RPB0062

Pathogen Description

Target Pathogen Pathogen Name NCBI Taxonomy ID Order Family Genus Species Pathogen type
SARS-CoV-2 SARS-CoV-2, 2019-nCoV, COVID-19, COVID-19 virus, SARS2, Wuhan coronavirus, Human coronavirus 2019, COVID19, HCoV-19, SARS-2, SARS-CoV4 2697049 Nidovirales Coronaviridae Betacoronavirus Severe acute respiratory syndrome-related coronavirus virus

Primer Description

Primer Name Sequence(5'-3') Length(bp) Primer Final Concentration(μM) GC Content(%) Predicted Melting Temperature(℃) Molecular Weight(g/moles) Positions in GenBank accession number
N-F CAGCAGTAGGGGAACTTCTCCTGCTAGAATGG 32 \ 53.1 65.09 9889.47 \
N-R TGGCCTTTACCAGACATTTTGCTCAAGCTG 30 \ 46.7 62.95 9147.99 \

Gene Description

Target Gene GenBank ID
RdRp and Ngene \

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
\ \ \ 30 42 CRISPR/Cas2a 2.5 copies/ul 100 100

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2021 One-tube SARS-CoV-2 detection platform based on RT-RPA and CRISPR/Cas12a. Sun, Yangyang; Yu, Lei; Liu, Chengxi; Ye, Shanting; Chen, Wei; Li, Dechang; Huang, Weiren; 19 J Transl Med 33593370 10.1186/s12967-021-02741-5

One-tube SARS-CoV-2 detection platform based on RT-RPA and CRISPR/Cas12a.

Author(s):

Sun, Yangyang; Yu, Lei; Liu, Chengxi; Ye, Shanting; Chen, Wei; Li, Dechang; Huang, Weiren;

Journal:

19 J Transl Med

Year:

2021

Abstract:

BACKGROUND:COVID-19 has spread rapidly around the world, affecting a large percentage of the population. When lifting certain mandatory measures for an economic restart, robust surveillance must be established and implemented, with nucleic acid detection for SARS-CoV-2 as an essential component.METHODS:We tried to develop a one-tube detection platform based on RT-RPA (Reverse Transcription and Recombinase Polymerase Isothermal Amplification) and DNA Endonuclease-Targeted CRISPR Trans Reporter (DETECTR) technology, termed OR-DETECTR, to detect SARS-CoV-2. We designed RT-RPA primers of the RdRp and N genes following the SARS-CoV-2 gene sequence. We optimized reaction components so that the detection process could be carried out in one tube. Specificity was demonstrated by detecting nucleic acid samples from pseudoviruses from seven human coronaviruses and Influenza A (H1N1). Clinical samples were used to validate the platform and all results were compared to rRT-PCR. RNA standards and pseudoviruses diluted by different gradients were used to demonstrate the detection limit. Additionally, we have developed a lateral flow assay based on OR-DETECTR for detecting COVID-19.RESULTS:The OR-DETECTR detection process can be completed in one tube, which takes approximately 50min. This method can specifically detect SARS-CoV-2 from seven human coronaviruses and Influenza A (H1N1), with a low detection limit of 2.5 copies/ul input (RNA standard) and 1 copy/ul input (pseudovirus). Results of six samples from SARS-CoV-2 patients, eight samples from patients with fever but no SARS-CoV-2 infection, and one mixed sample from 40 negative controls showed that OR-DETECTR is 100% consistent with rRT-PCR. The lateral flow assay based on OR-DETECTR can be used for the detection of COVID-19, and the detection limit is 2.5 copies/ul input.CONCLUSIONS:The OR-DETECTR platform for the detection of COVID-19 is rapid, accurate, tube closed, easy-to-operate, and free of large instruments.