RPB0158

Pathogen Description

Target Pathogen Pathogen Name NCBI Taxonomy ID Order Family Genus Species Pathogen type
Staphylococcus aureus Staphylococcus aureus, Micrococcus aureus, Staphylococcus pyogenes aureus 1280 Bacillales Staphylococcaceae Staphylococcus Staphylococcus aureus Bacterium

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
mecA-RPA-F3 TATGCAACAAGTCGTAAATAAAACACATAAAG 32 \ 28.1 53.31 9850.54 \
mecA-RPA-R2 TCATATGATATAAACCACCCAATTTGTCTGCC 32 \ 37.5 58.04 9702.39 \

Gene Description

Target Gene GenBank ID
mecA gene \

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
Detection for Methicillin-Resistant Staphylococcus aureus RPA-CRISPR/Cas12 \ 10 42 CRISPR system 10 copies for the fluorescence method and a range of 10-100 copies for the LFS \ \

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2022 Rapid One-Tube RPA-CRISPR/Cas12 Detection Platform for Methicillin-Resistant Staphylococcus aureus Yanan Li,Zhonglin Shi,Anzhong Hu,Junsheng Cui,Ke Yang,Yong Liu,Guoqing Deng,Cancan Zhu,Ling Zhu Diagnostics (Basel, Switzerland) 35453874 10.3390/diagnostics12040829

Rapid One-Tube RPA-CRISPR/Cas12 Detection Platform for Methicillin-Resistant Staphylococcus aureus

Author(s):

Yanan Li,Zhonglin Shi,Anzhong Hu,Junsheng Cui,Ke Yang,Yong Liu,Guoqing Deng,Cancan Zhu,Ling Zhu

Journal:

Diagnostics (Basel, Switzerland)

Year:

2022

Abstract:

Methicillin-resistant Staphylococcus aureus (MRSA) is a severe health threat causing high-level morbidity and mortality in health care environments and in community settings. Though existing diagnostic methods, including PCR and culture-based methods, are routinely used in clinical practice, they are not appropriate for rapid point-of-care testing (POCT). Recently, since the development of the CRISPR/Cas technology, new possibilities for rapid point-of-care detection have emerged. In this study, we developed a rapid, accurate, and contamination-free platform for MRSA detection by integrating recombinase polymerase amplification (RPA) with the Cas12 system into one tube. Using this approach, visual MRSA detection could be achieved in 20 min. Based on the one-tube RPA-CRISPR/Cas12a platform, the assay results are visualized by lateral flow test strips (LFS) and fluorescent-based methods, including real-time and end-point fluorescence. This platform allows specific MRSA detection with a sensitivity of 10 copies for the fluorescence method and a range of 10-100 copies for the LFS. The results of 23 samples from clinical MRSA isolates showed that the coincidence rate was 100% and 95.7% of the fluorescence method and LFS, respectively, compared to qPCR. In conclusion, the one-tube RPA-CRISPR/Cas12a platform is an effective method for MRSA detection with significant potential in future practical POCT applications.