throughput nucleic acid testing (NAT) to improve the containment of viral transmission during the epidemic, as well as provide a potential platform for the timely detection of other pathogens or viruses.
引用
收藏
页码:4135 / 4140
页数:6
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