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Epidemiologic, clinical, and virologic characteristics of human rhinovirus infection among otherwise healthy children and adults: Rhinovirus among adults and children

BACKGROUND: human rhinovirus (HRV) is a major cause of influenza-like illness (ILI) in adults and children. Differences in disease severity by HRV species have been described among hospitalized patients with underlying illness. Less is known about the clinical and virologic characteristics of HRV in...

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Autores principales: Chen, Wei-Ju, Arnold, John C., Fairchok, Mary P., Danaher, Patrick J., McDonough, Erin A., Blair, Patrick J., Garcia, Josefina, Halsey, Eric S., Schofield, Christina, Ottolini, Martin, Mor, Deepika, Ridoré, Michelande, Burgess, Timothy H., Millar, Eugene V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. Published by Elsevier B.V. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347877/
https://www.ncbi.nlm.nih.gov/pubmed/25728083
http://dx.doi.org/10.1016/j.jcv.2015.01.007
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author Chen, Wei-Ju
Arnold, John C.
Fairchok, Mary P.
Danaher, Patrick J.
McDonough, Erin A.
Blair, Patrick J.
Garcia, Josefina
Halsey, Eric S.
Schofield, Christina
Ottolini, Martin
Mor, Deepika
Ridoré, Michelande
Burgess, Timothy H.
Millar, Eugene V.
author_facet Chen, Wei-Ju
Arnold, John C.
Fairchok, Mary P.
Danaher, Patrick J.
McDonough, Erin A.
Blair, Patrick J.
Garcia, Josefina
Halsey, Eric S.
Schofield, Christina
Ottolini, Martin
Mor, Deepika
Ridoré, Michelande
Burgess, Timothy H.
Millar, Eugene V.
author_sort Chen, Wei-Ju
collection PubMed
description BACKGROUND: human rhinovirus (HRV) is a major cause of influenza-like illness (ILI) in adults and children. Differences in disease severity by HRV species have been described among hospitalized patients with underlying illness. Less is known about the clinical and virologic characteristics of HRV infection among otherwise healthy populations, particularly adults. OBJECTIVES: to characterize molecular epidemiology of HRV and association between HRV species and clinical presentation and viral shedding. STUDY DESIGN: observational, prospective, facility-based study of ILI was conducted from February 2010 to April 2012. Collection of nasopharyngeal specimens, patient symptoms, and clinical information occurred on days 0, 3, 7, and 28. Patients recorded symptom severity daily for the first 7 days of illness in a symptom diary. HRV was identified by RT-PCR and genotyped for species determination. Cases who were co-infected with other viral respiratory pathogens were excluded from the analysis. We evaluated the associations between HRV species, clinical severity, and patterns of viral shedding. RESULTS: eighty-four HRV cases were identified and their isolates genotyped. Of these, 62 (74%) were >18 years. Fifty-four were HRV-A, 11HRV-B, and 19HRV-C. HRV-C infection was more common among children than adults (59% vs. 10%, P < 0.001). Among adults, HRV-A was associated with higher severity of upper respiratory symptoms compared to HRV-B (P = 0.02), but no such association was found in children. In addition, adults shed HRV-A significantly longer than HRV-C (P trend = 0.01). CONCLUSIONS: among otherwise healthy adults with HRV infection, we observed species-specific differences in respiratory symptom severity and duration of viral shedding.
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spelling pubmed-43478772016-03-01 Epidemiologic, clinical, and virologic characteristics of human rhinovirus infection among otherwise healthy children and adults: Rhinovirus among adults and children Chen, Wei-Ju Arnold, John C. Fairchok, Mary P. Danaher, Patrick J. McDonough, Erin A. Blair, Patrick J. Garcia, Josefina Halsey, Eric S. Schofield, Christina Ottolini, Martin Mor, Deepika Ridoré, Michelande Burgess, Timothy H. Millar, Eugene V. J Clin Virol Article BACKGROUND: human rhinovirus (HRV) is a major cause of influenza-like illness (ILI) in adults and children. Differences in disease severity by HRV species have been described among hospitalized patients with underlying illness. Less is known about the clinical and virologic characteristics of HRV infection among otherwise healthy populations, particularly adults. OBJECTIVES: to characterize molecular epidemiology of HRV and association between HRV species and clinical presentation and viral shedding. STUDY DESIGN: observational, prospective, facility-based study of ILI was conducted from February 2010 to April 2012. Collection of nasopharyngeal specimens, patient symptoms, and clinical information occurred on days 0, 3, 7, and 28. Patients recorded symptom severity daily for the first 7 days of illness in a symptom diary. HRV was identified by RT-PCR and genotyped for species determination. Cases who were co-infected with other viral respiratory pathogens were excluded from the analysis. We evaluated the associations between HRV species, clinical severity, and patterns of viral shedding. RESULTS: eighty-four HRV cases were identified and their isolates genotyped. Of these, 62 (74%) were >18 years. Fifty-four were HRV-A, 11HRV-B, and 19HRV-C. HRV-C infection was more common among children than adults (59% vs. 10%, P < 0.001). Among adults, HRV-A was associated with higher severity of upper respiratory symptoms compared to HRV-B (P = 0.02), but no such association was found in children. In addition, adults shed HRV-A significantly longer than HRV-C (P trend = 0.01). CONCLUSIONS: among otherwise healthy adults with HRV infection, we observed species-specific differences in respiratory symptom severity and duration of viral shedding. Elsevier B.V. Published by Elsevier B.V. 2015-03 2015-01-13 /pmc/articles/PMC4347877/ /pubmed/25728083 http://dx.doi.org/10.1016/j.jcv.2015.01.007 Text en Copyright © 2015 Elsevier B.V. Published by Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Chen, Wei-Ju
Arnold, John C.
Fairchok, Mary P.
Danaher, Patrick J.
McDonough, Erin A.
Blair, Patrick J.
Garcia, Josefina
Halsey, Eric S.
Schofield, Christina
Ottolini, Martin
Mor, Deepika
Ridoré, Michelande
Burgess, Timothy H.
Millar, Eugene V.
Epidemiologic, clinical, and virologic characteristics of human rhinovirus infection among otherwise healthy children and adults: Rhinovirus among adults and children
title Epidemiologic, clinical, and virologic characteristics of human rhinovirus infection among otherwise healthy children and adults: Rhinovirus among adults and children
title_full Epidemiologic, clinical, and virologic characteristics of human rhinovirus infection among otherwise healthy children and adults: Rhinovirus among adults and children
title_fullStr Epidemiologic, clinical, and virologic characteristics of human rhinovirus infection among otherwise healthy children and adults: Rhinovirus among adults and children
title_full_unstemmed Epidemiologic, clinical, and virologic characteristics of human rhinovirus infection among otherwise healthy children and adults: Rhinovirus among adults and children
title_short Epidemiologic, clinical, and virologic characteristics of human rhinovirus infection among otherwise healthy children and adults: Rhinovirus among adults and children
title_sort epidemiologic, clinical, and virologic characteristics of human rhinovirus infection among otherwise healthy children and adults: rhinovirus among adults and children
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347877/
https://www.ncbi.nlm.nih.gov/pubmed/25728083
http://dx.doi.org/10.1016/j.jcv.2015.01.007
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