A dual-channel electrochemical biosensor enables concurrent detection of pathogens and antibiotic resistance.

E. coli secreted protein B Electrochemical biosensor Enteropathogenic E. coli Nitrocefin anti-EspB mAb β-lactamase

Journal

Biosensors & bioelectronics
ISSN: 1873-4235
Titre abrégé: Biosens Bioelectron
Pays: England
ID NLM: 9001289

Informations de publication

Date de publication:
20 Apr 2024
Historique:
received: 21 01 2024
revised: 04 04 2024
accepted: 17 04 2024
medline: 26 4 2024
pubmed: 26 4 2024
entrez: 25 4 2024
Statut: aheadofprint

Résumé

Diarrheagenic E. coli infections, commonly treated with β-lactam antibiotics, contribute to antibiotic resistance - a pressing public health concern. Rapid monitoring of pathogen antibiotic resistance is vital to combat antimicrobial spread. Current bacterial diagnosis methods identify pathogens or determine antibiotic resistance separately, necessitating multiple assays. There is an urgent need for tools that simultaneously identify infectious agents and their antibiotic resistance at the point of care (POC). We developed an integrated electrochemical chip-based biosensor for detecting enteropathogenic E. coli (EPEC), a major neonatal diarrheal pathogen, using an antibody against a virulence marker, termed EspB, and the β-lactam resistance marker, β-lactamase. A dual-channel microfabricated chip, bio-functionalized with a specific EspB monoclonal antibody, and nitrocefin, a β -lactamase substrate was utilized. The chip facilitated electrochemical impedance spectroscopy (EIS)-based detection of EspB antigen and EspB-expressing bacteria. For β-lactam resistance profiling, a second channel enabled differential-pulse voltammetric (DPV) measurement of hydrolyzed nitrocefin. EIS-based detection of EspB antigen was calibrated (LOD: 4.3 ng/mL ±1 and LOQ: 13.0 ng/mL ±3) as well as DPV-based detection of the antibiotic resistance marker, β-lactamase (LOD: 3.6 ng/mL ±1.65 and LOQ: 10 ng/mL ±4). The integrated EIS and DPV biosensor was employed for the simultaneous detection of EspB-expressing and β-lactamase-producing bacteria. The combined readout from both channels allowed the distinction between antibiotic-resistant and -sensitive pathogenic bacteria. The integrated electrochemical biosensor successfully achieved simultaneous, rapid detection of double positive EspB- and β-lactamase-expressing bacteria. Such distinction enabled by a portable device within a short assay time and a simplified sample preparation, may be highly valuable in mitigating the spread of AMR. This new diagnostic tool holds promise for the development of POC devices in clinical diagnosis.

Identifiants

pubmed: 38663325
pii: S0956-5663(24)00319-1
doi: 10.1016/j.bios.2024.116314
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

116314

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Sefi Vernick reports financial support was provided by The Israel Innovation Authority. Yariv Wine reports financial support was provided by The Ministry of Innovation, Science and Technology (MOST). Neta Sal-Man reports was provided by Israel Science Foundation. Yariv Wine reports financial support was provided by The Center for Combating Pandemics (TCCP), Tel Aviv University. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Dharanivasan Gunasekaran (D)

Department of Sensing, Information and Mechanization Engineering, Institute of Agricultural Engineering, Volcani Institute (ARO), Rishon LeZion, 5025001, Israel. Electronic address: dharanig@volcani.agri.gov.il.

Irina Rostovsky (I)

Department of Microbiology, Immunology and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, P.O. Box 653, Beer Sheva, 8410501, Israel. Electronic address: rostovsk@post.bgu.ac.il.

David Taussig (D)

The Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 69978, Israel; The Center for Combating Pandemics, Tel Aviv University, Tel Aviv, 69978, Israel. Electronic address: davidtaussig@mail.tau.ac.il.

Talya Bar-Am (T)

The Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 69978, Israel. Electronic address: talyabaram@mail.tau.ac.il.

Yariv Wine (Y)

The Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 69978, Israel; The Center for Combating Pandemics, Tel Aviv University, Tel Aviv, 69978, Israel; The Center for Nanoscience and Nanotechnology, Tel Aviv University, Tel Aviv, Israel. Electronic address: yarivwine@tauex.tau.ac.il.

Neta Sal-Man (N)

Department of Microbiology, Immunology and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, P.O. Box 653, Beer Sheva, 8410501, Israel. Electronic address: salmanne@bgu.ac.il.

Sefi Vernick (S)

Department of Sensing, Information and Mechanization Engineering, Institute of Agricultural Engineering, Volcani Institute (ARO), Rishon LeZion, 5025001, Israel. Electronic address: sefi@volcani.agri.gov.il.

Classifications MeSH