A Wireless, CRISPR-Polymer Dot Electrochemical Sensor for the Diagnosis of Bacterial Pneumonia and Multi-Drug Resistance.
San Hae ImAkhmad Irhas RobbyHeewon ChoiJu Yeon ChungYang Soo KimSung Young ParkHyun Jung ChungPublished in: ACS applied materials & interfaces (2024)
Rapid and accurate diagnosis is crucial for managing the global health threat posed by multidrug-resistant bacterial infections; however, current methods have limitations in either being time-consuming, labor-intensive, or requiring instruments with high costs. Addressing these challenges, we introduce a wireless electrochemical sensor integrating the CRISPR/Cas system with electroconductive polymer dot (PD) nanoparticles to rapidly detect bacterial pathogens from human sputum. To enhance the electroconductive properties, we synthesized copper-ion-immobilized PD (PD-Cu), followed by conjugation of the deactivated Cas9 protein (dCas9) onto PD-Cu-coated Si electrodes to generate the dCas9-PD-Cu sensor. The dCas9-PD-Cu sensor integrated with isothermal amplification can specifically detect target nucleic acids of multidrug-resistant bacteria, such as the antibiotic resistance genes kpc-2 and mecA . The dCas9-PD-Cu sensor exhibits high sensitivity, allowing for the detection of ∼54 femtograms of target nucleic acids, based on measuring the changes in resistivity of the Si electrodes through target capture by dCas9. Furthermore, a wireless sensing platform of the dCas9-PD-Cu sensor was established using a Bluetooth module and a microcontroller unit for detection using a smartphone. We demonstrate the feasibility of the platform in diagnosing multidrug-resistant bacterial pneumonia in patients' sputum samples, achieving 92% accuracy. The current study presents a versatile biosensor platform that can overcome the limitations of conventional diagnostics in the clinic.
Keyphrases
- multidrug resistant
- crispr cas
- genome editing
- label free
- gram negative
- gold nanoparticles
- drug resistant
- antibiotic resistance genes
- aqueous solution
- global health
- acinetobacter baumannii
- loop mediated isothermal amplification
- end stage renal disease
- metal organic framework
- primary care
- endothelial cells
- mycobacterium tuberculosis
- genome wide
- peritoneal dialysis
- intensive care unit
- escherichia coli
- small molecule
- ejection fraction
- ionic liquid
- pulmonary tuberculosis
- microbial community
- sensitive detection
- molecularly imprinted
- extracorporeal membrane oxygenation
- single cell
- simultaneous determination