Cargando…

Genome rearrangements in Escherichia coli during de novo acquisition of resistance to a single antibiotic or two antibiotics successively

BACKGROUND: The ability of bacteria to acquire resistance to antibiotics relies to a large extent on their capacity for genome modification. Prokaryotic genomes are highly plastic and can utilize horizontal gene transfer, point mutations, and gene deletions or amplifications to realize genome expans...

Descripción completa

Detalles Bibliográficos
Autores principales: Hoeksema, Marloes, Jonker, Martijs J., Bel, Keshia, Brul, Stanley, ter Kuile, Benno H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307192/
https://www.ncbi.nlm.nih.gov/pubmed/30591014
http://dx.doi.org/10.1186/s12864-018-5353-y
_version_ 1783382950078840832
author Hoeksema, Marloes
Jonker, Martijs J.
Bel, Keshia
Brul, Stanley
ter Kuile, Benno H.
author_facet Hoeksema, Marloes
Jonker, Martijs J.
Bel, Keshia
Brul, Stanley
ter Kuile, Benno H.
author_sort Hoeksema, Marloes
collection PubMed
description BACKGROUND: The ability of bacteria to acquire resistance to antibiotics relies to a large extent on their capacity for genome modification. Prokaryotic genomes are highly plastic and can utilize horizontal gene transfer, point mutations, and gene deletions or amplifications to realize genome expansion and rearrangements. The contribution of point mutations to de novo acquisition of antibiotic resistance is well-established. In this study, the internal genome rearrangement of Escherichia coli during to de novo acquisition of antibiotic resistance was investigated using whole-genome sequencing. RESULTS: Cells were made resistant to one of the four antibiotics and subsequently to one of the three remaining. This way the initial genetic rearrangements could be documented together with the effects of an altered genetic background on subsequent development of resistance. A DNA fragment including ampC was amplified by a factor sometimes exceeding 100 as a result of exposure to amoxicillin. Excision of prophage e14 was observed in many samples with a double exposure history, but not in cells exposed to a single antibiotic, indicating that the activation of the SOS stress response alone, normally the trigger for excision, was not sufficient to cause excision of prophage e14. Partial deletion of clpS and clpA occurred in strains exposed to enrofloxacin and tetracycline. Other deletions were observed in some strains, but not in replicates with the exact same exposure history. Various insertion sequence transpositions correlated with exposure to specific antibiotics. CONCLUSIONS: Many of the genome rearrangements have not been reported before to occur during resistance development. The observed correlation between genome rearrangements and specific antibiotic pressure, as well as their presence in independent replicates indicates that these events do not occur randomly. Taken together, the observed genome rearrangements illustrate the plasticity of the E. coli genome when exposed to antibiotic stress. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5353-y) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6307192
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-63071922019-01-02 Genome rearrangements in Escherichia coli during de novo acquisition of resistance to a single antibiotic or two antibiotics successively Hoeksema, Marloes Jonker, Martijs J. Bel, Keshia Brul, Stanley ter Kuile, Benno H. BMC Genomics Research Article BACKGROUND: The ability of bacteria to acquire resistance to antibiotics relies to a large extent on their capacity for genome modification. Prokaryotic genomes are highly plastic and can utilize horizontal gene transfer, point mutations, and gene deletions or amplifications to realize genome expansion and rearrangements. The contribution of point mutations to de novo acquisition of antibiotic resistance is well-established. In this study, the internal genome rearrangement of Escherichia coli during to de novo acquisition of antibiotic resistance was investigated using whole-genome sequencing. RESULTS: Cells were made resistant to one of the four antibiotics and subsequently to one of the three remaining. This way the initial genetic rearrangements could be documented together with the effects of an altered genetic background on subsequent development of resistance. A DNA fragment including ampC was amplified by a factor sometimes exceeding 100 as a result of exposure to amoxicillin. Excision of prophage e14 was observed in many samples with a double exposure history, but not in cells exposed to a single antibiotic, indicating that the activation of the SOS stress response alone, normally the trigger for excision, was not sufficient to cause excision of prophage e14. Partial deletion of clpS and clpA occurred in strains exposed to enrofloxacin and tetracycline. Other deletions were observed in some strains, but not in replicates with the exact same exposure history. Various insertion sequence transpositions correlated with exposure to specific antibiotics. CONCLUSIONS: Many of the genome rearrangements have not been reported before to occur during resistance development. The observed correlation between genome rearrangements and specific antibiotic pressure, as well as their presence in independent replicates indicates that these events do not occur randomly. Taken together, the observed genome rearrangements illustrate the plasticity of the E. coli genome when exposed to antibiotic stress. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5353-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-27 /pmc/articles/PMC6307192/ /pubmed/30591014 http://dx.doi.org/10.1186/s12864-018-5353-y Text en © The Author(s). 2018 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
Hoeksema, Marloes
Jonker, Martijs J.
Bel, Keshia
Brul, Stanley
ter Kuile, Benno H.
Genome rearrangements in Escherichia coli during de novo acquisition of resistance to a single antibiotic or two antibiotics successively
title Genome rearrangements in Escherichia coli during de novo acquisition of resistance to a single antibiotic or two antibiotics successively
title_full Genome rearrangements in Escherichia coli during de novo acquisition of resistance to a single antibiotic or two antibiotics successively
title_fullStr Genome rearrangements in Escherichia coli during de novo acquisition of resistance to a single antibiotic or two antibiotics successively
title_full_unstemmed Genome rearrangements in Escherichia coli during de novo acquisition of resistance to a single antibiotic or two antibiotics successively
title_short Genome rearrangements in Escherichia coli during de novo acquisition of resistance to a single antibiotic or two antibiotics successively
title_sort genome rearrangements in escherichia coli during de novo acquisition of resistance to a single antibiotic or two antibiotics successively
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307192/
https://www.ncbi.nlm.nih.gov/pubmed/30591014
http://dx.doi.org/10.1186/s12864-018-5353-y
work_keys_str_mv AT hoeksemamarloes genomerearrangementsinescherichiacoliduringdenovoacquisitionofresistancetoasingleantibioticortwoantibioticssuccessively
AT jonkermartijsj genomerearrangementsinescherichiacoliduringdenovoacquisitionofresistancetoasingleantibioticortwoantibioticssuccessively
AT belkeshia genomerearrangementsinescherichiacoliduringdenovoacquisitionofresistancetoasingleantibioticortwoantibioticssuccessively
AT brulstanley genomerearrangementsinescherichiacoliduringdenovoacquisitionofresistancetoasingleantibioticortwoantibioticssuccessively
AT terkuilebennoh genomerearrangementsinescherichiacoliduringdenovoacquisitionofresistancetoasingleantibioticortwoantibioticssuccessively