Genomic Epidemiology of Invasive Methicillin-Resistant Staphylococcus aureus Infections Among Hospitalized Individuals in Ontario, Canada

Author:

Guthrie Jennifer L1ORCID,Teatero Sarah1,Hirai Sotaro2,Fortuna Alex1,Rosen Daniel1,Mallo Gustavo V1,Campbell Jennifer3,Pelude Linda4,Golding George3,Simor Andrew E567,Patel Samir N17,McGeer Allison78,Fittipaldi Nahuel127,Delport Johan,Evans Gerald,Hota Susy,Katz Kevin,Lemieux Camille,Mertz Dominik,Science Michelle,Thampi Nisha,

Affiliation:

1. Public Health Ontario, Toronto Laboratory, Toronto, Ontario, Canada

2. Department of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada

3. National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada

4. Public Health Agency of Canada, Ottawa, Ontario, Canada

5. Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada

6. Department of Medicine, University of Toronto, Toronto, Ontario, Canada

7. Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada

8. Sinai Health System, Toronto, Ontario, Canada

Abstract

Abstract Background Prevention and control of methicillin-resistant Staphylococcus aureus (MRSA) infections remain challenging. In-depth surveillance integrating patient and isolate data can provide evidence to better inform infection control and public health practice. Methods We analyzed MRSA cases diagnosed in 2010 (n = 212) and 2016 (n = 214) by hospitals in Ontario, Canada. Case-level clinical and demographic data were integrated with isolate characteristics, including antimicrobial resistance (AMR), classic genotyping, and whole-genome sequencing results. Results Community-associated MRSA (epidemiologically defined) increased significantly from 23.6% in 2010 to 43.0% in 2016 (P < .001). The MRSA population structure changed over time, with a 1.5× increase in clonal complex (CC)8 strains and a concomitant decrease in CC5. The clonal shift was reflected in AMR patterns, with a decrease in erythromycin (86.7% to 78.4%, P = .036) and clindamycin resistance (84.3% to 47.9%, P < .001) and a >2-fold increase in fusidic acid resistance (9.0% to 22.5%, P < .001). Isolates within both CC5 and CC8 were relatively genetically diverse. We identified 6 small genomic clusters—3 potentially related to transmission in healthcare settings. Conclusions Community-associated MRSA is increasing among hospitalized individuals in Ontario. Clonal shifting from CC5 to CC8 has impacted AMR. We identified a relatively high genetic diversity and limited genomic clustering within these dominant CCs.

Funder

Public Health Ontario

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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