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Co-circulation of Four Human Coronaviruses (HCoVs) in Queensland Children with Acute Respiratory Tract Illnesses in 2004

Acute respiratory illnesses (ARIs) with unconfirmed infectious aetiologies peak at different times of the year. Molecular diagnostic assays reduce the number of unconfirmed ARIs compared to serology- or culture-based techniques. Screening of 888 inpatient and outpatient respiratory specimens spannin...

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Autores principales: Mackay, Ian M., Arden, Katherine E., Speicher, David J., O’Neil, Nicholas T., McErlean, Peter K., Greer, Ristan M., Nissen, Michael D., Sloots, Theo P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347326/
https://www.ncbi.nlm.nih.gov/pubmed/22590689
http://dx.doi.org/10.3390/v4040637
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author Mackay, Ian M.
Arden, Katherine E.
Speicher, David J.
O’Neil, Nicholas T.
McErlean, Peter K.
Greer, Ristan M.
Nissen, Michael D.
Sloots, Theo P.
author_facet Mackay, Ian M.
Arden, Katherine E.
Speicher, David J.
O’Neil, Nicholas T.
McErlean, Peter K.
Greer, Ristan M.
Nissen, Michael D.
Sloots, Theo P.
author_sort Mackay, Ian M.
collection PubMed
description Acute respiratory illnesses (ARIs) with unconfirmed infectious aetiologies peak at different times of the year. Molecular diagnostic assays reduce the number of unconfirmed ARIs compared to serology- or culture-based techniques. Screening of 888 inpatient and outpatient respiratory specimens spanning late autumn through to early spring, 2004, identified the presence of a human coronavirus (HCoV) on 74 occasions (8.3% of all specimens and 26.3% of all respiratory virus detections). Prevalence peaked in August (late winter in the southern hemisphere) when they were detected in 21.9% of specimens tested. HCoV-HKU1 and HCoV-OC43 comprised 82.4% of all HCoVs detected. Positive specimens were used to develop novel reverse transcriptase real-time PCRs (RT-rtPCRs) for HCoV detection. An objective clinical severity score was assigned to each positive HCoV patient. Severity scores were similar to those from a random selection of young children who were positive for respiratory syncytial virus at a different time but from the same specimen population. During the cooler months of 2004, sensitive and specific RT-rtPCRs identified the concurrent circulation of all four HCoVs, a quarter of which co-occurred with another virus and most of which were from children under the age of two years.
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spelling pubmed-33473262012-05-15 Co-circulation of Four Human Coronaviruses (HCoVs) in Queensland Children with Acute Respiratory Tract Illnesses in 2004 Mackay, Ian M. Arden, Katherine E. Speicher, David J. O’Neil, Nicholas T. McErlean, Peter K. Greer, Ristan M. Nissen, Michael D. Sloots, Theo P. Viruses Article Acute respiratory illnesses (ARIs) with unconfirmed infectious aetiologies peak at different times of the year. Molecular diagnostic assays reduce the number of unconfirmed ARIs compared to serology- or culture-based techniques. Screening of 888 inpatient and outpatient respiratory specimens spanning late autumn through to early spring, 2004, identified the presence of a human coronavirus (HCoV) on 74 occasions (8.3% of all specimens and 26.3% of all respiratory virus detections). Prevalence peaked in August (late winter in the southern hemisphere) when they were detected in 21.9% of specimens tested. HCoV-HKU1 and HCoV-OC43 comprised 82.4% of all HCoVs detected. Positive specimens were used to develop novel reverse transcriptase real-time PCRs (RT-rtPCRs) for HCoV detection. An objective clinical severity score was assigned to each positive HCoV patient. Severity scores were similar to those from a random selection of young children who were positive for respiratory syncytial virus at a different time but from the same specimen population. During the cooler months of 2004, sensitive and specific RT-rtPCRs identified the concurrent circulation of all four HCoVs, a quarter of which co-occurred with another virus and most of which were from children under the age of two years. MDPI 2012-04-23 /pmc/articles/PMC3347326/ /pubmed/22590689 http://dx.doi.org/10.3390/v4040637 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Mackay, Ian M.
Arden, Katherine E.
Speicher, David J.
O’Neil, Nicholas T.
McErlean, Peter K.
Greer, Ristan M.
Nissen, Michael D.
Sloots, Theo P.
Co-circulation of Four Human Coronaviruses (HCoVs) in Queensland Children with Acute Respiratory Tract Illnesses in 2004
title Co-circulation of Four Human Coronaviruses (HCoVs) in Queensland Children with Acute Respiratory Tract Illnesses in 2004
title_full Co-circulation of Four Human Coronaviruses (HCoVs) in Queensland Children with Acute Respiratory Tract Illnesses in 2004
title_fullStr Co-circulation of Four Human Coronaviruses (HCoVs) in Queensland Children with Acute Respiratory Tract Illnesses in 2004
title_full_unstemmed Co-circulation of Four Human Coronaviruses (HCoVs) in Queensland Children with Acute Respiratory Tract Illnesses in 2004
title_short Co-circulation of Four Human Coronaviruses (HCoVs) in Queensland Children with Acute Respiratory Tract Illnesses in 2004
title_sort co-circulation of four human coronaviruses (hcovs) in queensland children with acute respiratory tract illnesses in 2004
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347326/
https://www.ncbi.nlm.nih.gov/pubmed/22590689
http://dx.doi.org/10.3390/v4040637
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