RPB0241

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
nuc-F3 GTAGCTTCAAGTCTAAGTAGCTCAGCAAAT 30 10μM 40 57.85 9214.07 \
nuc-R3 GGTGTATCAACCAATAATAGTCTGAATGTC 30 10μM 36.67 54.79 9229.08 \
nuc-Probe 1 FAM-AACCCTGAATATCCAACAGTCGCGCTGTA-BHQ1 29 10μM 48.28 63.38 8830.81 \

Gene Description

Target Gene GenBank ID
nuc gene BX571856.1

Assay Description

Application Assay Primer Designing Software Reaction Time(min) Assay Temperature(℃) Readout System(s) Limit of Detection(LoD) Sensitivity(%) Specificity(%)
enhanced sensitivity, specificity, and identification efficacy for MRSA detection. RPA-PfAgo Primer Premier 5.0 55 mins 39°C PfAgo-based system 10²copies/μL \ \

Publication Description

Year of Publication Title Author(s) Journal PMID DOI
2024 Rapid and sensitive detection of methicillin-resistant Staphylococcus aureus through the RPA- Pf Ago system Weizhong Chen,Jiexiu Zhang,Huagui Wei,Jie Su,Jie Lin,Xueyan Liang,Jiangtao Chen,Rong Zhou,Lin Li,Zefang Lu,Guangyu Sun Front Microbiol 39234537 10.3389/fmicb.2024.1422574

Rapid and sensitive detection of methicillin-resistant Staphylococcus aureus through the RPA- Pf Ago system

Author(s):

Weizhong Chen,Jiexiu Zhang,Huagui Wei,Jie Su,Jie Lin,Xueyan Liang,Jiangtao Chen,Rong Zhou,Lin Li,Zefang Lu,Guangyu Sun

Journal:

Front Microbiol

Year:

2024

Abstract:

Introduction: Both the incidence and mortality rates associated with methicillin-resistant Staphylococcus aureus (MRSA) have progressively increased worldwide. A nucleic acid testing system was developed in response, enabling swift and precise detection of Staphylococcus aureus (S. aureus) and its MRSA infection status. This facilitates improved prevention and control of MRSA infections. Methods: In this work, we introduce a novel assay platform developed by integrating Pyrococcus furiosus Argonaute (PfAgo) with recombinase polymerase amplification (RPA), which was designed for the simultaneous detection of the nuc and mecA genes in MRSA. Results: This innovative approach enables visual MRSA detection within 55 mins, boasting a detection limit of 102 copies/μL. Characterized by its high specificity, the platform accurately identifies MRSA infections without cross-reactivity to other clinical pathogens, highlighting its unique capability for S. aureus infection diagnostics amidst bacterial diversity. Validation of this method was performed on 40 clinical isolates, demonstrating a 95.0% accuracy rate in comparison to the established Vitek2-COMPACT system. Discussion: The RPA-PfAgo platform has emerged as a superior diagnostic tool, offering enhanced sensitivity, specificity, and identification efficacy for MRSA detection. Our findings underscore the potential of this platform to significantly improve the diagnosis and management of MRSA infection.