Dramatic rise in the proportion of ESBL-producing Escherichia coli and Klebsiella pneumoniae among clinical isolates identified in Canadian hospital laboratories from 2007 to 2016

Author:

Denisuik Andrew J1,Karlowsky James A12,Adam Heather J13,Baxter Melanie R1,Lagacé-Wiens Philippe R S12,Mulvey Michael R14,Hoban Daryl J13,Zhanel George G1,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. Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, University of Manitoba, Room 543-745 Bannatyne Avenue, Winnipeg, Manitoba, Canada

2. Clinical Microbiology, St. Boniface Hospital/Diagnostic Services, Shared Health Manitoba, L4025-409 Taché Avenue, Winnipeg, Manitoba, Canada

3. Clinical Microbiology, Health Sciences Centre/Diagnostic Services, Shared Health, MS673-820 Sherbrook Street, Winnipeg, Manitoba, Canada

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

Abstract

Abstract Objectives To assess the prevalence, antimicrobial susceptibilities and molecular characteristics of ESBL-producing Escherichia coli and Klebsiella pneumoniae infecting patients receiving care in Canadian hospitals from January 2007 to December 2016. Methods Clinical isolates of E. coli (n = 8387) and K. pneumoniae (n = 2623) submitted to CANWARD, an ongoing Canadian national surveillance study, were tested using the CLSI reference broth microdilution method to determine their susceptibility to 15 antimicrobial agents. ESBL-producing E. coli and K. pneumoniae confirmed by the CLSI phenotypic method and putative AmpC-producing E. coli underwent PCR testing and DNA sequencing to identify resistance genes. Annual proportions of isolates harbouring ESBL and AmpC genes were assessed by the Cochran–Armitage test of trend. Results The annual proportion of isolates of E. coli that were ESBL producing increased from 3.4% in 2007 to 11.1% in 2016 (P < 0.0001); >95% of ESBL-producing E. coli were susceptible to amikacin, colistin, ertapenem, meropenem and tigecycline. The proportion of isolates of K. pneumoniae that were ESBL producing increased from 1.3% in 2007 to 9.7% in 2016 (P < 0.0001); >95% of ESBL-producing K. pneumoniae were susceptible to amikacin and meropenem. CTX-M-15 was the predominant genotype in both ESBL-producing E. coli (64.2% of isolates) and ESBL-producing K. pneumoniae (51.0%). The annual proportion of isolates of E. coli that were AmpC producing [annual proportion mean 1.9% (range 0.3%–3.1%)] was unchanged from 2007 to 2016 (P > 0.5). Conclusions The prevalence of both ESBL-producing E. coli and K. pneumoniae increased significantly in Canada during the study period while the prevalence of AmpC-producing E. coli remained low and stable.

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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