4.6 Article

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

Journal

DIAGNOSTICS
Volume 12, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/diagnostics12040829

Keywords

methicillin-resistant Staphylococcus aureus; mecA gene; RPA-CRISPR/Cas12a; one-tube; POCT

Funding

  1. National Natural Science Foundation of China [82002189]
  2. Natural Science Foundation of Anhui Province of China [2008085QF311]
  3. Key Research and Development Program of Anhui Province of China [202004d07020014]
  4. Youth Innovation Promotion Association of the Chinese Academy of Sciences [2018489, 2021442]
  5. Dean's Fund of Hefei Institute of Physical Science, China [YZJJ2020QN35, YZJJ2021QN03]

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In this study, a rapid and accurate platform for MRSA detection was developed by integrating recombinase polymerase amplification (RPA) with the Cas12 system. The platform allows specific MRSA detection with high sensitivity and can visualize the results within 20 minutes.
Methicillin-resistant Staphylococcus aureus (MRSA) is a severe health threat causing highlevel 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.

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