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Virome-wide detection of natural infection events and the associated antibody dynamics using longitudinal highly-multiplexed serology

Current methods for detecting infections either require a sample collected from an actively infected site, are limited in the number of agents they can query, and/or yield no information on the immune response. Here we present an approach that uses temporally coordinated changes in highly-multiplexe...

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Autores principales: Kelley, Erin J., Henson, Sierra N., Rahee, Fatima, Boyle, Annalee S., Engelbrektson, Anna L., Nelson, Georgia A., Mead, Heather L., Anderson, N. Leigh, Razavi, Morteza, Yip, Richard, Ladner, Jason T., Scriba, Thomas J., Altin, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10062260/
https://www.ncbi.nlm.nih.gov/pubmed/36997517
http://dx.doi.org/10.1038/s41467-023-37378-z
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author Kelley, Erin J.
Henson, Sierra N.
Rahee, Fatima
Boyle, Annalee S.
Engelbrektson, Anna L.
Nelson, Georgia A.
Mead, Heather L.
Anderson, N. Leigh
Razavi, Morteza
Yip, Richard
Ladner, Jason T.
Scriba, Thomas J.
Altin, John A.
author_facet Kelley, Erin J.
Henson, Sierra N.
Rahee, Fatima
Boyle, Annalee S.
Engelbrektson, Anna L.
Nelson, Georgia A.
Mead, Heather L.
Anderson, N. Leigh
Razavi, Morteza
Yip, Richard
Ladner, Jason T.
Scriba, Thomas J.
Altin, John A.
author_sort Kelley, Erin J.
collection PubMed
description Current methods for detecting infections either require a sample collected from an actively infected site, are limited in the number of agents they can query, and/or yield no information on the immune response. Here we present an approach that uses temporally coordinated changes in highly-multiplexed antibody measurements from longitudinal blood samples to monitor infection events at sub-species resolution across the human virome. In a longitudinally-sampled cohort of South African adolescents representing >100 person-years, we identify >650 events across 48 virus species and observe strong epidemic effects, including high-incidence waves of Aichivirus A and the D68 subtype of Enterovirus D earlier than their widespread circulation was appreciated. In separate cohorts of adults who were sampled at higher frequency using self-collected dried blood spots, we show that such events temporally correlate with symptoms and transient inflammatory biomarker elevations, and observe the responding antibodies to persist for periods ranging from ≤1 week to >5 years. Our approach generates a rich view of viral/host dynamics, supporting novel studies in immunology and epidemiology.
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spelling pubmed-100622602023-03-31 Virome-wide detection of natural infection events and the associated antibody dynamics using longitudinal highly-multiplexed serology Kelley, Erin J. Henson, Sierra N. Rahee, Fatima Boyle, Annalee S. Engelbrektson, Anna L. Nelson, Georgia A. Mead, Heather L. Anderson, N. Leigh Razavi, Morteza Yip, Richard Ladner, Jason T. Scriba, Thomas J. Altin, John A. Nat Commun Article Current methods for detecting infections either require a sample collected from an actively infected site, are limited in the number of agents they can query, and/or yield no information on the immune response. Here we present an approach that uses temporally coordinated changes in highly-multiplexed antibody measurements from longitudinal blood samples to monitor infection events at sub-species resolution across the human virome. In a longitudinally-sampled cohort of South African adolescents representing >100 person-years, we identify >650 events across 48 virus species and observe strong epidemic effects, including high-incidence waves of Aichivirus A and the D68 subtype of Enterovirus D earlier than their widespread circulation was appreciated. In separate cohorts of adults who were sampled at higher frequency using self-collected dried blood spots, we show that such events temporally correlate with symptoms and transient inflammatory biomarker elevations, and observe the responding antibodies to persist for periods ranging from ≤1 week to >5 years. Our approach generates a rich view of viral/host dynamics, supporting novel studies in immunology and epidemiology. Nature Publishing Group UK 2023-03-30 /pmc/articles/PMC10062260/ /pubmed/36997517 http://dx.doi.org/10.1038/s41467-023-37378-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kelley, Erin J.
Henson, Sierra N.
Rahee, Fatima
Boyle, Annalee S.
Engelbrektson, Anna L.
Nelson, Georgia A.
Mead, Heather L.
Anderson, N. Leigh
Razavi, Morteza
Yip, Richard
Ladner, Jason T.
Scriba, Thomas J.
Altin, John A.
Virome-wide detection of natural infection events and the associated antibody dynamics using longitudinal highly-multiplexed serology
title Virome-wide detection of natural infection events and the associated antibody dynamics using longitudinal highly-multiplexed serology
title_full Virome-wide detection of natural infection events and the associated antibody dynamics using longitudinal highly-multiplexed serology
title_fullStr Virome-wide detection of natural infection events and the associated antibody dynamics using longitudinal highly-multiplexed serology
title_full_unstemmed Virome-wide detection of natural infection events and the associated antibody dynamics using longitudinal highly-multiplexed serology
title_short Virome-wide detection of natural infection events and the associated antibody dynamics using longitudinal highly-multiplexed serology
title_sort virome-wide detection of natural infection events and the associated antibody dynamics using longitudinal highly-multiplexed serology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10062260/
https://www.ncbi.nlm.nih.gov/pubmed/36997517
http://dx.doi.org/10.1038/s41467-023-37378-z
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