4.7 Article

Populations of extended-spectrum β-lactamase-producing Escherichia coli and Klebsiella pneumoniae are different in human-polluted environment and food items: a multicentre European study

Journal

CLINICAL MICROBIOLOGY AND INFECTION
Volume 28, Issue 3, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cmi.2021.07.022

Keywords

Extended-spectrum beta-lactamase; Environment; Escherichia coli; Food; Klebsiella pneumoniae

Funding

  1. Instituto de Salud Carlos III [AC16/00076]
  2. Netherlands Organization for Health Research and Development [681055, 547001004]
  3. Swiss National Science Foundation [40AR40173608]
  4. German Federal Ministry of Education and Research [01KI1830]
  5. French Agence Nationale de la Recherche [ANR-16-JPEC-0007-03]
  6. Plan Nacional de IthornDthorni
  7. Instituto de Salud Carlos III
  8. Subdireccion General de Redes y Centros de Investigacion Cooperativa
  9. Ministerio de Ciencia, Innovacion y Universidades
  10. Spanish Network for Research in Infectious Diseases [REIPI RD16/0016/0001]
  11. European Development Regional Fund [2014e2020]

Ask authors/readers for more resources

This study in five European cities found that food items were not the main source of ESBL-Ec and ESBL-Kp, as the strains from contaminated environments were genetically distinct from those in food. The findings suggest that human-to-human transmission is possibly the most frequent route of ESBL-Ec and ESBL-Kp transmission in high-income countries.
Objectives: To assess the extent to which food items are a source of extended-spectrum beta-lactamase (ESBL) -producing Escherichia coli (ESBL-Ec) and ESBL-producing Klebsiella pneumoniae (ESBL-Kp) for humans in five European cities. Methods: We sampled 122 human polluted (hp)-environments (sewers and polluted rivers, as a proxy of human contamination) and 714 food items in Besancon (France), Geneva (Switzerland), Sevilla (Spain), Tubingen (Germany) and Utrecht (The Netherlands). A total of 254 ESBL-Ec and 39 ESBL-Kp isolates were cultured. All genomes were fully sequenced to compare their sequence types (ST) and core genomes, along with the distribution of bla(ESBL) genes and their genetic supports (i.e. chromosome or plasmid). Results: Sequence data revealed that ESBL-Ec and ESBL-Kp isolates from hp-environments were genetically different from those contaminating food items. ESBL-Ec ST131 was widespread in the hp-environment (21.5% of the isolates) but absent from the food items tested. ESBL-Ec ST10 was in similar proportions in hp-environments and food items (15 and 10 isolates, respectively) but mostly carried reservoir-specific bla(ESBL). bla(CTX-M-1) and bla(SHV-12) predominated in food-related E. coli isolates (32% and 34% of the isolates, respectively), whereas bla(CTX-M-15) and bla(CTX-M-27) predominated in isolates from hp-environments (52% and 15% of the isolates, respectively). Conclusions: We found a very limited connection between ESBL-Ec and ESBL-Kp populations retrieved in food items and from hp-environments and bla(ESBL). This suggests that human-to-human contamination, rather than the food chain, is possibly the most frequent route of ESBL-Ec and ESBL-Kp transmission in high-income countries. (C) 2021 The Authors. Published by Elsevier Ltd on behalf of European Society of Clinical Microbiology and Infectious Diseases.

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