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An engineered CRISPR-Cas12a variant and DNA-RNA hybrid guides enable robust and rapid COVID-19 testing.
Ooi, Kean Hean; Liu, Mengying Mandy; Tay, Jie Wen Douglas; Teo, Seok Yee; Kaewsapsak, Pornchai; Jin, Shengyang; Lee, Chun Kiat; Hou, Jingwen; Maurer-Stroh, Sebastian; Lin, Weisi; Yan, Benedict; Yan, Gabriel; Gao, Yong-Gui; Tan, Meng How.
  • Ooi KH; School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore, Singapore.
  • Liu MM; Genome Institute of Singapore, Agency for Science Technology and Research, Singapore, Singapore.
  • Tay JWD; School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore, Singapore.
  • Teo SY; Genome Institute of Singapore, Agency for Science Technology and Research, Singapore, Singapore.
  • Kaewsapsak P; School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore, Singapore.
  • Jin S; Genome Institute of Singapore, Agency for Science Technology and Research, Singapore, Singapore.
  • Lee CK; School of Biological Sciences, Nanyang Technological University, Singapore, Singapore.
  • Hou J; School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore, Singapore.
  • Maurer-Stroh S; Genome Institute of Singapore, Agency for Science Technology and Research, Singapore, Singapore.
  • Lin W; School of Biological Sciences, Nanyang Technological University, Singapore, Singapore.
  • Yan B; Genome Institute of Singapore, Agency for Science Technology and Research, Singapore, Singapore.
  • Yan G; School of Biological Sciences, Nanyang Technological University, Singapore, Singapore.
  • Gao YG; Department of Laboratory Medicine, National University Hospital, National University Health System, Singapore, Singapore.
  • Tan MH; School of Computer Science and Engineering, Nanyang Technological University, Singapore, Singapore.
Nat Commun ; 12(1): 1739, 2021 03 19.
Article in English | MEDLINE | ID: covidwho-1142438
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Guide, Kinetoplastida / COVID-19 Testing / SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Prognostic study Topics: Variants Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2021 Document Type: Article Affiliation country: S41467-021-21996-6

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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Guide, Kinetoplastida / COVID-19 Testing / SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Prognostic study Topics: Variants Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2021 Document Type: Article Affiliation country: S41467-021-21996-6