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Comparative analysis of core genome MLST and SNP typing within a European Salmonella serovar Enteritidis outbreak
Multi-country outbreaks of foodborne bacterial disease present challenges in their detection, tracking, and notification. As food is increasingly distributed across borders, such outbreaks are becoming more common. This increases the need for high-resolution, accessible, and replicable isolate typin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Publishers
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899760/ https://www.ncbi.nlm.nih.gov/pubmed/29574242 http://dx.doi.org/10.1016/j.ijfoodmicro.2018.02.023 |
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author | Pearce, Madison E. Alikhan, Nabil-Fareed Dallman, Timothy J. Zhou, Zhemin Grant, Kathie Maiden, Martin C.J. |
author_facet | Pearce, Madison E. Alikhan, Nabil-Fareed Dallman, Timothy J. Zhou, Zhemin Grant, Kathie Maiden, Martin C.J. |
author_sort | Pearce, Madison E. |
collection | PubMed |
description | Multi-country outbreaks of foodborne bacterial disease present challenges in their detection, tracking, and notification. As food is increasingly distributed across borders, such outbreaks are becoming more common. This increases the need for high-resolution, accessible, and replicable isolate typing schemes. Here we evaluate a core genome multilocus typing (cgMLST) scheme for the high-resolution reproducible typing of Salmonella enterica (S. enterica) isolates, by its application to a large European outbreak of S. enterica serovar Enteritidis. This outbreak had been extensively characterised using single nucleotide polymorphism (SNP)-based approaches. The cgMLST analysis was congruent with the original SNP-based analysis, the epidemiological data, and whole genome MLST (wgMLST) analysis. Combination of the cgMLST and epidemiological data confirmed that the genetic diversity among the isolates predated the outbreak, and was likely present at the infection source. There was consequently no link between country of isolation and genetic diversity, but the cgMLST clusters were congruent with date of isolation. Furthermore, comparison with publicly available Enteritidis isolate data demonstrated that the cgMLST scheme presented is highly scalable, enabling outbreaks to be contextualised within the Salmonella genus. The cgMLST scheme is therefore shown to be a standardised and scalable typing method, which allows Salmonella outbreaks to be analysed and compared across laboratories and jurisdictions. |
format | Online Article Text |
id | pubmed-5899760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-58997602018-06-02 Comparative analysis of core genome MLST and SNP typing within a European Salmonella serovar Enteritidis outbreak Pearce, Madison E. Alikhan, Nabil-Fareed Dallman, Timothy J. Zhou, Zhemin Grant, Kathie Maiden, Martin C.J. Int J Food Microbiol Article Multi-country outbreaks of foodborne bacterial disease present challenges in their detection, tracking, and notification. As food is increasingly distributed across borders, such outbreaks are becoming more common. This increases the need for high-resolution, accessible, and replicable isolate typing schemes. Here we evaluate a core genome multilocus typing (cgMLST) scheme for the high-resolution reproducible typing of Salmonella enterica (S. enterica) isolates, by its application to a large European outbreak of S. enterica serovar Enteritidis. This outbreak had been extensively characterised using single nucleotide polymorphism (SNP)-based approaches. The cgMLST analysis was congruent with the original SNP-based analysis, the epidemiological data, and whole genome MLST (wgMLST) analysis. Combination of the cgMLST and epidemiological data confirmed that the genetic diversity among the isolates predated the outbreak, and was likely present at the infection source. There was consequently no link between country of isolation and genetic diversity, but the cgMLST clusters were congruent with date of isolation. Furthermore, comparison with publicly available Enteritidis isolate data demonstrated that the cgMLST scheme presented is highly scalable, enabling outbreaks to be contextualised within the Salmonella genus. The cgMLST scheme is therefore shown to be a standardised and scalable typing method, which allows Salmonella outbreaks to be analysed and compared across laboratories and jurisdictions. Elsevier Science Publishers 2018-06-02 /pmc/articles/PMC5899760/ /pubmed/29574242 http://dx.doi.org/10.1016/j.ijfoodmicro.2018.02.023 Text en © 2018 The Authors. Published by Elsevier B.V. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pearce, Madison E. Alikhan, Nabil-Fareed Dallman, Timothy J. Zhou, Zhemin Grant, Kathie Maiden, Martin C.J. Comparative analysis of core genome MLST and SNP typing within a European Salmonella serovar Enteritidis outbreak |
title | Comparative analysis of core genome MLST and SNP typing within a European Salmonella serovar Enteritidis outbreak |
title_full | Comparative analysis of core genome MLST and SNP typing within a European Salmonella serovar Enteritidis outbreak |
title_fullStr | Comparative analysis of core genome MLST and SNP typing within a European Salmonella serovar Enteritidis outbreak |
title_full_unstemmed | Comparative analysis of core genome MLST and SNP typing within a European Salmonella serovar Enteritidis outbreak |
title_short | Comparative analysis of core genome MLST and SNP typing within a European Salmonella serovar Enteritidis outbreak |
title_sort | comparative analysis of core genome mlst and snp typing within a european salmonella serovar enteritidis outbreak |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899760/ https://www.ncbi.nlm.nih.gov/pubmed/29574242 http://dx.doi.org/10.1016/j.ijfoodmicro.2018.02.023 |
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