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Norovirus prevalence and estimated viral load in symptomatic and asymptomatic children from rural communities of Vhembe district, South Africa

BACKGROUND: Human Norovirus (NoV) is recognized as a major etiological agent of sporadic acute gastroenteritis worldwide. OBJECTIVES: This study describes the clinical features associated with Human NoV occurrence in children and determines the prevalence and estimated viral burden of NoV in symptom...

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Autores principales: Kabue, Jean Pierre, Meader, Emma, Hunter, Paul R., Potgieter, Natasha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099155/
https://www.ncbi.nlm.nih.gov/pubmed/27644014
http://dx.doi.org/10.1016/j.jcv.2016.09.005
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author Kabue, Jean Pierre
Meader, Emma
Hunter, Paul R.
Potgieter, Natasha
author_facet Kabue, Jean Pierre
Meader, Emma
Hunter, Paul R.
Potgieter, Natasha
author_sort Kabue, Jean Pierre
collection PubMed
description BACKGROUND: Human Norovirus (NoV) is recognized as a major etiological agent of sporadic acute gastroenteritis worldwide. OBJECTIVES: This study describes the clinical features associated with Human NoV occurrence in children and determines the prevalence and estimated viral burden of NoV in symptomatic and asymptomatic children in rural South Africa. STUDY DESIGN: Between July 2014 and April 2015, outpatient children under 5 years of age from rural communities of Vhembe district, South Africa, were enrolled for the study. A total of 303 stool specimens were collected from those with diarrhea (n = 253) and without (n = 50) diarrhea. NoVs were identified using real-time one-step RT-PCR. RESULTS: One hundred and four (41.1%) NoVs were detected (62[59.6%] GII, 16[15.4%] GI, and 26[25%] mixed GI/GII) in cases and 18 (36%) including 9(50%) GII, 2(11.1%) GI and 7(38.9%) mixed GI/GII in controls. NoV detection rates in symptomatic and asymptomatic children (OR = 1.24; 95% CI 0.66–2.33) were not significantly different. Comparison of the median C(T) values for NoV in symptomatic and asymptomatic children revealed significant statistical difference of estimated GII viral load from both groups, with a much higher viral burden in symptomatic children. CONCLUSIONS: Though not proven predictive of diarrhea disease in this study, the high detection rate of NoV reflects the substantial exposure of children from rural communities to enteric pathogens possibly due to poor sanitation and hygiene practices. The results suggest that the difference between asymptomatic and symptomatic children with NoV may be at the level of the viral load of NoV genogroups involved.
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spelling pubmed-50991552016-11-14 Norovirus prevalence and estimated viral load in symptomatic and asymptomatic children from rural communities of Vhembe district, South Africa Kabue, Jean Pierre Meader, Emma Hunter, Paul R. Potgieter, Natasha J Clin Virol Article BACKGROUND: Human Norovirus (NoV) is recognized as a major etiological agent of sporadic acute gastroenteritis worldwide. OBJECTIVES: This study describes the clinical features associated with Human NoV occurrence in children and determines the prevalence and estimated viral burden of NoV in symptomatic and asymptomatic children in rural South Africa. STUDY DESIGN: Between July 2014 and April 2015, outpatient children under 5 years of age from rural communities of Vhembe district, South Africa, were enrolled for the study. A total of 303 stool specimens were collected from those with diarrhea (n = 253) and without (n = 50) diarrhea. NoVs were identified using real-time one-step RT-PCR. RESULTS: One hundred and four (41.1%) NoVs were detected (62[59.6%] GII, 16[15.4%] GI, and 26[25%] mixed GI/GII) in cases and 18 (36%) including 9(50%) GII, 2(11.1%) GI and 7(38.9%) mixed GI/GII in controls. NoV detection rates in symptomatic and asymptomatic children (OR = 1.24; 95% CI 0.66–2.33) were not significantly different. Comparison of the median C(T) values for NoV in symptomatic and asymptomatic children revealed significant statistical difference of estimated GII viral load from both groups, with a much higher viral burden in symptomatic children. CONCLUSIONS: Though not proven predictive of diarrhea disease in this study, the high detection rate of NoV reflects the substantial exposure of children from rural communities to enteric pathogens possibly due to poor sanitation and hygiene practices. The results suggest that the difference between asymptomatic and symptomatic children with NoV may be at the level of the viral load of NoV genogroups involved. Elsevier Science 2016-11 /pmc/articles/PMC5099155/ /pubmed/27644014 http://dx.doi.org/10.1016/j.jcv.2016.09.005 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kabue, Jean Pierre
Meader, Emma
Hunter, Paul R.
Potgieter, Natasha
Norovirus prevalence and estimated viral load in symptomatic and asymptomatic children from rural communities of Vhembe district, South Africa
title Norovirus prevalence and estimated viral load in symptomatic and asymptomatic children from rural communities of Vhembe district, South Africa
title_full Norovirus prevalence and estimated viral load in symptomatic and asymptomatic children from rural communities of Vhembe district, South Africa
title_fullStr Norovirus prevalence and estimated viral load in symptomatic and asymptomatic children from rural communities of Vhembe district, South Africa
title_full_unstemmed Norovirus prevalence and estimated viral load in symptomatic and asymptomatic children from rural communities of Vhembe district, South Africa
title_short Norovirus prevalence and estimated viral load in symptomatic and asymptomatic children from rural communities of Vhembe district, South Africa
title_sort norovirus prevalence and estimated viral load in symptomatic and asymptomatic children from rural communities of vhembe district, south africa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099155/
https://www.ncbi.nlm.nih.gov/pubmed/27644014
http://dx.doi.org/10.1016/j.jcv.2016.09.005
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