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Colorimetric Test for Fast Detection of SARS-CoV-2 in Nasal and Throat Swabs
[Image: see text] Mass testing is fundamental to face the pandemic caused by the coronavirus SARS-CoV-2 discovered at the end of 2019. To this aim, it is necessary to establish reliable, fast, and cheap tools to detect viral particles in biological material so to identify the people capable of sprea...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534800/ https://www.ncbi.nlm.nih.gov/pubmed/32989986 http://dx.doi.org/10.1021/acssensors.0c01742 |
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author | Ventura, Bartolomeo Della Cennamo, Michele Minopoli, Antonio Campanile, Raffaele Censi, Sergio Bolletti Terracciano, Daniela Portella, Giuseppe Velotta, Raffaele |
author_facet | Ventura, Bartolomeo Della Cennamo, Michele Minopoli, Antonio Campanile, Raffaele Censi, Sergio Bolletti Terracciano, Daniela Portella, Giuseppe Velotta, Raffaele |
author_sort | Ventura, Bartolomeo Della |
collection | PubMed |
description | [Image: see text] Mass testing is fundamental to face the pandemic caused by the coronavirus SARS-CoV-2 discovered at the end of 2019. To this aim, it is necessary to establish reliable, fast, and cheap tools to detect viral particles in biological material so to identify the people capable of spreading the infection. We demonstrate that a colorimetric biosensor based on gold nanoparticle (AuNP) interaction induced by SARS-CoV-2 lends itself as an outstanding tool for detecting viral particles in nasal and throat swabs. The extinction spectrum of a colloidal solution of multiple viral-target gold nanoparticles—AuNPs functionalized with antibodies targeting three surface proteins of SARS-CoV-2 (spike, envelope, and membrane)—is red-shifted in few minutes when mixed with a solution containing the viral particle. The optical density of the mixed solution measured at 560 nm was compared to the threshold cycle (C(t)) of a real-time PCR (gold standard for detecting the presence of viruses) finding that the colorimetric method is able to detect very low viral load with a detection limit approaching that of the real-time PCR. Since the method is sensitive to the infecting viral particle rather than to its RNA, the achievements reported here open a new perspective not only in the context of the current and possible future pandemics, but also in microbiology, as the biosensor proves itself to be a powerful though simple tool for measuring the viral particle concentration. |
format | Online Article Text |
id | pubmed-7534800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-75348002020-10-05 Colorimetric Test for Fast Detection of SARS-CoV-2 in Nasal and Throat Swabs Ventura, Bartolomeo Della Cennamo, Michele Minopoli, Antonio Campanile, Raffaele Censi, Sergio Bolletti Terracciano, Daniela Portella, Giuseppe Velotta, Raffaele ACS Sens [Image: see text] Mass testing is fundamental to face the pandemic caused by the coronavirus SARS-CoV-2 discovered at the end of 2019. To this aim, it is necessary to establish reliable, fast, and cheap tools to detect viral particles in biological material so to identify the people capable of spreading the infection. We demonstrate that a colorimetric biosensor based on gold nanoparticle (AuNP) interaction induced by SARS-CoV-2 lends itself as an outstanding tool for detecting viral particles in nasal and throat swabs. The extinction spectrum of a colloidal solution of multiple viral-target gold nanoparticles—AuNPs functionalized with antibodies targeting three surface proteins of SARS-CoV-2 (spike, envelope, and membrane)—is red-shifted in few minutes when mixed with a solution containing the viral particle. The optical density of the mixed solution measured at 560 nm was compared to the threshold cycle (C(t)) of a real-time PCR (gold standard for detecting the presence of viruses) finding that the colorimetric method is able to detect very low viral load with a detection limit approaching that of the real-time PCR. Since the method is sensitive to the infecting viral particle rather than to its RNA, the achievements reported here open a new perspective not only in the context of the current and possible future pandemics, but also in microbiology, as the biosensor proves itself to be a powerful though simple tool for measuring the viral particle concentration. American Chemical Society 2020-09-29 2020-10-23 /pmc/articles/PMC7534800/ /pubmed/32989986 http://dx.doi.org/10.1021/acssensors.0c01742 Text en Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Ventura, Bartolomeo Della Cennamo, Michele Minopoli, Antonio Campanile, Raffaele Censi, Sergio Bolletti Terracciano, Daniela Portella, Giuseppe Velotta, Raffaele Colorimetric Test for Fast Detection of SARS-CoV-2 in Nasal and Throat Swabs |
title | Colorimetric Test for Fast Detection of SARS-CoV-2
in Nasal and Throat Swabs |
title_full | Colorimetric Test for Fast Detection of SARS-CoV-2
in Nasal and Throat Swabs |
title_fullStr | Colorimetric Test for Fast Detection of SARS-CoV-2
in Nasal and Throat Swabs |
title_full_unstemmed | Colorimetric Test for Fast Detection of SARS-CoV-2
in Nasal and Throat Swabs |
title_short | Colorimetric Test for Fast Detection of SARS-CoV-2
in Nasal and Throat Swabs |
title_sort | colorimetric test for fast detection of sars-cov-2
in nasal and throat swabs |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534800/ https://www.ncbi.nlm.nih.gov/pubmed/32989986 http://dx.doi.org/10.1021/acssensors.0c01742 |
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