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Virus Etiology, Diversity and Clinical Characteristics in South African Children Hospitalised with Gastroenteritis
Background: Viral gastroenteritis remains a major cause of hospitalisation in young children. This study aimed to determine the distribution and diversity of enteric viruses in children ≤5 years, hospitalised with gastroenteritis at Kalafong Provincial Tertiary Hospital, Pretoria, South Africa, betw...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911269/ https://www.ncbi.nlm.nih.gov/pubmed/33573340 http://dx.doi.org/10.3390/v13020215 |
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author | Rossouw, Esmari Brauer, Marieke Meyer, Pieter du Plessis, Nicolette M. Avenant, Theunis Mans, Janet |
author_facet | Rossouw, Esmari Brauer, Marieke Meyer, Pieter du Plessis, Nicolette M. Avenant, Theunis Mans, Janet |
author_sort | Rossouw, Esmari |
collection | PubMed |
description | Background: Viral gastroenteritis remains a major cause of hospitalisation in young children. This study aimed to determine the distribution and diversity of enteric viruses in children ≤5 years, hospitalised with gastroenteritis at Kalafong Provincial Tertiary Hospital, Pretoria, South Africa, between July 2016 and December 2017. Methods: Stool specimens (n = 205) were screened for norovirus GI and GII, rotavirus, sapovirus, astrovirus and adenovirus by multiplex RT-PCR. HIV exposure and FUT2 secretor status were evaluated. Secretor status was determined by FUT2 genotyping. Results: At least one gastroenteritis virus was detected in 47% (96/205) of children. Rotavirus predominated (46/205), followed by norovirus (32/205), adenovirus (15/205), sapovirus (9/205) and astrovirus (3/205). Norovirus genotypes GI.3, GII.2, GII.3, GII.4, GII.7, GII.12, GII.21, and rotavirus strains G1P[8], G2P[4], G2P[6], G3P[4], G3P[8], G8P[4], G8P[6], G9P[6], G9P[8] and sapovirus genotypes GI.1, GI.2, GII.1, GII.4, GII.8 were detected; norovirus GII.4[P31] and rotavirus G3P[4] predominated. Asymptomatic norovirus infection (GI.3, GI.7, GII.4, GII.6, GII.13) was detected in 22% of 46 six-week follow up stools. HIV exposure (30%) was not associated with more frequent or severe viral gastroenteritis hospitalisations compared to unexposed children. Rotavirus preferentially infected secretor children (p = 0.143) and norovirus infected 78% secretors and 22% non-secretors. Conclusion: Rotavirus was still the leading cause of gastroenteritis hospitalisations, but norovirus caused more severe symptoms. |
format | Online Article Text |
id | pubmed-7911269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79112692021-02-28 Virus Etiology, Diversity and Clinical Characteristics in South African Children Hospitalised with Gastroenteritis Rossouw, Esmari Brauer, Marieke Meyer, Pieter du Plessis, Nicolette M. Avenant, Theunis Mans, Janet Viruses Article Background: Viral gastroenteritis remains a major cause of hospitalisation in young children. This study aimed to determine the distribution and diversity of enteric viruses in children ≤5 years, hospitalised with gastroenteritis at Kalafong Provincial Tertiary Hospital, Pretoria, South Africa, between July 2016 and December 2017. Methods: Stool specimens (n = 205) were screened for norovirus GI and GII, rotavirus, sapovirus, astrovirus and adenovirus by multiplex RT-PCR. HIV exposure and FUT2 secretor status were evaluated. Secretor status was determined by FUT2 genotyping. Results: At least one gastroenteritis virus was detected in 47% (96/205) of children. Rotavirus predominated (46/205), followed by norovirus (32/205), adenovirus (15/205), sapovirus (9/205) and astrovirus (3/205). Norovirus genotypes GI.3, GII.2, GII.3, GII.4, GII.7, GII.12, GII.21, and rotavirus strains G1P[8], G2P[4], G2P[6], G3P[4], G3P[8], G8P[4], G8P[6], G9P[6], G9P[8] and sapovirus genotypes GI.1, GI.2, GII.1, GII.4, GII.8 were detected; norovirus GII.4[P31] and rotavirus G3P[4] predominated. Asymptomatic norovirus infection (GI.3, GI.7, GII.4, GII.6, GII.13) was detected in 22% of 46 six-week follow up stools. HIV exposure (30%) was not associated with more frequent or severe viral gastroenteritis hospitalisations compared to unexposed children. Rotavirus preferentially infected secretor children (p = 0.143) and norovirus infected 78% secretors and 22% non-secretors. Conclusion: Rotavirus was still the leading cause of gastroenteritis hospitalisations, but norovirus caused more severe symptoms. MDPI 2021-01-30 /pmc/articles/PMC7911269/ /pubmed/33573340 http://dx.doi.org/10.3390/v13020215 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 Rossouw, Esmari Brauer, Marieke Meyer, Pieter du Plessis, Nicolette M. Avenant, Theunis Mans, Janet Virus Etiology, Diversity and Clinical Characteristics in South African Children Hospitalised with Gastroenteritis |
title | Virus Etiology, Diversity and Clinical Characteristics in South African Children Hospitalised with Gastroenteritis |
title_full | Virus Etiology, Diversity and Clinical Characteristics in South African Children Hospitalised with Gastroenteritis |
title_fullStr | Virus Etiology, Diversity and Clinical Characteristics in South African Children Hospitalised with Gastroenteritis |
title_full_unstemmed | Virus Etiology, Diversity and Clinical Characteristics in South African Children Hospitalised with Gastroenteritis |
title_short | Virus Etiology, Diversity and Clinical Characteristics in South African Children Hospitalised with Gastroenteritis |
title_sort | virus etiology, diversity and clinical characteristics in south african children hospitalised with gastroenteritis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911269/ https://www.ncbi.nlm.nih.gov/pubmed/33573340 http://dx.doi.org/10.3390/v13020215 |
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