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Whole genome analysis of cephalosporin-resistant Escherichia coli from bloodstream infections in Australia, New Zealand and Singapore: high prevalence of CMY-2 producers and ST131 carrying blaCTX-M-15 and blaCTX-M-27.
Harris, Patrick N A; Ben Zakour, Nouri L; Roberts, Leah W; Wailan, Alexander M; Zowawi, Hosam M; Tambyah, Paul A; Lye, David C; Jureen, Roland; Lee, Tau H; Yin, Mo; Izharuddin, Ezlyn; Looke, David; Runnegar, Naomi; Rogers, Benjamin; Bhally, Hasan; Crowe, Amy; Schembri, Mark A; Beatson, Scott A; Paterson, David L.
Affiliation
  • Harris PNA; University of Queensland, UQ Centre for Clinical Research, Royal Brisbane & Women's Hospital, Queensland, Australia.
  • Ben Zakour NL; Microbiology Department, Central Laboratory, Pathology Queensland, Royal Brisbane & Women's Hospital, Queensland, Australia.
  • Roberts LW; School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, Australia.
  • Wailan AM; School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, Australia.
  • Zowawi HM; University of Queensland, UQ Centre for Clinical Research, Royal Brisbane & Women's Hospital, Queensland, Australia.
  • Tambyah PA; Infection Genomics, Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
  • Lye DC; University of Queensland, UQ Centre for Clinical Research, Royal Brisbane & Women's Hospital, Queensland, Australia.
  • Jureen R; College of Medicine, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Lee TH; WHO Collaborating Centre for Infection Prevention and Control, and GCC Centre for Infection Control, Riyadh, Saudi Arabia.
  • Yin M; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
  • Izharuddin E; Division of Infectious Diseases, Department of Medicine, National University Hospital, Singapore.
  • Looke D; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
  • Runnegar N; Communicable Disease Centre, Institute of Infectious Diseases and Epidemiology, Tan Tock Seng Hospital, Singapore.
  • Rogers B; Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore.
  • Bhally H; Department of Laboratory Medicine, Division of Microbiology, National University Hospital, Singapore.
  • Crowe A; Communicable Disease Centre, Institute of Infectious Diseases and Epidemiology, Tan Tock Seng Hospital, Singapore.
  • Schembri MA; Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore.
  • Beatson SA; Division of Infectious Diseases, Department of Medicine, National University Hospital, Singapore.
  • Paterson DL; Communicable Disease Centre, Institute of Infectious Diseases and Epidemiology, Tan Tock Seng Hospital, Singapore.
J Antimicrob Chemother ; 73(3): 634-642, 2018 03 01.
Article in En | MEDLINE | ID: mdl-29253152
ABSTRACT

Objectives:

To characterize MDR Escherichia coli from bloodstream infections (BSIs) in Australia, New Zealand and Singapore.

Methods:

We collected third-generation cephalosporin-resistant (3GC-R) E. coli from blood cultures in patients enrolled in a randomized controlled trial from February 2014 to August 2015. WGS was used to characterize antibiotic resistance genes, MLST, plasmids and phylogenetic relationships. Antibiotic susceptibility was determined using disc diffusion and Etest.

Results:

A total of 70 3GC-R E. coli were included, of which the majority were ST131 (61.4%). BSI was most frequently from a urinary source (69.6%), community associated (62.9%) and in older patients (median age 71 years). The median Pitt score was 1 and ICU admission was infrequent (3.1%). ST131 possessed more acquired resistance genes than non-ST131 (P = 0.003). Clade C1/C2 ST131 predominated (30.2% and 53.5% of ST131, respectively) and these were all ciprofloxacin resistant. All clade A ST131 (n = 6) were community associated. The predominant ESBL types were blaCTX-M (80.0%) and were strongly associated with ST131 (95% carried blaCTX-M), with the majority blaCTX-M-15. Clade C1 was associated with blaCTX-M-14 and blaCTX-M-27, whereas blaCTX-M-15 predominated in clade C2. Plasmid-mediated AmpC genes (mainly blaCMY-2) were frequent (17.1%) but were more common in non-ST131 (P < 0.001) isolates from Singapore and Brisbane. Two strains carried both blaCMY-2 and blaCTX-M. The majority of plasmid replicon types were IncF.

Conclusions:

In a prospective collection of 3GC-R E. coli causing BSI, community-associated Clade C1/C2 ST131 predominate in association with blaCTX-M ESBLs, although a significant proportion of non-ST131 strains carried blaCMY-2.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Beta-Lactamases / Cephalosporins / Bacteremia / Escherichia coli / Escherichia coli Infections Type of study: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Asia / Oceania Language: En Journal: J Antimicrob Chemother Year: 2018 Type: Article Affiliation country: Australia

Full text: 1 Database: MEDLINE Main subject: Beta-Lactamases / Cephalosporins / Bacteremia / Escherichia coli / Escherichia coli Infections Type of study: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Asia / Oceania Language: En Journal: J Antimicrob Chemother Year: 2018 Type: Article Affiliation country: Australia