Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/3044
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Type: Journal article
Title: A new family of potent AB5 cytotoxins produced by Shiga toxigenic Escherichia coli.
Author: Paton, A.
Srimanote, P.
Talbot, U.
Wang, H.
Paton, J.
Citation: Journal of Experimental Medicine, 2004; 200(1):35-46
Publisher: Rockefeller Univ Press
Issue Date: 2004
ISSN: 0022-1007
1540-9538
Statement of
Responsibility: 
Adrienne W. Paton, Potjanee Srimanote, Ursula M. Talbot, Hui Wang and James C. Paton
Abstract: The Shiga toxigenic Escherichia coli (STEC) O113:H21 strain 98NK2, which was responsible for an outbreak of hemolytic uremic syndrome, secretes a highly potent and lethal subtilase cytotoxin that is unrelated to any bacterial toxin described to date. It is the prototype of a new family of AB 5 toxins, comprising a single 35-kilodalton (kD) A subunit and a pentamer of 13-kD B subunits. The A subunit is a subtilase-like serine protease distantly related to the BA_2875 gene product of Bacillus anthracis . The B subunit is related to a putative exported protein from Yersinia pestis , and binds to a mimic of the ganglioside GM2. Subtilase cytotoxin is encoded by two closely linked, cotranscribed genes ( subA and subB ), which, in strain 98NK2, are located on a large, conjugative virulence plasmid. Homologues of the genes are present in 32 out of 68 other STEC strains tested. Intraperitoneal injection of purified subtilase cytotoxin was fatal for mice and resulted in extensive microvascular thrombosis, as well as necrosis in the brain, kidneys, and liver. Oral challenge of mice with E. coli K-12–expressing cloned subA and subB resulted in dramatic weight loss. These findings suggest that the toxin may contribute to the pathogenesis of human disease.
Keywords: subtilase; enterohemorrhagic E. coli; serine protease; hemolytic uremic syndrome; microvascular thrombosis
Description: Copyright © 2004 Rockefeller University Press
Provenance: An erratum to this article can be found at http://www.jem.org/cgi/content/full/200/11/1525. Please click on the description link below to view the erratum.
RMID: 0020040693
DOI: 10.1084/jem.20040392
Description (link): http://www.jem.org/cgi/content/full/200/11/1525
Published version: http://www.jem.org/cgi/content/abstract/200/1/35
Appears in Collections:Molecular and Biomedical Science publications

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