Author
Listed:
- Kean Hean Ooi
(Nanyang Technological University
Genome Institute of Singapore, Agency for Science Technology and Research)
- Mengying Mandy Liu
(Nanyang Technological University
Genome Institute of Singapore, Agency for Science Technology and Research)
- Jie Wen Douglas Tay
(Nanyang Technological University
Genome Institute of Singapore, Agency for Science Technology and Research
Nanyang Technological University)
- Seok Yee Teo
(Nanyang Technological University
Genome Institute of Singapore, Agency for Science Technology and Research
Nanyang Technological University)
- Pornchai Kaewsapsak
(Genome Institute of Singapore, Agency for Science Technology and Research)
- Shengyang Jin
(Nanyang Technological University)
- Chun Kiat Lee
(National University Health System)
- Jingwen Hou
(Nanyang Technological University)
- Sebastian Maurer-Stroh
(Bioinformatics Institute, Agency for Science Technology and Research)
- Weisi Lin
(Nanyang Technological University)
- Benedict Yan
(National University Health System)
- Gabriel Yan
(National University Hospital, National University Health System)
- Yong-Gui Gao
(Nanyang Technological University)
- Meng How Tan
(Nanyang Technological University
Genome Institute of Singapore, Agency for Science Technology and Research)
Abstract
Extensive testing is essential to break the transmission of SARS-CoV-2, which causes the ongoing COVID-19 pandemic. Here, we present a CRISPR-based diagnostic assay that is robust to viral genome mutations and temperature, produces results fast, can be applied directly on nasopharyngeal (NP) specimens without RNA purification, and incorporates a human internal control within the same reaction. Specifically, we show that the use of an engineered AsCas12a enzyme enables detection of wildtype and mutated SARS-CoV-2 and allows us to perform the detection step with loop-mediated isothermal amplification (LAMP) at 60-65 °C. We also find that the use of hybrid DNA-RNA guides increases the rate of reaction, enabling our test to be completed within 30 minutes. Utilizing clinical samples from 72 patients with COVID-19 infection and 57 healthy individuals, we demonstrate that our test exhibits a specificity and positive predictive value of 100% with a sensitivity of 50 and 1000 copies per reaction (or 2 and 40 copies per microliter) for purified RNA samples and unpurified NP specimens respectively.
Suggested Citation
Kean Hean Ooi & Mengying Mandy Liu & Jie Wen Douglas Tay & Seok Yee Teo & Pornchai Kaewsapsak & Shengyang Jin & Chun Kiat Lee & Jingwen Hou & Sebastian Maurer-Stroh & Weisi Lin & Benedict Yan & Gabrie, 2021.
"An engineered CRISPR-Cas12a variant and DNA-RNA hybrid guides enable robust and rapid COVID-19 testing,"
Nature Communications, Nature, vol. 12(1), pages 1-23, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21996-6
DOI: 10.1038/s41467-021-21996-6
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Citations
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Cited by:
- Santosh R. Rananaware & Emma K. Vesco & Grace M. Shoemaker & Swapnil S. Anekar & Luke Samuel W. Sandoval & Katelyn S. Meister & Nicolas C. Macaluso & Long T. Nguyen & Piyush K. Jain, 2023.
"Programmable RNA detection with CRISPR-Cas12a,"
Nature Communications, Nature, vol. 14(1), pages 1-14, December.
- Yin Liu & Xinyi Liu & Dongyi Wei & Lu Dang & Xiaoran Xu & Shisheng Huang & Liwen Li & Sanyun Wu & Jinxian Wu & Xiaoyan Liu & Wenjun Sun & Wanyu Tao & Yongchang Wei & Xingxu Huang & Kui Li & Xinjie Wan, 2024.
"CoHIT: a one-pot ultrasensitive ERA-CRISPR system for detecting multiple same-site indels,"
Nature Communications, Nature, vol. 15(1), pages 1-14, December.
- Jeong Moon & Changchun Liu, 2023.
"Asymmetric CRISPR enabling cascade signal amplification for nucleic acid detection by competitive crRNA,"
Nature Communications, Nature, vol. 14(1), pages 1-11, December.
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