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Molecular Epidemiology of Enterovirus in Children with Central Nervous System Infections

Limited recent molecular epidemiology data are available for pediatric Central Nervous System (CNS) infections in Europe. The aim of this study was to investigate the molecular epidemiology of enterovirus (EV) involved in CNS infections in children. Cerebrospinal fluid (CSF) from children (0–16 year...

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Autores principales: Posnakoglou, Lamprini, Tatsi, Elizabeth-Barbara, Chatzichristou, Panagiota, Siahanidou, Tania, Kanaka-Gantenbein, Christina, Syriopoulou, Vasiliki, Michos, Athanasios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828273/
https://www.ncbi.nlm.nih.gov/pubmed/33450832
http://dx.doi.org/10.3390/v13010100
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author Posnakoglou, Lamprini
Tatsi, Elizabeth-Barbara
Chatzichristou, Panagiota
Siahanidou, Tania
Kanaka-Gantenbein, Christina
Syriopoulou, Vasiliki
Michos, Athanasios
author_facet Posnakoglou, Lamprini
Tatsi, Elizabeth-Barbara
Chatzichristou, Panagiota
Siahanidou, Tania
Kanaka-Gantenbein, Christina
Syriopoulou, Vasiliki
Michos, Athanasios
author_sort Posnakoglou, Lamprini
collection PubMed
description Limited recent molecular epidemiology data are available for pediatric Central Nervous System (CNS) infections in Europe. The aim of this study was to investigate the molecular epidemiology of enterovirus (EV) involved in CNS infections in children. Cerebrospinal fluid (CSF) from children (0–16 years) with suspected meningitis–encephalitis (ME) who were hospitalized in the largest pediatric hospital of Greece from October 2017 to September 2020 was initially tested for 14 common pathogens using the multiplex PCR FilmArray(®) ME Panel (FA-ME). CSF samples positive for EV, as well as pharyngeal swabs and stools of the same children, were further genotyped employing Sanger sequencing. Of the 330 children tested with FA-ME, 75 (22.7%) were positive for EV and 50 different CSF samples were available for genotyping. The median age of children with EV CNS infection was 2 months (IQR: 1–60) and 44/75 (58.7%) of them were male. There was a seasonal distribution of EV CNS infections, with most cases detected between June and September (38/75, 50.7%). EV genotyping was successfully processed in 84/104 samples: CSF (n = 45/50), pharyngeal swabs (n = 15/29) and stools (n = 24/25). Predominant EV genotypes were CV-B5 (16/45, 35.6%), E30 (10/45, 22.2%), E16 (6/45, 13.3%) and E11 (5/45, 11.1%). However, significant phylogenetic differences from previous described isolates were detected. No unusual neurologic manifestations were observed, and all children recovered without obvious acute sequelae. Specific EV circulating genotypes are causing a significant number of pediatric CNS infections. Phylogenetic analysis of these predominant genotypes found genetic differences from already described EV isolates.
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spelling pubmed-78282732021-01-25 Molecular Epidemiology of Enterovirus in Children with Central Nervous System Infections Posnakoglou, Lamprini Tatsi, Elizabeth-Barbara Chatzichristou, Panagiota Siahanidou, Tania Kanaka-Gantenbein, Christina Syriopoulou, Vasiliki Michos, Athanasios Viruses Article Limited recent molecular epidemiology data are available for pediatric Central Nervous System (CNS) infections in Europe. The aim of this study was to investigate the molecular epidemiology of enterovirus (EV) involved in CNS infections in children. Cerebrospinal fluid (CSF) from children (0–16 years) with suspected meningitis–encephalitis (ME) who were hospitalized in the largest pediatric hospital of Greece from October 2017 to September 2020 was initially tested for 14 common pathogens using the multiplex PCR FilmArray(®) ME Panel (FA-ME). CSF samples positive for EV, as well as pharyngeal swabs and stools of the same children, were further genotyped employing Sanger sequencing. Of the 330 children tested with FA-ME, 75 (22.7%) were positive for EV and 50 different CSF samples were available for genotyping. The median age of children with EV CNS infection was 2 months (IQR: 1–60) and 44/75 (58.7%) of them were male. There was a seasonal distribution of EV CNS infections, with most cases detected between June and September (38/75, 50.7%). EV genotyping was successfully processed in 84/104 samples: CSF (n = 45/50), pharyngeal swabs (n = 15/29) and stools (n = 24/25). Predominant EV genotypes were CV-B5 (16/45, 35.6%), E30 (10/45, 22.2%), E16 (6/45, 13.3%) and E11 (5/45, 11.1%). However, significant phylogenetic differences from previous described isolates were detected. No unusual neurologic manifestations were observed, and all children recovered without obvious acute sequelae. Specific EV circulating genotypes are causing a significant number of pediatric CNS infections. Phylogenetic analysis of these predominant genotypes found genetic differences from already described EV isolates. MDPI 2021-01-13 /pmc/articles/PMC7828273/ /pubmed/33450832 http://dx.doi.org/10.3390/v13010100 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Posnakoglou, Lamprini
Tatsi, Elizabeth-Barbara
Chatzichristou, Panagiota
Siahanidou, Tania
Kanaka-Gantenbein, Christina
Syriopoulou, Vasiliki
Michos, Athanasios
Molecular Epidemiology of Enterovirus in Children with Central Nervous System Infections
title Molecular Epidemiology of Enterovirus in Children with Central Nervous System Infections
title_full Molecular Epidemiology of Enterovirus in Children with Central Nervous System Infections
title_fullStr Molecular Epidemiology of Enterovirus in Children with Central Nervous System Infections
title_full_unstemmed Molecular Epidemiology of Enterovirus in Children with Central Nervous System Infections
title_short Molecular Epidemiology of Enterovirus in Children with Central Nervous System Infections
title_sort molecular epidemiology of enterovirus in children with central nervous system infections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828273/
https://www.ncbi.nlm.nih.gov/pubmed/33450832
http://dx.doi.org/10.3390/v13010100
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