偏肺病毒
爆发
大流行
病毒学
传递率(结构动力学)
人口
传输(电信)
肺病毒科
生物
病毒
医学
2019年冠状病毒病(COVID-19)
呼吸道感染
病毒性疾病
呼吸系统
环境卫生
传染病(医学专业)
副粘病毒科
计算机科学
疾病
物理
病理
解剖
振动
电信
量子力学
隔振
作者
Emily Howerton,Thomas Williams,Jean‐Sébastien Casalegno,Samuel R. Dominguez,Rory Gunson,Kevin Messacar,C. Jessica E. Metcalf,Sang Woo Park,Cécile Viboud,Bryan T. Grenfell
标识
DOI:10.1038/s41467-025-62358-w
摘要
Abstract Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) are closely related pathogens responsible for a significant burden of acute respiratory infections. Interactions between RSV and hMPV have been hypothesized, but the mechanisms of interaction are largely unknown. Here, we use a mathematical model to quantify the likelihood of interactions from population-level surveillance data and investigate whether interactions could lead to increases in hMPV burden under RSV medical interventions, including active and passive immunization. In Scotland, Korea, and three regions of Canada, annual hMPV outbreaks lag RSV outbreaks by up to 18 weeks; two Canadian regions show patterns consistent with out-of-phase biennial outbreaks. Using a two-pathogen transmission model, we show that a negative effect of RSV infection on hMPV transmissibility can explain these dynamics. We use post-pandemic RSV-hMPV rebound dynamics as an out of sample test for our model, and the model with interactions better predicts this period than a model where the pathogens are assumed to be independent. Finally, our model suggests that hMPV peak timing and magnitude may change under RSV interventions. Our analysis provides a foundation for detecting possible RSV-hMPV interactions at the population level, although such a model oversimplifies important complexities about interaction mechanisms.
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