体能模型可在短期内准确预测 SARS-CoV-2 变异频率。

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS PLoS Computational Biology Pub Date : 2024-09-06 DOI:10.1371/journal.pcbi.1012443
Eslam Abousamra, Marlin Figgins, Trevor Bedford
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引用次数: 0

摘要

病原体进化的基因组监测对于公共卫生响应、治疗策略和疫苗开发至关重要。针对 SARS-COV-2 已经开发出多种模型,包括描述变异频率增长的多项式逻辑回归 (MLR),以及描述变异 Rt 的固定增长优势 (FGA)、增长优势随机漫步 (GARW) 和 Piantham 参数化。我们引入了一个评估变体频率实时预测的框架,并将这一框架应用于 2022 年期间 SARS-CoV-2 的演化过程,在这一过程中出现了多种新的病毒变体并在人群中迅速传播。我们对不同基因组监测强度的代表性国家的模型进行了比较。对模型准确性的回顾性评估表明,大多数变异频率模型表现良好,能够做出合理的预测。我们发现,简单的 MLR 模型在预测 30 天后具有强大基因组监测能力的国家时,中位绝对误差为 0.6%,平均绝对误差为 6%。我们研究了各国序列数量和质量对预测准确性的影响,并进行了系统性的降采样,确定每周 1000 个序列完全足以进行准确的短期预测。我们的结论是,适配性模型是短期进化预测的有用预报工具。
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Fitness models provide accurate short-term forecasts of SARS-CoV-2 variant frequency.

Genomic surveillance of pathogen evolution is essential for public health response, treatment strategies, and vaccine development. In the context of SARS-COV-2, multiple models have been developed including Multinomial Logistic Regression (MLR) describing variant frequency growth as well as Fixed Growth Advantage (FGA), Growth Advantage Random Walk (GARW) and Piantham parameterizations describing variant Rt. These models provide estimates of variant fitness and can be used to forecast changes in variant frequency. We introduce a framework for evaluating real-time forecasts of variant frequencies, and apply this framework to the evolution of SARS-CoV-2 during 2022 in which multiple new viral variants emerged and rapidly spread through the population. We compare models across representative countries with different intensities of genomic surveillance. Retrospective assessment of model accuracy highlights that most models of variant frequency perform well and are able to produce reasonable forecasts. We find that the simple MLR model provides ∼0.6% median absolute error and ∼6% mean absolute error when forecasting 30 days out for countries with robust genomic surveillance. We investigate impacts of sequence quantity and quality across countries on forecast accuracy and conduct systematic downsampling to identify that 1000 sequences per week is fully sufficient for accurate short-term forecasts. We conclude that fitness models represent a useful prognostic tool for short-term evolutionary forecasting.

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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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