Cargando…

Temporal dynamics of bacteria-plasmid coevolution under antibiotic selection

Horizontally acquired genes can be costly to express even if they encode useful traits, such as antibiotic resistance. We previously showed that when selected with tetracycline, Escherichia coli carrying the tetracycline-resistance plasmid RK2 evolved mutations on both replicons that together provid...

Descripción completa

Detalles Bibliográficos
Autores principales: Bottery, Michael J., Wood, A. Jamie, Brockhurst, Michael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330079/
https://www.ncbi.nlm.nih.gov/pubmed/30209344
http://dx.doi.org/10.1038/s41396-018-0276-9
_version_ 1783386921223847936
author Bottery, Michael J.
Wood, A. Jamie
Brockhurst, Michael A.
author_facet Bottery, Michael J.
Wood, A. Jamie
Brockhurst, Michael A.
author_sort Bottery, Michael J.
collection PubMed
description Horizontally acquired genes can be costly to express even if they encode useful traits, such as antibiotic resistance. We previously showed that when selected with tetracycline, Escherichia coli carrying the tetracycline-resistance plasmid RK2 evolved mutations on both replicons that together provided increased tetracycline resistance at reduced cost. Here we investigate the temporal dynamics of this intragenomic coevolution. Using genome sequencing we show that the order of adaptive mutations was highly repeatable across three independently evolving populations. Each population first gained a chromosomal mutation in ompF which shortened lag phase and increased tetracycline resistance. This was followed by mutations impairing the plasmid-encoded tetracycline efflux pump, and finally, additional resistance-associated chromosomal mutations. Thus, reducing the cost of the horizontally acquired tetracycline resistance was contingent on first evolving a degree of chromosomally encoded resistance. We conclude therefore that the trajectory of bacteria-plasmid coevolution was constrained to a single repeatable path.
format Online
Article
Text
id pubmed-6330079
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-63300792019-01-15 Temporal dynamics of bacteria-plasmid coevolution under antibiotic selection Bottery, Michael J. Wood, A. Jamie Brockhurst, Michael A. ISME J Brief Communication Horizontally acquired genes can be costly to express even if they encode useful traits, such as antibiotic resistance. We previously showed that when selected with tetracycline, Escherichia coli carrying the tetracycline-resistance plasmid RK2 evolved mutations on both replicons that together provided increased tetracycline resistance at reduced cost. Here we investigate the temporal dynamics of this intragenomic coevolution. Using genome sequencing we show that the order of adaptive mutations was highly repeatable across three independently evolving populations. Each population first gained a chromosomal mutation in ompF which shortened lag phase and increased tetracycline resistance. This was followed by mutations impairing the plasmid-encoded tetracycline efflux pump, and finally, additional resistance-associated chromosomal mutations. Thus, reducing the cost of the horizontally acquired tetracycline resistance was contingent on first evolving a degree of chromosomally encoded resistance. We conclude therefore that the trajectory of bacteria-plasmid coevolution was constrained to a single repeatable path. Nature Publishing Group UK 2018-09-12 2019-02 /pmc/articles/PMC6330079/ /pubmed/30209344 http://dx.doi.org/10.1038/s41396-018-0276-9 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 Brief Communication
Bottery, Michael J.
Wood, A. Jamie
Brockhurst, Michael A.
Temporal dynamics of bacteria-plasmid coevolution under antibiotic selection
title Temporal dynamics of bacteria-plasmid coevolution under antibiotic selection
title_full Temporal dynamics of bacteria-plasmid coevolution under antibiotic selection
title_fullStr Temporal dynamics of bacteria-plasmid coevolution under antibiotic selection
title_full_unstemmed Temporal dynamics of bacteria-plasmid coevolution under antibiotic selection
title_short Temporal dynamics of bacteria-plasmid coevolution under antibiotic selection
title_sort temporal dynamics of bacteria-plasmid coevolution under antibiotic selection
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330079/
https://www.ncbi.nlm.nih.gov/pubmed/30209344
http://dx.doi.org/10.1038/s41396-018-0276-9
work_keys_str_mv AT botterymichaelj temporaldynamicsofbacteriaplasmidcoevolutionunderantibioticselection
AT woodajamie temporaldynamicsofbacteriaplasmidcoevolutionunderantibioticselection
AT brockhurstmichaela temporaldynamicsofbacteriaplasmidcoevolutionunderantibioticselection