Rapid “mix and read” assay for scalable detection of SARS-CoV-2 antibodies in patient plasma
Abstract The human beta coronavirus SARS-CoV-2, causative virus of COVID-19, has infected more than 15 million people globally and continues to spread. Widespread, population level testing to detect active and past infections is critical to curb the COVID-19 pandemic. Antibody (serological) testing is the only option for detecting past infections outside the narrow window accessible to nucleic acid-based tests. However, currently available serological assays commonly lack scalability. Here, we describe the development of a rapid homogenous serological assay for the detection of antibodies to SARS-CoV-2 in patient plasma. We show that the fluorescence-based assay accurately detects seroconversion in COVID-19 patients from less than 1μL of plasma. Using a cohort of samples from COVID-19 infected or healthy individuals, we demonstrate detection with 100% sensitivity and specificity. This assay addresses an important need for a robust, low barrier to implementation, and scalable serological assay with complementary strengths to currently available serological platforms..
Medienart: |
Preprint |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
bioRxiv.org - (2024) vom: 23. Apr. Zur Gesamtaufnahme - year:2024 |
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Sprache: |
Englisch |
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Beteiligte Personen: |
Yue, Hong [VerfasserIn] |
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Links: |
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Themen: |
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doi: |
10.1101/2020.09.01.20184101 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
XBI018674836 |
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520 | |a Abstract The human beta coronavirus SARS-CoV-2, causative virus of COVID-19, has infected more than 15 million people globally and continues to spread. Widespread, population level testing to detect active and past infections is critical to curb the COVID-19 pandemic. Antibody (serological) testing is the only option for detecting past infections outside the narrow window accessible to nucleic acid-based tests. However, currently available serological assays commonly lack scalability. Here, we describe the development of a rapid homogenous serological assay for the detection of antibodies to SARS-CoV-2 in patient plasma. We show that the fluorescence-based assay accurately detects seroconversion in COVID-19 patients from less than 1μL of plasma. Using a cohort of samples from COVID-19 infected or healthy individuals, we demonstrate detection with 100% sensitivity and specificity. This assay addresses an important need for a robust, low barrier to implementation, and scalable serological assay with complementary strengths to currently available serological platforms. | ||
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700 | 1 | |a Nowak, Radosław P. |e verfasserin |0 (orcid)0000-0002-0605-0071 |4 aut | |
700 | 1 | |a Overwijn, Daan |e verfasserin |4 aut | |
700 | 1 | |a Payne, N. Connor |e verfasserin |4 aut | |
700 | 1 | |a Fischinger, Stephanie |e verfasserin |0 (orcid)0000-0003-2307-3379 |4 aut | |
700 | 1 | |a Atyeo, Caroline |e verfasserin |4 aut | |
700 | 1 | |a Baden, Lindsey R. |e verfasserin |4 aut | |
700 | 1 | |a Nilles, Eric J. |e verfasserin |0 (orcid)0000-0001-7044-5257 |4 aut | |
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700 | 1 | |a Alter, Galit |e verfasserin |4 aut | |
700 | 1 | |a Mazitschek, Ralph |e verfasserin |4 aut | |
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