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Origin of Public Memory B Cell Clones in Fish After Antiviral Vaccination
Vaccination induces “public” antibody clonotypes common to all individuals of a species, that may mediate universal protection against pathogens. Only few studies tried to trace back the origin of these public B-cell clones. Here we used Illumina sequencing and computational modeling to unveil the m...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170628/ https://www.ncbi.nlm.nih.gov/pubmed/30319606 http://dx.doi.org/10.3389/fimmu.2018.02115 |
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author | Magadan, Susana Jouneau, Luc Puelma Touzel, Maximilian Marillet, Simon Chara, Wahiba Six, Adrien Quillet, Edwige Mora, Thierry Walczak, Aleksandra M. Cazals, Frédéric Sunyer, Oriol Fillatreau, Simon Boudinot, Pierre |
author_facet | Magadan, Susana Jouneau, Luc Puelma Touzel, Maximilian Marillet, Simon Chara, Wahiba Six, Adrien Quillet, Edwige Mora, Thierry Walczak, Aleksandra M. Cazals, Frédéric Sunyer, Oriol Fillatreau, Simon Boudinot, Pierre |
author_sort | Magadan, Susana |
collection | PubMed |
description | Vaccination induces “public” antibody clonotypes common to all individuals of a species, that may mediate universal protection against pathogens. Only few studies tried to trace back the origin of these public B-cell clones. Here we used Illumina sequencing and computational modeling to unveil the mechanisms shaping the structure of the fish memory antibody response against an attenuated Viral Hemorrhagic Septicemia rhabdovirus. After vaccination, a persistent memory response with a public VH5JH5 IgM component was composed of dominant antibodies shared among all individuals. The rearrangement model showed that these public junctions occurred with high probability indicating that they were already favored before vaccination due to the recombination process, as shown in mammals. In addition, these clonotypes were in the naïve repertoire associated with larger similarity classes, composed of junctions differing only at one or two positions by amino acids with comparable properties. The model showed that this property was due to selective processes exerted between the recombination and the naive repertoire. Finally, our results showed that public clonotypes greatly expanded after vaccination displayed several VDJ junctions differing only by one or two amino acids with similar properties, highlighting a convergent response. The fish public memory antibody response to a virus is therefore shaped at three levels: by recombination biases, by selection acting on the formation of the pre-vaccination repertoire, and by convergent selection of functionally similar clonotypes during the response. We also show that naive repertoires of IgM and IgT have different structures and sharing between individuals, due to selection biases. In sum, our comparative approach identifies three conserved features of the antibody repertoire associated with public memory responses. These features were already present in the last common ancestors of fish and mammals, while other characteristics may represent species-specific solutions. |
format | Online Article Text |
id | pubmed-6170628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61706282018-10-12 Origin of Public Memory B Cell Clones in Fish After Antiviral Vaccination Magadan, Susana Jouneau, Luc Puelma Touzel, Maximilian Marillet, Simon Chara, Wahiba Six, Adrien Quillet, Edwige Mora, Thierry Walczak, Aleksandra M. Cazals, Frédéric Sunyer, Oriol Fillatreau, Simon Boudinot, Pierre Front Immunol Immunology Vaccination induces “public” antibody clonotypes common to all individuals of a species, that may mediate universal protection against pathogens. Only few studies tried to trace back the origin of these public B-cell clones. Here we used Illumina sequencing and computational modeling to unveil the mechanisms shaping the structure of the fish memory antibody response against an attenuated Viral Hemorrhagic Septicemia rhabdovirus. After vaccination, a persistent memory response with a public VH5JH5 IgM component was composed of dominant antibodies shared among all individuals. The rearrangement model showed that these public junctions occurred with high probability indicating that they were already favored before vaccination due to the recombination process, as shown in mammals. In addition, these clonotypes were in the naïve repertoire associated with larger similarity classes, composed of junctions differing only at one or two positions by amino acids with comparable properties. The model showed that this property was due to selective processes exerted between the recombination and the naive repertoire. Finally, our results showed that public clonotypes greatly expanded after vaccination displayed several VDJ junctions differing only by one or two amino acids with similar properties, highlighting a convergent response. The fish public memory antibody response to a virus is therefore shaped at three levels: by recombination biases, by selection acting on the formation of the pre-vaccination repertoire, and by convergent selection of functionally similar clonotypes during the response. We also show that naive repertoires of IgM and IgT have different structures and sharing between individuals, due to selection biases. In sum, our comparative approach identifies three conserved features of the antibody repertoire associated with public memory responses. These features were already present in the last common ancestors of fish and mammals, while other characteristics may represent species-specific solutions. Frontiers Media S.A. 2018-09-27 /pmc/articles/PMC6170628/ /pubmed/30319606 http://dx.doi.org/10.3389/fimmu.2018.02115 Text en Copyright © 2018 Magadan, Jouneau, Puelma Touzel, Marillet, Chara, Six, Quillet, Mora, Walczak, Cazals, Sunyer, Fillatreau and Boudinot. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Magadan, Susana Jouneau, Luc Puelma Touzel, Maximilian Marillet, Simon Chara, Wahiba Six, Adrien Quillet, Edwige Mora, Thierry Walczak, Aleksandra M. Cazals, Frédéric Sunyer, Oriol Fillatreau, Simon Boudinot, Pierre Origin of Public Memory B Cell Clones in Fish After Antiviral Vaccination |
title | Origin of Public Memory B Cell Clones in Fish After Antiviral Vaccination |
title_full | Origin of Public Memory B Cell Clones in Fish After Antiviral Vaccination |
title_fullStr | Origin of Public Memory B Cell Clones in Fish After Antiviral Vaccination |
title_full_unstemmed | Origin of Public Memory B Cell Clones in Fish After Antiviral Vaccination |
title_short | Origin of Public Memory B Cell Clones in Fish After Antiviral Vaccination |
title_sort | origin of public memory b cell clones in fish after antiviral vaccination |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170628/ https://www.ncbi.nlm.nih.gov/pubmed/30319606 http://dx.doi.org/10.3389/fimmu.2018.02115 |
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