Baicalin Inhibits the Lethality of Shiga-Like Toxin 2 in Mice
Author(s) -
Jing Dong,
Yong Zhang,
Yutao Chen,
Xiaodi Niu,
Yù Zhang,
Cheng Yang,
Quan Wang,
Xuemei Li,
Xuming Deng
Publication year - 2015
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.01416-15
Subject(s) - baicalin , stx2 , toxin , shiga toxin , escherichia coli , lethality , virulence , virulence factor , microbiology and biotechnology , chemistry , pharmacology , biology , biochemistry , toxicology , high performance liquid chromatography , chromatography , gene
Shiga-like toxins (Stxs), produced by pathogenic Escherichia coli, are a major virulence factor involved in severe diseases in human and animals. These toxins are ribosome-inactivating proteins, and treatment for diseases caused by them is not available. Therefore, there is an urgent need for agents capable of effectively targeting this lethal toxin. In this study, we identified baicalin, a flavonoid compound used in Chinese traditional medicine, as a compound against Shiga-like toxin 2 (Stx2). We found that baicalin significantly improves renal function and reduces Stx2-induced lethality in mice. Further experiments revealed that baicalin induces the formation of oligomers by the toxin by direct binding. We also identified the residues important for such interactions and analyzed their roles in binding baicalin by biophysical and biochemical analyses. Our results establish baicalin as a candidate compound for the development of therapeutics against diseases caused by Stxs.
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