Network Systems Science and Advanced Computing Division, Biocomplexity Institute, University of Virginia, Charlottesville, VA 22904.
Department of Computer Science, University of Virginia, Charlottesville, VA 22904.
Proc Natl Acad Sci U S A. 2023 Nov 28;120(48):e2305227120. doi: 10.1073/pnas.2305227120. Epub 2023 Nov 20.
Disease surveillance systems provide early warnings of disease outbreaks before they become public health emergencies. However, pandemics containment would be challenging due to the complex immunity landscape created by multiple variants. Genomic surveillance is critical for detecting novel variants with diverse characteristics and importation/emergence times. Yet, a systematic study incorporating genomic monitoring, situation assessment, and intervention strategies is lacking in the literature. We formulate an integrated computational modeling framework to study a realistic course of action based on sequencing, analysis, and response. We study the effects of the second variant's importation time, its infectiousness advantage and, its cross-infection on the novel variant's detection time, and the resulting intervention scenarios to contain epidemics driven by two-variants dynamics. Our results illustrate the limitation in the intervention's effectiveness due to the variants' competing dynamics and provide the following insights: i) There is a set of importation times that yields the worst detection time for the second variant, which depends on the first variant's basic reproductive number; ii) When the second variant is imported relatively early with respect to the first variant, the cross-infection level does not impact the detection time of the second variant. We found that depending on the target metric, the best outcomes are attained under different interventions' regimes. Our results emphasize the importance of sustained enforcement of Non-Pharmaceutical Interventions on preventing epidemic resurgence due to importation/emergence of novel variants. We also discuss how our methods can be used to study when a novel variant emerges within a population.
疾病监测系统在疾病爆发成为公共卫生紧急事件之前提供早期警报。然而,由于多种变异体所造成的复杂免疫景观,大流行的控制将具有挑战性。基因组监测对于检测具有不同特征和输入/出现时间的新型变体至关重要。然而,文献中缺乏包含基因组监测、情况评估和干预策略的系统研究。我们制定了一个综合的计算建模框架,以根据测序、分析和响应来研究现实的行动方案。我们研究了第二个变体的输入时间、传染性优势及其对新型变体检测时间的交叉感染的影响,以及由此产生的干预方案,以控制由两种变体动力学驱动的流行病。我们的研究结果说明了由于变体的竞争动态,干预措施的有效性存在局限性,并提供了以下见解:i)存在一组输入时间,这些时间会导致第二个变体的检测时间最长,这取决于第一个变体的基本繁殖数;ii)当第二个变体相对于第一个变体较早输入时,交叉感染水平不会影响第二个变体的检测时间。我们发现,根据目标指标,在不同的干预措施下可以获得最佳结果。我们的研究结果强调了由于新型变体的输入/出现,持续实施非药物干预措施对于防止流行病复发的重要性。我们还讨论了如何使用我们的方法来研究新型变体在人群中何时出现。