Greninger Alexander L, Naccache Samia N, Messacar Kevin, Clayton Anna, Yu Guixia, Somasekar Sneha, Federman Scot, Stryke Doug, Anderson Christopher, Yagi Shigeo, Messenger Sharon, Wadford Debra, Xia Dongxiang, Watt James P, Van Haren Keith, Dominguez Samuel R, Glaser Carol, Aldrovandi Grace, Chiu Charles Y
Department of Laboratory Medicine, University of California, San Francisco, San Francisco, CA, USA; UCSF-Abbott Viral Diagnostics and Discovery Center, San Francisco, CA, USA.
Department of Pediatrics, Children's Hospital Colorado and University of Colorado School of Medicine, Aurora, CO, USA.
Lancet Infect Dis. 2015 Jun;15(6):671-82. doi: 10.1016/S1473-3099(15)70093-9. Epub 2015 Mar 31.
Enterovirus D68 was implicated in a widespread outbreak of severe respiratory illness across the USA in 2014 and has also been reported sporadically in patients with acute flaccid myelitis. We aimed to investigate the association between enterovirus D68 infection and acute flaccid myelitis during the 2014 enterovirus D68 respiratory outbreak in the USA.
Patients with acute flaccid myelitis who presented to two hospitals in Colorado and California, USA, between Nov 24, 2013, and Oct 11, 2014, were included in the study. Additional cases identified from Jan 1, 2012, to Oct 4, 2014, via statewide surveillance were provided by the California Department of Public Health. We investigated the cause of these cases by metagenomic next-generation sequencing, viral genome recovery, and enterovirus D68 phylogenetic analysis. We compared patients with acute flaccid myelitis who were positive for enterovirus D68 with those with acute flaccid myelitis but negative for enterovirus D68 using the two-tailed Fisher's exact test, two-sample unpaired t test, and Mann-Whitney U test.
48 patients were included: 25 with acute flaccid myelitis, two with enterovirus-associated encephalitis, five with enterovirus-D68-associated upper respiratory illness, and 16 with aseptic meningitis or encephalitis who tested positive for enterovirus. Enterovirus D68 was detected in respiratory secretions from seven (64%) of 11 patients comprising two temporally and geographically linked acute flaccid myelitis clusters at the height of the 2014 outbreak, and from 12 (48%) of 25 patients with acute flaccid myelitis overall. Phylogenetic analysis revealed that all enterovirus D68 sequences associated with acute flaccid myelitis grouped into a clade B1 strain that emerged in 2010. Of six coding polymorphisms in the clade B1 enterovirus D68 polyprotein, five were present in neuropathogenic poliovirus or enterovirus D70, or both. One child with acute flaccid myelitis and a sibling with only upper respiratory illness were both infected by identical enterovirus D68 strains. Enterovirus D68 viraemia was identified in a child experiencing acute neurological progression of his paralytic illness. Deep metagenomic sequencing of cerebrospinal fluid from 14 patients with acute flaccid myelitis did not reveal evidence of an alternative infectious cause to enterovirus D68.
These findings strengthen the putative association between enterovirus D68 and acute flaccid myelitis and the contention that acute flaccid myelitis is a rare yet severe clinical manifestation of enterovirus D68 infection in susceptible hosts.
National Institutes of Health, University of California, Abbott Laboratories, and the Centers for Disease Control and Prevention.
2014年,肠道病毒D68引发了美国严重呼吸道疾病的广泛爆发,急性弛缓性脊髓炎患者中也有零星病例报告。我们旨在调查2014年美国肠道病毒D68呼吸道爆发期间,肠道病毒D68感染与急性弛缓性脊髓炎之间的关联。
2013年11月24日至2014年10月11日期间在美国科罗拉多州和加利福尼亚州两家医院就诊的急性弛缓性脊髓炎患者纳入本研究。加利福尼亚州公共卫生部提供了2012年1月1日至2014年10月4日期间通过全州监测发现的其他病例。我们通过宏基因组下一代测序、病毒基因组回收和肠道病毒D68系统发育分析来调查这些病例的病因。我们使用双尾Fisher精确检验、两样本不成对t检验和Mann-Whitney U检验,比较了肠道病毒D68检测呈阳性的急性弛缓性脊髓炎患者与肠道病毒D68检测呈阴性的急性弛缓性脊髓炎患者。
共纳入48例患者:25例急性弛缓性脊髓炎患者,2例肠道病毒相关脑炎患者,5例肠道病毒D68相关上呼吸道疾病患者,16例无菌性脑膜炎或脑炎患者,这些患者的肠道病毒检测呈阳性。在11例患者的呼吸道分泌物中检测到肠道病毒D68,其中7例(64%)来自2014年疫情高峰期两个在时间和地理上相关的急性弛缓性脊髓炎聚集性病例,25例急性弛缓性脊髓炎患者中共有12例(48%)检测到该病毒。系统发育分析显示,所有与急性弛缓性脊髓炎相关的肠道病毒D68序列均属于2010年出现的B1进化枝毒株。在B1进化枝肠道病毒D68多聚蛋白的6个编码多态性中,有5个存在于神经致病性脊髓灰质炎病毒或肠道病毒D70中,或两者都有。一名患有急性弛缓性脊髓炎的儿童和一名仅有上呼吸道疾病的兄弟姐妹均感染了相同的肠道病毒D68毒株。在一名经历麻痹性疾病急性神经进展的儿童中发现了肠道病毒D68病毒血症。对14例急性弛缓性脊髓炎患者的脑脊液进行深度宏基因组测序,未发现除肠道病毒D68以外的其他感染病因。
这些发现强化了肠道病毒D68与急性弛缓性脊髓炎之间的假定关联,以及急性弛缓性脊髓炎是肠道病毒D68感染在易感宿主中罕见但严重的临床表现这一观点。
美国国立卫生研究院、加利福尼亚大学、雅培实验室和疾病控制与预防中心。