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Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review
BACKGROUND: Whole genome sequencing (WGS) is becoming an important part of epidemiological investigations of infectious diseases due to greater resolution and cost reductions compared to traditional typing approaches. Many public health and clinical teams will increasingly use WGS to investigate clu...
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/PMC4804562/ https://www.ncbi.nlm.nih.gov/pubmed/27005433 http://dx.doi.org/10.1186/s12916-016-0566-x |
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author | Hatherell, Hollie-Ann Colijn, Caroline Stagg, Helen R. Jackson, Charlotte Winter, Joanne R. Abubakar, Ibrahim |
author_facet | Hatherell, Hollie-Ann Colijn, Caroline Stagg, Helen R. Jackson, Charlotte Winter, Joanne R. Abubakar, Ibrahim |
author_sort | Hatherell, Hollie-Ann |
collection | PubMed |
description | BACKGROUND: Whole genome sequencing (WGS) is becoming an important part of epidemiological investigations of infectious diseases due to greater resolution and cost reductions compared to traditional typing approaches. Many public health and clinical teams will increasingly use WGS to investigate clusters of potential pathogen transmission, making it crucial to understand the benefits and assumptions of the analytical methods for investigating the data. We aimed to understand how different approaches affect inferences of transmission dynamics and outline limitations of the methods. METHODS: We comprehensively searched electronic databases for studies that presented methods used to interpret WGS data for investigating tuberculosis (TB) transmission. Two authors independently selected studies for inclusion and extracted data. Due to considerable methodological heterogeneity between studies, we present summary data with accompanying narrative synthesis rather than pooled analyses. RESULTS: Twenty-five studies met our inclusion criteria. Despite the range of interpretation tools, the usefulness of WGS data in understanding TB transmission often depends on the amount of genetic diversity in the setting. Where diversity is small, distinguishing re-infections from relapses may be impossible; interpretation may be aided by the use of epidemiological data, examining minor variants and deep sequencing. Conversely, when within-host diversity is large, due to genetic hitchhiking or co-infection of two dissimilar strains, it is critical to understand how it arose. Greater understanding of microevolution and mixed infection will enhance interpretation of WGS data. CONCLUSIONS: As sequencing studies have sampled more intensely and integrated multiple sources of information, the understanding of TB transmission and diversity has grown, but there is still much to be learnt about the origins of diversity that will affect inferences from these data. Public health teams and researchers should combine epidemiological, clinical and WGS data to strengthen investigations of transmission. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-016-0566-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4804562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48045622016-03-24 Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review Hatherell, Hollie-Ann Colijn, Caroline Stagg, Helen R. Jackson, Charlotte Winter, Joanne R. Abubakar, Ibrahim BMC Med Research Article BACKGROUND: Whole genome sequencing (WGS) is becoming an important part of epidemiological investigations of infectious diseases due to greater resolution and cost reductions compared to traditional typing approaches. Many public health and clinical teams will increasingly use WGS to investigate clusters of potential pathogen transmission, making it crucial to understand the benefits and assumptions of the analytical methods for investigating the data. We aimed to understand how different approaches affect inferences of transmission dynamics and outline limitations of the methods. METHODS: We comprehensively searched electronic databases for studies that presented methods used to interpret WGS data for investigating tuberculosis (TB) transmission. Two authors independently selected studies for inclusion and extracted data. Due to considerable methodological heterogeneity between studies, we present summary data with accompanying narrative synthesis rather than pooled analyses. RESULTS: Twenty-five studies met our inclusion criteria. Despite the range of interpretation tools, the usefulness of WGS data in understanding TB transmission often depends on the amount of genetic diversity in the setting. Where diversity is small, distinguishing re-infections from relapses may be impossible; interpretation may be aided by the use of epidemiological data, examining minor variants and deep sequencing. Conversely, when within-host diversity is large, due to genetic hitchhiking or co-infection of two dissimilar strains, it is critical to understand how it arose. Greater understanding of microevolution and mixed infection will enhance interpretation of WGS data. CONCLUSIONS: As sequencing studies have sampled more intensely and integrated multiple sources of information, the understanding of TB transmission and diversity has grown, but there is still much to be learnt about the origins of diversity that will affect inferences from these data. Public health teams and researchers should combine epidemiological, clinical and WGS data to strengthen investigations of transmission. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-016-0566-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-23 /pmc/articles/PMC4804562/ /pubmed/27005433 http://dx.doi.org/10.1186/s12916-016-0566-x Text en © Hatherell 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 | Research Article Hatherell, Hollie-Ann Colijn, Caroline Stagg, Helen R. Jackson, Charlotte Winter, Joanne R. Abubakar, Ibrahim Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review |
title | Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review |
title_full | Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review |
title_fullStr | Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review |
title_full_unstemmed | Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review |
title_short | Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review |
title_sort | interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804562/ https://www.ncbi.nlm.nih.gov/pubmed/27005433 http://dx.doi.org/10.1186/s12916-016-0566-x |
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