Evolving landscape of carbapenem-resistant Pseudomonas aeruginosa at a single centre in the USA

Author:

Sakurai Aki1,Dinh An Q234,Hanson Blake M45ORCID,Shropshire William C6ORCID,Rizvi Samie A23,Rydell Kirsten23,Tran Truc T23,Wanger Audrey7,Arias Cesar A23,Miller William R23ORCID

Affiliation:

1. Department of Infectious Diseases and Microbiology, Fujita Health University School of Medicine , Toyoake, Aichi , Japan

2. Department of Internal Medicine, Division of Infectious Diseases, Houston Methodist Hospital , 6560 Fannin St, Scurlock Tower, Suite 1540, Houston, TX , USA

3. Center for Infectious Diseases, Houston Methodist Research Institute , Houston, TX , USA

4. Center for Infectious Diseases, University of Texas Health Science Center, School of Public Health , Houston, TX , USA

5. Center for Antimicrobial Resistance and Microbial Genomics, University of Texas Health Science Center, McGovern Medical School , Houston, TX , USA

6. Department of Infectious Diseases, Infection Control, and Employee Health, University of Texas M. D. Anderson Cancer Center , Houston, TX , USA

7. Department of Pathology and Laboratory Medicine, University of Texas Health Science Center, McGovern School of Medicine , Houston, TX , USA

Abstract

Abstract Objectives The increased identification of carbapenem-resistant Pseudomonas aeruginosa (CR-PA) is an ongoing concern. However, information on the evolving antimicrobial resistance profile and molecular epidemiology of CR-PA over time is scarce. Thus, we conducted a cross-sectional analysis to investigate the phenotypic and genotypic characteristics of CR-PA recovered over different time periods, focusing on the isolates exhibiting a ceftolozane/tazobactam resistance phenotype. Methods A total of 169 CR-PA isolated from clinical specimens at a single centre in Houston, TX, USA were studied. Among them, 61 isolates collected between 1999 and 2005 were defined as historical strains, and 108 collected between 2017 and 2018 were defined as contemporary strains. Antimicrobial susceptibilities against selected β-lactams was determined. WGS data were used for the identification of antimicrobial resistance determinants and phylogenetic analysis. Results Non-susceptibility to ceftolozane/tazobactam and ceftazidime/avibactam increased from 2% (1/59) to 17% (18/108) and from 7% (4/59) to 17% (18/108) from the historical to the contemporary collection, respectively. Carbapenemase genes, which were not identified in the historical collection, were harboured by 4.6% (5/108) of the contemporary strains, and the prevalence of ESBL genes also increased from 3.3% (2/61) to 16% (17/108). Genes encoding acquired β-lactamases were largely confined to the high-risk clones. Among ceftolozane/tazobactam-resistant isolates, non-susceptibility to ceftazidime/avibactam, imipenem/relebactam and cefiderocol was observed in 94% (15/16), 56% (9/16) and 12.5% (2/16), respectively. Resistance to ceftolozane/tazobactam and imipenem/relebactam was primarily associated with the presence of exogenous β-lactamases. Conclusions Acquisition of exogenous carbapenemases and ESBLs may be a worrisome trend in P. aeruginosa.

Funder

Infectious Diseases Society of America

National Institutes of Health

NIH/NIAID

Publisher

Oxford University Press (OUP)

Subject

Microbiology (medical),Infectious Diseases,Immunology and Allergy,Microbiology,Immunology

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