Cargando…
Pan-viral serology implicates enteroviruses in acute flaccid myelitis
Since 2012, the United States has experienced a biennial spike in pediatric acute flaccid myelitis (AFM).(1–6) Epidemiologic evidence suggests non-polio enteroviruses (EVs) are a potential etiology, yet EV RNA is rarely detected in cerebrospinal fluid (CSF).(2) We interrogated CSF from children with...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858576/ https://www.ncbi.nlm.nih.gov/pubmed/31636453 http://dx.doi.org/10.1038/s41591-019-0613-1 |
_version_ | 1783470980869390336 |
---|---|
author | Schubert, Ryan D. Hawes, Isobel A. Ramachandran, Prashanth S. Ramesh, Akshaya Crawford, Emily D. Pak, John E. Wu, Wesley Cheung, Carly K. O’Donovan, Brian D. Tato, Cristina M. Lyden, Amy Tan, Michelle Sit, Rene Sowa, Gavin A. Sample, Hannah A. Zorn, Kelsey C. Banerji, Debarko Khan, Lillian M. Bove, Riley Hauser, Stephen L. Gelfand, Amy A. Johnson-Kerner, Bethany Nash, Kendall Krishnamoorthy, Kalpathy S. Chitnis, Tanuja Ding, Joy Z. McMillan, Hugh J. Chiu, Charles Y. Briggs, Benjamin Glaser, Carol A. Yen, Cynthia Chu, Victoria Wadford, Debra A. Dominguez, Samuel R. Fei Fan Ng, Terry Marine, Rachel L. Lopez, Adriana S. Nix, W. Allan Soldatos, Ariane Gorman, Mark P. Benson, Leslie Messacar, Kevin Konopka-Anstadt, Jennifer L. Oberste, M. Steven DeRisi, Joseph L. Wilson, Michael R. |
author_facet | Schubert, Ryan D. Hawes, Isobel A. Ramachandran, Prashanth S. Ramesh, Akshaya Crawford, Emily D. Pak, John E. Wu, Wesley Cheung, Carly K. O’Donovan, Brian D. Tato, Cristina M. Lyden, Amy Tan, Michelle Sit, Rene Sowa, Gavin A. Sample, Hannah A. Zorn, Kelsey C. Banerji, Debarko Khan, Lillian M. Bove, Riley Hauser, Stephen L. Gelfand, Amy A. Johnson-Kerner, Bethany Nash, Kendall Krishnamoorthy, Kalpathy S. Chitnis, Tanuja Ding, Joy Z. McMillan, Hugh J. Chiu, Charles Y. Briggs, Benjamin Glaser, Carol A. Yen, Cynthia Chu, Victoria Wadford, Debra A. Dominguez, Samuel R. Fei Fan Ng, Terry Marine, Rachel L. Lopez, Adriana S. Nix, W. Allan Soldatos, Ariane Gorman, Mark P. Benson, Leslie Messacar, Kevin Konopka-Anstadt, Jennifer L. Oberste, M. Steven DeRisi, Joseph L. Wilson, Michael R. |
author_sort | Schubert, Ryan D. |
collection | PubMed |
description | Since 2012, the United States has experienced a biennial spike in pediatric acute flaccid myelitis (AFM).(1–6) Epidemiologic evidence suggests non-polio enteroviruses (EVs) are a potential etiology, yet EV RNA is rarely detected in cerebrospinal fluid (CSF).(2) We interrogated CSF from children with AFM (n=42) and pediatric other neurologic disease controls (n=58) for intrathecal anti-viral antibodies using a phage display library expressing 481,966 overlapping peptides derived from all known vertebrate and arboviruses (VirScan). We also performed metagenomic next-generation sequencing (mNGS) of AFM CSF RNA (n=20 cases), both unbiased and with targeted enrichment for EVs. Using VirScan, the only viral family significantly enriched by the CSF of AFM cases relative to controls was Picornaviridae, with the most enriched Picornaviridae peptides belonging to the genus Enterovirus (n=29/42 cases versus 4/58 controls). EV VP1 ELISA confirmed this finding (n=22/26 cases versus 7/50 controls). mNGS did not detect additional EV RNA. Despite rare detection of EV RNA, pan-viral serology identified frequently high levels of CSF EV-specific antibodies in AFM compared to controls, providing further evidence for a causal role of non-polio EVs in AFM. |
format | Online Article Text |
id | pubmed-6858576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-68585762020-04-21 Pan-viral serology implicates enteroviruses in acute flaccid myelitis Schubert, Ryan D. Hawes, Isobel A. Ramachandran, Prashanth S. Ramesh, Akshaya Crawford, Emily D. Pak, John E. Wu, Wesley Cheung, Carly K. O’Donovan, Brian D. Tato, Cristina M. Lyden, Amy Tan, Michelle Sit, Rene Sowa, Gavin A. Sample, Hannah A. Zorn, Kelsey C. Banerji, Debarko Khan, Lillian M. Bove, Riley Hauser, Stephen L. Gelfand, Amy A. Johnson-Kerner, Bethany Nash, Kendall Krishnamoorthy, Kalpathy S. Chitnis, Tanuja Ding, Joy Z. McMillan, Hugh J. Chiu, Charles Y. Briggs, Benjamin Glaser, Carol A. Yen, Cynthia Chu, Victoria Wadford, Debra A. Dominguez, Samuel R. Fei Fan Ng, Terry Marine, Rachel L. Lopez, Adriana S. Nix, W. Allan Soldatos, Ariane Gorman, Mark P. Benson, Leslie Messacar, Kevin Konopka-Anstadt, Jennifer L. Oberste, M. Steven DeRisi, Joseph L. Wilson, Michael R. Nat Med Article Since 2012, the United States has experienced a biennial spike in pediatric acute flaccid myelitis (AFM).(1–6) Epidemiologic evidence suggests non-polio enteroviruses (EVs) are a potential etiology, yet EV RNA is rarely detected in cerebrospinal fluid (CSF).(2) We interrogated CSF from children with AFM (n=42) and pediatric other neurologic disease controls (n=58) for intrathecal anti-viral antibodies using a phage display library expressing 481,966 overlapping peptides derived from all known vertebrate and arboviruses (VirScan). We also performed metagenomic next-generation sequencing (mNGS) of AFM CSF RNA (n=20 cases), both unbiased and with targeted enrichment for EVs. Using VirScan, the only viral family significantly enriched by the CSF of AFM cases relative to controls was Picornaviridae, with the most enriched Picornaviridae peptides belonging to the genus Enterovirus (n=29/42 cases versus 4/58 controls). EV VP1 ELISA confirmed this finding (n=22/26 cases versus 7/50 controls). mNGS did not detect additional EV RNA. Despite rare detection of EV RNA, pan-viral serology identified frequently high levels of CSF EV-specific antibodies in AFM compared to controls, providing further evidence for a causal role of non-polio EVs in AFM. 2019-10-21 2019-11 /pmc/articles/PMC6858576/ /pubmed/31636453 http://dx.doi.org/10.1038/s41591-019-0613-1 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Schubert, Ryan D. Hawes, Isobel A. Ramachandran, Prashanth S. Ramesh, Akshaya Crawford, Emily D. Pak, John E. Wu, Wesley Cheung, Carly K. O’Donovan, Brian D. Tato, Cristina M. Lyden, Amy Tan, Michelle Sit, Rene Sowa, Gavin A. Sample, Hannah A. Zorn, Kelsey C. Banerji, Debarko Khan, Lillian M. Bove, Riley Hauser, Stephen L. Gelfand, Amy A. Johnson-Kerner, Bethany Nash, Kendall Krishnamoorthy, Kalpathy S. Chitnis, Tanuja Ding, Joy Z. McMillan, Hugh J. Chiu, Charles Y. Briggs, Benjamin Glaser, Carol A. Yen, Cynthia Chu, Victoria Wadford, Debra A. Dominguez, Samuel R. Fei Fan Ng, Terry Marine, Rachel L. Lopez, Adriana S. Nix, W. Allan Soldatos, Ariane Gorman, Mark P. Benson, Leslie Messacar, Kevin Konopka-Anstadt, Jennifer L. Oberste, M. Steven DeRisi, Joseph L. Wilson, Michael R. Pan-viral serology implicates enteroviruses in acute flaccid myelitis |
title | Pan-viral serology implicates enteroviruses in acute flaccid myelitis |
title_full | Pan-viral serology implicates enteroviruses in acute flaccid myelitis |
title_fullStr | Pan-viral serology implicates enteroviruses in acute flaccid myelitis |
title_full_unstemmed | Pan-viral serology implicates enteroviruses in acute flaccid myelitis |
title_short | Pan-viral serology implicates enteroviruses in acute flaccid myelitis |
title_sort | pan-viral serology implicates enteroviruses in acute flaccid myelitis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858576/ https://www.ncbi.nlm.nih.gov/pubmed/31636453 http://dx.doi.org/10.1038/s41591-019-0613-1 |
work_keys_str_mv | AT schubertryand panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT hawesisobela panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT ramachandranprashanths panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT rameshakshaya panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT crawfordemilyd panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT pakjohne panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT wuwesley panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT cheungcarlyk panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT odonovanbriand panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT tatocristinam panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT lydenamy panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT tanmichelle panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT sitrene panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT sowagavina panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT samplehannaha panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT zornkelseyc panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT banerjidebarko panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT khanlillianm panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT boveriley panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT hauserstephenl panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT gelfandamya panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT johnsonkernerbethany panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT nashkendall panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT krishnamoorthykalpathys panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT chitnistanuja panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT dingjoyz panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT mcmillanhughj panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT chiucharlesy panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT briggsbenjamin panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT glasercarola panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT yencynthia panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT chuvictoria panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT wadforddebraa panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT dominguezsamuelr panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT feifanngterry panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT marinerachell panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT lopezadrianas panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT nixwallan panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT soldatosariane panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT gormanmarkp panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT bensonleslie panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT messacarkevin panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT konopkaanstadtjenniferl panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT oberstemsteven panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT derisijosephl panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis AT wilsonmichaelr panviralserologyimplicatesenterovirusesinacuteflaccidmyelitis |