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Illumina sequencing of clinical samples for virus detection in a public health laboratory

High-throughput sequencing (HTS) provides the opportunity, once a diagnostic result is obtained, to extract additional information from a virus-containing sample. Hence, it offers advantages over established quantitative amplification technology, such as quantitative PCR, particularly in a public he...

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Autores principales: Huang, Bixing, Jennison, Amy, Whiley, David, McMahon, Jamie, Hewitson, Glen, Graham, Rikki, De Jong, Amanda, Warrilow, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443674/
https://www.ncbi.nlm.nih.gov/pubmed/30931974
http://dx.doi.org/10.1038/s41598-019-41830-w
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author Huang, Bixing
Jennison, Amy
Whiley, David
McMahon, Jamie
Hewitson, Glen
Graham, Rikki
De Jong, Amanda
Warrilow, David
author_facet Huang, Bixing
Jennison, Amy
Whiley, David
McMahon, Jamie
Hewitson, Glen
Graham, Rikki
De Jong, Amanda
Warrilow, David
author_sort Huang, Bixing
collection PubMed
description High-throughput sequencing (HTS) provides the opportunity, once a diagnostic result is obtained, to extract additional information from a virus-containing sample. Hence, it offers advantages over established quantitative amplification technology, such as quantitative PCR, particularly in a public health environment. At this early stage of its clinical application, there have been limited studies comparing HTS performance to that of the more established quantitative PCR technology for direct detection of viruses. In this pilot-scale study, we tested HTS with a range of viruses and sample types routinely encountered in a public health virology laboratory. In comparison with quantitative PCR, our HTS method was able to sensitively (92%) detect all viruses in any sample type with the exception of certain tissues. Moreover, sufficient nucleotide sequence information was obtained to enable genotyping of strains detected, thus providing additional useful epidemiological information. While HTS sensitivity may not yet match that of PCR, the added value through enhanced epidemiological data has considerable potential to enable real-time surveillance of circulating strains so as to facilitate rapid and appropriate response to outbreaks and virus zoonotic spillover events.
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spelling pubmed-64436742019-04-05 Illumina sequencing of clinical samples for virus detection in a public health laboratory Huang, Bixing Jennison, Amy Whiley, David McMahon, Jamie Hewitson, Glen Graham, Rikki De Jong, Amanda Warrilow, David Sci Rep Article High-throughput sequencing (HTS) provides the opportunity, once a diagnostic result is obtained, to extract additional information from a virus-containing sample. Hence, it offers advantages over established quantitative amplification technology, such as quantitative PCR, particularly in a public health environment. At this early stage of its clinical application, there have been limited studies comparing HTS performance to that of the more established quantitative PCR technology for direct detection of viruses. In this pilot-scale study, we tested HTS with a range of viruses and sample types routinely encountered in a public health virology laboratory. In comparison with quantitative PCR, our HTS method was able to sensitively (92%) detect all viruses in any sample type with the exception of certain tissues. Moreover, sufficient nucleotide sequence information was obtained to enable genotyping of strains detected, thus providing additional useful epidemiological information. While HTS sensitivity may not yet match that of PCR, the added value through enhanced epidemiological data has considerable potential to enable real-time surveillance of circulating strains so as to facilitate rapid and appropriate response to outbreaks and virus zoonotic spillover events. Nature Publishing Group UK 2019-04-01 /pmc/articles/PMC6443674/ /pubmed/30931974 http://dx.doi.org/10.1038/s41598-019-41830-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Huang, Bixing
Jennison, Amy
Whiley, David
McMahon, Jamie
Hewitson, Glen
Graham, Rikki
De Jong, Amanda
Warrilow, David
Illumina sequencing of clinical samples for virus detection in a public health laboratory
title Illumina sequencing of clinical samples for virus detection in a public health laboratory
title_full Illumina sequencing of clinical samples for virus detection in a public health laboratory
title_fullStr Illumina sequencing of clinical samples for virus detection in a public health laboratory
title_full_unstemmed Illumina sequencing of clinical samples for virus detection in a public health laboratory
title_short Illumina sequencing of clinical samples for virus detection in a public health laboratory
title_sort illumina sequencing of clinical samples for virus detection in a public health laboratory
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443674/
https://www.ncbi.nlm.nih.gov/pubmed/30931974
http://dx.doi.org/10.1038/s41598-019-41830-w
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