Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/44452
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Type: Journal article
Title: Pathologic changes in mice induced by subtilase cytotoxin, a potent new Escherichia coli AB₅ toxin that targets the endoplasmic reticulum
Other Titles: Pathologic changes in mice induced by subtilase cytotoxin, a potent new Escherichia coli AB(5) toxin that targets the endoplasmic reticulum
Author: Wang, H.
Paton, J.
Paton, A.
Citation: Journal of Infectious Diseases, 2007; 196(7):1093-1101
Publisher: Univ Chicago Press
Issue Date: 2007
ISSN: 0022-1899
1537-6613
Statement of
Responsibility: 
Hui Wang, James C. Paton, and Adrienne W. Paton
Abstract: Subtilase cytotoxin (SubAB) is the prototype of a recently discovered AB₅ cytotoxin family produced by certain strains of Shiga toxigenic Escherichia coli (STEC). The catalytic A subunit is a highly specific subtilase-like serine protease that cleaves the endoplasmic reticulum chaperone BiP. The toxin is lethal for mice, but the pathology it induces is poorly understood. Here, we show that intraperitoneal injection of SubAB causes microangiopathic hemolytic anemia, thrombocytopenia, and renal impairment in mice-characteristics typical of Shiga toxin-induced hemolytic uremic syndrome. SubAB caused extensive microvascular thrombosis and other histologic damage in the brain, kidneys, and liver, as well as dramatic splenic atrophy. Peripheral blood leukocyte levels were increased at 24 h; there was also significant neutrophil infiltration in the liver, kidneys, and spleen and toxin-induced apoptosis at these sites. These findings raise the possibility that SubAB directly contributes to pathology in humans infected with strains of STEC that produce both Shiga toxin and SubAB.
Keywords: Liver; Kidney; Brain; Spleen; Endoplasmic Reticulum; Animals; Mice, Inbred BALB C; Humans; Mice; Escherichia coli; Anemia, Hemolytic; Thrombocytopenia; Escherichia coli Proteins; Protein Subunits; Shiga Toxins; Cytotoxins; Apoptosis; Male
Rights: © 2007 by the Infectious Diseases Society of America. All rights reserved.
RMID: 0020072876
DOI: 10.1086/521364
Published version: http://www.journals.uchicago.edu/doi/abs/10.1086/521364
Appears in Collections:Molecular and Biomedical Science publications

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