Inhibition of Shiga toxin-converting bacteriophage development by novel antioxidant compounds

J Enzyme Inhib Med Chem. 2018 Dec;33(1):639-650. doi: 10.1080/14756366.2018.1444610.

Abstract

Oxidative stress may be the major cause of induction of Shiga toxin-converting (Stx) prophages from chromosomes of Shiga toxin-producing Escherichia coli (STEC) in human intestine. Thus, we aimed to test a series of novel antioxidant compounds for their activities against prophage induction, thus, preventing pathogenicity of STEC. Forty-six compounds (derivatives of carbazole, indazole, triazole, quinolone, ninhydrine, and indenoindole) were tested. Fifteen of them gave promising results and were further characterized. Eleven compounds had acceptable profiles in cytotoxicity tests with human HEK-293 and HDFa cell lines. Three of them (selected for molecular studies) prevent the prophage induction at the level of expression of specific phage genes. In bacterial cells treated with hydrogen peroxide, expression of genes involved in the oxidative stress response was significantly less efficient in the presence of the tested compounds. Therefore, they apparently reduce the oxidative stress, which prevents induction of Stx prophage in E. coli.

Keywords: Shiga toxin-converting bacteriophage; Shiga toxin-producing Escherichia coli; antioxidants; heterocyclic compounds; oxidative stress.

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Antioxidants / chemical synthesis
  • Antioxidants / chemistry
  • Antioxidants / pharmacology*
  • Cell Line
  • Cell Survival / drug effects
  • Dose-Response Relationship, Drug
  • HEK293 Cells
  • Humans
  • Molecular Structure
  • Oxidative Stress / drug effects
  • Shiga Toxin / antagonists & inhibitors*
  • Shiga Toxin / genetics
  • Shiga Toxin / metabolism
  • Shiga-Toxigenic Escherichia coli / cytology
  • Shiga-Toxigenic Escherichia coli / drug effects*
  • Shiga-Toxigenic Escherichia coli / metabolism
  • Structure-Activity Relationship

Substances

  • Anti-Bacterial Agents
  • Antioxidants
  • Shiga Toxin

Grants and funding

This work was supported by University of Gdansk, task [grant no. 530-L140-D242–17-1 A].