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Diminazene aceturate: An antibacterial agent for Shiga-toxin-producing Escherichia coli O157:H7

Authors
Wu, S.-Y.Park, G.-Y.Kim, S.-H.Hulme, J.An, S.S.A.
Issue Date
Oct-2016
Publisher
Dove Medical Press Ltd.
Keywords
Berenil©; E. coli O157; Enterohemorrhagic; Protease; Reversible; ROS
Citation
Drug Design, Development and Therapy, v.10, pp.3363 - 3378
Journal Title
Drug Design, Development and Therapy
Volume
10
Start Page
3363
End Page
3378
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/8872
DOI
10.2147/DDDT.S114832
ISSN
1177-8881
Abstract
The aim of this study was to investigate the bacteriostatic and bactericidal effects of diminazene aceturate (DA) against five strains of pathogenic bacteria and two strains of nonpathogenic bacteria. The results showed that 5 µg/mL of DA suppressed the growth of pathogenic Escherichia coli by as much as 77% compared with the controls. Enterohemorrhagic E. coli EDL933 (an E. coli O157:H7 strain) was the most sensitive to DA with a minimum inhibitory concentration of 20 µg/mL. Additional investigations showed that DA induced the highest level of intracellular reactive oxygen species in EDL933. A positive correlation between the reactive oxygen species levels and DA concentration was demonstrated. DA (5 µg/mL) was also a potent uncoupler, inducing a stationary phase collapse (70%–75%) in both strains of E. coli O157:H7. Further investigation showed that the collapse was due to the NaCl:DA ratio in the broth and was potassium ion dependent. A protease screening assay was conducted to elucidate the underlying mechanism. It was found that at neutral pH, the hydrolysis of H-Asp-pNA increased by a factor of 2–3 in the presence of DA, implying that DA causes dysregulation of the proton motive force and a decrease in cellular pH. Finally, a commercial verotoxin test showed that DA did not significantly increase toxin production in EDL933 and was a suitable antibacterial agent for Shiga-toxin-producing E. coli. © 2016 Wu et al.
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