Using a multi-strain infectious disease model with physical information neural networks to study the time dependence of SARS-CoV-2 variants of concern.

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS PLoS Computational Biology Pub Date : 2025-02-14 eCollection Date: 2025-02-01 DOI:10.1371/journal.pcbi.1012778
Wenxuan Li, Xu Chen, Suli Liu, Chiyu Zhang, Guyue Liu
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Abstract

With the ongoing evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its increasing adaptation to humans, several variants of concern (VOCs) and variants of interest (VOIs) have been identified since late 2020. These include Alpha, Beta, Gamma, Delta, Omicron parent lineage, and other variants. These variants may show distinct levels of virulence, antigenicity, and infectivity, which require specific defense and control measures. In this study, we propose an [Formula: see text] infectious disease model to simulate the spread of SARS-CoV-2 variants among the human population. We combine the proposed epidemic model and reported infected data of variants with physical information neural networks (PINNs) to develop a novel mechanism called VOCs-informed neural network (VOCs-INN). In our experiments, we found that this algorithm can accurately fit the reported data of the British Columbia (BC) province and its five internal health agencies in Canada. Furthermore, it can simulate observed or unobserved dynamics, infer time-dependent parameters, and enable short-term predictions. The experimental results also reveal variations in the intensity of control strategies implemented across these regions. VOCs-INN performs well in fitting and forecasting when analyzing long-term or multi-wave data.

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利用具有物理信息神经网络的多株传染病模型研究SARS-CoV-2变异关注的时间依赖性。
随着严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的持续演变及其对人类的日益适应,自2020年底以来,已经确定了几种关注变体(VOCs)和感兴趣变体(voi)。这些包括Alpha, Beta, Gamma, Delta, Omicron亲本血统和其他变体。这些变异可能表现出不同程度的毒力、抗原性和传染性,需要采取特定的防御和控制措施。在这项研究中,我们提出了一个[公式:见文本]传染病模型来模拟SARS-CoV-2变体在人群中的传播。我们将提出的流行模型和报告的变异感染数据与物理信息神经网络(pinn)相结合,建立了一种新的机制,称为VOCs-informed神经网络(VOCs-INN)。在我们的实验中,我们发现该算法可以准确地拟合加拿大不列颠哥伦比亚省(BC)及其五个内部卫生机构的报告数据。此外,它还可以模拟观察到的或未观察到的动态,推断与时间相关的参数,并实现短期预测。实验结果还揭示了在这些区域实施的控制策略强度的变化。VOCs-INN在分析长期或多波数据时具有良好的拟合和预测能力。
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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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