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Antimicrobial susceptibility of E. coli causing urinary tract infections in dogs in Saskatchewan, Canada

Date

2025-03-04

Journal Title

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Publisher

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Type

Thesis

Degree Level

Masters

Abstract

Background: E. coli is the most common cause of urinary infections in dogs. Antimicrobials are the primary treatment for these infections. However, the emergence of antimicrobial resistance globally is resulting in limited therapeutic options available to veterinarians and physicians. Since 2013, we have conducted a longitudinal passive surveillance project targeting E. coli causing UTIs in dogs isolated by a regional diagnostic lab. The objectives of this study were to describe the antimicrobial susceptibility of E. coli isolates from Oct 2018-Oct 2022 (n = 576) and the frequency of epidemiologically important resistance genes. Methodology: Laboratory records were reviewed to ensure that only one isolate per dog was included. Antimicrobial minimum inhibitory concentrations (MICs) were determined by broth microdilution and agar dilution. Based on the susceptibility profile, isolates were screened for broad-spectrum β-lactamases (ESBL and AmpC enzymes) and plasmid-mediated quinolone resistance determinants (PMQRs) by PCR, amplicons were then sequenced to identify gene alleles. Isolates possessing these genes were sequence typed by multi-locus sequence typing (MLST) to identify resistant clones. Results: Overall, 76.9% of the isolates were pan-susceptible while 4.3% were multidrug-resistant (resistant to 3 or more drug classes) according to the CLSI guidelines and the breakpoints for E. coli in urine. Ampicillin resistance, identified in 13.9% of isolates, was the most common. Resistance to amoxicillin-clavulanic acid, cefazolin, chloramphenicol, nalidixic acid, and tetracycline was identified in between 5 10% of isolates. Fewer than 5% of isolates were resistant to cefoxitin, ceftriaxone, cefepime, ciprofloxacin, gentamicin, amikacin, tobramycin, or trimethoprim iii sulfamethoxazole. Broad-spectrum β-lactamases were identified among fewer than 5% of the isolates; the AmpC type enzymes were most common. Three isolates possessed a PMQR determinant. Two isolates possessed qnrS8 and a single isolate possessed aac(6’)-lb-cr. Discussion: Over the 9-year study period, no significant changes in the frequency of resistance to ampicillin, amoxicillin-clavulanic acid, cefazolin (only a 4 year period), nalidixic acid, tetracycline, or chloramphenicol were identified. However, significant increases in the MICs of ampicillin, nalidixic acid, and chloramphenicol were found, similar trends were not identified for other drugs. Analysis of MICs over time provides information about any underlying changes that you cannot find by only analyzing resistance frequencies. This serves as an early warning for a possible step-wise increase in MIC which does not occur adjacent to the resistance breakpoint. Conclusions: This study demonstrates that although E. coli causing canine UTIs remain susceptible in this region, temporal increases in the MICs to some drugs may indicate the emergence of resistance. These results support the use of first-line therapies such as amoxicillin or trimethoprim-sulfamethoxazole recommended by the ISCAID guidelines in Saskatchewan, Canada. Finally, continued surveillance is warranted to identify emerging resistance trends and guide future empiric therapy.

Description

Keywords

AMR, E. coli, UTI, Dogs, Veterinary, Resistance genes, MICs, Resistance frequencies, surveillance

Citation

Degree

Master of Science (M.Sc.)

Department

Veterinary Microbiology

Program

Veterinary Microbiology

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DOI

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