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Electrochemical Strategy for Low-Cost Viral Detection
[Image: see text] Sexually transmitted infections, including the human immunodeficiency virus (HIV) and the human papillomavirus (HPV), disproportionally impact those in low-resource settings. Early diagnosis is essential for managing HIV. Similarly, HPV causes nearly all cases of cervical cancer, t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227598/ https://www.ncbi.nlm.nih.gov/pubmed/34235257 http://dx.doi.org/10.1021/acscentsci.1c00186 |
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author | Zamani, Marjon Robson, James M. Fan, Andy Bono, Michael S. Furst, Ariel L. Klapperich, Catherine M. |
author_facet | Zamani, Marjon Robson, James M. Fan, Andy Bono, Michael S. Furst, Ariel L. Klapperich, Catherine M. |
author_sort | Zamani, Marjon |
collection | PubMed |
description | [Image: see text] Sexually transmitted infections, including the human immunodeficiency virus (HIV) and the human papillomavirus (HPV), disproportionally impact those in low-resource settings. Early diagnosis is essential for managing HIV. Similarly, HPV causes nearly all cases of cervical cancer, the majority (90%) of which occur in low-resource settings. Importantly, infection with HPV is six times more likely to progress to cervical cancer in women who are HIV-positive. An inexpensive, adaptable point-of-care test for viral infections would make screening for these viruses more accessible to a broader set of the population. Here, we report a novel, cost-effective electrochemical platform using gold leaf electrodes to detect clinically relevant viral loads. We have combined this platform with loop-mediated isothermal amplification and a CRISPR-based recognition assay to detect HPV. Lower limits of detection were demonstrated down to 10(4) total copies of input nucleic acids, which is a clinically relevant viral load for HPV DNA. Further, proof-of-concept experiments with cervical swab samples, extracted using standard extraction protocols, demonstrated that the strategy is extendable to complex human samples. This adaptable technology could be applied to detect any viral infection rapidly and cost-effectively. |
format | Online Article Text |
id | pubmed-8227598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82275982021-07-06 Electrochemical Strategy for Low-Cost Viral Detection Zamani, Marjon Robson, James M. Fan, Andy Bono, Michael S. Furst, Ariel L. Klapperich, Catherine M. ACS Cent Sci [Image: see text] Sexually transmitted infections, including the human immunodeficiency virus (HIV) and the human papillomavirus (HPV), disproportionally impact those in low-resource settings. Early diagnosis is essential for managing HIV. Similarly, HPV causes nearly all cases of cervical cancer, the majority (90%) of which occur in low-resource settings. Importantly, infection with HPV is six times more likely to progress to cervical cancer in women who are HIV-positive. An inexpensive, adaptable point-of-care test for viral infections would make screening for these viruses more accessible to a broader set of the population. Here, we report a novel, cost-effective electrochemical platform using gold leaf electrodes to detect clinically relevant viral loads. We have combined this platform with loop-mediated isothermal amplification and a CRISPR-based recognition assay to detect HPV. Lower limits of detection were demonstrated down to 10(4) total copies of input nucleic acids, which is a clinically relevant viral load for HPV DNA. Further, proof-of-concept experiments with cervical swab samples, extracted using standard extraction protocols, demonstrated that the strategy is extendable to complex human samples. This adaptable technology could be applied to detect any viral infection rapidly and cost-effectively. American Chemical Society 2021-05-12 2021-06-23 /pmc/articles/PMC8227598/ /pubmed/34235257 http://dx.doi.org/10.1021/acscentsci.1c00186 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Zamani, Marjon Robson, James M. Fan, Andy Bono, Michael S. Furst, Ariel L. Klapperich, Catherine M. Electrochemical Strategy for Low-Cost Viral Detection |
title | Electrochemical Strategy for Low-Cost Viral Detection |
title_full | Electrochemical Strategy for Low-Cost Viral Detection |
title_fullStr | Electrochemical Strategy for Low-Cost Viral Detection |
title_full_unstemmed | Electrochemical Strategy for Low-Cost Viral Detection |
title_short | Electrochemical Strategy for Low-Cost Viral Detection |
title_sort | electrochemical strategy for low-cost viral detection |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227598/ https://www.ncbi.nlm.nih.gov/pubmed/34235257 http://dx.doi.org/10.1021/acscentsci.1c00186 |
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