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Molecular diversity and biennial circulation of enterovirus D68: a systematic screening study in Lyon, France, 2010 to 2016

机译:肠道病毒D68的分子多样性和两年一次的循环:2010年至2016年在法国里昂进行的系统筛选研究

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Background Understanding enterovirus D68 (EV-D68) circulation patterns as well as risk factors for severe respiratory and neurological illness is important for developing preventive strategies. Methods : Between 2010 and 2016, 11,132 respiratory specimens from hospitalised patients in Lyon, France, were screened for EV-D68 by PCR. Phylogenetic relationships of the viral-protein-1 sequences were reconstructed using maximum-likelihood and Bayesian-Markov-Chain-Monte-Carlo approaches. Results: Overall, 171 infections with a biennial pattern were detected, including seven, one, 55, none, 42, one and 65 cases annually during 2010–16. Children (&?16 years-old; n?=?150) were mostly affected and 71% (n?=?121) of the total patients were under 5 years-old. In 146 patients with medical reviews, 73% (n?=?107) presented with acute respiratory distress. Among paediatric patients with medical reviews (n?=?133), 55% (n=73) had an asthma/wheezing history, while among adults (n?=?13), 11 had underlying diseases. In total, 45 patients had severe infections and 28 patients needed intensive care unit stays. No acute flaccid myelitis (AFM) was detected. We found genotypes A, B1, B2 B3 and D circulating, and no associations between these and clinical presentations. During the study, new genotypes continuously emerged, being replaced over time. We estimated that ancestors of currently circulating genotypes emerged in the late-1990s to 2010. Rises of the EV-D68 effective population size in Lyon coincided with infection upsurges. Phylogenetic analyses showed ongoing diversification of EV-D68 worldwide, coinciding with more infections in recent years and increases of reported AFM paediatric cases. Conclusions: Reinforcement of diagnostic capacities and clinical-based surveillance of EV-D68 infections is needed in Europe to assess the EV-D68 burden.
机译:背景技术了解肠道病毒D68(EV-D68)的循环模式以及严重呼吸道和神经系统疾病的危险因素对于制定预防策略很重要。方法:2010年至2016年,通过PCR对法国里昂住院患者的11132例呼吸道标本进行了EV-D68筛查。使用最大似然和贝叶斯-马尔可夫-链-蒙特-卡洛方法重建病毒蛋白-1序列的系统发生关系。结果:总体上,在2010-16年期间,每年检测到171例呈两年期感染,包括每年7例,1例,55例,无,42例,1例和65例。儿童(≤16岁; n = 150)受疾病影响最大,总患者中有71%(n = 121)在5岁以下。在146例接受医学检查的患者中,有73%(n?=?107)表现为急性呼吸窘迫。在接受医学检查的小儿患者中(n = 133),55%(n = 73)有哮喘/喘息史,而在成年人(n = 13)中,有11位患有基础疾病。共有45例严重感染,28例需要重症监护病房。未检测到急性弛缓性脊髓炎(AFM)。我们发现基因型A,B1,B2,B3和D在循环,并且这些与临床表现之间没有关联。在研究过程中,新的基因型不断出现,并随着时间的推移而被取代。我们估计当前流行的基因型的祖先出现在1990年代后期至2010年。里昂EV-D68有效种群数量的上升与感染的增加相吻合。系统发育分析表明,EV-D68在全球范围内正在持续多样化,这与近年来的更多感染和报告的AFM儿科病例的增加相吻合。结论:在欧洲,需要增强诊断能力和对EV-D68感染进行临床监测以评估EV-D68负担。

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