RPB0131

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-F3 TAATACGACTCACTATAGGGAACACATAAAGAAGATATTTATAGATCTTATGCAA 55 0.1 29.1 59.73 16965.15 \
mecA-R1 TTGGCATTGTAGCTAGCCATTCCTTTATCTTGTAC 35 0.1 40 60.87 10668.97 \

Gene Description

Target Gene GenBank ID
mecA KC243783.1

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
detection of methicillin-resistant Staphylococcus aureus RPA-CRISPR Cas12a/Cas13a primer premier software 5.0 15 39 CRISPR Cas12a/Cas13a 5 copies/μL

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2023 One-tube RPA-CRISPR Cas12a/Cas13a rapid detection of methicillin-resistant Staphylococcus aureus Yujie Liu,Hui Liu,Guanliu Yu,Wenbo Sun,Muhammad Aizaz,Guiwen Yang,Lei Chen Analytica chimica acta 37709482 10.1016/j.aca.2023.341757

One-tube RPA-CRISPR Cas12a/Cas13a rapid detection of methicillin-resistant Staphylococcus aureus

Author(s):

Yujie Liu,Hui Liu,Guanliu Yu,Wenbo Sun,Muhammad Aizaz,Guiwen Yang,Lei Chen

Journal:

Analytica chimica acta

Year:

2023

Abstract:

At present, methicillin-resistant Staphylococcus aureus (MRSA) has caused a serious impact on a global scale. The infection and carrier rate of MRSA in the community is increasing year by year, but there is still no convenient detection system for on-site rapid detection. It is very important to select a rapid detection system to accurately and quickly detect patients infected with MRSA. We have developed a high-efficient single-tube detection platform based on RPA and CRISPR reaction system to detect the genes of mecA and clfA of MRSA. Using this detection platform, visual MRSA detection could be achieved in 30 min. It was observed that this detection platform was capable to successfully detect the target genomic as low as 5 copies μL-1, and the reaction was completed in one step without opening the lid. This detection platform could only detect MRSA, but not other common clinical pathogenic bacteria, such as Salmonella, Pseudomonas aeruginosa, Staphylococcus xylosus, Aeromonas hydrophila, Escherichia coli and Staphylococcus warneri, indicated its satisfactory selectivity for MRSA without interference from other bacteria. The results of clinical samples show that the platform has outstanding advantages in sensitivity, specificity and identification of methicillin resistance. The entire reaction can be completed in one step in the handheld instrument without opening the cover, avoiding aerosol pollution during the reaction. The detection platform combined with handheld instruments will have great application potential in point-of-care testing.