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Next-generation diagnostic test for dengue virus detection using an ultrafast plasmonic colorimetric RT-PCR strategy

The current global COVID-19 pandemic once again highlighted the urgent need for a simple, cost-effective, and sensitive diagnostic platform that can be rapidly developed for distribution and easy access in resource-limited areas. Here, we present a simple and low-cost plasmonic photothermal (PPT)-re...

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Autores principales: Jiang, Kunlun, Lee, Jung-Hoon, Fung, To Sing, Wu, Jingrui, Liu, Congnuan, Mi, Hua, Rajapakse, R.P.V. Jayanthe, Balasuriya, Udeni B.R., Peng, Yung-Kang, Go, Yun Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291885/
https://www.ncbi.nlm.nih.gov/pubmed/37455070
http://dx.doi.org/10.1016/j.aca.2023.341565
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author Jiang, Kunlun
Lee, Jung-Hoon
Fung, To Sing
Wu, Jingrui
Liu, Congnuan
Mi, Hua
Rajapakse, R.P.V. Jayanthe
Balasuriya, Udeni B.R.
Peng, Yung-Kang
Go, Yun Young
author_facet Jiang, Kunlun
Lee, Jung-Hoon
Fung, To Sing
Wu, Jingrui
Liu, Congnuan
Mi, Hua
Rajapakse, R.P.V. Jayanthe
Balasuriya, Udeni B.R.
Peng, Yung-Kang
Go, Yun Young
author_sort Jiang, Kunlun
collection PubMed
description The current global COVID-19 pandemic once again highlighted the urgent need for a simple, cost-effective, and sensitive diagnostic platform that can be rapidly developed for distribution and easy access in resource-limited areas. Here, we present a simple and low-cost plasmonic photothermal (PPT)-reverse transcription-colorimetric polymerase chain reaction (RTcPCR) for molecular diagnosis of dengue virus (DENV) infection. The assay can be completed within 54 min with an estimated detection limit of 1.6 copies/μL of viral nucleic acid. The analytical sensitivity and specificity of PPT-RTcPCR were comparable to that of the reference RT-qPCR assay. Moreover, the clinical performance of PPT-RTcPCR was evaluated and validated using 158 plasma samples collected from patients suspected of dengue infection. The results showed a diagnostic agreement of 97.5% compared to the reference RT-qPCR and demonstrated a clinical sensitivity and specificity of 97.0% and 100%, respectively. The simplicity and reliability of our PPT-RTcPCR strategy suggest it can provide a foundation for developing a field-deployable diagnostic assay for dengue and other infectious diseases.
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spelling pubmed-102918852023-06-27 Next-generation diagnostic test for dengue virus detection using an ultrafast plasmonic colorimetric RT-PCR strategy Jiang, Kunlun Lee, Jung-Hoon Fung, To Sing Wu, Jingrui Liu, Congnuan Mi, Hua Rajapakse, R.P.V. Jayanthe Balasuriya, Udeni B.R. Peng, Yung-Kang Go, Yun Young Anal Chim Acta Article The current global COVID-19 pandemic once again highlighted the urgent need for a simple, cost-effective, and sensitive diagnostic platform that can be rapidly developed for distribution and easy access in resource-limited areas. Here, we present a simple and low-cost plasmonic photothermal (PPT)-reverse transcription-colorimetric polymerase chain reaction (RTcPCR) for molecular diagnosis of dengue virus (DENV) infection. The assay can be completed within 54 min with an estimated detection limit of 1.6 copies/μL of viral nucleic acid. The analytical sensitivity and specificity of PPT-RTcPCR were comparable to that of the reference RT-qPCR assay. Moreover, the clinical performance of PPT-RTcPCR was evaluated and validated using 158 plasma samples collected from patients suspected of dengue infection. The results showed a diagnostic agreement of 97.5% compared to the reference RT-qPCR and demonstrated a clinical sensitivity and specificity of 97.0% and 100%, respectively. The simplicity and reliability of our PPT-RTcPCR strategy suggest it can provide a foundation for developing a field-deployable diagnostic assay for dengue and other infectious diseases. Published by Elsevier B.V. 2023-09-15 2023-06-26 /pmc/articles/PMC10291885/ /pubmed/37455070 http://dx.doi.org/10.1016/j.aca.2023.341565 Text en © 2023 Published by Elsevier B.V. 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
Jiang, Kunlun
Lee, Jung-Hoon
Fung, To Sing
Wu, Jingrui
Liu, Congnuan
Mi, Hua
Rajapakse, R.P.V. Jayanthe
Balasuriya, Udeni B.R.
Peng, Yung-Kang
Go, Yun Young
Next-generation diagnostic test for dengue virus detection using an ultrafast plasmonic colorimetric RT-PCR strategy
title Next-generation diagnostic test for dengue virus detection using an ultrafast plasmonic colorimetric RT-PCR strategy
title_full Next-generation diagnostic test for dengue virus detection using an ultrafast plasmonic colorimetric RT-PCR strategy
title_fullStr Next-generation diagnostic test for dengue virus detection using an ultrafast plasmonic colorimetric RT-PCR strategy
title_full_unstemmed Next-generation diagnostic test for dengue virus detection using an ultrafast plasmonic colorimetric RT-PCR strategy
title_short Next-generation diagnostic test for dengue virus detection using an ultrafast plasmonic colorimetric RT-PCR strategy
title_sort next-generation diagnostic test for dengue virus detection using an ultrafast plasmonic colorimetric rt-pcr strategy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291885/
https://www.ncbi.nlm.nih.gov/pubmed/37455070
http://dx.doi.org/10.1016/j.aca.2023.341565
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