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Genotyping of clinically relevant human adenoviruses by array‐in‐well hybridization assay
Clin Microbiol Infect ABSTRACT: A robust oligonucleotide array‐in‐well hybridization assay using novel up‐converting phosphor reporter technology was applied for genotyping clinically relevant human adenovirus types. A total of 231 adenovirus‐positive respiratory, ocular swab, stool and other specim...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129513/ https://www.ncbi.nlm.nih.gov/pubmed/22712766 http://dx.doi.org/10.1111/j.1469-0691.2012.03926.x |
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author | Ylihärsilä, M. Harju, E. Arppe, R. Hattara, L. Hölsä, J. Saviranta, P. Soukka, T. Waris, M. |
author_facet | Ylihärsilä, M. Harju, E. Arppe, R. Hattara, L. Hölsä, J. Saviranta, P. Soukka, T. Waris, M. |
author_sort | Ylihärsilä, M. |
collection | PubMed |
description | Clin Microbiol Infect ABSTRACT: A robust oligonucleotide array‐in‐well hybridization assay using novel up‐converting phosphor reporter technology was applied for genotyping clinically relevant human adenovirus types. A total of 231 adenovirus‐positive respiratory, ocular swab, stool and other specimens from 219 patients collected between April 2010 and April 2011 were included in the study. After a real‐time PCR amplification targeting the adenovirus hexon gene, the array‐in‐well assay identified the presence of B03 (n = 122; 57.5% of patients), E04 (29; 13.7%), C02 (21; 9.9%), D37 (14; 6.6%), C01 (12; 5.7%), C05 (5; 2.4%), D19 (4; 1.9%), C06 (2; 0.9%), D08 (1; 0.5%), A31 (1; 0.5%) and F41 (1; 0.5%) genotypes among the clinical sample panel. The typing result was obtained for all specimens that could be amplified (n = 223; 97%), and specificity of the typing was confirmed by sequencing specimens representing each of the different genotypes. No hybridization signal was obtained in adenovirus‐negative specimens or specimens with other viruses (n = 30). The array‐in‐well hybridization assay has great potential as a rapid and multiplex platform for the typing of clinically relevant human adenovirus genotypes in different specimen types. |
format | Online Article Text |
id | pubmed-7129513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-71295132020-04-08 Genotyping of clinically relevant human adenoviruses by array‐in‐well hybridization assay Ylihärsilä, M. Harju, E. Arppe, R. Hattara, L. Hölsä, J. Saviranta, P. Soukka, T. Waris, M. Clin Microbiol Infect VIROLOGY Clin Microbiol Infect ABSTRACT: A robust oligonucleotide array‐in‐well hybridization assay using novel up‐converting phosphor reporter technology was applied for genotyping clinically relevant human adenovirus types. A total of 231 adenovirus‐positive respiratory, ocular swab, stool and other specimens from 219 patients collected between April 2010 and April 2011 were included in the study. After a real‐time PCR amplification targeting the adenovirus hexon gene, the array‐in‐well assay identified the presence of B03 (n = 122; 57.5% of patients), E04 (29; 13.7%), C02 (21; 9.9%), D37 (14; 6.6%), C01 (12; 5.7%), C05 (5; 2.4%), D19 (4; 1.9%), C06 (2; 0.9%), D08 (1; 0.5%), A31 (1; 0.5%) and F41 (1; 0.5%) genotypes among the clinical sample panel. The typing result was obtained for all specimens that could be amplified (n = 223; 97%), and specificity of the typing was confirmed by sequencing specimens representing each of the different genotypes. No hybridization signal was obtained in adenovirus‐negative specimens or specimens with other viruses (n = 30). The array‐in‐well hybridization assay has great potential as a rapid and multiplex platform for the typing of clinically relevant human adenovirus genotypes in different specimen types. Blackwell Publishing Ltd 2012-06-19 2013-06 /pmc/articles/PMC7129513/ /pubmed/22712766 http://dx.doi.org/10.1111/j.1469-0691.2012.03926.x Text en © 2012 The Authors. Clinical Microbiology and Infection © 2012 European Society of Clinical Microbiology and Infectious Diseases 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 | VIROLOGY Ylihärsilä, M. Harju, E. Arppe, R. Hattara, L. Hölsä, J. Saviranta, P. Soukka, T. Waris, M. Genotyping of clinically relevant human adenoviruses by array‐in‐well hybridization assay |
title | Genotyping of clinically relevant human adenoviruses by array‐in‐well hybridization assay |
title_full | Genotyping of clinically relevant human adenoviruses by array‐in‐well hybridization assay |
title_fullStr | Genotyping of clinically relevant human adenoviruses by array‐in‐well hybridization assay |
title_full_unstemmed | Genotyping of clinically relevant human adenoviruses by array‐in‐well hybridization assay |
title_short | Genotyping of clinically relevant human adenoviruses by array‐in‐well hybridization assay |
title_sort | genotyping of clinically relevant human adenoviruses by array‐in‐well hybridization assay |
topic | VIROLOGY |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129513/ https://www.ncbi.nlm.nih.gov/pubmed/22712766 http://dx.doi.org/10.1111/j.1469-0691.2012.03926.x |
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