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Prevalence and molecular characterisation of human adenovirus in diarrhoeic children in Tanzania; a case control study

BACKGROUND: Human adenovirus (HAdV) causes acute diarrhoea sporadically, as well as in outbreaks. Understanding the prevalence and types of HAdV in diarrhoea is important for control and preventive measures, especially in the African region where there is a high burden of diarrhoeal disease. The pre...

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Autores principales: Moyo, Sabrina John, Hanevik, Kurt, Blomberg, Bjørn, Kommedal, Oyvind, Nordbø, Svein Arne, Maselle, Samuel, Langeland, Nina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266963/
https://www.ncbi.nlm.nih.gov/pubmed/25495029
http://dx.doi.org/10.1186/s12879-014-0666-1
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author Moyo, Sabrina John
Hanevik, Kurt
Blomberg, Bjørn
Kommedal, Oyvind
Nordbø, Svein Arne
Maselle, Samuel
Langeland, Nina
author_facet Moyo, Sabrina John
Hanevik, Kurt
Blomberg, Bjørn
Kommedal, Oyvind
Nordbø, Svein Arne
Maselle, Samuel
Langeland, Nina
author_sort Moyo, Sabrina John
collection PubMed
description BACKGROUND: Human adenovirus (HAdV) causes acute diarrhoea sporadically, as well as in outbreaks. Understanding the prevalence and types of HAdV in diarrhoea is important for control and preventive measures, especially in the African region where there is a high burden of diarrhoeal disease. The present study assessed the prevalence, molecular characteristics, seasonality and associated clinical features of HAdV infection Tanzanian children below two years of age with and without diarrhoea between 2010–2011. METHODS: Stool specimens, demographic and clinical information were collected in 690 cases and 545 controls. All stool samples were screened for HAdV-antigen using ELISA. Positive samples subsequently underwent real-time PCR and sequencing for molecular typing. RESULTS: HAdV was detected in 37 children, corresponding to a prevalence of 3.5% (24/690) in diarrhoeic and 2.4% (13/545) in non-diarrhoeic children (P > 0.05). Among HAdV-infected children, the median age was significantly lower in diarrhoeic than in non-diarrhoeic children (10 vs. 14 months, P˂0.001). More than half of HAdV infected (54.2%) were dehydrated as compared to diarrhoeic children without HAdV (45.8%, P = 0.01). The proportion of the enteric HAdV type 40/41 in diarrhoeic and non-diarrhoeic children was (50.0%, 12/24) and (46.2%, 6/13) respectively. Other HAdV types detected were; 1, 2, 7, 18, 19 and 31. The prevalence of adenovirus was not significantly different between rainy and dry seasons. HAdV was not detected in the 33 known HIV positive children. There was no significant association between HAdV infection and gender, nutritional status of the child and parent educational level. CONCLUSION: The present study provides further evidence of the contribution of adenovirus in causing gastroenteritis in young children, with symptomatic infection being significantly more prevalent in children below one year. We found similar prevalence of adenovirus in non-diarrhoeic children and in diarrhoeic children. This first report on molecular epidemiology of human adenovirus in Tanzania observed diversity of HAdV types that circulate the study setting. The study findings suggest that HAdV is not an important cause of diarrhoea in young HIV-positive children. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-014-0666-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-42669632014-12-16 Prevalence and molecular characterisation of human adenovirus in diarrhoeic children in Tanzania; a case control study Moyo, Sabrina John Hanevik, Kurt Blomberg, Bjørn Kommedal, Oyvind Nordbø, Svein Arne Maselle, Samuel Langeland, Nina BMC Infect Dis Research Article BACKGROUND: Human adenovirus (HAdV) causes acute diarrhoea sporadically, as well as in outbreaks. Understanding the prevalence and types of HAdV in diarrhoea is important for control and preventive measures, especially in the African region where there is a high burden of diarrhoeal disease. The present study assessed the prevalence, molecular characteristics, seasonality and associated clinical features of HAdV infection Tanzanian children below two years of age with and without diarrhoea between 2010–2011. METHODS: Stool specimens, demographic and clinical information were collected in 690 cases and 545 controls. All stool samples were screened for HAdV-antigen using ELISA. Positive samples subsequently underwent real-time PCR and sequencing for molecular typing. RESULTS: HAdV was detected in 37 children, corresponding to a prevalence of 3.5% (24/690) in diarrhoeic and 2.4% (13/545) in non-diarrhoeic children (P > 0.05). Among HAdV-infected children, the median age was significantly lower in diarrhoeic than in non-diarrhoeic children (10 vs. 14 months, P˂0.001). More than half of HAdV infected (54.2%) were dehydrated as compared to diarrhoeic children without HAdV (45.8%, P = 0.01). The proportion of the enteric HAdV type 40/41 in diarrhoeic and non-diarrhoeic children was (50.0%, 12/24) and (46.2%, 6/13) respectively. Other HAdV types detected were; 1, 2, 7, 18, 19 and 31. The prevalence of adenovirus was not significantly different between rainy and dry seasons. HAdV was not detected in the 33 known HIV positive children. There was no significant association between HAdV infection and gender, nutritional status of the child and parent educational level. CONCLUSION: The present study provides further evidence of the contribution of adenovirus in causing gastroenteritis in young children, with symptomatic infection being significantly more prevalent in children below one year. We found similar prevalence of adenovirus in non-diarrhoeic children and in diarrhoeic children. This first report on molecular epidemiology of human adenovirus in Tanzania observed diversity of HAdV types that circulate the study setting. The study findings suggest that HAdV is not an important cause of diarrhoea in young HIV-positive children. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-014-0666-1) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-12 /pmc/articles/PMC4266963/ /pubmed/25495029 http://dx.doi.org/10.1186/s12879-014-0666-1 Text en © Moyo et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Moyo, Sabrina John
Hanevik, Kurt
Blomberg, Bjørn
Kommedal, Oyvind
Nordbø, Svein Arne
Maselle, Samuel
Langeland, Nina
Prevalence and molecular characterisation of human adenovirus in diarrhoeic children in Tanzania; a case control study
title Prevalence and molecular characterisation of human adenovirus in diarrhoeic children in Tanzania; a case control study
title_full Prevalence and molecular characterisation of human adenovirus in diarrhoeic children in Tanzania; a case control study
title_fullStr Prevalence and molecular characterisation of human adenovirus in diarrhoeic children in Tanzania; a case control study
title_full_unstemmed Prevalence and molecular characterisation of human adenovirus in diarrhoeic children in Tanzania; a case control study
title_short Prevalence and molecular characterisation of human adenovirus in diarrhoeic children in Tanzania; a case control study
title_sort prevalence and molecular characterisation of human adenovirus in diarrhoeic children in tanzania; a case control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266963/
https://www.ncbi.nlm.nih.gov/pubmed/25495029
http://dx.doi.org/10.1186/s12879-014-0666-1
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