Genomic and serologic characterization of enterovirus A71 brainstem encephalitis
| العنوان: | Genomic and serologic characterization of enterovirus A71 brainstem encephalitis |
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| المؤلفون: | Leon KE, Schubert RD, Casas-Alba D, Hawes IA, Ramachandran PS, Ramesh A, Pak JE, Wu W, Cheung CK, Crawford ED, Khan LM, Launes-Montana C, Sample HA, Zorn KC, Cabrerizo M, Valero-Rello A, Langelier C, Munoz-Almagro C, DeRisi JL, Wilson MR |
| المصدر: | NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu instname r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu Fundació Sant Joan de Déu |
| بيانات النشر: | Lippincott Williams and Wilkins, 2020. |
| سنة النشر: | 2020 |
| الوصف: | OBJECTIVE: In 2016, Catalonia experienced a pediatric brainstem encephalitis outbreak caused by enterovirus A71 (EV-A71). Conventional testing identified EV in the periphery but rarely in CSF. Metagenomic next-generation sequencing (mNGS) and CSF pan-viral serology (VirScan) were deployed to enhance viral detection and characterization. METHODS: RNA was extracted from the CSF (n = 20), plasma (n = 9), stool (n = 15), and nasopharyngeal samples (n = 16) from 10 children with brainstem encephalitis and 10 children with meningitis or encephalitis. Pathogens were identified using mNGS. Available CSF from cases (n = 12) and pediatric other neurologic disease controls (n = 54) were analyzed with VirScan with a subset (n = 9 and n = 50) validated by ELISA. RESULTS: mNGS detected EV in all samples positive by quantitative reverse transcription polymerase chain reaction (qRT-PCR) (n = 25). In qRT-PCR-negative samples (n = 35), mNGS found virus in 23% (n = 8, 3 CSF samples). Overall, mNGS enhanced EV detection from 42% (25/60) to 57% (33/60) (p-value = 0.013). VirScan and ELISA increased detection to 92% (11/12) compared with 46% (4/12) for CSF mNGS and qRT-PCR (p-value = 0.023). Phylogenetic analysis confirmed the EV-A71 strain clustered with a neurovirulent German EV-A71. A single amino acid substitution (S241P) in the EVA71 VP1 protein was exclusive to the CNS in one subject. CONCLUSION: mNGS with VirScan significantly increased the CNS detection of EVs relative to qRT-PCR, and the latter generated an antigenic profile of the acute EV-A71 immune response. Genomic analysis confirmed the close relation of the outbreak EV-A71 and neuroinvasive German EV-A71. A S241P substitution in VP1 was found exclusively in the CSF. |
| تدمد: | 2332-7812 |
| URL الوصول: | https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e9c9ab1ba76a804178277718b397193c http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=17492 |
| حقوق: | OPEN |
| رقم الأكسشن: | edsair.dedup.wf.001..e9c9ab1ba76a804178277718b397193c |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 23327812 |
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