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Clinical use of whole genome sequencing for Mycobacterium tuberculosis
Drug-resistant tuberculosis (TB) remains a major challenge to global health and to healthcare in the UK. In 2014, a total of 6,520 cases of TB were recorded in England, of which 1.4 % were multidrug-resistant TB (MDR-TB). Extensively drug-resistant TB (XDR-TB) occurs at a much lower rate, but the im...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804576/ https://www.ncbi.nlm.nih.gov/pubmed/27004841 http://dx.doi.org/10.1186/s12916-016-0598-2 |
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author | Witney, Adam A. Cosgrove, Catherine A. Arnold, Amber Hinds, Jason Stoker, Neil G. Butcher, Philip D. |
author_facet | Witney, Adam A. Cosgrove, Catherine A. Arnold, Amber Hinds, Jason Stoker, Neil G. Butcher, Philip D. |
author_sort | Witney, Adam A. |
collection | PubMed |
description | Drug-resistant tuberculosis (TB) remains a major challenge to global health and to healthcare in the UK. In 2014, a total of 6,520 cases of TB were recorded in England, of which 1.4 % were multidrug-resistant TB (MDR-TB). Extensively drug-resistant TB (XDR-TB) occurs at a much lower rate, but the impact on the patient and hospital is severe. Current diagnostic methods such as drug susceptibility testing and targeted molecular tests are slow to return or examine only a limited number of target regions, respectively. Faster, more comprehensive diagnostics will enable earlier use of the most appropriate drug regimen, thus improving patient outcomes and reducing overall healthcare costs. Whole genome sequencing (WGS) has been shown to provide a rapid and comprehensive view of the genotype of the organism, and thus enable reliable prediction of the drug susceptibility phenotype within a clinically relevant timeframe. In addition, it provides the highest resolution when investigating transmission events in possible outbreak scenarios. However, robust software and database tools need to be developed for the full potential to be realized in this specialized area of medicine. |
format | Online Article Text |
id | pubmed-4804576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48045762016-03-24 Clinical use of whole genome sequencing for Mycobacterium tuberculosis Witney, Adam A. Cosgrove, Catherine A. Arnold, Amber Hinds, Jason Stoker, Neil G. Butcher, Philip D. BMC Med Review Drug-resistant tuberculosis (TB) remains a major challenge to global health and to healthcare in the UK. In 2014, a total of 6,520 cases of TB were recorded in England, of which 1.4 % were multidrug-resistant TB (MDR-TB). Extensively drug-resistant TB (XDR-TB) occurs at a much lower rate, but the impact on the patient and hospital is severe. Current diagnostic methods such as drug susceptibility testing and targeted molecular tests are slow to return or examine only a limited number of target regions, respectively. Faster, more comprehensive diagnostics will enable earlier use of the most appropriate drug regimen, thus improving patient outcomes and reducing overall healthcare costs. Whole genome sequencing (WGS) has been shown to provide a rapid and comprehensive view of the genotype of the organism, and thus enable reliable prediction of the drug susceptibility phenotype within a clinically relevant timeframe. In addition, it provides the highest resolution when investigating transmission events in possible outbreak scenarios. However, robust software and database tools need to be developed for the full potential to be realized in this specialized area of medicine. BioMed Central 2016-03-23 /pmc/articles/PMC4804576/ /pubmed/27004841 http://dx.doi.org/10.1186/s12916-016-0598-2 Text en © Witney et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Witney, Adam A. Cosgrove, Catherine A. Arnold, Amber Hinds, Jason Stoker, Neil G. Butcher, Philip D. Clinical use of whole genome sequencing for Mycobacterium tuberculosis |
title | Clinical use of whole genome sequencing for Mycobacterium tuberculosis |
title_full | Clinical use of whole genome sequencing for Mycobacterium tuberculosis |
title_fullStr | Clinical use of whole genome sequencing for Mycobacterium tuberculosis |
title_full_unstemmed | Clinical use of whole genome sequencing for Mycobacterium tuberculosis |
title_short | Clinical use of whole genome sequencing for Mycobacterium tuberculosis |
title_sort | clinical use of whole genome sequencing for mycobacterium tuberculosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804576/ https://www.ncbi.nlm.nih.gov/pubmed/27004841 http://dx.doi.org/10.1186/s12916-016-0598-2 |
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