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An Optimized High-Throughput Immuno-Plaque Assay for SARS-CoV-2

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has been identified as the causative agent of coronavirus disease 2019 and is capable of human-to-human transmission and rapid global spread. The rapid emergence and global spread of SARS-CoV-2 has encouraged the establishment of a rapid,...

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Autores principales: Amarilla, Alberto A., Modhiran, Naphak, Setoh, Yin Xiang, Peng, Nias Y. G., Sng, Julian D. J., Liang, Benjamin, McMillan, Christopher L. D., Freney, Morgan E., Cheung, Stacey T. M., Chappell, Keith J., Khromykh, Alexander A., Young, Paul R., Watterson, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906992/
https://www.ncbi.nlm.nih.gov/pubmed/33643253
http://dx.doi.org/10.3389/fmicb.2021.625136
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author Amarilla, Alberto A.
Modhiran, Naphak
Setoh, Yin Xiang
Peng, Nias Y. G.
Sng, Julian D. J.
Liang, Benjamin
McMillan, Christopher L. D.
Freney, Morgan E.
Cheung, Stacey T. M.
Chappell, Keith J.
Khromykh, Alexander A.
Young, Paul R.
Watterson, Daniel
author_facet Amarilla, Alberto A.
Modhiran, Naphak
Setoh, Yin Xiang
Peng, Nias Y. G.
Sng, Julian D. J.
Liang, Benjamin
McMillan, Christopher L. D.
Freney, Morgan E.
Cheung, Stacey T. M.
Chappell, Keith J.
Khromykh, Alexander A.
Young, Paul R.
Watterson, Daniel
author_sort Amarilla, Alberto A.
collection PubMed
description Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has been identified as the causative agent of coronavirus disease 2019 and is capable of human-to-human transmission and rapid global spread. The rapid emergence and global spread of SARS-CoV-2 has encouraged the establishment of a rapid, sensitive, and reliable viral detection and quantification methodology. Here, we present an alternative assay, termed immuno-plaque assay (iPA), which utilizes a combination of plaque assay and immunofluorescence techniques. We have extensively optimized the conditions for SARS-CoV-2 infection and demonstrated the great flexibility of iPA detection using several antibodies and dual-probing with two distinct epitope-specific antibodies. In addition, we showed that iPA could be utilized for ultra-high-throughput viral titration and neutralization assay within 24 h and is amenable to a 384-well format. These advantages will significantly accelerate SARS-CoV-2 research outcomes during this pandemic period.
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spelling pubmed-79069922021-02-27 An Optimized High-Throughput Immuno-Plaque Assay for SARS-CoV-2 Amarilla, Alberto A. Modhiran, Naphak Setoh, Yin Xiang Peng, Nias Y. G. Sng, Julian D. J. Liang, Benjamin McMillan, Christopher L. D. Freney, Morgan E. Cheung, Stacey T. M. Chappell, Keith J. Khromykh, Alexander A. Young, Paul R. Watterson, Daniel Front Microbiol Microbiology Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has been identified as the causative agent of coronavirus disease 2019 and is capable of human-to-human transmission and rapid global spread. The rapid emergence and global spread of SARS-CoV-2 has encouraged the establishment of a rapid, sensitive, and reliable viral detection and quantification methodology. Here, we present an alternative assay, termed immuno-plaque assay (iPA), which utilizes a combination of plaque assay and immunofluorescence techniques. We have extensively optimized the conditions for SARS-CoV-2 infection and demonstrated the great flexibility of iPA detection using several antibodies and dual-probing with two distinct epitope-specific antibodies. In addition, we showed that iPA could be utilized for ultra-high-throughput viral titration and neutralization assay within 24 h and is amenable to a 384-well format. These advantages will significantly accelerate SARS-CoV-2 research outcomes during this pandemic period. Frontiers Media S.A. 2021-02-12 /pmc/articles/PMC7906992/ /pubmed/33643253 http://dx.doi.org/10.3389/fmicb.2021.625136 Text en Copyright © 2021 Amarilla, Modhiran, Setoh, Peng, Sng, Liang, McMillan, Freney, Cheung, Chappell, Khromykh, Young and Watterson. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Amarilla, Alberto A.
Modhiran, Naphak
Setoh, Yin Xiang
Peng, Nias Y. G.
Sng, Julian D. J.
Liang, Benjamin
McMillan, Christopher L. D.
Freney, Morgan E.
Cheung, Stacey T. M.
Chappell, Keith J.
Khromykh, Alexander A.
Young, Paul R.
Watterson, Daniel
An Optimized High-Throughput Immuno-Plaque Assay for SARS-CoV-2
title An Optimized High-Throughput Immuno-Plaque Assay for SARS-CoV-2
title_full An Optimized High-Throughput Immuno-Plaque Assay for SARS-CoV-2
title_fullStr An Optimized High-Throughput Immuno-Plaque Assay for SARS-CoV-2
title_full_unstemmed An Optimized High-Throughput Immuno-Plaque Assay for SARS-CoV-2
title_short An Optimized High-Throughput Immuno-Plaque Assay for SARS-CoV-2
title_sort optimized high-throughput immuno-plaque assay for sars-cov-2
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906992/
https://www.ncbi.nlm.nih.gov/pubmed/33643253
http://dx.doi.org/10.3389/fmicb.2021.625136
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