Digital Microfluidic Multiplex RT-qPCR for SARS-CoV-2 Detection and Variants Discrimination

被引:2
作者
Ho, Kuan-Lun [1 ]
Ding, Jing [1 ]
Fan, Jia-Shao [2 ]
Tsui, Wai Ning Tiffany [3 ]
Bai, Jianfa [3 ,4 ]
Fan, Shih-Kang [1 ]
机构
[1] Kansas State Univ, Dept Mech & Nucl Engn, Manhattan, KS 66506 USA
[2] Kansas State Univ, Dept Elect & Comp Engn, Manhattan, KS 66506 USA
[3] Kansas State Univ, Kansas State Vet Diagnost Lab, Manhattan, KS 66506 USA
[4] Kansas State Univ, Dept Diagnost Med Pathobiol, Manhattan, KS 66506 USA
关键词
SARS-CoV-2; COVID-19; Delta variant; Omicron variant; RT-qPCR; digital microfluidics; electrowetting; POINT; PCR;
D O I
10.3390/mi14081627
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Continuous mutations have occurred in the genome of the SARS-CoV-2 virus since the onset of the COVID-19 pandemic. The increased transmissibility of the mutated viruses has not only imposed medical burdens but also prolonged the duration of the pandemic. A point-of-care (POC) platform that provides multitarget detection will help to track and reduce disease transmissions. Here we detected and discriminated three genotypes of SARS-CoV-2, including the wildtype and two variants of concern (VOCs), the Delta variant and Omicron variant, through reverse transcription quantitative polymerase chain reaction (RT-qPCR) on a digital microfluidics (DMF)-based cartridge. Upon evaluating with the RNA samples of Omicron variant, the DMF RT-qPCR presented a sensitivity of 10 copies/mu L and an amplification efficiency of 96.1%, capable for clinical diagnosis. When spiking with SARS-CoV-2 RNA (wildtype, Delta variant, or Omicron variant) and 18S rDNA, the clinical analog samples demonstrated accurate detection and discrimination of different SARS-CoV-2 strains in 49 min.
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页数:11
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