4.7 Article

Rapid, Sensitive, and Specific Severe Acute Respiratory Syndrome Coronavirus 2 Detection: A Multicenter Comparison Between Standard Quantitative Reverse-Transcriptase Polymerase Chain Reaction and CRISPR-Based DETECTR

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 223, 期 2, 页码 206-213

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiaa641

关键词

COVID-19; DETECTR; qRT-PCR; SARS-CoV-2

资金

  1. Nederlands Organisatie voor Wetenschappelijk Onderzoek-Zorgonderzoek Nederland Medische Wetenschappen (NWO-ZONMW) creative solutions to battle COVID-19 Grant from the Dutch Government [5000.9954]

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Research indicates that DETECTR and qRT-PCR show similar sensitivity in detecting SARS-CoV-2, with DETECTR potentially serving as a complementary approach to qRT-PCR. DETECTR also demonstrates 100% specificity and higher analytical sensitivity, making it suitable for clinical point-of-care testing.
Background. Recent advances in CRISPR-based diagnostics suggest that DETECTR, a combination of reverse-transcriptase loop-mediated isothermal amplification (RT-LAMP) and subsequent Cas12 bystander nuclease activation by amplicon-targeting ribonucicoprotein complexes, could be a faster and cheaper alternative to quantitative reverse-transcription polymerase chain reaction (qRT-PCR) without sacrificing sensitivity and/or specificity. Methods. In this study, we compare DETECTR with qRT-PCR to diagnose coronavirus disease 2019 on 378 patient samples. Patient sample dilution assays suggest a higher analytical sensitivity of DETECTR compared with qRT-PCR; however, this was not confirmed in this large patient cohort, where we report 95% reproducibility between the 2 tests. Results. These data showed that both techniques are equally sensitive in detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) providing additional value of DETECTR to the currently used qRT-PCR platforms. For DETECTR, different guide ribonucleic acids can be used simultaneously to obviate negative results due to mutations in N-gene. Lateral flow strips, suitable as a point-of-care test, showed a 100% correlation to the high-throughput DETECTR assay. More importantly, DETECTR was 100% specific for SARS-CoV-2 relative to other human coronaviruses. Conclusions. Because there is no need for specialized equipment, DETECTR could be rapidly implemented as a complementary technically independent approach to qRT-PCR thereby increasing the testing capacity of medical microbiological laboratories and relieving the existent PCR platforms for routine non-SARS-CoV-2 diagnostic testing.

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