Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1783407879669153792 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6443674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT huangbixing illuminasequencingofclinicalsamplesforvirusdetectioninapublichealthlaboratory AT jennisonamy illuminasequencingofclinicalsamplesforvirusdetectioninapublichealthlaboratory AT whileydavid illuminasequencingofclinicalsamplesforvirusdetectioninapublichealthlaboratory AT mcmahonjamie illuminasequencingofclinicalsamplesforvirusdetectioninapublichealthlaboratory AT hewitsonglen illuminasequencingofclinicalsamplesforvirusdetectioninapublichealthlaboratory AT grahamrikki illuminasequencingofclinicalsamplesforvirusdetectioninapublichealthlaboratory AT dejongamanda illuminasequencingofclinicalsamplesforvirusdetectioninapublichealthlaboratory AT warrilowdavid illuminasequencingofclinicalsamplesforvirusdetectioninapublichealthlaboratory |