Cargando…

A scalable model for simulating multi-round antibody evolution and benchmarking of clonal tree reconstruction methods

Affinity maturation (AM) of B cells through somatic hypermutations (SHMs) enables the immune system to evolve to recognize diverse pathogens. The accumulation of SHMs leads to the formation of clonal lineages of antibody-secreting b cells that have evolved from a common naïve B cell. Advances in hig...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Chao, Bzikadze, Andrey V., Safonova, Yana, Mirarab, Siavash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815712/
https://www.ncbi.nlm.nih.gov/pubmed/36618367
http://dx.doi.org/10.3389/fimmu.2022.1014439
_version_ 1784864383514443776
author Zhang, Chao
Bzikadze, Andrey V.
Safonova, Yana
Mirarab, Siavash
author_facet Zhang, Chao
Bzikadze, Andrey V.
Safonova, Yana
Mirarab, Siavash
author_sort Zhang, Chao
collection PubMed
description Affinity maturation (AM) of B cells through somatic hypermutations (SHMs) enables the immune system to evolve to recognize diverse pathogens. The accumulation of SHMs leads to the formation of clonal lineages of antibody-secreting b cells that have evolved from a common naïve B cell. Advances in high-throughput sequencing have enabled deep scans of B cell receptor repertoires, paving the way for reconstructing clonal trees. However, it is not clear if clonal trees, which capture microevolutionary time scales, can be reconstructed using traditional phylogenetic reconstruction methods with adequate accuracy. In fact, several clonal tree reconstruction methods have been developed to fix supposed shortcomings of phylogenetic methods. Nevertheless, no consensus has been reached regarding the relative accuracy of these methods, partially because evaluation is challenging. Benchmarking the performance of existing methods and developing better methods would both benefit from realistic models of clonal lineage evolution specifically designed for emulating B cell evolution. In this paper, we propose a model for modeling B cell clonal lineage evolution and use this model to benchmark several existing clonal tree reconstruction methods. Our model, designed to be extensible, has several features: by evolving the clonal tree and sequences simultaneously, it allows modeling selective pressure due to changes in affinity binding; it enables scalable simulations of large numbers of cells; it enables several rounds of infection by an evolving pathogen; and, it models building of memory. In addition, we also suggest a set of metrics for comparing clonal trees and measuring their properties. Our results show that while maximum likelihood phylogenetic reconstruction methods can fail to capture key features of clonal tree expansion if applied naively, a simple post-processing of their results, where short branches are contracted, leads to inferences that are better than alternative methods.
format Online
Article
Text
id pubmed-9815712
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-98157122023-01-06 A scalable model for simulating multi-round antibody evolution and benchmarking of clonal tree reconstruction methods Zhang, Chao Bzikadze, Andrey V. Safonova, Yana Mirarab, Siavash Front Immunol Immunology Affinity maturation (AM) of B cells through somatic hypermutations (SHMs) enables the immune system to evolve to recognize diverse pathogens. The accumulation of SHMs leads to the formation of clonal lineages of antibody-secreting b cells that have evolved from a common naïve B cell. Advances in high-throughput sequencing have enabled deep scans of B cell receptor repertoires, paving the way for reconstructing clonal trees. However, it is not clear if clonal trees, which capture microevolutionary time scales, can be reconstructed using traditional phylogenetic reconstruction methods with adequate accuracy. In fact, several clonal tree reconstruction methods have been developed to fix supposed shortcomings of phylogenetic methods. Nevertheless, no consensus has been reached regarding the relative accuracy of these methods, partially because evaluation is challenging. Benchmarking the performance of existing methods and developing better methods would both benefit from realistic models of clonal lineage evolution specifically designed for emulating B cell evolution. In this paper, we propose a model for modeling B cell clonal lineage evolution and use this model to benchmark several existing clonal tree reconstruction methods. Our model, designed to be extensible, has several features: by evolving the clonal tree and sequences simultaneously, it allows modeling selective pressure due to changes in affinity binding; it enables scalable simulations of large numbers of cells; it enables several rounds of infection by an evolving pathogen; and, it models building of memory. In addition, we also suggest a set of metrics for comparing clonal trees and measuring their properties. Our results show that while maximum likelihood phylogenetic reconstruction methods can fail to capture key features of clonal tree expansion if applied naively, a simple post-processing of their results, where short branches are contracted, leads to inferences that are better than alternative methods. Frontiers Media S.A. 2022-12-06 /pmc/articles/PMC9815712/ /pubmed/36618367 http://dx.doi.org/10.3389/fimmu.2022.1014439 Text en Copyright © 2022 Zhang, Bzikadze, Safonova and Mirarab https://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
Zhang, Chao
Bzikadze, Andrey V.
Safonova, Yana
Mirarab, Siavash
A scalable model for simulating multi-round antibody evolution and benchmarking of clonal tree reconstruction methods
title A scalable model for simulating multi-round antibody evolution and benchmarking of clonal tree reconstruction methods
title_full A scalable model for simulating multi-round antibody evolution and benchmarking of clonal tree reconstruction methods
title_fullStr A scalable model for simulating multi-round antibody evolution and benchmarking of clonal tree reconstruction methods
title_full_unstemmed A scalable model for simulating multi-round antibody evolution and benchmarking of clonal tree reconstruction methods
title_short A scalable model for simulating multi-round antibody evolution and benchmarking of clonal tree reconstruction methods
title_sort scalable model for simulating multi-round antibody evolution and benchmarking of clonal tree reconstruction methods
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815712/
https://www.ncbi.nlm.nih.gov/pubmed/36618367
http://dx.doi.org/10.3389/fimmu.2022.1014439
work_keys_str_mv AT zhangchao ascalablemodelforsimulatingmultiroundantibodyevolutionandbenchmarkingofclonaltreereconstructionmethods
AT bzikadzeandreyv ascalablemodelforsimulatingmultiroundantibodyevolutionandbenchmarkingofclonaltreereconstructionmethods
AT safonovayana ascalablemodelforsimulatingmultiroundantibodyevolutionandbenchmarkingofclonaltreereconstructionmethods
AT mirarabsiavash ascalablemodelforsimulatingmultiroundantibodyevolutionandbenchmarkingofclonaltreereconstructionmethods
AT zhangchao scalablemodelforsimulatingmultiroundantibodyevolutionandbenchmarkingofclonaltreereconstructionmethods
AT bzikadzeandreyv scalablemodelforsimulatingmultiroundantibodyevolutionandbenchmarkingofclonaltreereconstructionmethods
AT safonovayana scalablemodelforsimulatingmultiroundantibodyevolutionandbenchmarkingofclonaltreereconstructionmethods
AT mirarabsiavash scalablemodelforsimulatingmultiroundantibodyevolutionandbenchmarkingofclonaltreereconstructionmethods