Ratnavale Saikanth, Hepp Crystal, Doerry Eck, Mihaljevic Joseph R
School of Informatics, Computing, and Cyber Systems, Northern Arizona University, Flagstaff, AZ, United States of America.
Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ, United States of America.
PLOS Glob Public Health. 2022 Sep 15;2(9):e0001058. doi: 10.1371/journal.pgph.0001058. eCollection 2022.
The implementation of non-pharmaceutical public health interventions can have simultaneous impacts on pathogen transmission rates as well as host mobility rates. For instance, with SARS-CoV-2, masking can influence host-to-host transmission, while stay-at-home orders can influence mobility. Importantly, variations in transmission rates and mobility patterns can influence pathogen-induced hospitalization rates. This poses a significant challenge for the use of mathematical models of disease dynamics in forecasting the spread of a pathogen; to create accurate forecasts in spatial models of disease spread, we must simultaneously account for time-varying rates of transmission and host movement. In this study, we develop a statistical model-fitting algorithm to estimate dynamic rates of SARS-CoV-2 transmission and host movement from geo-referenced hospitalization data. Using simulated data sets, we then test whether our method can accurately estimate these time-varying rates simultaneously, and how this accuracy is influenced by the spatial population structure. Our model-fitting method relies on a highly parallelized process of grid search and a sliding window technique that allows us to estimate time-varying transmission rates with high accuracy and precision, as well as movement rates with somewhat lower precision. Estimated parameters also had lower precision in more rural data sets, due to lower hospitalization rates (i.e., these areas are less data-rich). This model-fitting routine could easily be generalized to any stochastic, spatially-explicit modeling framework, offering a flexible and efficient method to estimate time-varying parameters from geo-referenced data sets.
实施非药物公共卫生干预措施可能会对病原体传播率以及宿主流动率同时产生影响。例如,对于严重急性呼吸综合征冠状病毒2(SARS-CoV-2),戴口罩可影响人际传播,而居家令则可影响流动性。重要的是,传播率和流动模式的变化会影响病原体导致的住院率。这给在预测病原体传播时使用疾病动态数学模型带来了重大挑战;为了在疾病传播的空间模型中做出准确预测,我们必须同时考虑随时间变化的传播率和宿主移动情况。在本研究中,我们开发了一种统计模型拟合算法,以从地理参考的住院数据中估计SARS-CoV-2的动态传播率和宿主移动情况。然后,我们使用模拟数据集测试我们的方法是否能够同时准确估计这些随时间变化的率,以及这种准确性如何受到空间人口结构的影响。我们的模型拟合方法依赖于高度并行化的网格搜索过程和滑动窗口技术,这使我们能够高精度地估计随时间变化的传播率,以及精度稍低的移动率。由于住院率较低(即这些地区的数据丰富度较低),在农村数据集中估计的参数精度也较低。这种模型拟合程序可以很容易地推广到任何随机的、空间明确的建模框架,提供一种灵活高效的方法,从地理参考数据集中估计随时间变化的参数。