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Acute gastroenteritis and enteric viruses in hospitalised children in southern Brazil: aetiology, seasonality and clinical outcomes
Viral acute gastroenteritis (AG) is a significant cause of hospitalisation in children younger than five years. Group A rotavirus (RVA) is responsible for 30% of these cases. Following the introduction of RVA immunisation in Brazil in 2006, a decreased circulation of this virus has been observed. Ho...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Instituto Oswaldo Cruz, Ministério da Saúde
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155843/ https://www.ncbi.nlm.nih.gov/pubmed/25075782 http://dx.doi.org/10.1590/0074-0276140066 |
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author | Raboni, Sonia Maria Damasio, Guilherme Augusto Costa Ferreira, Carla EO Pereira, Luciane A Nogueira, Meri B Vidal, Luine R Cruz, Cristina R Almeida, Sergio M |
author_facet | Raboni, Sonia Maria Damasio, Guilherme Augusto Costa Ferreira, Carla EO Pereira, Luciane A Nogueira, Meri B Vidal, Luine R Cruz, Cristina R Almeida, Sergio M |
author_sort | Raboni, Sonia Maria |
collection | PubMed |
description | Viral acute gastroenteritis (AG) is a significant cause of hospitalisation in children younger than five years. Group A rotavirus (RVA) is responsible for 30% of these cases. Following the introduction of RVA immunisation in Brazil in 2006, a decreased circulation of this virus has been observed. However, AG remains an important cause of hospitalisation of paediatric patients and only limited data are available regarding the role of other enteric viruses in these cases. We conducted a prospective study of paediatric patients hospitalised for AG. Stool samples were collected to investigate human adenovirus (HAdV), RVA, norovirus (NoV) and astrovirus (AstV). NoV typing was performed by nucleotide sequencing and phylogenetic analysis. From the 225 samples tested, 60 (26%) were positive for at least one viral agent. HAdV, NoV, RVA and AstV were detected in 16%, 8%, 6% and 0% of the samples, respectively. Mixed infections were found in nine patients: HAdV/RVA (5), HAdV/NoV (3) and HAdV/NoV/RVA (1). The frequency of fever and lymphocytosis was significantly higher in virus-infected patients. Phylogenetic analysis of NoV indicated that all of these viruses belonged to genotype GII.4. The significant frequency of these pathogens in patients with AG highlights the need to routinely implement laboratory investigations. |
format | Online Article Text |
id | pubmed-4155843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Instituto Oswaldo Cruz, Ministério da Saúde |
record_format | MEDLINE/PubMed |
spelling | pubmed-41558432014-09-11 Acute gastroenteritis and enteric viruses in hospitalised children in southern Brazil: aetiology, seasonality and clinical outcomes Raboni, Sonia Maria Damasio, Guilherme Augusto Costa Ferreira, Carla EO Pereira, Luciane A Nogueira, Meri B Vidal, Luine R Cruz, Cristina R Almeida, Sergio M Mem Inst Oswaldo Cruz Articles Viral acute gastroenteritis (AG) is a significant cause of hospitalisation in children younger than five years. Group A rotavirus (RVA) is responsible for 30% of these cases. Following the introduction of RVA immunisation in Brazil in 2006, a decreased circulation of this virus has been observed. However, AG remains an important cause of hospitalisation of paediatric patients and only limited data are available regarding the role of other enteric viruses in these cases. We conducted a prospective study of paediatric patients hospitalised for AG. Stool samples were collected to investigate human adenovirus (HAdV), RVA, norovirus (NoV) and astrovirus (AstV). NoV typing was performed by nucleotide sequencing and phylogenetic analysis. From the 225 samples tested, 60 (26%) were positive for at least one viral agent. HAdV, NoV, RVA and AstV were detected in 16%, 8%, 6% and 0% of the samples, respectively. Mixed infections were found in nine patients: HAdV/RVA (5), HAdV/NoV (3) and HAdV/NoV/RVA (1). The frequency of fever and lymphocytosis was significantly higher in virus-infected patients. Phylogenetic analysis of NoV indicated that all of these viruses belonged to genotype GII.4. The significant frequency of these pathogens in patients with AG highlights the need to routinely implement laboratory investigations. Instituto Oswaldo Cruz, Ministério da Saúde 2014-07 /pmc/articles/PMC4155843/ /pubmed/25075782 http://dx.doi.org/10.1590/0074-0276140066 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Raboni, Sonia Maria Damasio, Guilherme Augusto Costa Ferreira, Carla EO Pereira, Luciane A Nogueira, Meri B Vidal, Luine R Cruz, Cristina R Almeida, Sergio M Acute gastroenteritis and enteric viruses in hospitalised children in southern Brazil: aetiology, seasonality and clinical outcomes |
title | Acute gastroenteritis and enteric viruses in hospitalised children in
southern Brazil: aetiology, seasonality and clinical outcomes |
title_full | Acute gastroenteritis and enteric viruses in hospitalised children in
southern Brazil: aetiology, seasonality and clinical outcomes |
title_fullStr | Acute gastroenteritis and enteric viruses in hospitalised children in
southern Brazil: aetiology, seasonality and clinical outcomes |
title_full_unstemmed | Acute gastroenteritis and enteric viruses in hospitalised children in
southern Brazil: aetiology, seasonality and clinical outcomes |
title_short | Acute gastroenteritis and enteric viruses in hospitalised children in
southern Brazil: aetiology, seasonality and clinical outcomes |
title_sort | acute gastroenteritis and enteric viruses in hospitalised children in
southern brazil: aetiology, seasonality and clinical outcomes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155843/ https://www.ncbi.nlm.nih.gov/pubmed/25075782 http://dx.doi.org/10.1590/0074-0276140066 |
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