Automated amplification-free digital RNA detection platform for rapid and sensitive SARS-CoV-2 diagnosis

Author:

Shinoda Hajime,Iida TatsuyaORCID,Makino Asami,Yoshimura Mami,Ishikawa Junichiro,Ando Jun,Murai Kazue,Sugiyama Katsumi,Muramoto YukikoORCID,Nakano MasahiroORCID,Kiga Kotaro,Cui Longzhu,Nureki OsamuORCID,Takeuchi Hiroaki,Noda Takeshi,Nishimasu HiroshiORCID,Watanabe RikiyaORCID

Abstract

AbstractIn the ongoing COVID-19 pandemic, rapid and sensitive diagnosis of viral infection is a critical deterrent to the spread of SARS-CoV-2. To this end, we developed an automated amplification-free digital RNA detection platform using CRISPR-Cas13a and microchamber device (opn-SATORI), which automatically completes a detection process from sample mixing to RNA quantification in clinical specimens within ~9 min. Using the optimal Cas13a enzyme and magnetic beads technology, opn-SATORI detected SARS-CoV-2 genomic RNA with a LoD of < 6.5 aM (3.9 copies μL−1), comparable to RT-qPCR. Additionally, opn-SATORI discriminated between SARS-CoV-2 variants of concern, including alpha, delta, and omicron, with 98% accuracy. Thus, opn-SATORI can serve as a rapid and convenient diagnostic platform for identifying several types of viral infections.

Funder

MEXT | Japan Science and Technology Agency

MEXT | Japan Society for the Promotion of Science

Japan Agency for Medical Research and Development

Publisher

Springer Science and Business Media LLC

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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