Antibodies to Enteroviruses in Cerebrospinal Fluid of Patients with Acute Flaccid Myelitis

被引:68
作者
Mishra, Nischay [1 ]
Ng, Terry Fei Fan [2 ]
Marine, Rachel L. [2 ]
Jain, Komal [1 ]
Ng, James [1 ]
Thakkar, Riddhi [1 ]
Caciula, Adrian [1 ]
Price, Adam [1 ]
Garcia, Joel A. [1 ]
Burns, Jane C. [3 ]
Thakur, Kiran T. [4 ]
Hetzler, Kimbell L. [5 ]
Routh, Janell A. [2 ]
Konopka-Anstadt, Jennifer L. [2 ]
Nix, W. Allan [2 ]
Tokarz, Rafal [1 ]
Briese, Thomas [1 ]
Oberste, M. Steven [2 ]
Lipkin, W. Ian [1 ]
机构
[1] Columbia Univ, Mailman Sch Publ Hlth, Ctr Infect & Immun, New York, NY USA
[2] Ctr Dis Control & Prevent, Div Viral Dis, Atlanta, GA USA
[3] Univ Calif San Diego, Sch Med, Dept Pediat, La Jolla, CA 92093 USA
[4] Columbia Irving Univ, Med Ctr, Dept Neurol, Div Crit Care & Hospitalist Neurol, New York, NY USA
[5] Ctr Dis Control & Prevent, Div Viral Dis, Atlanta, GA USA
来源
MBIO | 2019年 / 10卷 / 04期
基金
美国国家卫生研究院;
关键词
VirCapSeq-VERT; acute flaccid myelitis; antibodies; enterovirus; enterovirus D-68; peptide array; serology; UNITED-STATES; D68; OUTBREAK; PCR;
D O I
10.1128/mBio.01903-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Acute flaccid myelitis (AFM) has caused motor paralysis in >560 children in the United States since 2014. The temporal association of enterovirus (EV) outbreaks with increases in AFM cases and reports of fever, respiratory, or gastrointestinal illness prior to AFM in >90% of cases suggest a role for infectious agents. Cerebrospinal fluid (CSF) from 14 AFM and 5 non-AFM patients with central nervous system (CNS) diseases in 2018 were investigated by viral-capture high-throughput sequencing (VirCapSeq-VERT system). These CSF and serum samples, as well as multiple controls, were tested for antibodies to human EVs using peptide microarrays. EV RNA was confirmed in CSF from only 1 adult AFM case and 1 non-AFM case. In contrast, antibodies to EV peptides were present in CSF of 11 of 14 AFM patients (79%), significantly higher than controls, including non-AFM patients (1/5 [20%]), children with Kawasaki disease (0/10), and adults with non-AFM CNS diseases (2/11 [18%]) (P = 0.023, 0.0001, and 0.0028, respectively). Six of 14 CSF samples (43%) and 8 of 11 sera (73%) from AFM patients were immunoreactive to an EV-D68-specific peptide, whereas the three control groups were not immunoreactive in either CSF (0/5, 0/10, and 0/11; P = 0.008, 0.0003, and 0.035, respectively) or sera (0/2, 0/8, and 0/5; P = 0.139, 0.002, and 0.009, respectively). IMPORTANCE The presence in cerebrospinal fluid of antibodies to EV peptides at higher levels than non-AFM controls supports the plausibility of a link between EV infection and AFM that warrants further investigation and has the potential to lead to strategies for diagnosis and prevention of disease.
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页数:10
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