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Molecular epidemiology of human adenovirus infections in Denmark, 2011–2016

BACKGROUND: Human adenoviruses (HAdVs) can cause respiratory tract infections, conjunctivitis, diarrhoea and outbreaks have been reported. However, little is known about the disease burden and the molecular epidemiology of HAdV. OBJECTIVES: To retrospectively perform a molecular characterization of...

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Autores principales: Barnadas, Céline, Schmidt, Dennis Jelsbak, Fischer, Thea K., Fonager, Jannik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106356/
https://www.ncbi.nlm.nih.gov/pubmed/29704734
http://dx.doi.org/10.1016/j.jcv.2018.04.012
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author Barnadas, Céline
Schmidt, Dennis Jelsbak
Fischer, Thea K.
Fonager, Jannik
author_facet Barnadas, Céline
Schmidt, Dennis Jelsbak
Fischer, Thea K.
Fonager, Jannik
author_sort Barnadas, Céline
collection PubMed
description BACKGROUND: Human adenoviruses (HAdVs) can cause respiratory tract infections, conjunctivitis, diarrhoea and outbreaks have been reported. However, little is known about the disease burden and the molecular epidemiology of HAdV. OBJECTIVES: To retrospectively perform a molecular characterization of HAdV positive samples received at Statens Serum Institut during the period 2011–2016 and to compare this with demographic information, geographic location, sample collection date and type and co-infection with other viral pathogens. STUDY DESIGN: 152 HAdV positive samples were genotyped by Sanger sequencing of a fragment of the hexon gene using published primers along with a newly developed primer set for enhanced genotyping of HAdV D. Phylogenetic analysis was used for genotyping and genotypes were compared with epidemiological information. In addition, HAdV burden and co-infection was evaluated for samples tested in laboratory analysis packages. RESULTS: Six out of seven HAdV species were identified and represented by 13 types. Young children (<5 years old) were more likely to be positive for HAdV and co-infections with other gastrointestinal or respiratory viruses were common. Possible outbreaks of ocular infections due to HAdV D could not be confirmed. CONCLUSION: A diverse set of HAdV species were circulating in Denmark in the study period and although possible transmission clusters were identified, this could not be verified with current genotyping methods Young children were commonly affected by HAdV infection and co-infections with other viral pathogens were frequent suggesting a possible underestimation of the real HAdV burden.
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spelling pubmed-71063562020-03-31 Molecular epidemiology of human adenovirus infections in Denmark, 2011–2016 Barnadas, Céline Schmidt, Dennis Jelsbak Fischer, Thea K. Fonager, Jannik J Clin Virol Article BACKGROUND: Human adenoviruses (HAdVs) can cause respiratory tract infections, conjunctivitis, diarrhoea and outbreaks have been reported. However, little is known about the disease burden and the molecular epidemiology of HAdV. OBJECTIVES: To retrospectively perform a molecular characterization of HAdV positive samples received at Statens Serum Institut during the period 2011–2016 and to compare this with demographic information, geographic location, sample collection date and type and co-infection with other viral pathogens. STUDY DESIGN: 152 HAdV positive samples were genotyped by Sanger sequencing of a fragment of the hexon gene using published primers along with a newly developed primer set for enhanced genotyping of HAdV D. Phylogenetic analysis was used for genotyping and genotypes were compared with epidemiological information. In addition, HAdV burden and co-infection was evaluated for samples tested in laboratory analysis packages. RESULTS: Six out of seven HAdV species were identified and represented by 13 types. Young children (<5 years old) were more likely to be positive for HAdV and co-infections with other gastrointestinal or respiratory viruses were common. Possible outbreaks of ocular infections due to HAdV D could not be confirmed. CONCLUSION: A diverse set of HAdV species were circulating in Denmark in the study period and although possible transmission clusters were identified, this could not be verified with current genotyping methods Young children were commonly affected by HAdV infection and co-infections with other viral pathogens were frequent suggesting a possible underestimation of the real HAdV burden. Elsevier B.V. 2018-07 2018-04-21 /pmc/articles/PMC7106356/ /pubmed/29704734 http://dx.doi.org/10.1016/j.jcv.2018.04.012 Text en © 2018 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Barnadas, Céline
Schmidt, Dennis Jelsbak
Fischer, Thea K.
Fonager, Jannik
Molecular epidemiology of human adenovirus infections in Denmark, 2011–2016
title Molecular epidemiology of human adenovirus infections in Denmark, 2011–2016
title_full Molecular epidemiology of human adenovirus infections in Denmark, 2011–2016
title_fullStr Molecular epidemiology of human adenovirus infections in Denmark, 2011–2016
title_full_unstemmed Molecular epidemiology of human adenovirus infections in Denmark, 2011–2016
title_short Molecular epidemiology of human adenovirus infections in Denmark, 2011–2016
title_sort molecular epidemiology of human adenovirus infections in denmark, 2011–2016
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106356/
https://www.ncbi.nlm.nih.gov/pubmed/29704734
http://dx.doi.org/10.1016/j.jcv.2018.04.012
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