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Electrochemical genosensor for the specific detection of SARS-CoV-2
Infection caused by Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) is responsible for the Coronavirus disease (COVID-19) and the current pandemic. Its mortality rate increases, demonstrating the imperative need for acute and rapid diagnostic tools as an alternative to current serologic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012668/ https://www.ncbi.nlm.nih.gov/pubmed/35462140 http://dx.doi.org/10.1016/j.talanta.2022.123482 |
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author | Cajigas, Sebastian Alzate, Daniel Fernández, Maritza Muskus, Carlos Orozco, Jahir |
author_facet | Cajigas, Sebastian Alzate, Daniel Fernández, Maritza Muskus, Carlos Orozco, Jahir |
author_sort | Cajigas, Sebastian |
collection | PubMed |
description | Infection caused by Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) is responsible for the Coronavirus disease (COVID-19) and the current pandemic. Its mortality rate increases, demonstrating the imperative need for acute and rapid diagnostic tools as an alternative to current serological tests and molecular techniques. Features of electrochemical genosensor devices make them amenable for fast and accurate testing closer to the patient. This work reports on a specific electrochemical genosensor for SARS-CoV-2 detection and discrimination against homologous respiratory viruses. The electrochemical biosensor was assembled by immobilizing thiolated capture probes on top of maleimide-coated magnetic particles, followed by specific target hybridization between the capture and biotinylated signaling probes in a sandwich-type manner. The probes were rigorously designed bioinformatically and tested in vitro. Enzymatic complexes based on streptavidin-horseradish peroxidase linked the biotinylated signaling probe to render the biosensor electrochemical response. The genosensor showed to reach a sensitivity of 174.4 μA fM(−1) and a limit of detection of 807 fM when using streptavidin poly-HRP20 enzymatic complex, detected SARS-CoV-2 specifically and discriminated it against homologous viruses in spiked samples and samples from SARS-CoV-2 cell cultures, a step forward to detect SARS-CoV-2 closer to the patient as a promising way for diagnosis and surveillance of COVID-19. |
format | Online Article Text |
id | pubmed-9012668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90126682022-04-18 Electrochemical genosensor for the specific detection of SARS-CoV-2 Cajigas, Sebastian Alzate, Daniel Fernández, Maritza Muskus, Carlos Orozco, Jahir Talanta Article Infection caused by Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) is responsible for the Coronavirus disease (COVID-19) and the current pandemic. Its mortality rate increases, demonstrating the imperative need for acute and rapid diagnostic tools as an alternative to current serological tests and molecular techniques. Features of electrochemical genosensor devices make them amenable for fast and accurate testing closer to the patient. This work reports on a specific electrochemical genosensor for SARS-CoV-2 detection and discrimination against homologous respiratory viruses. The electrochemical biosensor was assembled by immobilizing thiolated capture probes on top of maleimide-coated magnetic particles, followed by specific target hybridization between the capture and biotinylated signaling probes in a sandwich-type manner. The probes were rigorously designed bioinformatically and tested in vitro. Enzymatic complexes based on streptavidin-horseradish peroxidase linked the biotinylated signaling probe to render the biosensor electrochemical response. The genosensor showed to reach a sensitivity of 174.4 μA fM(−1) and a limit of detection of 807 fM when using streptavidin poly-HRP20 enzymatic complex, detected SARS-CoV-2 specifically and discriminated it against homologous viruses in spiked samples and samples from SARS-CoV-2 cell cultures, a step forward to detect SARS-CoV-2 closer to the patient as a promising way for diagnosis and surveillance of COVID-19. Elsevier B.V. 2022-08-01 2022-04-16 /pmc/articles/PMC9012668/ /pubmed/35462140 http://dx.doi.org/10.1016/j.talanta.2022.123482 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Cajigas, Sebastian Alzate, Daniel Fernández, Maritza Muskus, Carlos Orozco, Jahir Electrochemical genosensor for the specific detection of SARS-CoV-2 |
title | Electrochemical genosensor for the specific detection of SARS-CoV-2 |
title_full | Electrochemical genosensor for the specific detection of SARS-CoV-2 |
title_fullStr | Electrochemical genosensor for the specific detection of SARS-CoV-2 |
title_full_unstemmed | Electrochemical genosensor for the specific detection of SARS-CoV-2 |
title_short | Electrochemical genosensor for the specific detection of SARS-CoV-2 |
title_sort | electrochemical genosensor for the specific detection of sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012668/ https://www.ncbi.nlm.nih.gov/pubmed/35462140 http://dx.doi.org/10.1016/j.talanta.2022.123482 |
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