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An electrochemical biosensor for the detection of Mycobacterium tuberculosis DNA from sputum and urine samples

Tuberculosis (TB) is a major global public health problem with high mortality and morbidity. In low-middle income countries (LMIC) a large number of respiratory symptomatic cases that require TB screening per year demands more accurate, fast and affordable testing for TB diagnostics. Sputum smear is...

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Autores principales: Ramos-Sono, Daniel, Laureano, Raúl, Rueda, Daniel, Gilman, Robert H., La Rosa, Adolfo, Ruiz, Jesús, León, Raúl, Sheen, Patricia, Zimic, Mirko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7592764/
https://www.ncbi.nlm.nih.gov/pubmed/33112923
http://dx.doi.org/10.1371/journal.pone.0241067
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author Ramos-Sono, Daniel
Laureano, Raúl
Rueda, Daniel
Gilman, Robert H.
La Rosa, Adolfo
Ruiz, Jesús
León, Raúl
Sheen, Patricia
Zimic, Mirko
author_facet Ramos-Sono, Daniel
Laureano, Raúl
Rueda, Daniel
Gilman, Robert H.
La Rosa, Adolfo
Ruiz, Jesús
León, Raúl
Sheen, Patricia
Zimic, Mirko
author_sort Ramos-Sono, Daniel
collection PubMed
description Tuberculosis (TB) is a major global public health problem with high mortality and morbidity. In low-middle income countries (LMIC) a large number of respiratory symptomatic cases that require TB screening per year demands more accurate, fast and affordable testing for TB diagnostics. Sputum smear is the initial screening test in LMICs, however, its sensitivity is limited in patients with low sputum bacilli load. The same limitation is observed in the currently available molecular tests. We designed, standardized and evaluated an electrochemical biosensor that detects the highly specific DNA insertion element 6110 (IS6110). A PCR amplified DNA product is hybridized on the surface of the working electrode built on FTO-Glass with immobilized specific DNA probes, after which cyclic voltammetry is performed with an Ag/AgCl reference electrode and a platinum counter electrode. The response of the sensor was measured by the ratio (cathodic peak current of the hybridized sensor) / (cathodic peak current of the non-hybridized sensor). We tested the biosensor, using positive hybridization control sequences, genomic DNA extracted from M. tuberculosis strains and sputum of TB patients, and extracted DNA from the urine of healthy controls spiked with M. tuberculosis DNA. This biosensor was effective for the detection of M. tuberculosis DNA with a detection limit of 16 fM in sputum sample and 1 fM in spiked urine samples. The low cost and the relatively brief duration of the assay make this an important TB screening tool in the fight against tuberculosis.
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spelling pubmed-75927642020-11-02 An electrochemical biosensor for the detection of Mycobacterium tuberculosis DNA from sputum and urine samples Ramos-Sono, Daniel Laureano, Raúl Rueda, Daniel Gilman, Robert H. La Rosa, Adolfo Ruiz, Jesús León, Raúl Sheen, Patricia Zimic, Mirko PLoS One Research Article Tuberculosis (TB) is a major global public health problem with high mortality and morbidity. In low-middle income countries (LMIC) a large number of respiratory symptomatic cases that require TB screening per year demands more accurate, fast and affordable testing for TB diagnostics. Sputum smear is the initial screening test in LMICs, however, its sensitivity is limited in patients with low sputum bacilli load. The same limitation is observed in the currently available molecular tests. We designed, standardized and evaluated an electrochemical biosensor that detects the highly specific DNA insertion element 6110 (IS6110). A PCR amplified DNA product is hybridized on the surface of the working electrode built on FTO-Glass with immobilized specific DNA probes, after which cyclic voltammetry is performed with an Ag/AgCl reference electrode and a platinum counter electrode. The response of the sensor was measured by the ratio (cathodic peak current of the hybridized sensor) / (cathodic peak current of the non-hybridized sensor). We tested the biosensor, using positive hybridization control sequences, genomic DNA extracted from M. tuberculosis strains and sputum of TB patients, and extracted DNA from the urine of healthy controls spiked with M. tuberculosis DNA. This biosensor was effective for the detection of M. tuberculosis DNA with a detection limit of 16 fM in sputum sample and 1 fM in spiked urine samples. The low cost and the relatively brief duration of the assay make this an important TB screening tool in the fight against tuberculosis. Public Library of Science 2020-10-28 /pmc/articles/PMC7592764/ /pubmed/33112923 http://dx.doi.org/10.1371/journal.pone.0241067 Text en © 2020 Ramos-Sono et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ramos-Sono, Daniel
Laureano, Raúl
Rueda, Daniel
Gilman, Robert H.
La Rosa, Adolfo
Ruiz, Jesús
León, Raúl
Sheen, Patricia
Zimic, Mirko
An electrochemical biosensor for the detection of Mycobacterium tuberculosis DNA from sputum and urine samples
title An electrochemical biosensor for the detection of Mycobacterium tuberculosis DNA from sputum and urine samples
title_full An electrochemical biosensor for the detection of Mycobacterium tuberculosis DNA from sputum and urine samples
title_fullStr An electrochemical biosensor for the detection of Mycobacterium tuberculosis DNA from sputum and urine samples
title_full_unstemmed An electrochemical biosensor for the detection of Mycobacterium tuberculosis DNA from sputum and urine samples
title_short An electrochemical biosensor for the detection of Mycobacterium tuberculosis DNA from sputum and urine samples
title_sort electrochemical biosensor for the detection of mycobacterium tuberculosis dna from sputum and urine samples
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7592764/
https://www.ncbi.nlm.nih.gov/pubmed/33112923
http://dx.doi.org/10.1371/journal.pone.0241067
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