Identification and Characterization of Novel Compounds Blocking Shiga Toxin Expression in Escherichia coli O157:H7

Alejandro Huerta-uribe, Zoe R. Marjenberg, Nao Yamaguchi, Stephen Fitzgerald, James P. R. Connolly, Nuria Carpena, Hanna Uvell, Gillian Douce, Michael Elofsson, Olwyn Byron, Rudi Marquez, David L. Gally, Andrew J. Roe

Research output: Contribution to journalArticlepeer-review

Abstract

Infections caused by Shiga toxin (Stx)-producing E. coli strains constitute a health problem, as they are problematic to treat. Stx production is a key virulence factor associated with the pathogenicity of enterohaemorrhagic E. coli (EHEC) and can result in the development of haemolytic uremic syndrome in infected patients. The genes encoding Stx are located on temperate lysogenic phages integrated into the bacterial chromosome and expression of the toxin is generally coupled to phage induction through the SOS response. We aimed to find new compounds capable of blocking expression of Stx type 2 (Stx2) as this subtype of Stx is more strongly associated with human disease. High-throughput screening of a small-molecule library identified a lead compound that reduced Stx2 expression in a dose-dependent manner. We show that the optimized compound interferes with the SOS response by directly affecting the activity and oligomerization of RecA, thus limiting phage activation and Stx2 expression. Our work suggests that RecA is highly susceptible to inhibition and that targeting this protein is a viable approach to limiting production of Stx2 by EHEC. This type of approach has the potential to limit production and transfer of other phage induced and transduced determinants.
Original languageEnglish
Article number1930
JournalFrontiers in Microbiology
Volume7
Early online date30 Nov 2016
DOIs
Publication statusE-pub ahead of print - 30 Nov 2016

Keywords

  • Shiga toxin
  • E. coli
  • RecA
  • phage
  • expression

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