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Comparative Sequence Analysis of Multidrug-Resistant IncA/C Plasmids from Salmonella enterica

Determinants of multidrug resistance (MDR) are often encoded on mobile elements, such as plasmids, transposons, and integrons, which have the potential to transfer among foodborne pathogens, as well as to other virulent pathogens, increasing the threats these traits pose to human and veterinary heal...

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Autores principales: Hoffmann, Maria, Pettengill, James B., Gonzalez-Escalona, Narjol, Miller, John, Ayers, Sherry L., Zhao, Shaohua, Allard, Marc W., McDermott, Patrick F., Brown, Eric W., Monday, Steven R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545573/
https://www.ncbi.nlm.nih.gov/pubmed/28824587
http://dx.doi.org/10.3389/fmicb.2017.01459
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author Hoffmann, Maria
Pettengill, James B.
Gonzalez-Escalona, Narjol
Miller, John
Ayers, Sherry L.
Zhao, Shaohua
Allard, Marc W.
McDermott, Patrick F.
Brown, Eric W.
Monday, Steven R.
author_facet Hoffmann, Maria
Pettengill, James B.
Gonzalez-Escalona, Narjol
Miller, John
Ayers, Sherry L.
Zhao, Shaohua
Allard, Marc W.
McDermott, Patrick F.
Brown, Eric W.
Monday, Steven R.
author_sort Hoffmann, Maria
collection PubMed
description Determinants of multidrug resistance (MDR) are often encoded on mobile elements, such as plasmids, transposons, and integrons, which have the potential to transfer among foodborne pathogens, as well as to other virulent pathogens, increasing the threats these traits pose to human and veterinary health. Our understanding of MDR among Salmonella has been limited by the lack of closed plasmid genomes for comparisons across resistance phenotypes, due to difficulties in effectively separating the DNA of these high-molecular weight, low-copy-number plasmids from chromosomal DNA. To resolve this problem, we demonstrate an efficient protocol for isolating, sequencing and closing IncA/C plasmids from Salmonella sp. using single molecule real-time sequencing on a Pacific Biosciences (Pacbio) RS II Sequencer. We obtained six Salmonella enterica isolates from poultry, representing six different serovars, each exhibiting the MDR-Ampc resistance profile. Salmonella plasmids were obtained using a modified mini preparation and transformed with Escherichia coli DH10Br. A Qiagen Large-Construct kit™ was used to recover highly concentrated and purified plasmid DNA that was sequenced using PacBio technology. These six closed IncA/C plasmids ranged in size from 104 to 191 kb and shared a stable, conserved backbone containing 98 core genes, with only six differences among those core genes. The plasmids encoded a number of antimicrobial resistance genes, including those for quaternary ammonium compounds and mercury. We then compared our six IncA/C plasmid sequences: first with 14 IncA/C plasmids derived from S. enterica available at the National Center for Biotechnology Information (NCBI), and then with an additional 38 IncA/C plasmids derived from different taxa. These comparisons allowed us to build an evolutionary picture of how antimicrobial resistance may be mediated by this common plasmid backbone. Our project provides detailed genetic information about resistance genes in plasmids, advances in plasmid sequencing, and phylogenetic analyses, and important insights about how MDR evolution occurs across diverse serotypes from different animal sources, particularly in agricultural settings where antimicrobial drug use practices vary.
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spelling pubmed-55455732017-08-18 Comparative Sequence Analysis of Multidrug-Resistant IncA/C Plasmids from Salmonella enterica Hoffmann, Maria Pettengill, James B. Gonzalez-Escalona, Narjol Miller, John Ayers, Sherry L. Zhao, Shaohua Allard, Marc W. McDermott, Patrick F. Brown, Eric W. Monday, Steven R. Front Microbiol Microbiology Determinants of multidrug resistance (MDR) are often encoded on mobile elements, such as plasmids, transposons, and integrons, which have the potential to transfer among foodborne pathogens, as well as to other virulent pathogens, increasing the threats these traits pose to human and veterinary health. Our understanding of MDR among Salmonella has been limited by the lack of closed plasmid genomes for comparisons across resistance phenotypes, due to difficulties in effectively separating the DNA of these high-molecular weight, low-copy-number plasmids from chromosomal DNA. To resolve this problem, we demonstrate an efficient protocol for isolating, sequencing and closing IncA/C plasmids from Salmonella sp. using single molecule real-time sequencing on a Pacific Biosciences (Pacbio) RS II Sequencer. We obtained six Salmonella enterica isolates from poultry, representing six different serovars, each exhibiting the MDR-Ampc resistance profile. Salmonella plasmids were obtained using a modified mini preparation and transformed with Escherichia coli DH10Br. A Qiagen Large-Construct kit™ was used to recover highly concentrated and purified plasmid DNA that was sequenced using PacBio technology. These six closed IncA/C plasmids ranged in size from 104 to 191 kb and shared a stable, conserved backbone containing 98 core genes, with only six differences among those core genes. The plasmids encoded a number of antimicrobial resistance genes, including those for quaternary ammonium compounds and mercury. We then compared our six IncA/C plasmid sequences: first with 14 IncA/C plasmids derived from S. enterica available at the National Center for Biotechnology Information (NCBI), and then with an additional 38 IncA/C plasmids derived from different taxa. These comparisons allowed us to build an evolutionary picture of how antimicrobial resistance may be mediated by this common plasmid backbone. Our project provides detailed genetic information about resistance genes in plasmids, advances in plasmid sequencing, and phylogenetic analyses, and important insights about how MDR evolution occurs across diverse serotypes from different animal sources, particularly in agricultural settings where antimicrobial drug use practices vary. Frontiers Media S.A. 2017-08-07 /pmc/articles/PMC5545573/ /pubmed/28824587 http://dx.doi.org/10.3389/fmicb.2017.01459 Text en Copyright © 2017 Hoffmann, Pettengill, Gonzalez-Escalona, Miller, Ayers, Zhao, Allard, McDermott, Brown and Monday. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Hoffmann, Maria
Pettengill, James B.
Gonzalez-Escalona, Narjol
Miller, John
Ayers, Sherry L.
Zhao, Shaohua
Allard, Marc W.
McDermott, Patrick F.
Brown, Eric W.
Monday, Steven R.
Comparative Sequence Analysis of Multidrug-Resistant IncA/C Plasmids from Salmonella enterica
title Comparative Sequence Analysis of Multidrug-Resistant IncA/C Plasmids from Salmonella enterica
title_full Comparative Sequence Analysis of Multidrug-Resistant IncA/C Plasmids from Salmonella enterica
title_fullStr Comparative Sequence Analysis of Multidrug-Resistant IncA/C Plasmids from Salmonella enterica
title_full_unstemmed Comparative Sequence Analysis of Multidrug-Resistant IncA/C Plasmids from Salmonella enterica
title_short Comparative Sequence Analysis of Multidrug-Resistant IncA/C Plasmids from Salmonella enterica
title_sort comparative sequence analysis of multidrug-resistant inca/c plasmids from salmonella enterica
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545573/
https://www.ncbi.nlm.nih.gov/pubmed/28824587
http://dx.doi.org/10.3389/fmicb.2017.01459
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