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The Role of European Starlings (Sturnus vulgaris) in the Dissemination of Multidrug-Resistant Escherichia coli among Concentrated Animal Feeding Operations

Antimicrobial use in livestock production is a driver for the development and proliferation of antimicrobial resistance (AMR). Wildlife interactions with livestock, acquiring associated AMR bacteria and genes, and wildlife’s subsequent dispersal across the landscape are hypothesized to play an impor...

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Autores principales: Chandler, Jeffrey C., Anders, Jennifer E., Blouin, Nicolas A., Carlson, James C., LeJeune, Jeffrey T., Goodridge, Lawrence D., Wang, Baolin, Day, Leslie A., Mangan, Anna M., Reid, Dustin A., Coleman, Shannon M., Hopken, Matthew W., Bisha, Bledar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229194/
https://www.ncbi.nlm.nih.gov/pubmed/32415136
http://dx.doi.org/10.1038/s41598-020-64544-w
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author Chandler, Jeffrey C.
Anders, Jennifer E.
Blouin, Nicolas A.
Carlson, James C.
LeJeune, Jeffrey T.
Goodridge, Lawrence D.
Wang, Baolin
Day, Leslie A.
Mangan, Anna M.
Reid, Dustin A.
Coleman, Shannon M.
Hopken, Matthew W.
Bisha, Bledar
author_facet Chandler, Jeffrey C.
Anders, Jennifer E.
Blouin, Nicolas A.
Carlson, James C.
LeJeune, Jeffrey T.
Goodridge, Lawrence D.
Wang, Baolin
Day, Leslie A.
Mangan, Anna M.
Reid, Dustin A.
Coleman, Shannon M.
Hopken, Matthew W.
Bisha, Bledar
author_sort Chandler, Jeffrey C.
collection PubMed
description Antimicrobial use in livestock production is a driver for the development and proliferation of antimicrobial resistance (AMR). Wildlife interactions with livestock, acquiring associated AMR bacteria and genes, and wildlife’s subsequent dispersal across the landscape are hypothesized to play an important role in the ecology of AMR. Here, we examined priority AMR phenotypes and genotypes of Escherichia coli isolated from the gastrointestinal tracts of European starlings (Sturnus vulgaris) found on concentrated animal feeding operations (CAFOs). European starlings may be present in high numbers on CAFOs (>100,000 birds), interact with urban environments, and can migrate distances exceeding 1,500 km in North America. In this study, 1,477 European starlings from 31 feedlots in five U.S. states were sampled for E. coli resistant to third generation cephalosporins (3G-C) and fluoroquinolones. The prevalence of 3G-C and fluoroquinolone-resistant E. coli was 4% and 10%, respectively. Multidrug resistance in the E. coli isolates collected (n = 236) was common, with the majority of isolates displaying resistance to six or more classes of antibiotics. Genetic analyses of a subset of these isolates identified 94 genes putatively contributing to AMR, including seven class A and C β-lactamases as well as mutations in gyrA and parC recognized to confer resistance to quinolones. Phylogenetic and subtyping assessments showed that highly similar isolates (≥99.4% shared core genome, ≥99.6% shared coding sequence) with priority AMR were found in birds on feedlots separated by distances exceeding 150 km, suggesting that European starlings could be involved in the interstate dissemination of priority AMR bacteria.
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spelling pubmed-72291942020-05-26 The Role of European Starlings (Sturnus vulgaris) in the Dissemination of Multidrug-Resistant Escherichia coli among Concentrated Animal Feeding Operations Chandler, Jeffrey C. Anders, Jennifer E. Blouin, Nicolas A. Carlson, James C. LeJeune, Jeffrey T. Goodridge, Lawrence D. Wang, Baolin Day, Leslie A. Mangan, Anna M. Reid, Dustin A. Coleman, Shannon M. Hopken, Matthew W. Bisha, Bledar Sci Rep Article Antimicrobial use in livestock production is a driver for the development and proliferation of antimicrobial resistance (AMR). Wildlife interactions with livestock, acquiring associated AMR bacteria and genes, and wildlife’s subsequent dispersal across the landscape are hypothesized to play an important role in the ecology of AMR. Here, we examined priority AMR phenotypes and genotypes of Escherichia coli isolated from the gastrointestinal tracts of European starlings (Sturnus vulgaris) found on concentrated animal feeding operations (CAFOs). European starlings may be present in high numbers on CAFOs (>100,000 birds), interact with urban environments, and can migrate distances exceeding 1,500 km in North America. In this study, 1,477 European starlings from 31 feedlots in five U.S. states were sampled for E. coli resistant to third generation cephalosporins (3G-C) and fluoroquinolones. The prevalence of 3G-C and fluoroquinolone-resistant E. coli was 4% and 10%, respectively. Multidrug resistance in the E. coli isolates collected (n = 236) was common, with the majority of isolates displaying resistance to six or more classes of antibiotics. Genetic analyses of a subset of these isolates identified 94 genes putatively contributing to AMR, including seven class A and C β-lactamases as well as mutations in gyrA and parC recognized to confer resistance to quinolones. Phylogenetic and subtyping assessments showed that highly similar isolates (≥99.4% shared core genome, ≥99.6% shared coding sequence) with priority AMR were found in birds on feedlots separated by distances exceeding 150 km, suggesting that European starlings could be involved in the interstate dissemination of priority AMR bacteria. Nature Publishing Group UK 2020-05-15 /pmc/articles/PMC7229194/ /pubmed/32415136 http://dx.doi.org/10.1038/s41598-020-64544-w Text en © The Author(s) 2020 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
Chandler, Jeffrey C.
Anders, Jennifer E.
Blouin, Nicolas A.
Carlson, James C.
LeJeune, Jeffrey T.
Goodridge, Lawrence D.
Wang, Baolin
Day, Leslie A.
Mangan, Anna M.
Reid, Dustin A.
Coleman, Shannon M.
Hopken, Matthew W.
Bisha, Bledar
The Role of European Starlings (Sturnus vulgaris) in the Dissemination of Multidrug-Resistant Escherichia coli among Concentrated Animal Feeding Operations
title The Role of European Starlings (Sturnus vulgaris) in the Dissemination of Multidrug-Resistant Escherichia coli among Concentrated Animal Feeding Operations
title_full The Role of European Starlings (Sturnus vulgaris) in the Dissemination of Multidrug-Resistant Escherichia coli among Concentrated Animal Feeding Operations
title_fullStr The Role of European Starlings (Sturnus vulgaris) in the Dissemination of Multidrug-Resistant Escherichia coli among Concentrated Animal Feeding Operations
title_full_unstemmed The Role of European Starlings (Sturnus vulgaris) in the Dissemination of Multidrug-Resistant Escherichia coli among Concentrated Animal Feeding Operations
title_short The Role of European Starlings (Sturnus vulgaris) in the Dissemination of Multidrug-Resistant Escherichia coli among Concentrated Animal Feeding Operations
title_sort role of european starlings (sturnus vulgaris) in the dissemination of multidrug-resistant escherichia coli among concentrated animal feeding operations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229194/
https://www.ncbi.nlm.nih.gov/pubmed/32415136
http://dx.doi.org/10.1038/s41598-020-64544-w
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