Characterization of carbapenem-resistant and XDR Pseudomonas aeruginosa in Canada: results of the CANWARD 2007–16 study

Author:

McCracken Melissa G1,Adam Heather J23,Blondeau Joseph M4,Walkty Andrew J23,Karlowsky James A23,Hoban Daryl J23,Zhanel George G2,Mulvey Michael R1,Zhanel George G,Hoban Daryl J,Adam Heather J,Baxter Melanie R,Nichol Kimberly A,Lagacé-Wiens Philippe R S,Walkty Andrew,Karlowsky James A,Blondeau J,Slinger R,Davidson R,Zhanel G,Hoban D,Delport J,Ellis C,Laverdière M,Loo V,Poutanen S,Fuller J,Roscoe D,Desjardins M,Matukas L,Goyette M,Lee C,Carignan A,Bergevin M,Pelletier R,

Affiliation:

1. National Microbiology Laboratory, Public Health Agency of Canada, 1015 Arlington Street, Winnipeg, Manitoba, Canada

2. Department of Medical Microbiology/Infectious Diseases, Max Rady College of Medicine, University of Manitoba, Room 543-745 Bannatyne Avenue, Winnipeg, Manitoba, Canada

3. Clinical Microbiology, Diagnostic Services Manitoba, MS673-820 Sherbrook Street, Winnipeg, Manitoba, Canada

4. Division of Clinical Microbiology, Royal University Hospital and the Saskatoon Health Region and Departments of Microbiology and Immunology, Pathology, and Ophthalmology, University of Saskatchewan, Saskatoon, Canada

Abstract

Abstract Objectives Carbapenem-resistant Pseudomonas aeruginosa are emerging worldwide with increasing reports of carbapenemase-producing isolates. Carbapenem-resistant isolates may also be XDR. This study characterized carbapenem-resistant and XDR P. aeruginosa isolated from patients receiving care at Canadian hospitals from 2007 to 2016. Methods Antimicrobial susceptibility testing was performed using CLSI broth microdilution methods. PCR was used to detect carbapenemases (GES, KPC, NDM, IMP, VIM, OXA-48) and other resistance markers; specific carbapenemase gene variants were identified by DNA sequencing. Genetic relatedness was assessed by MLST and PFGE. Results From 2007 to 2016, 3864 isolates of P. aeruginosa were collected; 466 (12.1%) isolates were carbapenem resistant. The prevalence of carbapenem-resistant P. aeruginosa reached a peak of 17.3% in 2014. Colistin (94% susceptible) and ceftolozane/tazobactam (92.5%) were the most active agents against carbapenem-resistant P. aeruginosa. XDR P. aeruginosa comprised 4.5% of isolates; they were found to be genetically diverse and remained susceptible to colistin and ceftolozane/tazobactam. Only 4.3% (n = 20) of carbapenem-resistant P. aeruginosa harboured a carbapenemase; most were blaGES-5 (35%, n = 7). Wide genetic diversity was observed among carbapenem-resistant P. aeruginosa with >200 different sequence types identified. Conclusions Although the prevalence of carbapenem-resistant P. aeruginosa in Canada spiked in 2014 and 2015, carbapenemase-producing P. aeruginosa remain rare with only 20 (4.3%) isolates identified over a 10 year period. Broad genetic diversity was observed among both carbapenem-resistant and XDR phenotypes of P. aeruginosa. Pan-drug-resistant P. aeruginosa have not yet been identified in Canada.

Funder

University of Manitoba

Diagnostic Services Manitoba

National Microbiology Laboratory

Astellas

Merck

Pfizer

Sunovion

The Medicines Company

Abbott

Achaogen

Cubist

Paladin Labs

Bayer

Janssen Ortho/Ortho McNeil

Affinium

Basilea

AstraZeneca

Paratek

Tetraphase

Theravance

Sanofi-Aventis and Zoetis

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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