Bioinformatics and Systems Biology, University of California, San Diego, San Diego, CA, United States.
Computer Science and Engineering Department, University of California, San Diego, San Diego, CA, United States.
Front Immunol. 2022 Dec 6;13:1014439. doi: 10.3389/fimmu.2022.1014439. eCollection 2022.
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.
通过体细胞超突变(SHM),B 细胞的亲和力成熟(AM)使免疫系统能够进化以识别各种病原体。SHM 的积累导致了从共同的幼稚 B 细胞进化而来的分泌抗体的 B 细胞克隆谱系的形成。高通量测序的进步使得深入扫描 B 细胞受体库成为可能,为构建克隆树铺平了道路。然而,尚不清楚是否可以使用传统的系统发育重建方法以足够的准确性来重建捕捉微观进化时间尺度的克隆树。事实上,已经开发了几种克隆树重建方法来纠正系统发育方法的假设缺陷。然而,由于评估具有挑战性,这些方法的相对准确性尚未达成共识。基准测试现有方法的性能并开发更好的方法都将受益于专门设计用于模拟 B 细胞进化的克隆谱系进化的现实模型。在本文中,我们提出了一种用于建模 B 细胞克隆谱系进化的模型,并使用该模型对几种现有的克隆树重建方法进行了基准测试。我们的模型旨在具有可扩展性,具有以下几个特点:通过同时进化克隆树和序列,它允许对由于亲和力结合变化引起的选择压力进行建模;它能够对大量细胞进行可扩展的模拟;它能够进行多次进化病原体的感染;并且,它可以对记忆的建立进行建模。此外,我们还提出了一组用于比较克隆树和测量其属性的指标。我们的结果表明,虽然最大似然系统发育重建方法如果盲目应用可能无法捕捉到克隆树扩展的关键特征,但对其结果进行简单的后处理,即缩短短分支,可以得出比替代方法更好的推断。