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Horizontal antimicrobial resistance transfer drives epidemics of multiple Shigella species
Horizontal gene transfer has played a role in developing the global public health crisis of antimicrobial resistance (AMR). However, the dynamics of AMR transfer through bacterial populations and its direct impact on human disease is poorly elucidated. Here, we study parallel epidemic emergences of...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899146/ https://www.ncbi.nlm.nih.gov/pubmed/29654279 http://dx.doi.org/10.1038/s41467-018-03949-8 |
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author | Baker, Kate S. Dallman, Timothy J. Field, Nigel Childs, Tristan Mitchell, Holly Day, Martin Weill, François-Xavier Lefèvre, Sophie Tourdjman, Mathieu Hughes, Gwenda Jenkins, Claire Thomson, Nicholas |
author_facet | Baker, Kate S. Dallman, Timothy J. Field, Nigel Childs, Tristan Mitchell, Holly Day, Martin Weill, François-Xavier Lefèvre, Sophie Tourdjman, Mathieu Hughes, Gwenda Jenkins, Claire Thomson, Nicholas |
author_sort | Baker, Kate S. |
collection | PubMed |
description | Horizontal gene transfer has played a role in developing the global public health crisis of antimicrobial resistance (AMR). However, the dynamics of AMR transfer through bacterial populations and its direct impact on human disease is poorly elucidated. Here, we study parallel epidemic emergences of multiple Shigella species, a priority AMR organism, in men who have sex with men to gain insight into AMR emergence and spread. Using genomic epidemiology, we show that repeated horizontal transfer of a single AMR plasmid among Shigella enhanced existing and facilitated new epidemics. These epidemic patterns contrasted with slighter, slower increases in disease caused by organisms with vertically inherited (chromosomally encoded) AMR. This demonstrates that horizontal transfer of AMR directly affects epidemiological outcomes of globally important AMR pathogens and highlights the need for integration of genomic analyses into all areas of AMR research, surveillance and management. |
format | Online Article Text |
id | pubmed-5899146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58991462018-04-16 Horizontal antimicrobial resistance transfer drives epidemics of multiple Shigella species Baker, Kate S. Dallman, Timothy J. Field, Nigel Childs, Tristan Mitchell, Holly Day, Martin Weill, François-Xavier Lefèvre, Sophie Tourdjman, Mathieu Hughes, Gwenda Jenkins, Claire Thomson, Nicholas Nat Commun Article Horizontal gene transfer has played a role in developing the global public health crisis of antimicrobial resistance (AMR). However, the dynamics of AMR transfer through bacterial populations and its direct impact on human disease is poorly elucidated. Here, we study parallel epidemic emergences of multiple Shigella species, a priority AMR organism, in men who have sex with men to gain insight into AMR emergence and spread. Using genomic epidemiology, we show that repeated horizontal transfer of a single AMR plasmid among Shigella enhanced existing and facilitated new epidemics. These epidemic patterns contrasted with slighter, slower increases in disease caused by organisms with vertically inherited (chromosomally encoded) AMR. This demonstrates that horizontal transfer of AMR directly affects epidemiological outcomes of globally important AMR pathogens and highlights the need for integration of genomic analyses into all areas of AMR research, surveillance and management. Nature Publishing Group UK 2018-04-13 /pmc/articles/PMC5899146/ /pubmed/29654279 http://dx.doi.org/10.1038/s41467-018-03949-8 Text en © The Author(s) 2018 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 Baker, Kate S. Dallman, Timothy J. Field, Nigel Childs, Tristan Mitchell, Holly Day, Martin Weill, François-Xavier Lefèvre, Sophie Tourdjman, Mathieu Hughes, Gwenda Jenkins, Claire Thomson, Nicholas Horizontal antimicrobial resistance transfer drives epidemics of multiple Shigella species |
title | Horizontal antimicrobial resistance transfer drives epidemics of multiple Shigella species |
title_full | Horizontal antimicrobial resistance transfer drives epidemics of multiple Shigella species |
title_fullStr | Horizontal antimicrobial resistance transfer drives epidemics of multiple Shigella species |
title_full_unstemmed | Horizontal antimicrobial resistance transfer drives epidemics of multiple Shigella species |
title_short | Horizontal antimicrobial resistance transfer drives epidemics of multiple Shigella species |
title_sort | horizontal antimicrobial resistance transfer drives epidemics of multiple shigella species |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899146/ https://www.ncbi.nlm.nih.gov/pubmed/29654279 http://dx.doi.org/10.1038/s41467-018-03949-8 |
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