Uncovering Epistatic Interactions in SARS-CoV-2 Evolution Through Hidden Markov Models.

IF 1.3 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS
Journal of Computational Biology Pub Date : 2026-05-01 Epub Date: 2026-02-20 DOI:10.1177/15578666261423963
Ayotomiwa Ezekiel Adeniyi, Akshay Juyal, Pavel Skums, Murray Patterson, Alex Zelikovsky
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引用次数: 0

Abstract

Understanding epistatic interactions, where mutations collectively influence viral fitness, is critical for predicting pathogen evolution. We present a hidden Markov model (HMM) framework that captures the temporal dynamics of epistatic relationships in SARS-CoV-2, addressing limitations of static network-based approaches. Our method models single amino acid variant pairs as a two-state system (linked/unlinked), with emission probabilities derived from linkage disequilibrium theory and transition probabilities optimized via the Baum-Welch algorithm. We implement permutation-based validation with temporal order noise reduction (>80% agreement across five iterations) to distinguish biological signals from stochastic noise. Applied to 2,192,008 spike protein sequences from the United States (March 2020-December 2021), our approach identified three classes of epistatic dynamics: permanent (0.3%), transient (0.3%), and oscillating (0.7%) linkages. Analysis of Alpha variant positions revealed 78% epistatic linkage compared with 1.3% across all spike protein position pairs, with 60% exhibiting oscillating patterns suggestive of frequency-dependent selection. We detected all 17 previously reported epistatic pairs plus 18 novel interactions, including critical connections between positions 69-70 and other functional sites. Notably, Alpha variant epistatic networks were detectable as early as April 2020, months before widespread circulation. Our framework scales to variant-wide analysis, revealing distinct patterns across variants: Delta (96% linkage, 71% oscillating) and Omicron (87% linkage, 56% oscillating). The computational pipeline, implemented with parallelized HMM training and Viterbi decoding, processes hundreds of thousands of position pairs efficiently. By transforming epistasis detection from static to temporal analysis, this work provides computational tools for early variant detection and demonstrates how probabilistic modeling can capture evolutionary dynamics in real-time genomic surveillance systems.

利用隐马尔可夫模型揭示SARS-CoV-2进化中的上位相互作用。
了解上位相互作用,其中突变集体影响病毒适应性,是预测病原体进化的关键。我们提出了一个隐马尔可夫模型(HMM)框架,该框架捕捉了SARS-CoV-2中上位关系的时间动态,解决了基于静态网络的方法的局限性。我们的方法将单个氨基酸变异对建模为两态系统(连接/未连接),发射概率由链接不平衡理论推导,转移概率通过Baum-Welch算法优化。我们实现了基于排列的时序降噪验证(五次迭代的一致性约为80%),以区分生物信号和随机噪声。应用于来自美国的2192008个刺突蛋白序列(2020年3月- 2021年12月),我们的方法确定了三类上位动力学:永久(0.3%)、瞬态(0.3%)和振荡(0.7%)连接。α变异位点分析显示78%的上位性连锁,而所有刺突蛋白位点对的这一比例为1.3%,其中60%表现出频率依赖选择的振荡模式。我们检测到所有17个先前报道的上位性对和18个新的相互作用,包括位置69-70和其他功能位点之间的关键连接。值得注意的是,早在2020年4月就可以检测到α变体上位网络,比广泛传播早了几个月。我们的框架扩展到变体范围的分析,揭示了不同变体之间的不同模式:Delta(96%连锁,71%振荡)和Omicron(87%连锁,56%振荡)。计算管道采用并行HMM训练和Viterbi解码实现,可以高效地处理数十万个位置对。通过将上位性检测从静态转换为时间分析,这项工作为早期变异检测提供了计算工具,并展示了概率建模如何在实时基因组监测系统中捕获进化动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Computational Biology
Journal of Computational Biology 生物-计算机:跨学科应用
CiteScore
3.60
自引率
5.90%
发文量
113
审稿时长
6-12 weeks
期刊介绍: Journal of Computational Biology is the leading peer-reviewed journal in computational biology and bioinformatics, publishing in-depth statistical, mathematical, and computational analysis of methods, as well as their practical impact. Available only online, this is an essential journal for scientists and students who want to keep abreast of developments in bioinformatics. Journal of Computational Biology coverage includes: -Genomics -Mathematical modeling and simulation -Distributed and parallel biological computing -Designing biological databases -Pattern matching and pattern detection -Linking disparate databases and data -New tools for computational biology -Relational and object-oriented database technology for bioinformatics -Biological expert system design and use -Reasoning by analogy, hypothesis formation, and testing by machine -Management of biological databases
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