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从血清流行率数据推断英格兰肠道病毒 D68(EV-D68)传播的变化。

Changes in transmission of Enterovirus D68 (EV-D68) in England inferred from seroprevalence data.

机构信息

MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, United Kingdom.

Department of Computer Science, University of Oxford, Oxford, United Kingdom.

出版信息

Elife. 2023 Jun 9;12:e76609. doi: 10.7554/eLife.76609.

Abstract

The factors leading to the global emergence of Enterovirus D68 (EV-D68) in 2014 as a cause of acute flaccid myelitis (AFM) in children are unknown. To investigate potential changes in virus transmissibility or population susceptibility, we measured the seroprevalence of EV-D68-specific neutralising antibodies in serum samples collected in England in 2006, 2011, and 2017. Using catalytic mathematical models, we estimate an approximately 50% increase in the annual probability of infection over the 10-year study period, coinciding with the emergence of clade B around 2009. Despite such increase in transmission, seroprevalence data suggest that the virus was already widely circulating before the AFM outbreaks and the increase of infections by age cannot explain the observed number of AFM cases. Therefore, the acquisition of or an increase in neuropathogenicity would be additionally required to explain the emergence of outbreaks of AFM. Our results provide evidence that changes in enterovirus phenotypes cause major changes in disease epidemiology.

摘要

导致肠道病毒 D68(EV-D68)在 2014 年作为儿童急性弛缓性脊髓炎(AFM)的病因在全球出现的因素尚不清楚。为了研究病毒传播能力或人群易感性的潜在变化,我们测量了 2006 年、2011 年和 2017 年在英国采集的血清样本中针对 EV-D68 的特异性中和抗体的血清阳性率。使用催化数学模型,我们估计在 10 年的研究期间,感染的年概率大约增加了 50%,这与 2009 年左右出现的 B 谱系相符。尽管传播有所增加,但血清阳性率数据表明,在 AFM 爆发之前,该病毒已经广泛传播,并且感染人数的增加并不能解释观察到的 AFM 病例数。因此,需要获得或增加神经致病性,才能解释 AFM 爆发的出现。我们的结果提供了证据,表明肠道病毒表型的变化导致了疾病流行病学的重大变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d49/10259368/2c774620b3fc/elife-76609-fig1.jpg

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