Rapid and sensitive detection of methicillin-resistant through the RPA-Ago system.

INTRODUCTION

Both the incidence and mortality rates associated with methicillin-resistant (MRSA) have progressively increased worldwide. A nucleic acid testing system was developed in response, enabling swift and precise detection of () 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 Argonaute (Ago) with recombinase polymerase amplification (RPA), which was designed for the simultaneous detection of the and genes in MRSA.

RESULTS

This innovative approach enables visual MRSA detection within 55 mins, boasting a detection limit of 10 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 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-Ago 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.