Serological profiles of pan-coronavirus-specific responses in COVID-19 patients using a multiplexed electro-chemiluminescence-based testing platform.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 06 01 2021
accepted: 19 05 2021
entrez: 3 6 2021
pubmed: 4 6 2021
medline: 29 6 2021
Statut: epublish

Résumé

Serological assessment of SARS-CoV-2 specific responses are an essential tool for determining the prevalence of past SARS-CoV-2 infections in the population especially when testing occurs after symptoms have developed and limited contact tracing is in place. The goal of our study was to test a new 10-plex electro-chemiluminescence-based assay to measure IgM and IgG responses to the spike proteins from multiple human coronaviruses including SARS-CoV-2, assess the epitope specificity of the SARS-CoV-2 antibody response against full-length spike protein, receptor-binding domain and N-terminal domain of the spike protein, and the nucleocapsid protein. We carried out the assay on samples collected from three sample groups: subjects diagnosed with COVID-19 from the U.S. Army hospital at Camp Humphreys in Pyeongtaek, South Korea; healthcare administrators from the same hospital but with no reported diagnosis of COVID-19; and pre-pandemic samples. We found that the new CoV-specific multiplex assay was highly sensitive allowing plasma samples to be diluted 1:30,000 with a robust signal. The reactivity of IgG responses to SARS-CoV-2 nucleocapsid protein and IgM responses to SARS-CoV-2 spike protein could distinguish COVID-19 samples from non-COVID-19 and pre-pandemic samples. The data from the three sample groups also revealed a unique pattern of cross-reactivity between SARS-CoV-2 and SARS-CoV-1, MERS-CoV, and seasonal coronaviruses HKU1 and OC43. Our findings show that the CoV-2 IgM response is highly specific while the CoV-2 IgG response is more cross-reactive across a range of human CoVs and also showed that IgM and IgG responses show distinct patterns of epitope specificity. In summary, this multiplex assay was able to distinguish samples by COVID-19 status and characterize distinct trends in terms of cross-reactivity and fine-specificity in antibody responses, underscoring its potential value in diagnostic or serosurveillance efforts.

Identifiants

pubmed: 34081747
doi: 10.1371/journal.pone.0252628
pii: PONE-D-21-00516
pmc: PMC8174743
doi:

Substances chimiques

Antibodies, Viral 0
Immunoglobulin G 0
Immunoglobulin M 0
Nucleocapsid Proteins 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0252628

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Sidhartha Chaudhury (S)

Center Enabling Capabilities, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.

Jack Hutter (J)

Clinical Trials Center, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.

Jessica S Bolton (JS)

Immunology Core, Malaria Biologics Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.
Henry M. Jackson Foundation for The Advancement of Military Medicine, Bethesda, MD, United States of America.

Shilpa Hakre (S)

Emerging Infectious Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.

Evelyn Mose (E)

Brian D. Allgood Army Community Hospital, Camp Humphreys, Pyeongtaek, South Korea.

Amy Wooten (A)

Brian D. Allgood Army Community Hospital, Camp Humphreys, Pyeongtaek, South Korea.

William O'Connell (W)

Brian D. Allgood Army Community Hospital, Camp Humphreys, Pyeongtaek, South Korea.

Joseph Hudak (J)

Brian D. Allgood Army Community Hospital, Camp Humphreys, Pyeongtaek, South Korea.

Shelly J Krebs (SJ)

Emerging Infectious Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.

Janice M Darden (JM)

Henry M. Jackson Foundation for The Advancement of Military Medicine, Bethesda, MD, United States of America.

Jason A Regules (JA)

Immunology Core, Malaria Biologics Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.

Clinton K Murray (CK)

United States Forces Korea Surgeon, Camp Humphreys, South Korea.

Kayvon Modjarrad (K)

Emerging Infectious Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.

Paul Scott (P)

Emerging Infectious Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.

Sheila Peel (S)

Diagnostics and Countermeasures Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.

Elke S Bergmann-Leitner (ES)

Immunology Core, Malaria Biologics Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.

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Classifications MeSH