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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2020
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.
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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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