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Genomic and functional characterisation of IncX3 plasmids encoding bla(SHV-12) in Escherichia coli from human and animal origin

The bla(SHV-12) β-lactamase gene is one of the most prevalent genes conferring resistance to extended-spectrum β-lactams in Enterobacteriaceae disseminating within and between reservoirs, mostly via plasmid-mediated horizontal gene transfer. Yet, studies regarding the biology of plasmids encoding bl...

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Autores principales: Liakopoulos, Apostolos, van der Goot, Jeanet, Bossers, Alex, Betts, Jonathan, Brouwer, Michael S. M., Kant, Arie, Smith, Hilde, Ceccarelli, Daniela, Mevius, Dik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955891/
https://www.ncbi.nlm.nih.gov/pubmed/29769695
http://dx.doi.org/10.1038/s41598-018-26073-5
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author Liakopoulos, Apostolos
van der Goot, Jeanet
Bossers, Alex
Betts, Jonathan
Brouwer, Michael S. M.
Kant, Arie
Smith, Hilde
Ceccarelli, Daniela
Mevius, Dik
author_facet Liakopoulos, Apostolos
van der Goot, Jeanet
Bossers, Alex
Betts, Jonathan
Brouwer, Michael S. M.
Kant, Arie
Smith, Hilde
Ceccarelli, Daniela
Mevius, Dik
author_sort Liakopoulos, Apostolos
collection PubMed
description The bla(SHV-12) β-lactamase gene is one of the most prevalent genes conferring resistance to extended-spectrum β-lactams in Enterobacteriaceae disseminating within and between reservoirs, mostly via plasmid-mediated horizontal gene transfer. Yet, studies regarding the biology of plasmids encoding bla(SHV-12) are very limited. In this study, we revealed the emergence of IncX3 plasmids alongside IncI1α/γ in bla(SHV-12) in animal-related Escherichia coli isolates. Four representative bla(SHV-12)-encoding IncX3 plasmids were selected for genome sequencing and further genetic and functional characterization. We report here the first complete sequences of IncX3 plasmids of animal origin and show that IncX3 plasmids exhibit remarkable synteny in their backbone, while the major differences lie in their bla(SHV-12)-flanking region. Our findings indicate that plasmids of this subgroup are conjugative and highly stable, while they exert no fitness cost on their bacterial host. These favourable features might have contributed to the emergence of IncX3 amongst SHV-12-producing E. coli in the Netherlands, highlighting the epidemic potential of these plasmids.
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spelling pubmed-59558912018-05-21 Genomic and functional characterisation of IncX3 plasmids encoding bla(SHV-12) in Escherichia coli from human and animal origin Liakopoulos, Apostolos van der Goot, Jeanet Bossers, Alex Betts, Jonathan Brouwer, Michael S. M. Kant, Arie Smith, Hilde Ceccarelli, Daniela Mevius, Dik Sci Rep Article The bla(SHV-12) β-lactamase gene is one of the most prevalent genes conferring resistance to extended-spectrum β-lactams in Enterobacteriaceae disseminating within and between reservoirs, mostly via plasmid-mediated horizontal gene transfer. Yet, studies regarding the biology of plasmids encoding bla(SHV-12) are very limited. In this study, we revealed the emergence of IncX3 plasmids alongside IncI1α/γ in bla(SHV-12) in animal-related Escherichia coli isolates. Four representative bla(SHV-12)-encoding IncX3 plasmids were selected for genome sequencing and further genetic and functional characterization. We report here the first complete sequences of IncX3 plasmids of animal origin and show that IncX3 plasmids exhibit remarkable synteny in their backbone, while the major differences lie in their bla(SHV-12)-flanking region. Our findings indicate that plasmids of this subgroup are conjugative and highly stable, while they exert no fitness cost on their bacterial host. These favourable features might have contributed to the emergence of IncX3 amongst SHV-12-producing E. coli in the Netherlands, highlighting the epidemic potential of these plasmids. Nature Publishing Group UK 2018-05-16 /pmc/articles/PMC5955891/ /pubmed/29769695 http://dx.doi.org/10.1038/s41598-018-26073-5 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
Liakopoulos, Apostolos
van der Goot, Jeanet
Bossers, Alex
Betts, Jonathan
Brouwer, Michael S. M.
Kant, Arie
Smith, Hilde
Ceccarelli, Daniela
Mevius, Dik
Genomic and functional characterisation of IncX3 plasmids encoding bla(SHV-12) in Escherichia coli from human and animal origin
title Genomic and functional characterisation of IncX3 plasmids encoding bla(SHV-12) in Escherichia coli from human and animal origin
title_full Genomic and functional characterisation of IncX3 plasmids encoding bla(SHV-12) in Escherichia coli from human and animal origin
title_fullStr Genomic and functional characterisation of IncX3 plasmids encoding bla(SHV-12) in Escherichia coli from human and animal origin
title_full_unstemmed Genomic and functional characterisation of IncX3 plasmids encoding bla(SHV-12) in Escherichia coli from human and animal origin
title_short Genomic and functional characterisation of IncX3 plasmids encoding bla(SHV-12) in Escherichia coli from human and animal origin
title_sort genomic and functional characterisation of incx3 plasmids encoding bla(shv-12) in escherichia coli from human and animal origin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955891/
https://www.ncbi.nlm.nih.gov/pubmed/29769695
http://dx.doi.org/10.1038/s41598-018-26073-5
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