Accurate, Sensitive, and Rapid Detection of Pseudomonas aeruginosa Based on CRISPR/Cas12b with One Fluid-Handling

Xiaotong Qiu1, Xueping Liu2, Ruixue Wang3

  • 1State Key Laboratory for Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.

Microbiology Spectrum
|January 9, 2023
PubMed

Insights

A new clustered regularly interspaced short palindromic repeats testing in one pot (CRISPR-top) assay rapidly detects Pseudomonas aeruginosa. This highly sensitive and specific method is ideal for resource-limited settings.

Area of Science:

  • Molecular Biology
  • Diagnostic Assays
  • Microbiology

Background:

  • Pseudomonas aeruginosa is a significant cause of hospital-acquired infections and mortality, particularly in cystic fibrosis patients.
  • Rapid and accurate detection of P. aeruginosa is crucial for effective infection control and patient management.
  • Existing diagnostic methods may lack the speed, sensitivity, or accessibility required for all clinical settings.

Purpose of the Study:

  • To develop and validate a novel, rapid, and sensitive assay for the detection of P. aeruginosa.
  • To establish a clustered regularly interspaced short palindromic repeats testing in one pot (CRISPR-top) assay for P. aeruginosa identification.
  • To evaluate the performance of the CRISPR-top assay using clinical samples and compare it with quantitative real-time PCR (qPCR).

Main Methods:

  • Developed a one-pot, isothermal CRISPR-top assay for P. aeruginosa detection, requiring a single fluid-handling step.
  • Optimized reaction conditions, including primer concentrations, reporter molecule concentration, and incubation temperature (55°C).
  • Validated assay specificity using 48 bacterial strains and determined the limit of detection (10 copies/reaction). Tested 46 human sputum specimens.

Main Results:

  • The assay demonstrated 100% inclusivity and exclusivity against 48 tested strains.
  • The limit of detection was as low as 10 copies per reaction mixture.
  • In sputum samples, the assay showed 85.3% sensitivity and 100% specificity compared to qPCR, with a positive predictive value of 100%.

Conclusions:

  • The developed P. aeruginosa CRISPR-top assay is a highly efficient tool for accurate and rapid detection.
  • The assay's isothermal nature and single-step procedure make it suitable for on-site testing, especially in resource-limited environments.
  • This CRISPR-top assay offers a valuable alternative diagnostic method comparable to qPCR for P. aeruginosa detection.

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