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Differential human antibody repertoires following Zika infection and the implications for serodiagnostics and disease outcome

Zika virus (ZIKV) outbreak in Americas led to extensive efforts to develop vaccines and ZIKV-specific diagnostics. In the current study, we use whole genome phage display library spanning the entire ZIKV genome (ZIKV-GFPDL) for in-depth immune profiling of IgG and IgM antibody repertoires in serum a...

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Autores principales: Ravichandran, Supriya, Hahn, Megan, Belaunzarán-Zamudio, Pablo F., Ramos-Castañeda, José, Nájera-Cancino, Gabriel, Caballero-Sosa, Sandra, Navarro-Fuentes, Karla R., Ruiz-Palacios, Guillermo, Golding, Hana, Beigel, John H., Khurana, Surender
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486612/
https://www.ncbi.nlm.nih.gov/pubmed/31028263
http://dx.doi.org/10.1038/s41467-019-09914-3
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author Ravichandran, Supriya
Hahn, Megan
Belaunzarán-Zamudio, Pablo F.
Ramos-Castañeda, José
Nájera-Cancino, Gabriel
Caballero-Sosa, Sandra
Navarro-Fuentes, Karla R.
Ruiz-Palacios, Guillermo
Golding, Hana
Beigel, John H.
Khurana, Surender
author_facet Ravichandran, Supriya
Hahn, Megan
Belaunzarán-Zamudio, Pablo F.
Ramos-Castañeda, José
Nájera-Cancino, Gabriel
Caballero-Sosa, Sandra
Navarro-Fuentes, Karla R.
Ruiz-Palacios, Guillermo
Golding, Hana
Beigel, John H.
Khurana, Surender
author_sort Ravichandran, Supriya
collection PubMed
description Zika virus (ZIKV) outbreak in Americas led to extensive efforts to develop vaccines and ZIKV-specific diagnostics. In the current study, we use whole genome phage display library spanning the entire ZIKV genome (ZIKV-GFPDL) for in-depth immune profiling of IgG and IgM antibody repertoires in serum and urine longitudinal samples from individuals acutely infected with ZIKV. We observe a very diverse IgM immune repertoire encompassing the entire ZIKV polyprotein on day 0 in both serum and urine. ZIKV-specific IgG antibodies increase 10-fold between day 0 and day 7 in serum, but not in urine; these are highly focused on prM/E, NS1 and NS2B. Differential antibody affinity maturation is observed against ZIKV structural E protein compared with nonstructural protein NS1. Serum antibody affinity to ZIKV-E protein inversely correlates with ZIKV disease symptoms. Our study provides insight into unlinked evolution of immune response to ZIKV infection and identified unique targets for ZIKV serodiagnostics.
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spelling pubmed-64866122019-04-29 Differential human antibody repertoires following Zika infection and the implications for serodiagnostics and disease outcome Ravichandran, Supriya Hahn, Megan Belaunzarán-Zamudio, Pablo F. Ramos-Castañeda, José Nájera-Cancino, Gabriel Caballero-Sosa, Sandra Navarro-Fuentes, Karla R. Ruiz-Palacios, Guillermo Golding, Hana Beigel, John H. Khurana, Surender Nat Commun Article Zika virus (ZIKV) outbreak in Americas led to extensive efforts to develop vaccines and ZIKV-specific diagnostics. In the current study, we use whole genome phage display library spanning the entire ZIKV genome (ZIKV-GFPDL) for in-depth immune profiling of IgG and IgM antibody repertoires in serum and urine longitudinal samples from individuals acutely infected with ZIKV. We observe a very diverse IgM immune repertoire encompassing the entire ZIKV polyprotein on day 0 in both serum and urine. ZIKV-specific IgG antibodies increase 10-fold between day 0 and day 7 in serum, but not in urine; these are highly focused on prM/E, NS1 and NS2B. Differential antibody affinity maturation is observed against ZIKV structural E protein compared with nonstructural protein NS1. Serum antibody affinity to ZIKV-E protein inversely correlates with ZIKV disease symptoms. Our study provides insight into unlinked evolution of immune response to ZIKV infection and identified unique targets for ZIKV serodiagnostics. Nature Publishing Group UK 2019-04-26 /pmc/articles/PMC6486612/ /pubmed/31028263 http://dx.doi.org/10.1038/s41467-019-09914-3 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2019 2019 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/.
spellingShingle Article
Ravichandran, Supriya
Hahn, Megan
Belaunzarán-Zamudio, Pablo F.
Ramos-Castañeda, José
Nájera-Cancino, Gabriel
Caballero-Sosa, Sandra
Navarro-Fuentes, Karla R.
Ruiz-Palacios, Guillermo
Golding, Hana
Beigel, John H.
Khurana, Surender
Differential human antibody repertoires following Zika infection and the implications for serodiagnostics and disease outcome
title Differential human antibody repertoires following Zika infection and the implications for serodiagnostics and disease outcome
title_full Differential human antibody repertoires following Zika infection and the implications for serodiagnostics and disease outcome
title_fullStr Differential human antibody repertoires following Zika infection and the implications for serodiagnostics and disease outcome
title_full_unstemmed Differential human antibody repertoires following Zika infection and the implications for serodiagnostics and disease outcome
title_short Differential human antibody repertoires following Zika infection and the implications for serodiagnostics and disease outcome
title_sort differential human antibody repertoires following zika infection and the implications for serodiagnostics and disease outcome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486612/
https://www.ncbi.nlm.nih.gov/pubmed/31028263
http://dx.doi.org/10.1038/s41467-019-09914-3
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