Digital RT-PCR Chip method for detection of SARS-CoV-2 virus

被引:4
|
作者
Dioni, Laura [1 ]
Orlandi, Annarosa [2 ]
Renteria, Sara Uceda [2 ]
Favero, Chiara [1 ]
Solazzo, Giulia [1 ]
Oggioni, Massimo [2 ]
Bollati, Valentina [1 ,3 ]
机构
[1] Univ Milan, Dept Clin Sci & Community Hlth, EPIGET Lab, Milan, Italy
[2] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Virol Unit, Milan, Italy
[3] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Occupat Hlth Unit, Milan, Italy
关键词
UNICORN; SARS-CoV-2; Digital RT-PCR; Chip; Viral load;
D O I
10.1016/j.jim.2022.113339
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The "gold standard" method for detection of SARS-CoV-2 is the real time reverse transcription-polymerase chain reaction, but due to pre-analytical and technical limitations, biological samples with low viral load are not sometimes detected. For this purpose a digital RT-PCR method on-chip was developed for detection of the SARS-CoV-2 virus, using two TaqMan T Assays for quantification of the N Protein (Nucleocapsid) and the S Protein (Spike), and the QuantStudio T 3D Digital PCR instrument. The method was applied to assess the nasopharyngeal swabs of asymptomatic subjects recruited in the UNICORN Study. The digital RT-PCR method is characterized by a higher sensitivity than the RT-qPCR method, even if performed with the same TaqMan T, and could be a promising tool for SARS-CoV-2 viral load quantification.
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页数:4
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