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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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).
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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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