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Rapid and universal detection of SARS‐CoV‐2 and influenza A virus using a reusable dual‐channel optic fiber immunosensor

Establishment of rapid on‐site detection technology capable of concurrently detecting SARS‐Cov‐2 and influenza A virus is urgent to effectively control the epidemic from these two types of important viruses. Accordingly, we developed a reusable dual‐channel optical fiber immunosensor (DOFIS), which...

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Autores principales: Yang, Yi, Zhao, Rongtao, Wang, Yule, Song, Dan, Jiang, Bo, Guo, Xudong, Liu, Wanying, Long, Feng, Song, Hongbin, Hao, Rongzhang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349508/
https://www.ncbi.nlm.nih.gov/pubmed/35859097
http://dx.doi.org/10.1002/jmv.28015
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author Yang, Yi
Zhao, Rongtao
Wang, Yule
Song, Dan
Jiang, Bo
Guo, Xudong
Liu, Wanying
Long, Feng
Song, Hongbin
Hao, Rongzhang
author_facet Yang, Yi
Zhao, Rongtao
Wang, Yule
Song, Dan
Jiang, Bo
Guo, Xudong
Liu, Wanying
Long, Feng
Song, Hongbin
Hao, Rongzhang
author_sort Yang, Yi
collection PubMed
description Establishment of rapid on‐site detection technology capable of concurrently detecting SARS‐Cov‐2 and influenza A virus is urgent to effectively control the epidemic from these two types of important viruses. Accordingly, we developed a reusable dual‐channel optical fiber immunosensor (DOFIS), which utilized the evanescent wave‐sensing properties and tandem detection mode of the mobile phase, effectively accelerating the detection process such that it can be completed within 10 min. It could detect the nucleoprotein of multiple influenza A viruses (H1N1, H3N2, and H7N9), as well as the spike proteins of the SARS‐CoV‐2 Omicron and Delta variants, and could respond to 20 TCID(50)/ml SARS‐CoV‐2 pseudovirus and 100 TCID(50)/ml influenza A (A/PR/8/H1N1), presenting lower limit of detection and wider linear range than enzyme‐linked immunosorbent assay. The detection results on 26 clinical samples for SARS‐CoV‐2 demonstrated its specificity (100%) and sensitivity (94%), much higher than the sensitivity of commercial colloidal gold test strip (35%). Particularly, DOFIS might be reused more than 80 times, showing not only cost‐saving but also potential in real‐time monitoring of the pathogenic viruses. Therefore, this newly‐developed DOFIS platform is low cost, simple to operate, and has broad spectrum detection capabilities for SARS‐CoV‐2 mutations and multiple influenza A strains. It may prove suitable for deployment as a rapid on‐site screening and surveillance technique for infectious disease.
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spelling pubmed-93495082022-08-04 Rapid and universal detection of SARS‐CoV‐2 and influenza A virus using a reusable dual‐channel optic fiber immunosensor Yang, Yi Zhao, Rongtao Wang, Yule Song, Dan Jiang, Bo Guo, Xudong Liu, Wanying Long, Feng Song, Hongbin Hao, Rongzhang J Med Virol Research Articles Establishment of rapid on‐site detection technology capable of concurrently detecting SARS‐Cov‐2 and influenza A virus is urgent to effectively control the epidemic from these two types of important viruses. Accordingly, we developed a reusable dual‐channel optical fiber immunosensor (DOFIS), which utilized the evanescent wave‐sensing properties and tandem detection mode of the mobile phase, effectively accelerating the detection process such that it can be completed within 10 min. It could detect the nucleoprotein of multiple influenza A viruses (H1N1, H3N2, and H7N9), as well as the spike proteins of the SARS‐CoV‐2 Omicron and Delta variants, and could respond to 20 TCID(50)/ml SARS‐CoV‐2 pseudovirus and 100 TCID(50)/ml influenza A (A/PR/8/H1N1), presenting lower limit of detection and wider linear range than enzyme‐linked immunosorbent assay. The detection results on 26 clinical samples for SARS‐CoV‐2 demonstrated its specificity (100%) and sensitivity (94%), much higher than the sensitivity of commercial colloidal gold test strip (35%). Particularly, DOFIS might be reused more than 80 times, showing not only cost‐saving but also potential in real‐time monitoring of the pathogenic viruses. Therefore, this newly‐developed DOFIS platform is low cost, simple to operate, and has broad spectrum detection capabilities for SARS‐CoV‐2 mutations and multiple influenza A strains. It may prove suitable for deployment as a rapid on‐site screening and surveillance technique for infectious disease. John Wiley and Sons Inc. 2022-07-26 2022-11 /pmc/articles/PMC9349508/ /pubmed/35859097 http://dx.doi.org/10.1002/jmv.28015 Text en © 2022 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Yang, Yi
Zhao, Rongtao
Wang, Yule
Song, Dan
Jiang, Bo
Guo, Xudong
Liu, Wanying
Long, Feng
Song, Hongbin
Hao, Rongzhang
Rapid and universal detection of SARS‐CoV‐2 and influenza A virus using a reusable dual‐channel optic fiber immunosensor
title Rapid and universal detection of SARS‐CoV‐2 and influenza A virus using a reusable dual‐channel optic fiber immunosensor
title_full Rapid and universal detection of SARS‐CoV‐2 and influenza A virus using a reusable dual‐channel optic fiber immunosensor
title_fullStr Rapid and universal detection of SARS‐CoV‐2 and influenza A virus using a reusable dual‐channel optic fiber immunosensor
title_full_unstemmed Rapid and universal detection of SARS‐CoV‐2 and influenza A virus using a reusable dual‐channel optic fiber immunosensor
title_short Rapid and universal detection of SARS‐CoV‐2 and influenza A virus using a reusable dual‐channel optic fiber immunosensor
title_sort rapid and universal detection of sars‐cov‐2 and influenza a virus using a reusable dual‐channel optic fiber immunosensor
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349508/
https://www.ncbi.nlm.nih.gov/pubmed/35859097
http://dx.doi.org/10.1002/jmv.28015
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