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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.
Abstract:
Pseudomonas aeruginosa is a major bacterial pathogen causing nosocomial infections and accounts for morbidity and mortality among patients with cystic fibrosis. An accurate, sensitive, and rapid method to detect P. aeruginosa is critical for the early control of infection and patient management. In this study, we established a P. aeruginosa clustered regularly interspaced short palindromic repeats testing in one pot (CRISPR-top) assay which detected P. aeruginosa with one fluid-handling step in one tube. The reaction was performed isothermally within 1 h; thus, specific instruments were not required. The optimal reaction conditions of this assay were determined to be a temperature of 55°C; working concentrations of 1 μM for the forward inner primer and backward inner primer, 0.5 μM for the loop forward primer and loop backward primer, and 0.25 μM for the forward outer primer and backward outer primer; as well as a 2 μM concentration single-stranded DNA reporter molecules. In terms of specificity, our assay showed 100% inclusivity and exclusivity among 48 strains, including 15 P. aeruginosa clinical isolates and 33 non-P. aeruginosa strains. The limit of detection of our method was 10 copies per reaction mixture. Forty-six human sputum specimens from patients with respiratory symptoms were tested. Using the results of quantitative real-time PCR as the gold standard, our method showed 85.3% (29/34) sensitivity, 100% (12/12) specificity, a positive predictive value of 100% (29/29), and a negative predictive value of 70.6% (12/17). In summary, the P. aeruginosa CRISPR-top assay developed in the present study is a high-efficiency alternative tool for the accurate and rapid detection of P. aeruginosa, especially in resource-limited settings. IMPORTANCE This study reports a P. aeruginosa CRISPR-top assay which can precisely identify P. aeruginosa using nucleic acids from pure cultures or clinical samples in one pot with one fluid-handling step. The P. aeruginosa CRISPR-top reaction is suitable for on-site testing, and its diagnostic performance can be compared with that of qPCR.
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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