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Population Structure and Antimicrobial Resistance of Canine Uropathogenic Escherichia coli.

Authors :
LeCuyer TE
Byrne BA
Daniels JB
Diaz-Campos DV
Hammac GK
Miller CB
Besser TE
Davis MA
Source :
Journal of clinical microbiology [J Clin Microbiol] 2018 Aug 27; Vol. 56 (9). Date of Electronic Publication: 2018 Aug 27 (Print Publication: 2018).
Publication Year :
2018

Abstract

Escherichia coli is the most common cause of human and canine urinary tract infection (UTI). Clonal groups, often with high levels of antimicrobial resistance, are a major component of the E. coli population that causes human UTI. While little is known about the population structure of E. coli that causes UTI in dogs, there is evidence that dogs and humans can share fecal strains of E. coli and that human-associated strains can cause disease in dogs. In order to better characterize the E. coli strains that cause canine UTI, we analyzed 295 E. coli isolates obtained from canine urine samples from five veterinary diagnostic laboratories and analyzed their multilocus sequence types, phenotypic and genotypic antimicrobial resistance profiles, and virulence-associated gene repertoires. Sequence type 372 (ST372), an infrequent human pathogen, was the predominant sequence type in dogs at all locations. Extended-spectrum β-lactamase-producing isolates with bla <subscript>CTX-M</subscript> genes were uncommon in canine isolates but when present were often associated with sequence types that have been described in human infections. This provides support for occasional cross-host-species sharing of strains that cause extraintestinal disease and highlights the importance of understanding the role of companion animals in the overall transmission patterns of extraintestinal pathogenic E. coli .<br /> (Copyright © 2018 American Society for Microbiology.)

Details

Language :
English
ISSN :
1098-660X
Volume :
56
Issue :
9
Database :
MEDLINE
Journal :
Journal of clinical microbiology
Publication Type :
Academic Journal
Accession number :
29997200
Full Text :
https://doi.org/10.1128/JCM.00788-18