Dual Synthetic Receptor-Based Sandwich Electrochemical Sensor for Highly Selective and Ultrasensitive Detection of Pathogenic Bacteria at the Single-Cell Level

• Published in: Analytical chemistry (Washington) Vol. 95; no. 13; pp. 5561 - 5567
• Main Authors: Lin, Xiaohui, Liu, Ping Ping, Yan, Juan, Luan, Donglei, Sun, Tao, Bian, Xiaojun
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 04-04-2023
• Subjects: Aptamers; Aptamers, Nucleotide; Bacteria; Biosensing Techniques; Buffer solutions; Chemical sensors; Chemistry; Dilution; Electrochemical Techniques; Electrochemistry; Electrodes; Food safety; Gold; Imprinted polymers; Infectious diseases; Limit of Detection; Metal Nanoparticles; Microorganisms; Nanoparticles; Polymer films; Polymerization; Polymers; Public safety; Receptors, Artificial; Selectivity; Sensors; Staphylococcus aureus
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.2c04657

Sensitive and rapid detection of pathogenic bacteria is essential for effective source control and prevention of microbial infectious diseases. However, it remains a substantial challenge to rapidly detect bacteria at the single-cell level. Herein, we present an electrochemical sandwich sensor for highly selective and ultrasensitive detection of a single bacterial cell based on dual recognition by the bacteria-imprinted polymer film (BIF) and aptamer. The BIF was used as the capture probe, which was in situ fabricated on the electrode surface within 15 min via electropolymerization. The aptamer and electroactive 6-(Ferrocenyl)­hexanethiol cofunctionalized gold nanoparticles (Au@Fc-Apt) were employed as the signal probe. Once the target bacteria were anchored on the BIF-modified electrode, the Au@Fc-Apt was further specifically bound to the bacteria, generating enhanced current signals for ultrasensitive detection of Staphylococcus aureus down to a single cell in phosphate buffer solution. Even in the complex milk samples, the sensor could detect as low as 10 CFU mL–1 of S. aureus without any complicated pretreatment except for 10-fold dilution. Moreover, the current response to the target bacteria was hardly affected by the coexisting multiple interfering bacteria, whose number is 30 times higher than the target, demonstrating the excellent selectivity of the sensor. Compared with most reported sandwich-type electrochemical sensors, this assay is more sensitive and more rapid, requiring less time (1.5 h) for the sensing interface construction. By virtue of its sensitivity, rapidity, selectivity, and cost-effectiveness, the sensor can serve as a universal detection platform for monitoring pathogenic bacteria in fields of food/public safety.