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September 10, 2025Microbiology Spectrum13 citationsOpen Access

Development of a rapid and sensitive RPA-CRISPR/Cas12a-based assay for the detection of Brucella melitensis

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YSYu ShenCYChenchen YiHWHeng Wang

Key Points

  • The RPA-CRISPR/Cas12a-FL assay showed a remarkable detection limit of 1 copy/μL, enhancing diagnostic sensitivity.
  • Clinical validation with serum samples revealed a 100% concordance with serological results, confirming clinical reliability.
  • This method integrates fluorescence and lateral flow strip detection, providing dual capabilities for brucella detection.
  • The assay demonstrates strong specificity for Brucella, avoiding cross-reactivity with other bacterial species.

Abstract

Brucellosis, a zoonotic disease caused by Brucella species, presents significant public health challenges due to its complex diagnosis and the limited availability of rapid detection methods. To address these challenges, we developed a novel detection method that integrates recombinase polymerase amplification (RPA) with the CRISPR/Cas12a system, enabling dual readout through fluorescence (FL) and lateral flow strip (LFS) detection. The RPA-CRISPR/Cas12a-FL assay demonstrated an impressive detection limit of 1 copy/μL, which is 10 times more sensitive than quantitative polymerase chain reaction, while the RPA-CRISPR/Cas12a-LFS method achieved a detection limit of 10 copies/μL, comparable to nested PCR. Specificity testing confirmed the robustness of the assay, as it produced strong signals exclusively for Brucella without cross-reactivity with other bacterial species. Clinical validation using serum samples from 24 confirmed brucellosis patients and six healthy controls demonstrated a 100% concordance with serological results, underscoring the reliability of this method for clinical applications. This assay provides a rapid, sensitive, and specific tool for Brucella detection, suitable for both laboratory and field settings, and holds significant potential for enhancing the diagnosis and control of brucellosis.IMPORTANCEBrucellosis is a significant zoonotic disease, and rapid and accurate diagnosis is crucial for its treatment and control. To address this need, we developed a novel detection method that combines recombinant enzyme polymerase amplification with a CRISPR/Cas12a system, achieving dual readout through fluorescence and lateral flow strips. The test demonstrates excellent sensitivity and specificity, with clinical validation confirming complete concordance with serological results. This approach offers a fast, reliable, and field-deployable solution for brucellosis diagnosis, significantly enhancing disease management and public health outcomes.

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Cite This Study

Shen et al. (2025) studied this question.

synapsesocial.com/papers/68c1d5f754b1d3bfb60f90b4https://doi.org/10.1128/spectrum.00998-25
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  3. 3Laboratory-based diagnosis of brucellosis--a review of the literature. Part II: serological tests for brucellosis.2003 · 245 citations
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  5. 5CRISPR-Cas12a test strip (CRISPR/CAST) package: In-situ detection of Brucella from infected livestock2023 · 20 citations