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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...

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Autores principales: Zamani, Marjon, Robson, James M., Fan, Andy, Bono, Michael S., Furst, Ariel L., Klapperich, Catherine M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
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.
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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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