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Deconvoluting virome-wide antibody epitope reactivity profiles
BACKGROUND: Comprehensive characterization of exposures and immune responses to viral infections is critical to a basic understanding of human health and disease. We previously developed the VirScan system, a programmable phage-display technology for profiling antibody binding to a library of peptid...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688874/ https://www.ncbi.nlm.nih.gov/pubmed/34922324 http://dx.doi.org/10.1016/j.ebiom.2021.103747 |
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author | Monaco, Daniel R. Kottapalli, Sanjay V. Breitwieser, Florian P. Anderson, Danielle E. Wijaya, Limin Tan, Kevin Chia, Wan Ni Kammers, Kai Caturegli, Patrizio Waugh, Kathleen Roederer, Mario Petri, Michelle Goldman, Daniel W. Rewers, Marian Wang, Lin-Fa Larman, H. Benjamin |
author_facet | Monaco, Daniel R. Kottapalli, Sanjay V. Breitwieser, Florian P. Anderson, Danielle E. Wijaya, Limin Tan, Kevin Chia, Wan Ni Kammers, Kai Caturegli, Patrizio Waugh, Kathleen Roederer, Mario Petri, Michelle Goldman, Daniel W. Rewers, Marian Wang, Lin-Fa Larman, H. Benjamin |
author_sort | Monaco, Daniel R. |
collection | PubMed |
description | BACKGROUND: Comprehensive characterization of exposures and immune responses to viral infections is critical to a basic understanding of human health and disease. We previously developed the VirScan system, a programmable phage-display technology for profiling antibody binding to a library of peptides designed to span the human virome. Previous VirScan analytical approaches did not carefully account for antibody cross-reactivity among sequences shared by related viruses or for the disproportionate representation of individual viruses in the library. METHODS: Here we present the AntiViral Antibody Response Deconvolution Algorithm (AVARDA), a multi-module software package for analyzing VirScan datasets. AVARDA provides a probabilistic assessment of infection with species-level resolution by considering sequence alignment of all library peptides to each other and to all human viruses. We employed AVARDA to analyze VirScan data from a cohort of encephalitis patients with either known viral infections or undiagnosed etiologies. We further assessed AVARDA's utility in associating viral infection with type 1 diabetes and lupus. FINDINGS: By comparing acute and convalescent sera, AVARDA successfully confirmed or detected encephalitis-associated responses to human herpesviruses 1, 3, 4, 5, and 6, improving the rate of diagnosing viral encephalitis in this cohort by 44%. AVARDA analyses of VirScan data from the type 1 diabetes and lupus cohorts implicated enterovirus and herpesvirus infections, respectively. INTERPRETATION: AVARDA, in combination with VirScan and other pan-pathogen serological techniques, is likely to find broad utility in the epidemiology and diagnosis of infectious diseases. FUNDING: This work was made possible by support from the National Institutes of Health (NIH), the US Army Research Office, the Singapore Infectious Diseases Initiative (SIDI), the Singapore Ministry of Health's National Medical Research Council (NMRC) and the Singapore National Research Foundation (NRF). |
format | Online Article Text |
id | pubmed-8688874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-86888742021-12-30 Deconvoluting virome-wide antibody epitope reactivity profiles Monaco, Daniel R. Kottapalli, Sanjay V. Breitwieser, Florian P. Anderson, Danielle E. Wijaya, Limin Tan, Kevin Chia, Wan Ni Kammers, Kai Caturegli, Patrizio Waugh, Kathleen Roederer, Mario Petri, Michelle Goldman, Daniel W. Rewers, Marian Wang, Lin-Fa Larman, H. Benjamin EBioMedicine Article BACKGROUND: Comprehensive characterization of exposures and immune responses to viral infections is critical to a basic understanding of human health and disease. We previously developed the VirScan system, a programmable phage-display technology for profiling antibody binding to a library of peptides designed to span the human virome. Previous VirScan analytical approaches did not carefully account for antibody cross-reactivity among sequences shared by related viruses or for the disproportionate representation of individual viruses in the library. METHODS: Here we present the AntiViral Antibody Response Deconvolution Algorithm (AVARDA), a multi-module software package for analyzing VirScan datasets. AVARDA provides a probabilistic assessment of infection with species-level resolution by considering sequence alignment of all library peptides to each other and to all human viruses. We employed AVARDA to analyze VirScan data from a cohort of encephalitis patients with either known viral infections or undiagnosed etiologies. We further assessed AVARDA's utility in associating viral infection with type 1 diabetes and lupus. FINDINGS: By comparing acute and convalescent sera, AVARDA successfully confirmed or detected encephalitis-associated responses to human herpesviruses 1, 3, 4, 5, and 6, improving the rate of diagnosing viral encephalitis in this cohort by 44%. AVARDA analyses of VirScan data from the type 1 diabetes and lupus cohorts implicated enterovirus and herpesvirus infections, respectively. INTERPRETATION: AVARDA, in combination with VirScan and other pan-pathogen serological techniques, is likely to find broad utility in the epidemiology and diagnosis of infectious diseases. FUNDING: This work was made possible by support from the National Institutes of Health (NIH), the US Army Research Office, the Singapore Infectious Diseases Initiative (SIDI), the Singapore Ministry of Health's National Medical Research Council (NMRC) and the Singapore National Research Foundation (NRF). Elsevier 2021-12-16 /pmc/articles/PMC8688874/ /pubmed/34922324 http://dx.doi.org/10.1016/j.ebiom.2021.103747 Text en © 2021 Published by Elsevier B.V. https://creativecommons.org/licenses/by/3.0/igo/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/igo/). |
spellingShingle | Article Monaco, Daniel R. Kottapalli, Sanjay V. Breitwieser, Florian P. Anderson, Danielle E. Wijaya, Limin Tan, Kevin Chia, Wan Ni Kammers, Kai Caturegli, Patrizio Waugh, Kathleen Roederer, Mario Petri, Michelle Goldman, Daniel W. Rewers, Marian Wang, Lin-Fa Larman, H. Benjamin Deconvoluting virome-wide antibody epitope reactivity profiles |
title | Deconvoluting virome-wide antibody epitope reactivity profiles |
title_full | Deconvoluting virome-wide antibody epitope reactivity profiles |
title_fullStr | Deconvoluting virome-wide antibody epitope reactivity profiles |
title_full_unstemmed | Deconvoluting virome-wide antibody epitope reactivity profiles |
title_short | Deconvoluting virome-wide antibody epitope reactivity profiles |
title_sort | deconvoluting virome-wide antibody epitope reactivity profiles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688874/ https://www.ncbi.nlm.nih.gov/pubmed/34922324 http://dx.doi.org/10.1016/j.ebiom.2021.103747 |
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