Identification of Antibiotics That Diminish Disease in a Murine Model of Enterohemorrhagic Escherichia coli Infection

Antimicrob Agents Chemother. 2020 Mar 24;64(4):e02159-19. doi: 10.1128/AAC.02159-19. Print 2020 Mar 24.

Abstract

Infections with enterohemorrhagic Escherichia coli (EHEC) cause disease ranging from mild diarrhea to hemolytic-uremic syndrome (HUS) and are the most common cause of renal failure in children in high-income countries. The severity of the disease derives from the release of Shiga toxins (Stx). The use of antibiotics to treat EHEC infections is generally avoided, as it can result in increased stx expression. Here, we systematically tested different classes of antibiotics and found that their influence on stx expression and release varies significantly. We assessed a selection of these antibiotics in vivo using the Citrobacter rodentium ϕstx2dact mouse model and show that stx2d-inducing antibiotics resulted in weight loss and kidney damage despite clearance of the infection. However, several non-Stx-inducing antibiotics cleared bacterial infection without causing Stx-mediated pathology. Our results suggest that these antibiotics might be useful in the treatment of EHEC-infected human patients and decrease the risk of HUS development.

Keywords: Citrobacter rodentium; EHEC; Shiga toxin; antibiotics; mouse model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Kidney Injury / microbiology
  • Acute Kidney Injury / prevention & control*
  • Animals
  • Anti-Bacterial Agents / therapeutic use*
  • Citrobacter rodentium / genetics
  • Citrobacter rodentium / metabolism
  • Disease Models, Animal
  • Enterohemorrhagic Escherichia coli / drug effects*
  • Enterohemorrhagic Escherichia coli / pathogenicity
  • Escherichia coli Infections / drug therapy*
  • Escherichia coli Infections / microbiology
  • Escherichia coli Infections / pathology
  • Female
  • Hemolytic-Uremic Syndrome / drug therapy
  • Hemolytic-Uremic Syndrome / microbiology
  • Mice
  • Mice, Inbred C57BL
  • Shiga Toxin 2 / genetics
  • Shiga Toxin 2 / metabolism*
  • Shiga Toxin 2 / toxicity

Substances

  • Anti-Bacterial Agents
  • Shiga Toxin 2