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Detection of four human coronaviruses in respiratory infections in children: A one‐year study in Colorado

Lower respiratory tract infections are the leading cause of death in children worldwide. Studies on the epidemiology and clinical associations of the four human non‐SARS human coronaviruses (HCoVs) using sensitive polymerase chain reaction (PCR) assays are needed to evaluate the clinical significanc...

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Detalles Bibliográficos
Autores principales: Dominguez, Samuel R., Robinson, Christine C., Holmes, Kathryn V.
Formato: Texto
Lenguaje:English
Publicado: Wiley Subscription Services, Inc., A Wiley Company 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2879166/
https://www.ncbi.nlm.nih.gov/pubmed/19626607
http://dx.doi.org/10.1002/jmv.21541
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author Dominguez, Samuel R.
Robinson, Christine C.
Holmes, Kathryn V.
author_facet Dominguez, Samuel R.
Robinson, Christine C.
Holmes, Kathryn V.
author_sort Dominguez, Samuel R.
collection PubMed
description Lower respiratory tract infections are the leading cause of death in children worldwide. Studies on the epidemiology and clinical associations of the four human non‐SARS human coronaviruses (HCoVs) using sensitive polymerase chain reaction (PCR) assays are needed to evaluate the clinical significance of HCoV infections worldwide. Pediatric respiratory specimens (1,683) submitted to a diagnostic virology laboratory over a 1‐year period (December 2004–November 2005) that were negative for seven respiratory viruses by conventional methods were tested for RNA of four HCoVs using sensitive RT‐PCR assays. Coronavirus RNAs were detected in 84 (5.0%) specimens: HCoV‐NL63 in 37 specimens, HCoV‐OC43 in 34, HCoV‐229E in 11, and HCoV‐HKU1 in 2. The majority of HCoV infections occurred during winter months, and over 62% were in previously healthy children. Twenty‐six (41%) coronavirus positive patients had evidence of a lower respiratory tract infection (LRTI), 17 (26%) presented with vomiting and/or diarrhea, and 5 (8%) presented with meningoencephalitis or seizures. Respiratory specimens from one immunocompromised patient were persistently positive for HCoV‐229E RNA for 3 months. HCoV‐NL63‐positive patients were nearly twice as likely to be hospitalized (P = 0.02) and to have a LRTI (P = 0.04) than HCoV‐OC43‐positive patients. HCoVs are associated with a small, but significant number (at least 2.4% of total samples submitted), of both upper and lower respiratory tract illnesses in children in Colorado. Our data raise the possibility that HCoV may play a role in gastrointestinal and CNS disease. Additional studies are needed to investigate the potential roles of HCoVs in these diseases. J. Med. Virol. 81:1597–1604, 2009. © 2009 Wiley‐Liss, Inc.
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spelling pubmed-28791662010-06-01 Detection of four human coronaviruses in respiratory infections in children: A one‐year study in Colorado Dominguez, Samuel R. Robinson, Christine C. Holmes, Kathryn V. J Med Virol Article Lower respiratory tract infections are the leading cause of death in children worldwide. Studies on the epidemiology and clinical associations of the four human non‐SARS human coronaviruses (HCoVs) using sensitive polymerase chain reaction (PCR) assays are needed to evaluate the clinical significance of HCoV infections worldwide. Pediatric respiratory specimens (1,683) submitted to a diagnostic virology laboratory over a 1‐year period (December 2004–November 2005) that were negative for seven respiratory viruses by conventional methods were tested for RNA of four HCoVs using sensitive RT‐PCR assays. Coronavirus RNAs were detected in 84 (5.0%) specimens: HCoV‐NL63 in 37 specimens, HCoV‐OC43 in 34, HCoV‐229E in 11, and HCoV‐HKU1 in 2. The majority of HCoV infections occurred during winter months, and over 62% were in previously healthy children. Twenty‐six (41%) coronavirus positive patients had evidence of a lower respiratory tract infection (LRTI), 17 (26%) presented with vomiting and/or diarrhea, and 5 (8%) presented with meningoencephalitis or seizures. Respiratory specimens from one immunocompromised patient were persistently positive for HCoV‐229E RNA for 3 months. HCoV‐NL63‐positive patients were nearly twice as likely to be hospitalized (P = 0.02) and to have a LRTI (P = 0.04) than HCoV‐OC43‐positive patients. HCoVs are associated with a small, but significant number (at least 2.4% of total samples submitted), of both upper and lower respiratory tract illnesses in children in Colorado. Our data raise the possibility that HCoV may play a role in gastrointestinal and CNS disease. Additional studies are needed to investigate the potential roles of HCoVs in these diseases. J. Med. Virol. 81:1597–1604, 2009. © 2009 Wiley‐Liss, Inc. Wiley Subscription Services, Inc., A Wiley Company 2009-07-22 2009-09 /pmc/articles/PMC2879166/ /pubmed/19626607 http://dx.doi.org/10.1002/jmv.21541 Text en Copyright © 2009 Wiley‐Liss, Inc. This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.
spellingShingle Article
Dominguez, Samuel R.
Robinson, Christine C.
Holmes, Kathryn V.
Detection of four human coronaviruses in respiratory infections in children: A one‐year study in Colorado
title Detection of four human coronaviruses in respiratory infections in children: A one‐year study in Colorado
title_full Detection of four human coronaviruses in respiratory infections in children: A one‐year study in Colorado
title_fullStr Detection of four human coronaviruses in respiratory infections in children: A one‐year study in Colorado
title_full_unstemmed Detection of four human coronaviruses in respiratory infections in children: A one‐year study in Colorado
title_short Detection of four human coronaviruses in respiratory infections in children: A one‐year study in Colorado
title_sort detection of four human coronaviruses in respiratory infections in children: a one‐year study in colorado
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2879166/
https://www.ncbi.nlm.nih.gov/pubmed/19626607
http://dx.doi.org/10.1002/jmv.21541
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