Inhibition of Shiga toxin-converting bacteriophage development by novel antioxidant compounds.
Sylwia BlochBożena Nejman-FaleńczykKarolina PierzynowskaEwa PiotrowskaAlicja WęgrzynChristelle MarminonZouhair BouazizPascal NeboisJoachim JoseMarc Le BorgneSarmistha SahaGrzegorz WegrzynPublished in: Journal of enzyme inhibition and medicinal chemistry (2018)
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.
Keyphrases
- escherichia coli
- oxidative stress
- hydrogen peroxide
- induced apoptosis
- endothelial cells
- biofilm formation
- poor prognosis
- klebsiella pneumoniae
- dna damage
- nitric oxide
- induced pluripotent stem cells
- pseudomonas aeruginosa
- pluripotent stem cells
- ischemia reperfusion injury
- long non coding rna
- cell cycle arrest
- genome wide
- binding protein
- cell death
- cystic fibrosis
- transcription factor
- heat stress
- pi k akt
- mouse model