Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Department of Mathematics, College of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter, United Kingdom.
PLoS Pathog. 2024 Nov 20;20(11):e1012703. doi: 10.1371/journal.ppat.1012703. eCollection 2024 Nov.
Enterovirus A71 (EV-A71) and coxsackievirus A6 (CVA6) primarily cause hand, foot and mouth disease and have emerged to cause potential fatal neurological and systemic manifestations. However, limited surveillance data collected through passive surveillance systems hampers characterization of their epidemiological dynamics. We fit a series of catalytic models to age-stratified seroprevalence data for EV-A71 and CVA6 collected in England at three time points (2006, 2011 and 2017) to estimate the force of infection (FOI) over time and assess possible changes in transmission. For both serotypes, model comparison does not support the occurrence of important changes in transmission over the study period, and we find that a declining risk of infection with age and / or seroreversion are needed to explain the seroprevalence data. Furthermore, we provide evidence that the increased number of reports of CVA6 during 2006-2017 is unlikely to be explained by changes in surveillance. Therefore, we hypothesize that the increased number of CVA6 cases observed since 2011 must be explained by increased virus pathogenicity. Further studies of seroprevalence data from other countries would allow to confirm this. Our results underscore the value of seroprevalence data to unravel changes in the circulation dynamics of pathogens with weak surveillance systems and large number of asymptomatic infections.
肠道病毒 A71(EV-A71)和柯萨奇病毒 A6(CVA6)主要引起手足口病,并已出现导致潜在致命的神经和全身表现的情况。然而,通过被动监测系统收集的有限监测数据阻碍了对其流行病学动态的特征描述。我们对在英格兰三个时间点(2006 年、2011 年和 2017 年)收集的针对 EV-A71 和 CVA6 的按年龄分层血清流行率数据拟合了一系列催化模型,以估计随时间推移的感染力(FOI)并评估可能发生的传播变化。对于这两种血清型,模型比较均不支持在研究期间发生重要的传播变化,我们发现需要降低感染风险的年龄和/或血清学逆转才能解释血清流行率数据。此外,我们提供的证据表明,2006 年至 2017 年期间 CVA6 报告病例数的增加不太可能是由于监测变化引起的。因此,我们假设自 2011 年以来观察到的 CVA6 病例数的增加必须归因于病毒致病性的增加。对来自其他国家的血清流行率数据的进一步研究将能够证实这一点。我们的研究结果强调了血清流行率数据对于在具有较弱监测系统和大量无症状感染的情况下揭示病原体循环动力学变化的价值。