RPB0399

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
FP CCTACGGGTCTGTATCACGAGCAAGCGGC 29 0.32 μM 62.07 68.79 8903.82 28,274-29,533
RP CGTAGCTGTCGAGCGCATCATTTTTGGAG 29 0.32 μM 51.72 63.75 8939.84 28,274-29,533

Gene Description

Target Gene GenBank ID
N gene \

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
highly sensitive and specific one-tube, rapid (30 min), and visual detection of nucleic acids. RPA-CRISPR\Cas12 \ 30 min 37°C CRISPR\Cas12 0.2 copies/μL of DNA and 0.4 copies/μL of RNA \ \

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2023 Fast and visual detection of nucleic acids using a one-step RPA-CRISPR detection (ORCD) system unrestricted by the PAM Kangfeng Lin,Jianguang Guo,Xiangju Guo,Qinghan Li,Xiao Li,Zhen Sun,Zehang Zhao,Jiao Weng,Jinzhun Wu,Rui Zhang,Boan Li Analytica Chimica Acta 36813457 10.1016/j.aca.2023.340938

Fast and visual detection of nucleic acids using a one-step RPA-CRISPR detection (ORCD) system unrestricted by the PAM

Author(s):

Kangfeng Lin,Jianguang Guo,Xiangju Guo,Qinghan Li,Xiao Li,Zhen Sun,Zehang Zhao,Jiao Weng,Jinzhun Wu,Rui Zhang,Boan Li

Journal:

Analytica Chimica Acta

Year:

2023

Abstract:

CRISPR-Cas12a (Cpf1) is widely used for pathogen detection. However, most Cas12a nucleic acid detection methods are limited by a PAM sequence requirement. Moreover, preamplification and Cas12a cleavage are separate. Here, we developed a one-step RPA-CRISPR detection (ORCD) system unrestricted by the PAM sequence with high sensitivity and specificity that offers one-tube, rapid, and visually observable detection of nucleic acids. In this system, Cas12a detection and RPA amplification are performed simultaneously, without separate preamplification and product transfer steps, and 0.2 copies/μL of DNA and 0.4 copies/μL of RNA can be detected. In the ORCD system, the activity of Cas12a is the key to the nucleic acid detection; specifically, reducing Cas12a activity increases the sensitivity of ORCD assay detection of the PAM target. Furthermore, by combining this detection technique with a nucleic acid extraction-free method, our ORCD system can be used to extract, amplify and detect samples within 30 min, as verified with tests of 82 Bordetella pertussis clinical samples with a sensitivity and specificity of 97.30% and 100% compared with PCR. We also tested 13 SARS-CoV-2 samples with RT-ORCD, and the results were consistent with RT-PCR.