High-throughput quantitation of SARS-CoV-2 antibodies in a single-dilution homogeneous assay

Abstract SARS-CoV-2 emerged in late 2019 and has since spread around the world, causing a pandemic of the respiratory disease COVID-19. Detecting antibodies against the virus is an essential tool for tracking infections and developing vaccines. Such tests, primarily utilizing the enzyme-linked immun...

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Autores principales: Markus H. Kainulainen, Eric Bergeron, Payel Chatterjee, Asheley P. Chapman, Joo Lee, Asiya Chida, Xiaoling Tang, Rebekah E. Wharton, Kristina B. Mercer, Marla Petway, Harley M. Jenks, Timothy D. Flietstra, Amy J. Schuh, Panayampalli S. Satheshkumar, Jasmine M. Chaitram, S. Michele Owen, Laura K. McMullan, Mike Flint, M. G. Finn, Jason M. Goldstein, Joel M. Montgomery, Christina F. Spiropoulou
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:27dfd414a1384a84aa5cb8b2992de9c12021-12-02T17:30:46ZHigh-throughput quantitation of SARS-CoV-2 antibodies in a single-dilution homogeneous assay10.1038/s41598-021-91300-52045-2322https://doaj.org/article/27dfd414a1384a84aa5cb8b2992de9c12021-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-91300-5https://doaj.org/toc/2045-2322Abstract SARS-CoV-2 emerged in late 2019 and has since spread around the world, causing a pandemic of the respiratory disease COVID-19. Detecting antibodies against the virus is an essential tool for tracking infections and developing vaccines. Such tests, primarily utilizing the enzyme-linked immunosorbent assay (ELISA) principle, can be either qualitative (reporting positive/negative results) or quantitative (reporting a value representing the quantity of specific antibodies). Quantitation is vital for determining stability or decline of antibody titers in convalescence, efficacy of different vaccination regimens, and detection of asymptomatic infections. Quantitation typically requires two-step ELISA testing, in which samples are first screened in a qualitative assay and positive samples are subsequently analyzed as a dilution series. To overcome the throughput limitations of this approach, we developed a simpler and faster system that is highly automatable and achieves quantitation in a single-dilution screening format with sensitivity and specificity comparable to those of ELISA.Markus H. KainulainenEric BergeronPayel ChatterjeeAsheley P. ChapmanJoo LeeAsiya ChidaXiaoling TangRebekah E. WhartonKristina B. MercerMarla PetwayHarley M. JenksTimothy D. FlietstraAmy J. SchuhPanayampalli S. SatheshkumarJasmine M. ChaitramS. Michele OwenLaura K. McMullanMike FlintM. G. FinnJason M. GoldsteinJoel M. MontgomeryChristina F. SpiropoulouNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Markus H. Kainulainen
Eric Bergeron
Payel Chatterjee
Asheley P. Chapman
Joo Lee
Asiya Chida
Xiaoling Tang
Rebekah E. Wharton
Kristina B. Mercer
Marla Petway
Harley M. Jenks
Timothy D. Flietstra
Amy J. Schuh
Panayampalli S. Satheshkumar
Jasmine M. Chaitram
S. Michele Owen
Laura K. McMullan
Mike Flint
M. G. Finn
Jason M. Goldstein
Joel M. Montgomery
Christina F. Spiropoulou
High-throughput quantitation of SARS-CoV-2 antibodies in a single-dilution homogeneous assay
description Abstract SARS-CoV-2 emerged in late 2019 and has since spread around the world, causing a pandemic of the respiratory disease COVID-19. Detecting antibodies against the virus is an essential tool for tracking infections and developing vaccines. Such tests, primarily utilizing the enzyme-linked immunosorbent assay (ELISA) principle, can be either qualitative (reporting positive/negative results) or quantitative (reporting a value representing the quantity of specific antibodies). Quantitation is vital for determining stability or decline of antibody titers in convalescence, efficacy of different vaccination regimens, and detection of asymptomatic infections. Quantitation typically requires two-step ELISA testing, in which samples are first screened in a qualitative assay and positive samples are subsequently analyzed as a dilution series. To overcome the throughput limitations of this approach, we developed a simpler and faster system that is highly automatable and achieves quantitation in a single-dilution screening format with sensitivity and specificity comparable to those of ELISA.
format article
author Markus H. Kainulainen
Eric Bergeron
Payel Chatterjee
Asheley P. Chapman
Joo Lee
Asiya Chida
Xiaoling Tang
Rebekah E. Wharton
Kristina B. Mercer
Marla Petway
Harley M. Jenks
Timothy D. Flietstra
Amy J. Schuh
Panayampalli S. Satheshkumar
Jasmine M. Chaitram
S. Michele Owen
Laura K. McMullan
Mike Flint
M. G. Finn
Jason M. Goldstein
Joel M. Montgomery
Christina F. Spiropoulou
author_facet Markus H. Kainulainen
Eric Bergeron
Payel Chatterjee
Asheley P. Chapman
Joo Lee
Asiya Chida
Xiaoling Tang
Rebekah E. Wharton
Kristina B. Mercer
Marla Petway
Harley M. Jenks
Timothy D. Flietstra
Amy J. Schuh
Panayampalli S. Satheshkumar
Jasmine M. Chaitram
S. Michele Owen
Laura K. McMullan
Mike Flint
M. G. Finn
Jason M. Goldstein
Joel M. Montgomery
Christina F. Spiropoulou
author_sort Markus H. Kainulainen
title High-throughput quantitation of SARS-CoV-2 antibodies in a single-dilution homogeneous assay
title_short High-throughput quantitation of SARS-CoV-2 antibodies in a single-dilution homogeneous assay
title_full High-throughput quantitation of SARS-CoV-2 antibodies in a single-dilution homogeneous assay
title_fullStr High-throughput quantitation of SARS-CoV-2 antibodies in a single-dilution homogeneous assay
title_full_unstemmed High-throughput quantitation of SARS-CoV-2 antibodies in a single-dilution homogeneous assay
title_sort high-throughput quantitation of sars-cov-2 antibodies in a single-dilution homogeneous assay
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/27dfd414a1384a84aa5cb8b2992de9c1
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