Prevalence and characteristics of multidrug-resistant Escherichia coli sequence type ST131 at two academic centers in Boston and Minneapolis, USA

Mélanie T. Mahoney, Hunter Brigman, Brian D Johnston, James R Johnson, Elizabeth B. Hirsch

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Background: Escherichia coli sequence type (ST) ST131, with its emergent resistance-associated H30Rx, H30R1, and C1-M27 clonal subsets, accounts for the greatest share of extraintestinal E. coli infections and most extended-spectrum β-lactamase (ESBL)-producing E. coli. Methods: We characterized and compared consecutive E. coli urine isolates from two geographically distinct medical centers in Minneapolis, Minnesota (n = 172) and Boston, Massachusetts (n = 143) for ESBL phenotype, CTX-M-type ESBL genes, phylogenetic groups, selected ST131 subclones, and 40 extraintestinal virulence genes. Results: Whereas the Boston vs. Minneapolis isolates had a similar prevalence of phylogenetic groups (mainly B2: 79% vs 73%), ST131 (34% vs 28%), H30 (28% vs 21%), and H30Rx (6% vs 5%), the emerging C1-M27 subclone occurred uniquely among Boston (6%) isolates. ESBL production was more prevalent among Boston isolates (15% vs 8%) and among ST131 isolates. Identified ESBL genes included blaCTX-M-27 (Boston only) and blaCTX-M-15. Ciprofloxacin resistance was ST131-associated and similarly prevalent across centers. Boston isolates had higher virulence gene scores. Conclusions: Despite numerous similarities to Minneapolis isolates, Boston ST131 isolates demonstrated more prevalent ESBL production, higher virulence gene scores, and, uniquely, the C1-M27 subclone and blaCTX-M-27. Broader surveillance is needed to define the prevalence of ST131′s globally successful C1-M27 subclone across the U.S.

Original languageEnglish (US)
Pages (from-to)434-439
Number of pages6
JournalAmerican journal of infection control
Volume51
Issue number4
DOIs
StatePublished - Apr 2023

Bibliographical note

Funding Information:
Funding/Support: This research was supported in part by Office of Research and Development, Department of Veteran Affairs , grant # 2I01CX000920-04 (J.R.J).

Funding Information:
Conflicts of interest: Elizabeth B. Hirsch has received research funding from Merck and advisory board honorarium from Melinta, MeMed, and Merck. James R. Johnson has had research grants and/or consultancies involving Achaogen, Allergan, Crucell/Janssen, Melinta, Merck, Shionogi, Syntiron, and Tetraphase, and has patent applications for tests to detect specific E. coli strains. All other authors declare no conflicts of interest.

Funding Information:
Funding/Support: This research was supported in part by Office of Research and Development, Department of Veteran Affairs, grant # 2I01CX000920-04 (J.R.J). Conflicts of interest: Elizabeth B. Hirsch has received research funding from Merck and advisory board honorarium from Melinta, MeMed, and Merck. James R. Johnson has had research grants and/or consultancies involving Achaogen, Allergan, Crucell/Janssen, Melinta, Merck, Shionogi, Syntiron, and Tetraphase, and has patent applications for tests to detect specific E. coli strains. All other authors declare no conflicts of interest.

Publisher Copyright:
© 2022 Association for Professionals in Infection Control and Epidemiology, Inc.

Keywords

  • E. coli
  • ESBL
  • ST131
  • Urinary tract infection
  • Virulence

PubMed: MeSH publication types

  • Journal Article
  • Research Support, U.S. Gov't, Non-P.H.S.

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