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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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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 |
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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 |
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