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Characterisation of a newly identified human rhinovirus, HRV-QPM, discovered in infants with bronchiolitis

BACKGROUND: Human rhinoviruses (HRVs) are some of the earliest identified and most commonly detected viruses associated with acute respiratory tract infections (ARTIs) and yet the molecular epidemiology and genomic variation of individual serotypes remains undefined. OBJECTIVES: To molecularly chara...

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Detalles Bibliográficos
Autores principales: McErlean, P., Shackelton, L.A., Lambert, S.B., Nissen, M.D., Sloots, T.P., Mackay, I.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172271/
https://www.ncbi.nlm.nih.gov/pubmed/17482871
http://dx.doi.org/10.1016/j.jcv.2007.03.012
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author McErlean, P.
Shackelton, L.A.
Lambert, S.B.
Nissen, M.D.
Sloots, T.P.
Mackay, I.M.
author_facet McErlean, P.
Shackelton, L.A.
Lambert, S.B.
Nissen, M.D.
Sloots, T.P.
Mackay, I.M.
author_sort McErlean, P.
collection PubMed
description BACKGROUND: Human rhinoviruses (HRVs) are some of the earliest identified and most commonly detected viruses associated with acute respiratory tract infections (ARTIs) and yet the molecular epidemiology and genomic variation of individual serotypes remains undefined. OBJECTIVES: To molecularly characterise a novel HRV and determine its prevalence and clinical impact on a predominantly paediatric population. STUDY DESIGN: Nucleotide sequencing was employed to determine the complete HRV-QPM coding sequence. Two novel real-time RT-PCR diagnostic assays were designed and employed to retrospectively screen a well-defined population of 1244 specimen extracts to identify the prevalence of HRV-QPM during 2003. RESULTS: Phylogenetic studies of complete coding sequences defined HRV-QPM as a novel member the genus Rhinovirus residing within the previously described HRV-A2 sub-lineage. Investigation of the relatively short VP1 sequence suggest that the virus is resistant to Pleconaril, setting it apart from the HRV A species. Sixteen additional HRV-QPM strains were detected (1.4% of specimens) often as the sole micro-organism present among infants with suspected bronchiolitis. HRV-QPM was also detected in Europe during 2006, and a closely related virus circulated in the United States during 2004. CONCLUSIONS: We present the molecular characterisation and preliminary clinical impact of a newly identified HRV along with sequences representing additional new HRVs.
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spelling pubmed-71722712020-04-22 Characterisation of a newly identified human rhinovirus, HRV-QPM, discovered in infants with bronchiolitis McErlean, P. Shackelton, L.A. Lambert, S.B. Nissen, M.D. Sloots, T.P. Mackay, I.M. J Clin Virol Article BACKGROUND: Human rhinoviruses (HRVs) are some of the earliest identified and most commonly detected viruses associated with acute respiratory tract infections (ARTIs) and yet the molecular epidemiology and genomic variation of individual serotypes remains undefined. OBJECTIVES: To molecularly characterise a novel HRV and determine its prevalence and clinical impact on a predominantly paediatric population. STUDY DESIGN: Nucleotide sequencing was employed to determine the complete HRV-QPM coding sequence. Two novel real-time RT-PCR diagnostic assays were designed and employed to retrospectively screen a well-defined population of 1244 specimen extracts to identify the prevalence of HRV-QPM during 2003. RESULTS: Phylogenetic studies of complete coding sequences defined HRV-QPM as a novel member the genus Rhinovirus residing within the previously described HRV-A2 sub-lineage. Investigation of the relatively short VP1 sequence suggest that the virus is resistant to Pleconaril, setting it apart from the HRV A species. Sixteen additional HRV-QPM strains were detected (1.4% of specimens) often as the sole micro-organism present among infants with suspected bronchiolitis. HRV-QPM was also detected in Europe during 2006, and a closely related virus circulated in the United States during 2004. CONCLUSIONS: We present the molecular characterisation and preliminary clinical impact of a newly identified HRV along with sequences representing additional new HRVs. Elsevier B.V. 2007-06 2007-05-07 /pmc/articles/PMC7172271/ /pubmed/17482871 http://dx.doi.org/10.1016/j.jcv.2007.03.012 Text en Copyright © 2007 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
McErlean, P.
Shackelton, L.A.
Lambert, S.B.
Nissen, M.D.
Sloots, T.P.
Mackay, I.M.
Characterisation of a newly identified human rhinovirus, HRV-QPM, discovered in infants with bronchiolitis
title Characterisation of a newly identified human rhinovirus, HRV-QPM, discovered in infants with bronchiolitis
title_full Characterisation of a newly identified human rhinovirus, HRV-QPM, discovered in infants with bronchiolitis
title_fullStr Characterisation of a newly identified human rhinovirus, HRV-QPM, discovered in infants with bronchiolitis
title_full_unstemmed Characterisation of a newly identified human rhinovirus, HRV-QPM, discovered in infants with bronchiolitis
title_short Characterisation of a newly identified human rhinovirus, HRV-QPM, discovered in infants with bronchiolitis
title_sort characterisation of a newly identified human rhinovirus, hrv-qpm, discovered in infants with bronchiolitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172271/
https://www.ncbi.nlm.nih.gov/pubmed/17482871
http://dx.doi.org/10.1016/j.jcv.2007.03.012
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