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No evidence for an association between infections with WU and KI polyomaviruses and respiratory disease
BACKGROUND: WU virus (WUV) and KI polyomavirus (KIPyV) are newly discovered related human polyomaviruses detected in respiratory samples. To investigate their potential role in respiratory disease, we determined their frequencies of detection, clinical presentations and epidemiological characteristi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172997/ https://www.ncbi.nlm.nih.gov/pubmed/17997354 http://dx.doi.org/10.1016/j.jcv.2007.09.008 |
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author | Norja, P. Ubillos, I. Templeton, K. Simmonds, P. |
author_facet | Norja, P. Ubillos, I. Templeton, K. Simmonds, P. |
author_sort | Norja, P. |
collection | PubMed |
description | BACKGROUND: WU virus (WUV) and KI polyomavirus (KIPyV) are newly discovered related human polyomaviruses detected in respiratory samples. To investigate their potential role in respiratory disease, we determined their frequencies of detection, clinical presentations and epidemiological characteristics among samples referred for diagnostic respiratory virus testing. METHODS: Anonymised samples and accompanying study subject information were obtained from the Edinburgh respiratory specimen archive. Samples were screened by nested PCR using two sets of primers conserved between WUV and KIPyV, as well for other respiratory viruses (respiratory syncytial virus [RSV], adenoviruses [AdV], influenza A/B and parainfluenza viruses 1–3, human bocavirus, B19). RESULTS AND CONCLUSIONS: WUV and KIPyV were detected in 10 and 14 samples, respectively from 983 specimens (from 9 to 10 different individuals from 612 study subjects). Infections occurred in two types of study subject; those who were young (<2 years) with lower respiratory tract infections (n = 8), and almost invariably co-infected with other respiratory viruses (RSV, AdV), and a second, generally older group either without respiratory disease (n = 6) or with mild upper respiratory tract infections (n = 5) but who were generally clinically severely immunosuppressed from leukaemia or transplant therapy. Findings from either group do not support an aetiological link between infection with WUV or KIPyV and respiratory disease. |
format | Online Article Text |
id | pubmed-7172997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71729972020-04-22 No evidence for an association between infections with WU and KI polyomaviruses and respiratory disease Norja, P. Ubillos, I. Templeton, K. Simmonds, P. J Clin Virol Article BACKGROUND: WU virus (WUV) and KI polyomavirus (KIPyV) are newly discovered related human polyomaviruses detected in respiratory samples. To investigate their potential role in respiratory disease, we determined their frequencies of detection, clinical presentations and epidemiological characteristics among samples referred for diagnostic respiratory virus testing. METHODS: Anonymised samples and accompanying study subject information were obtained from the Edinburgh respiratory specimen archive. Samples were screened by nested PCR using two sets of primers conserved between WUV and KIPyV, as well for other respiratory viruses (respiratory syncytial virus [RSV], adenoviruses [AdV], influenza A/B and parainfluenza viruses 1–3, human bocavirus, B19). RESULTS AND CONCLUSIONS: WUV and KIPyV were detected in 10 and 14 samples, respectively from 983 specimens (from 9 to 10 different individuals from 612 study subjects). Infections occurred in two types of study subject; those who were young (<2 years) with lower respiratory tract infections (n = 8), and almost invariably co-infected with other respiratory viruses (RSV, AdV), and a second, generally older group either without respiratory disease (n = 6) or with mild upper respiratory tract infections (n = 5) but who were generally clinically severely immunosuppressed from leukaemia or transplant therapy. Findings from either group do not support an aetiological link between infection with WUV or KIPyV and respiratory disease. Elsevier B.V. 2007-12 2007-11-07 /pmc/articles/PMC7172997/ /pubmed/17997354 http://dx.doi.org/10.1016/j.jcv.2007.09.008 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 Norja, P. Ubillos, I. Templeton, K. Simmonds, P. No evidence for an association between infections with WU and KI polyomaviruses and respiratory disease |
title | No evidence for an association between infections with WU and KI polyomaviruses and respiratory disease |
title_full | No evidence for an association between infections with WU and KI polyomaviruses and respiratory disease |
title_fullStr | No evidence for an association between infections with WU and KI polyomaviruses and respiratory disease |
title_full_unstemmed | No evidence for an association between infections with WU and KI polyomaviruses and respiratory disease |
title_short | No evidence for an association between infections with WU and KI polyomaviruses and respiratory disease |
title_sort | no evidence for an association between infections with wu and ki polyomaviruses and respiratory disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172997/ https://www.ncbi.nlm.nih.gov/pubmed/17997354 http://dx.doi.org/10.1016/j.jcv.2007.09.008 |
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