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Analysis of Serologic Cross-Reactivity Between Common Human Coronaviruses and SARS-CoV-2 Using Coronavirus Antigen Microarray
The current practice for diagnosis of SARS-CoV-2 infection relies on PCR testing of nasopharyngeal or respiratory specimens in a symptomatic patient at high epidemiologic risk. This testing strategy likely underestimates the true prevalence of infection, creating the need for serologic methods to de...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239054/ https://www.ncbi.nlm.nih.gov/pubmed/32511324 http://dx.doi.org/10.1101/2020.03.24.006544 |
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author | Khan, Saahir Nakajima, Rie Jain, Aarti de Assis, Rafael Ramiro Jasinskas, Al Obiero, Joshua M. Adenaiye, Oluwasanmi Tai, Sheldon Hong, Filbert Milton, Donald K. Davies, Huw Felgner, Philip L. |
author_facet | Khan, Saahir Nakajima, Rie Jain, Aarti de Assis, Rafael Ramiro Jasinskas, Al Obiero, Joshua M. Adenaiye, Oluwasanmi Tai, Sheldon Hong, Filbert Milton, Donald K. Davies, Huw Felgner, Philip L. |
author_sort | Khan, Saahir |
collection | PubMed |
description | The current practice for diagnosis of SARS-CoV-2 infection relies on PCR testing of nasopharyngeal or respiratory specimens in a symptomatic patient at high epidemiologic risk. This testing strategy likely underestimates the true prevalence of infection, creating the need for serologic methods to detect infections missed by the limited testing to date. Here, we describe the development of a coronavirus antigen microarray containing immunologically significant antigens from SARS-CoV-2, in addition to SARS-CoV, MERS-CoV, common human coronavirus strains, and other common respiratory viruses. A preliminary study of human sera collected prior to the SARS-CoV-2 pandemic demonstrates overall high IgG reactivity to common human coronaviruses and low IgG reactivity to epidemic coronaviruses including SARS-CoV-2, with some cross-reactivity of conserved antigenic domains including S2 domain of spike protein and nucleocapsid protein. This array can be used to answer outstanding questions regarding SARS-CoV-2 infection, including whether baseline serology for other coronaviruses impacts disease course, how the antibody response to infection develops over time, and what antigens would be optimal for vaccine development. |
format | Online Article Text |
id | pubmed-7239054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-72390542020-06-07 Analysis of Serologic Cross-Reactivity Between Common Human Coronaviruses and SARS-CoV-2 Using Coronavirus Antigen Microarray Khan, Saahir Nakajima, Rie Jain, Aarti de Assis, Rafael Ramiro Jasinskas, Al Obiero, Joshua M. Adenaiye, Oluwasanmi Tai, Sheldon Hong, Filbert Milton, Donald K. Davies, Huw Felgner, Philip L. bioRxiv Article The current practice for diagnosis of SARS-CoV-2 infection relies on PCR testing of nasopharyngeal or respiratory specimens in a symptomatic patient at high epidemiologic risk. This testing strategy likely underestimates the true prevalence of infection, creating the need for serologic methods to detect infections missed by the limited testing to date. Here, we describe the development of a coronavirus antigen microarray containing immunologically significant antigens from SARS-CoV-2, in addition to SARS-CoV, MERS-CoV, common human coronavirus strains, and other common respiratory viruses. A preliminary study of human sera collected prior to the SARS-CoV-2 pandemic demonstrates overall high IgG reactivity to common human coronaviruses and low IgG reactivity to epidemic coronaviruses including SARS-CoV-2, with some cross-reactivity of conserved antigenic domains including S2 domain of spike protein and nucleocapsid protein. This array can be used to answer outstanding questions regarding SARS-CoV-2 infection, including whether baseline serology for other coronaviruses impacts disease course, how the antibody response to infection develops over time, and what antigens would be optimal for vaccine development. Cold Spring Harbor Laboratory 2020-03-25 /pmc/articles/PMC7239054/ /pubmed/32511324 http://dx.doi.org/10.1101/2020.03.24.006544 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Khan, Saahir Nakajima, Rie Jain, Aarti de Assis, Rafael Ramiro Jasinskas, Al Obiero, Joshua M. Adenaiye, Oluwasanmi Tai, Sheldon Hong, Filbert Milton, Donald K. Davies, Huw Felgner, Philip L. Analysis of Serologic Cross-Reactivity Between Common Human Coronaviruses and SARS-CoV-2 Using Coronavirus Antigen Microarray |
title | Analysis of Serologic Cross-Reactivity Between Common Human Coronaviruses and SARS-CoV-2 Using Coronavirus Antigen Microarray |
title_full | Analysis of Serologic Cross-Reactivity Between Common Human Coronaviruses and SARS-CoV-2 Using Coronavirus Antigen Microarray |
title_fullStr | Analysis of Serologic Cross-Reactivity Between Common Human Coronaviruses and SARS-CoV-2 Using Coronavirus Antigen Microarray |
title_full_unstemmed | Analysis of Serologic Cross-Reactivity Between Common Human Coronaviruses and SARS-CoV-2 Using Coronavirus Antigen Microarray |
title_short | Analysis of Serologic Cross-Reactivity Between Common Human Coronaviruses and SARS-CoV-2 Using Coronavirus Antigen Microarray |
title_sort | analysis of serologic cross-reactivity between common human coronaviruses and sars-cov-2 using coronavirus antigen microarray |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239054/ https://www.ncbi.nlm.nih.gov/pubmed/32511324 http://dx.doi.org/10.1101/2020.03.24.006544 |
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