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Gene mobility promotes the spread of resistance in bacterial populations
Theory predicts that horizontal gene transfer (HGT) expands the selective conditions under which genes spread in bacterial populations. Whereas vertically inherited genes can only spread by positively selected clonal expansion, mobile genetic elements can drive fixation of genes by infectious HGT. W...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496671/ https://www.ncbi.nlm.nih.gov/pubmed/28362724 http://dx.doi.org/10.1038/ismej.2017.42 |
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author | Stevenson, Cagla Hall, James PJ Harrison, Ellie Wood, AJamie Brockhurst, Michael A |
author_facet | Stevenson, Cagla Hall, James PJ Harrison, Ellie Wood, AJamie Brockhurst, Michael A |
author_sort | Stevenson, Cagla |
collection | PubMed |
description | Theory predicts that horizontal gene transfer (HGT) expands the selective conditions under which genes spread in bacterial populations. Whereas vertically inherited genes can only spread by positively selected clonal expansion, mobile genetic elements can drive fixation of genes by infectious HGT. We tested this using populations of Pseudomonas fluorescens and the conjugative mercury resistance (Hg(R)) plasmid pQBR57. HGT expanded the selective conditions allowing the spread of Hg(R): Chromosomal Hg(R) only increased in frequency under positive selection, whereas plasmid-encoded Hg(R) reached fixation with or without positive selection. Tracking plasmid dynamics over time revealed that the mode of Hg(R) inheritance varied across mercury environments. Under mercury selection, the spread of Hg(R) was driven primarily by clonal expansion while in the absence of mercury Hg(R) dynamics were dominated by infectious transfer. Thus, HGT is most likely to drive the spread of resistance genes in environments where resistance is useless. |
format | Online Article Text |
id | pubmed-5496671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54966712017-08-24 Gene mobility promotes the spread of resistance in bacterial populations Stevenson, Cagla Hall, James PJ Harrison, Ellie Wood, AJamie Brockhurst, Michael A ISME J Short Communication Theory predicts that horizontal gene transfer (HGT) expands the selective conditions under which genes spread in bacterial populations. Whereas vertically inherited genes can only spread by positively selected clonal expansion, mobile genetic elements can drive fixation of genes by infectious HGT. We tested this using populations of Pseudomonas fluorescens and the conjugative mercury resistance (Hg(R)) plasmid pQBR57. HGT expanded the selective conditions allowing the spread of Hg(R): Chromosomal Hg(R) only increased in frequency under positive selection, whereas plasmid-encoded Hg(R) reached fixation with or without positive selection. Tracking plasmid dynamics over time revealed that the mode of Hg(R) inheritance varied across mercury environments. Under mercury selection, the spread of Hg(R) was driven primarily by clonal expansion while in the absence of mercury Hg(R) dynamics were dominated by infectious transfer. Thus, HGT is most likely to drive the spread of resistance genes in environments where resistance is useless. Nature Publishing Group 2017-08 2017-03-31 /pmc/articles/PMC5496671/ /pubmed/28362724 http://dx.doi.org/10.1038/ismej.2017.42 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Short Communication Stevenson, Cagla Hall, James PJ Harrison, Ellie Wood, AJamie Brockhurst, Michael A Gene mobility promotes the spread of resistance in bacterial populations |
title | Gene mobility promotes the spread of resistance in bacterial populations |
title_full | Gene mobility promotes the spread of resistance in bacterial populations |
title_fullStr | Gene mobility promotes the spread of resistance in bacterial populations |
title_full_unstemmed | Gene mobility promotes the spread of resistance in bacterial populations |
title_short | Gene mobility promotes the spread of resistance in bacterial populations |
title_sort | gene mobility promotes the spread of resistance in bacterial populations |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496671/ https://www.ncbi.nlm.nih.gov/pubmed/28362724 http://dx.doi.org/10.1038/ismej.2017.42 |
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