Simple and low‐cost antibiotic susceptibility testing for Mycobacterium tuberculosis using screen‐printed electrodes

Author:

Ghorbanpoor Hamed12345ORCID,Akcakoca Iremnur6,Norouz Dizaji Araz2ORCID,Butterworth Adrian7,Corrigan Damion78,Kocagoz Tanil910,Ebrahimi Aliakbar245,Avci Huseyin34511,Dogan Guzel Fatma2ORCID

Affiliation:

1. Department of Biomedical Engineering Eskisehir Osmangazi University Eskisehir Turkey

2. Department of Biomedical Engineering Ankara Yildirim Beyazit University Ankara Turkey

3. Department of Metallurgical and Materials Engineering Eskisehir Osmangazi University Eskisehir Turkey

4. Cellular Therapy and Stem Cell Research Center Eskisehir Osmangazi University Eskisehir Turkey

5. AvciBio Research Group Eskisehir Osmangazi University Eskisehir Turkey

6. Department of Metallurgical and Material Engineering Yildirim Beyazit University Ankara Turkey

7. Department of Biomedical Engineering University of Strathclyde Glasgow UK

8. Department of Pure and Applied Chemistry University of Strathclyde Glasgow UK

9. Department of Medical Biotechnology Institute of Health Sciences Istanbul Turkey

10. Department of Medical Microbiology School of Medicine Acibadem Mehmet Ali Aydinlar University Istanbul Turkey

11. Translational Medicine Research and Clinical Center Eskisehir Osmangazi University Eskisehir Turkey

Abstract

AbstractOne quarter of the global population is thought to be latently infected by Mycobacterium tuberculosis (TB) with it estimated that 1 in 10 of those people will go on to develop active disease. Due to the fact that M. tuberculosis (TB) is a disease most often associated with low‐ and middle‐income countries, it is critical that low‐cost and easy‐to‐use technological solutions are developed, which can have a direct impact on diagnosis and prescribing practice for TB. One area where intervention could be particularly useful is antibiotic susceptibility testing (AST). This work presents a low‐cost, simple‐to‐use AST sensor that can detect drug susceptibility on the basis of changing RNA abundance for the typically slow‐growing M. tuberculosis (TB) pathogen in 96 h using screen‐printed electrodes and standard molecular biology laboratory reactionware. In order to find out the sensitivity of applied sensor platform, a different concentration (108–103 CFU/mL) of M. tuberculosis was performed, and limit of detection and limit of quantitation were calculated as 103.82 and 1011.59 CFU/mL, respectively. The results display that it was possible to detect TB sequences and distinguish antibiotic‐treated cells from untreated cells with a label‐free molecular detection. These findings pave the way for the development of a comprehensive, low‐cost, and simple‐to‐use AST system for prescribing in TB and multidrug‐resistant tuberculosis.

Publisher

Wiley

Subject

Process Chemistry and Technology,Drug Discovery,Applied Microbiology and Biotechnology,Biomedical Engineering,Molecular Medicine,General Medicine,Bioengineering,Biotechnology

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