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PlaScope: a targeted approach to assess the plasmidome from genome assemblies at the species level

Plasmid prediction may be of great interest when studying bacteria of medical importance such as Enterobacteriaceae as well as Staphylococcus aureus or Enterococcus. Indeed, many resistance and virulence genes are located on such replicons with major impact in terms of pathogenicity and spreading ca...

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Detalles Bibliográficos
Autores principales: Royer, G., Decousser, J. W., Branger, C., Dubois, M., Médigue, C., Denamur, E., Vallenet, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202455/
https://www.ncbi.nlm.nih.gov/pubmed/30265232
http://dx.doi.org/10.1099/mgen.0.000211
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author Royer, G.
Decousser, J. W.
Branger, C.
Dubois, M.
Médigue, C.
Denamur, E.
Vallenet, D.
author_facet Royer, G.
Decousser, J. W.
Branger, C.
Dubois, M.
Médigue, C.
Denamur, E.
Vallenet, D.
author_sort Royer, G.
collection PubMed
description Plasmid prediction may be of great interest when studying bacteria of medical importance such as Enterobacteriaceae as well as Staphylococcus aureus or Enterococcus. Indeed, many resistance and virulence genes are located on such replicons with major impact in terms of pathogenicity and spreading capacities. Beyond strain outbreak, plasmid outbreaks have been reported in particular for some extended-spectrum beta-lactamase- or carbapenemase-producing Enterobacteriaceae. Several tools are now available to explore the ‘plasmidome’ from whole-genome sequences with various approaches, but none of them are able to combine high sensitivity and specificity. With this in mind, we developed PlaScope, a targeted approach to recover plasmidic sequences in genome assemblies at the species or genus level. Based on Centrifuge, a metagenomic classifier, and a custom database containing complete sequences of chromosomes and plasmids from various curated databases, PlaScope classifies contigs from an assembly according to their predicted location. Compared to other plasmid classifiers, PlasFlow and cBar, it achieves better recall (0.87), specificity (0.99), precision (0.96) and accuracy (0.98) on a dataset of 70 genomes of Escherichia coli containing plasmids. In a second part, we identified 20 of the 21 chromosomal integrations of the extended-spectrum beta-lactamase coding gene in a clinical dataset of E. coli strains. In addition, we predicted virulence gene and operon locations in agreement with the literature. We also built a database for Klebsiella and correctly assigned the location for the majority of resistance genes from a collection of 12 Klebsiella pneumoniae strains. Similar approaches could also be developed for other well-characterized bacteria.
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spelling pubmed-62024552018-10-31 PlaScope: a targeted approach to assess the plasmidome from genome assemblies at the species level Royer, G. Decousser, J. W. Branger, C. Dubois, M. Médigue, C. Denamur, E. Vallenet, D. Microb Genom Methods Paper Plasmid prediction may be of great interest when studying bacteria of medical importance such as Enterobacteriaceae as well as Staphylococcus aureus or Enterococcus. Indeed, many resistance and virulence genes are located on such replicons with major impact in terms of pathogenicity and spreading capacities. Beyond strain outbreak, plasmid outbreaks have been reported in particular for some extended-spectrum beta-lactamase- or carbapenemase-producing Enterobacteriaceae. Several tools are now available to explore the ‘plasmidome’ from whole-genome sequences with various approaches, but none of them are able to combine high sensitivity and specificity. With this in mind, we developed PlaScope, a targeted approach to recover plasmidic sequences in genome assemblies at the species or genus level. Based on Centrifuge, a metagenomic classifier, and a custom database containing complete sequences of chromosomes and plasmids from various curated databases, PlaScope classifies contigs from an assembly according to their predicted location. Compared to other plasmid classifiers, PlasFlow and cBar, it achieves better recall (0.87), specificity (0.99), precision (0.96) and accuracy (0.98) on a dataset of 70 genomes of Escherichia coli containing plasmids. In a second part, we identified 20 of the 21 chromosomal integrations of the extended-spectrum beta-lactamase coding gene in a clinical dataset of E. coli strains. In addition, we predicted virulence gene and operon locations in agreement with the literature. We also built a database for Klebsiella and correctly assigned the location for the majority of resistance genes from a collection of 12 Klebsiella pneumoniae strains. Similar approaches could also be developed for other well-characterized bacteria. Microbiology Society 2018-09-28 /pmc/articles/PMC6202455/ /pubmed/30265232 http://dx.doi.org/10.1099/mgen.0.000211 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Paper
Royer, G.
Decousser, J. W.
Branger, C.
Dubois, M.
Médigue, C.
Denamur, E.
Vallenet, D.
PlaScope: a targeted approach to assess the plasmidome from genome assemblies at the species level
title PlaScope: a targeted approach to assess the plasmidome from genome assemblies at the species level
title_full PlaScope: a targeted approach to assess the plasmidome from genome assemblies at the species level
title_fullStr PlaScope: a targeted approach to assess the plasmidome from genome assemblies at the species level
title_full_unstemmed PlaScope: a targeted approach to assess the plasmidome from genome assemblies at the species level
title_short PlaScope: a targeted approach to assess the plasmidome from genome assemblies at the species level
title_sort plascope: a targeted approach to assess the plasmidome from genome assemblies at the species level
topic Methods Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202455/
https://www.ncbi.nlm.nih.gov/pubmed/30265232
http://dx.doi.org/10.1099/mgen.0.000211
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