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Predictors of influenza a molecular viral shedding in Hutterite communities

BACKGROUND: Patterns of influenza molecular viral shedding following influenza infection have been well established; predictors of viral shedding however remain uncertain. OBJECTIVES: We sought to determine factors associated with peak molecular viral load, duration of shedding, and viral area under...

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Autores principales: Wang, Biao, Russell, Margaret L., Fonseca, Kevin, Earn, David J. D., Horsman, Gregory, Van Caeseele, Paul, Chokani, Khami, Vooght, Mark, Babiuk, Lorne, Walter, Stephen D., Loeb, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5410723/
https://www.ncbi.nlm.nih.gov/pubmed/28207989
http://dx.doi.org/10.1111/irv.12448
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author Wang, Biao
Russell, Margaret L.
Fonseca, Kevin
Earn, David J. D.
Horsman, Gregory
Van Caeseele, Paul
Chokani, Khami
Vooght, Mark
Babiuk, Lorne
Walter, Stephen D.
Loeb, Mark
author_facet Wang, Biao
Russell, Margaret L.
Fonseca, Kevin
Earn, David J. D.
Horsman, Gregory
Van Caeseele, Paul
Chokani, Khami
Vooght, Mark
Babiuk, Lorne
Walter, Stephen D.
Loeb, Mark
author_sort Wang, Biao
collection PubMed
description BACKGROUND: Patterns of influenza molecular viral shedding following influenza infection have been well established; predictors of viral shedding however remain uncertain. OBJECTIVES: We sought to determine factors associated with peak molecular viral load, duration of shedding, and viral area under the curve (AUC) in children and adult Hutterite colony members with laboratory‐confirmed influenza. METHODS: A cohort study was conducted in Hutterite colonies in Alberta, Canada. Flocked nasal swabs were collected during three influenza seasons (2007‐2008 to 2009‐2010) from both symptomatic and asymptomatic individuals infected with influenza. Samples were tested by real‐time reverse‐transcription polymerase chain reaction for influenza A and influenza B, and the viral load was determined for influenza A‐positive samples. RESULTS: For seasonal H1N1, younger age was associated with a larger AUC, female sex was associated with decreased peak viral load and reduced viral shedding duration, while the presence of comorbidity was associated with increased peak viral load. For H3N2, younger age was associated with increased peak viral load and increased AUC. For pandemic H1N1, younger age was associated with increased peak viral load and increased viral AUC, female sex was associated with reduced peak viral load, while inapparent infection was associated with reduced peak viral load, reduced viral shedding duration, and reduced viral AUC. CONCLUSIONS: Patterns of molecular viral shedding vary by age, sex, comorbidity, and the presence of symptoms. Predictor variables vary by influenza A subtype.
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spelling pubmed-54107232017-05-03 Predictors of influenza a molecular viral shedding in Hutterite communities Wang, Biao Russell, Margaret L. Fonseca, Kevin Earn, David J. D. Horsman, Gregory Van Caeseele, Paul Chokani, Khami Vooght, Mark Babiuk, Lorne Walter, Stephen D. Loeb, Mark Influenza Other Respir Viruses Original Articles BACKGROUND: Patterns of influenza molecular viral shedding following influenza infection have been well established; predictors of viral shedding however remain uncertain. OBJECTIVES: We sought to determine factors associated with peak molecular viral load, duration of shedding, and viral area under the curve (AUC) in children and adult Hutterite colony members with laboratory‐confirmed influenza. METHODS: A cohort study was conducted in Hutterite colonies in Alberta, Canada. Flocked nasal swabs were collected during three influenza seasons (2007‐2008 to 2009‐2010) from both symptomatic and asymptomatic individuals infected with influenza. Samples were tested by real‐time reverse‐transcription polymerase chain reaction for influenza A and influenza B, and the viral load was determined for influenza A‐positive samples. RESULTS: For seasonal H1N1, younger age was associated with a larger AUC, female sex was associated with decreased peak viral load and reduced viral shedding duration, while the presence of comorbidity was associated with increased peak viral load. For H3N2, younger age was associated with increased peak viral load and increased AUC. For pandemic H1N1, younger age was associated with increased peak viral load and increased viral AUC, female sex was associated with reduced peak viral load, while inapparent infection was associated with reduced peak viral load, reduced viral shedding duration, and reduced viral AUC. CONCLUSIONS: Patterns of molecular viral shedding vary by age, sex, comorbidity, and the presence of symptoms. Predictor variables vary by influenza A subtype. John Wiley and Sons Inc. 2017-03-16 2017-05 /pmc/articles/PMC5410723/ /pubmed/28207989 http://dx.doi.org/10.1111/irv.12448 Text en © 2017 The Authors. Influenza and Other Respiratory Viruses Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Wang, Biao
Russell, Margaret L.
Fonseca, Kevin
Earn, David J. D.
Horsman, Gregory
Van Caeseele, Paul
Chokani, Khami
Vooght, Mark
Babiuk, Lorne
Walter, Stephen D.
Loeb, Mark
Predictors of influenza a molecular viral shedding in Hutterite communities
title Predictors of influenza a molecular viral shedding in Hutterite communities
title_full Predictors of influenza a molecular viral shedding in Hutterite communities
title_fullStr Predictors of influenza a molecular viral shedding in Hutterite communities
title_full_unstemmed Predictors of influenza a molecular viral shedding in Hutterite communities
title_short Predictors of influenza a molecular viral shedding in Hutterite communities
title_sort predictors of influenza a molecular viral shedding in hutterite communities
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5410723/
https://www.ncbi.nlm.nih.gov/pubmed/28207989
http://dx.doi.org/10.1111/irv.12448
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