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Spread and clinical severity of respiratory syncytial virus A genotype ON1 in Germany, 2011–2017

BACKGROUND: The Respiratory Syncytial Virus (RSV) A genotype ON1, which was first detected in Ontario (Canada) in 2010/11, appeared in Germany in 2011/12. Preliminary observations suggested a higher clinical severity in children infected with this new genotype. We investigated spread and disease sev...

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Autores principales: Streng, Andrea, Goettler, David, Haerlein, Miriam, Lehmann, Lisa, Ulrich, Kristina, Prifert, Christiane, Krempl, Christine, Weißbrich, Benedikt, Liese, Johannes G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624929/
https://www.ncbi.nlm.nih.gov/pubmed/31299924
http://dx.doi.org/10.1186/s12879-019-4266-y
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author Streng, Andrea
Goettler, David
Haerlein, Miriam
Lehmann, Lisa
Ulrich, Kristina
Prifert, Christiane
Krempl, Christine
Weißbrich, Benedikt
Liese, Johannes G.
author_facet Streng, Andrea
Goettler, David
Haerlein, Miriam
Lehmann, Lisa
Ulrich, Kristina
Prifert, Christiane
Krempl, Christine
Weißbrich, Benedikt
Liese, Johannes G.
author_sort Streng, Andrea
collection PubMed
description BACKGROUND: The Respiratory Syncytial Virus (RSV) A genotype ON1, which was first detected in Ontario (Canada) in 2010/11, appeared in Germany in 2011/12. Preliminary observations suggested a higher clinical severity in children infected with this new genotype. We investigated spread and disease severity of RSV-A ON1 in pediatric in- and outpatient settings. METHODS: During 2010/11 to 2016/17, clinical characteristics and respiratory samples from children with acute respiratory tract infections (RTI) were obtained from ongoing surveillance studies in 33 pediatric practices (PP), one pediatric hospital ward (PW) and 23 pediatric intensive care units (PICU) in Germany. RSV was detected in the respiratory samples by PCR; genotypes were identified by sequencing. Within each setting, clinical severity markers were compared between RSV-A ON1 and RSV-A non-ON1 genotypes. RESULTS: A total of 603 children with RSV-RTI were included (132 children in PP, 288 in PW, and 183 in PICU). Of these children, 341 (56.6%) were infected with RSV-A, 235 (39.0%) with RSV-B, and one child (0.2%) with both RSV-A and RSV-B; in 26 (4.3%) children, the subtype could not be identified. In the 341 RSV-A positive samples, genotype ON1 was detected in 247 (72.4%), NA1 in 92 (26.9%), and GA5 in 2 children (0.6%). RSV-A ON1, rarely observed in 2011/12, was the predominant RSV-A genotype in all settings by 2012/13 and remained predominant until 2016/17. Children in PP or PW infected with RSV-A ON1 did not show a more severe clinical course of disease compared with RSV-A non-ON1 infections. In the PICU group, hospital stay was one day longer (median 8 days, inter-quartile range (IQR) 7–12 vs. 7 days, IQR 5–9; p = 0.02) and duration of oxygen treatment two days longer (median 6 days, IQR 4–9 vs. 4 days, IQR 2–6; p = 0.03) for children infected with RSV-A ON1. CONCLUSIONS: In children, RSV-A ON1 largely replaced RSV-A non-ON1 genotypes within two seasons and remained the predominant RSV-A genotype in Germany during subsequent seasons. A higher clinical severity of RSV-A ON1 was observed within the group of children receiving PICU treatment, whereas in other settings clinical severity of RSV-A ON1 and non-ON1 genotypes was largely similar. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-019-4266-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-66249292019-07-23 Spread and clinical severity of respiratory syncytial virus A genotype ON1 in Germany, 2011–2017 Streng, Andrea Goettler, David Haerlein, Miriam Lehmann, Lisa Ulrich, Kristina Prifert, Christiane Krempl, Christine Weißbrich, Benedikt Liese, Johannes G. BMC Infect Dis Research Article BACKGROUND: The Respiratory Syncytial Virus (RSV) A genotype ON1, which was first detected in Ontario (Canada) in 2010/11, appeared in Germany in 2011/12. Preliminary observations suggested a higher clinical severity in children infected with this new genotype. We investigated spread and disease severity of RSV-A ON1 in pediatric in- and outpatient settings. METHODS: During 2010/11 to 2016/17, clinical characteristics and respiratory samples from children with acute respiratory tract infections (RTI) were obtained from ongoing surveillance studies in 33 pediatric practices (PP), one pediatric hospital ward (PW) and 23 pediatric intensive care units (PICU) in Germany. RSV was detected in the respiratory samples by PCR; genotypes were identified by sequencing. Within each setting, clinical severity markers were compared between RSV-A ON1 and RSV-A non-ON1 genotypes. RESULTS: A total of 603 children with RSV-RTI were included (132 children in PP, 288 in PW, and 183 in PICU). Of these children, 341 (56.6%) were infected with RSV-A, 235 (39.0%) with RSV-B, and one child (0.2%) with both RSV-A and RSV-B; in 26 (4.3%) children, the subtype could not be identified. In the 341 RSV-A positive samples, genotype ON1 was detected in 247 (72.4%), NA1 in 92 (26.9%), and GA5 in 2 children (0.6%). RSV-A ON1, rarely observed in 2011/12, was the predominant RSV-A genotype in all settings by 2012/13 and remained predominant until 2016/17. Children in PP or PW infected with RSV-A ON1 did not show a more severe clinical course of disease compared with RSV-A non-ON1 infections. In the PICU group, hospital stay was one day longer (median 8 days, inter-quartile range (IQR) 7–12 vs. 7 days, IQR 5–9; p = 0.02) and duration of oxygen treatment two days longer (median 6 days, IQR 4–9 vs. 4 days, IQR 2–6; p = 0.03) for children infected with RSV-A ON1. CONCLUSIONS: In children, RSV-A ON1 largely replaced RSV-A non-ON1 genotypes within two seasons and remained the predominant RSV-A genotype in Germany during subsequent seasons. A higher clinical severity of RSV-A ON1 was observed within the group of children receiving PICU treatment, whereas in other settings clinical severity of RSV-A ON1 and non-ON1 genotypes was largely similar. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-019-4266-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-12 /pmc/articles/PMC6624929/ /pubmed/31299924 http://dx.doi.org/10.1186/s12879-019-4266-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Streng, Andrea
Goettler, David
Haerlein, Miriam
Lehmann, Lisa
Ulrich, Kristina
Prifert, Christiane
Krempl, Christine
Weißbrich, Benedikt
Liese, Johannes G.
Spread and clinical severity of respiratory syncytial virus A genotype ON1 in Germany, 2011–2017
title Spread and clinical severity of respiratory syncytial virus A genotype ON1 in Germany, 2011–2017
title_full Spread and clinical severity of respiratory syncytial virus A genotype ON1 in Germany, 2011–2017
title_fullStr Spread and clinical severity of respiratory syncytial virus A genotype ON1 in Germany, 2011–2017
title_full_unstemmed Spread and clinical severity of respiratory syncytial virus A genotype ON1 in Germany, 2011–2017
title_short Spread and clinical severity of respiratory syncytial virus A genotype ON1 in Germany, 2011–2017
title_sort spread and clinical severity of respiratory syncytial virus a genotype on1 in germany, 2011–2017
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624929/
https://www.ncbi.nlm.nih.gov/pubmed/31299924
http://dx.doi.org/10.1186/s12879-019-4266-y
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