Shiga Toxins: Pathogenicity and Therapeutic Applications

A special issue of Toxins (ISSN 2072-6651). This special issue belongs to the section "Bacterial Toxins".

Deadline for manuscript submissions: closed (31 December 2020) | Viewed by 3705

Special Issue Editor


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Guest Editor
1. Department of Biomolecular Science, KRIBB School of Bioscience, Korea University of Science and Technology (UST), 127 Gajeong-ro, Yuseong-gu, Daejeon 34113, Republic of Korea
2. Environmental Diseases Research Center, Korea Research Institute of Bioscience and Biotechnology, 125 Gwahak-ro, Daejeon 34141, Republic of Korea
Interests: Bacterial toxins; Shiga toxin-producing E.coli; Shiga toxins; hemolytic uremic syndrome
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Special Issue Information

Dear Colleagues,

Shigellosis caused by Shiga toxin (Stx)-producing Shigella dysenteriae serotype 1 or Stx-producing Escherichia coli (STEC) continues to be a major public health threat and is a particular concern because of the potential to develop life-threatening extra-intestinal complications, such as acute renal failure (hemolytic uremic syndrome; HUS), and CNS complications, such as seizures, paralysis, and death. Once Shiga toxins (Stxs) are internalized following the toxin-receptor binding on host cellular surface, they are trafficked into the Golgi apparatus and to the ER in a retrograde manner to enter the host cell cytosol, leading to various host cellular responses, including protein synthesis inhibition, apoptosis through ER stress, autophagy, and inflammation. Distinct investigations on host cell signaling responses activated by Stxs as multifunctional proteins are necessary to identify novel targets for intervention in pathogenesis. Moreover, many studies present compelling and strong evidence regarding therapeutic applications to target particular diseases, such as tumors, by engineering the toxins.

At the molecular, cellular or clinical level, an improved understanding of the pathogenesis of the diseases’ bacillary dysentery and hemorrhagic colitis, and the subsequent development of extra-intestinal/extrarenal complications caused by STEC, will be necessary to develop effective protective and interventional therapies to treat patients infected with the organism.

This Special Issue of Toxins will focus on recent advances to consider unexplored mechanisms of STEC-mediated pathogenesis, current therapeutic applications or STEC genetics contributing to pathogenicity.

Prof. Dr. Moo-Seung Lee
Guest Editor

Manuscript Submission Information

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Keywords

  • Shiga toxins
  • Shiga toxin-producing Shigella species
  • Shiga toxin-producing Escherichia coli
  • hemolytic uremic syndrome
  • Shiga toxins-mediated pathogenesis
  • cancer therapeutics
  • toxin engineering

Published Papers (1 paper)

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Research

14 pages, 3819 KiB  
Article
Baicalein Inhibits Stx1 and 2 of EHE: Effects of Baicalein on the Cytotoxicity, Production, and Secretion of Shiga Toxins of Enterohaemorrhagic Escherichia coli
by Pham Thi Vinh, Yui Shinohara, Akifumi Yamada, Hoang Minh Duc, Motokazu Nakayama, Tadahiro Ozawa, Jun Sato, Yoshimitsu Masuda, Ken-Ichi Honjoh and Takahisa Miyamoto
Toxins 2019, 11(9), 505; https://0-doi-org.brum.beds.ac.uk/10.3390/toxins11090505 - 29 Aug 2019
Cited by 12 | Viewed by 3416
Abstract
Shiga toxin-producing enterohaemorrhagic Escherichia coli (EHEC) O157:H7 is an important foodborne pathogen. Baicalein (5,6,7-trihydroxylflavone), a flavone isolated from the roots of Scutellaria baicalensis, is considered as a potential antibacterial agent to control foodborne pathogens. Among seven compounds selected by in silico screening [...] Read more.
Shiga toxin-producing enterohaemorrhagic Escherichia coli (EHEC) O157:H7 is an important foodborne pathogen. Baicalein (5,6,7-trihydroxylflavone), a flavone isolated from the roots of Scutellaria baicalensis, is considered as a potential antibacterial agent to control foodborne pathogens. Among seven compounds selected by in silico screening of the natural compound database, baicalein inhibited the cytotoxicity of both Shiga toxins 1 and 2 (Stx1 and Stx2) against Vero cells after pretreatment at 0.13 mmol/L. In addition, baicalein reduced the susceptibility of Vero cells to both Stx1 and Stx2. Real-time qPCR showed that baicalein increased transcription of stx1 but not of stx2. However, baicalein had no effects on production or secretion of Stx1 or Stx2. Docking models suggested that baicalein formed a stable structure with StxB pentamer with low intramolecular energy. The results demonstrate that inhibitory activity of baicalein against the cytotoxicity of both Stx1 and Stx2 might be due to of the formation of a binding structure inside the pocket of the Stx1B and Stx2B pentamers. Full article
(This article belongs to the Special Issue Shiga Toxins: Pathogenicity and Therapeutic Applications)
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