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Veterinary Hospital Dissemination of CTX-M-15 Extended-Spectrum Beta-Lactamase–Producing Escherichia coli ST410 in the United Kingdom
We characterized extended-spectrum beta-lactamases (ESBLs) and plasmid-mediated quinolone resistance (PMQR) in 32 Escherichia coli extended spectrum cephalosporin (ESC)-resistant clinical isolates from UK companion animals from several clinics. In addition, to investigate the possible dissemination...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073239/ https://www.ncbi.nlm.nih.gov/pubmed/27314838 http://dx.doi.org/10.1089/mdr.2016.0036 |
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author | Timofte, Dorina Maciuca, Iuliana Elena Williams, Nicola J. Wattret, Andrew Schmidt, Vanessa |
author_facet | Timofte, Dorina Maciuca, Iuliana Elena Williams, Nicola J. Wattret, Andrew Schmidt, Vanessa |
author_sort | Timofte, Dorina |
collection | PubMed |
description | We characterized extended-spectrum beta-lactamases (ESBLs) and plasmid-mediated quinolone resistance (PMQR) in 32 Escherichia coli extended spectrum cephalosporin (ESC)-resistant clinical isolates from UK companion animals from several clinics. In addition, to investigate the possible dissemination of ESBL clinical isolates within a veterinary hospital, two ESBL-producing E. coli isolates from a dog with septic peritonitis and a cluster of environmental ESC-resistant E. coli isolates obtained from the same clinic and during the same time period, as these two particular ESBL-positive clinical isolates, were also included in the study. Molecular characterization identified bla(CTX-M) to be the most prevalent gene in ESC-resistant isolates, where 66% and 27% of clinical isolates carried bla(CTX-M-15) and bla(CTX-M-14,) respectively. The only PMQR gene detected was aac(6')-Ib-cr, being found in 34% of the ESC E. coli isolates and was associated with the carriage of bla(CTX-M-15). The clinical and environmental isolates investigated for hospital dissemination had a common ESBL/AmpC phenotype, carried bla(CTX-M-15), and co-harbored bla(OXA-1,) bla(TEM-1,) bla(CMY-2,) and aac(6')-Ib-cr. Multilocus sequence typing identified them all as ST410, while pulse-field gel electrophoresis demonstrated 100% homology of clinical and environmental isolates, suggesting hospital environmental dissemination of CTX-M-15–producing E. coli ST410. |
format | Online Article Text |
id | pubmed-5073239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Mary Ann Liebert, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50732392016-10-26 Veterinary Hospital Dissemination of CTX-M-15 Extended-Spectrum Beta-Lactamase–Producing Escherichia coli ST410 in the United Kingdom Timofte, Dorina Maciuca, Iuliana Elena Williams, Nicola J. Wattret, Andrew Schmidt, Vanessa Microb Drug Resist Veterinary Microbiology We characterized extended-spectrum beta-lactamases (ESBLs) and plasmid-mediated quinolone resistance (PMQR) in 32 Escherichia coli extended spectrum cephalosporin (ESC)-resistant clinical isolates from UK companion animals from several clinics. In addition, to investigate the possible dissemination of ESBL clinical isolates within a veterinary hospital, two ESBL-producing E. coli isolates from a dog with septic peritonitis and a cluster of environmental ESC-resistant E. coli isolates obtained from the same clinic and during the same time period, as these two particular ESBL-positive clinical isolates, were also included in the study. Molecular characterization identified bla(CTX-M) to be the most prevalent gene in ESC-resistant isolates, where 66% and 27% of clinical isolates carried bla(CTX-M-15) and bla(CTX-M-14,) respectively. The only PMQR gene detected was aac(6')-Ib-cr, being found in 34% of the ESC E. coli isolates and was associated with the carriage of bla(CTX-M-15). The clinical and environmental isolates investigated for hospital dissemination had a common ESBL/AmpC phenotype, carried bla(CTX-M-15), and co-harbored bla(OXA-1,) bla(TEM-1,) bla(CMY-2,) and aac(6')-Ib-cr. Multilocus sequence typing identified them all as ST410, while pulse-field gel electrophoresis demonstrated 100% homology of clinical and environmental isolates, suggesting hospital environmental dissemination of CTX-M-15–producing E. coli ST410. Mary Ann Liebert, Inc. 2016-10-01 2016-10-01 /pmc/articles/PMC5073239/ /pubmed/27314838 http://dx.doi.org/10.1089/mdr.2016.0036 Text en © Dorina Timofte et al., 2016; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Veterinary Microbiology Timofte, Dorina Maciuca, Iuliana Elena Williams, Nicola J. Wattret, Andrew Schmidt, Vanessa Veterinary Hospital Dissemination of CTX-M-15 Extended-Spectrum Beta-Lactamase–Producing Escherichia coli ST410 in the United Kingdom |
title | Veterinary Hospital Dissemination of CTX-M-15 Extended-Spectrum Beta-Lactamase–Producing Escherichia coli ST410 in the United Kingdom |
title_full | Veterinary Hospital Dissemination of CTX-M-15 Extended-Spectrum Beta-Lactamase–Producing Escherichia coli ST410 in the United Kingdom |
title_fullStr | Veterinary Hospital Dissemination of CTX-M-15 Extended-Spectrum Beta-Lactamase–Producing Escherichia coli ST410 in the United Kingdom |
title_full_unstemmed | Veterinary Hospital Dissemination of CTX-M-15 Extended-Spectrum Beta-Lactamase–Producing Escherichia coli ST410 in the United Kingdom |
title_short | Veterinary Hospital Dissemination of CTX-M-15 Extended-Spectrum Beta-Lactamase–Producing Escherichia coli ST410 in the United Kingdom |
title_sort | veterinary hospital dissemination of ctx-m-15 extended-spectrum beta-lactamase–producing escherichia coli st410 in the united kingdom |
topic | Veterinary Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073239/ https://www.ncbi.nlm.nih.gov/pubmed/27314838 http://dx.doi.org/10.1089/mdr.2016.0036 |
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