RPB0449

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
F cctctaatacgactcactataggAAGTCTAATCTCAAACCTTTTGAGAGAGATATTT 57 125 nM 35.09 62.77 17468.43 \
R ACAAACAGTTGCTGGTGCATGTAGAAGTTC 30 125 nM 43.33 60.95 9270.09 \

Gene Description

Target Gene GenBank ID
T478K \

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
rapid, ultrasensitive, and accurate nucleic acid analysis technology. RT-RPA-CRISPR\Cas13 Primer Premier 5 with NCBI BLAST 30 min 37 °C CRISPR\Cas13 1 copy/μL \ \

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2023 CESSAT: A chemical additive-enhanced single-step accurate CRISPR\Cas13 testing system for field-deployable ultrasensitive detection and genotyping of SARS-CoV-2 variants of concern Yunxiang Wang,Hong Chen,Huixia Gao,Hongjuan Wei,Yuling Wang,Kai Mu,Liyan Liu,Erhei Dai,Zhen Rong,Shengqi Wang Biosensors and Bioelectronics 36958206 10.1016/j.bios.2023.115238

CESSAT: A chemical additive-enhanced single-step accurate CRISPR\Cas13 testing system for field-deployable ultrasensitive detection and genotyping of SARS-CoV-2 variants of concern

Author(s):

Yunxiang Wang,Hong Chen,Huixia Gao,Hongjuan Wei,Yuling Wang,Kai Mu,Liyan Liu,Erhei Dai,Zhen Rong,Shengqi Wang

Journal:

Biosensors and Bioelectronics

Year:

2023

Abstract:

The continued emergence of SARS-CoV-2 variants of concern (VOCs) has raised great challenges for epidemic prevention and control. A rapid, sensitive, and on-site SARS-CoV-2 genotyping technique is urgently needed for individual diagnosis and routine surveillance. Here, a field-deployable ultrasensitive CRISPR-based diagnostics system, called Chemical additive-Enhanced Single-Step Accurate CRISPR/Cas13 Testing system (CESSAT), for simultaneous screening of SARS-CoV-2 and its five VOCs (Alpha, Beta, Gamma, Delta, and Omicron) within 40 min was reported. In this system, a single-step reverse transcription recombinase polymerase amplification-CRISPR/Cas13a assay was incorporated with optimized extraction-free viral lysis and reagent lyophilization, which could eliminate complicated sample processing steps and rigorous reagent storage conditions. Remarkably, 10% glycine as a chemical additive could improve the assay sensitivity by 10 times, making the limit of detection as low as 1 copy/μL (5 copies/reaction). A compact optic fiber-integrated smartphone-based device was developed for sample lysis, assay incubation, fluorescence imaging, and result interpretation. CESSAT could specifically differentiate the synthetic pseudovirus of SARS-CoV-2 and its five VOCs. The genotyping results for 40 clinical samples were in 100% concordance with standard method. We believe this simple but efficient enhancement strategy can be widely incorporated with existing Cas13a-based assays, thus leading a substantial progress in the development and application of rapid, ultrasensitive, and accurate nucleic acid analysis technology.