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Applied and Environmental Microbiology, February 2003, p. 1059-1066, Vol. 69, No. 2
0099-2240/03/$08.00+0     DOI: 10.1128/AEM.69.2.1059-1066.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Comparison of Shiga Toxin Production by Hemolytic-Uremic Syndrome-Associated and Bovine-Associated Shiga Toxin-Producing Escherichia coli Isolates

Jenny M. Ritchie,1* Patrick L. Wagner,1,2 David W. K. Acheson,3 and Matthew K. Waldor1,2

Division of Geographic Medicine and Infectious Diseases,1 Howard Hughes Medical Institute, Tufts-New England Medical Center, Boston, Massachusetts 02111,2 Department of Epidemiology and Preventive Medicine, University of Maryland, Baltimore, Maryland 212013

Received 5 September 2002/ Accepted 22 November 2002

There is considerable diversity among Shiga toxin (Stx)-producing Escherichia coli (STEC) bacteria, and only a subset of these organisms are thought to be human pathogens. The characteristics that distinguish STEC bacteria that give rise to human disease are not well understood. Stxs, the principal virulence determinants of STEC, are thought to account for hemolytic-uremic syndrome (HUS), a severe clinical consequence of STEC infection. Stxs are typically bacteriophage encoded, and their production has been shown to be enhanced by prophage-inducing agents such as mitomycin C in a limited number of clinical STEC isolates. Low iron concentrations also enhance Stx production by some clinical isolates; however, little is known regarding whether and to what extent these stimuli regulate Stx production by STEC associated with cattle, the principal environmental reservoir of STEC. In this study, we investigated whether toxin production differed between HUS- and bovine-associated STEC strains. Basal production of Stx by HUS-associated STEC exceeded that of bovine-associated STEC. In addition, following mitomycin C treatment, Stx2 production by HUS-associated STEC was significantly greater than that by bovine-associated STEC. Unexpectedly, mitomycin C treatment had a minimal effect on Stx1 production by both HUS- and bovine-associated STEC. However, Stx1 production was induced by growth in low-iron medium, and induction was more marked for HUS-associated STEC than for bovine-associated STEC. These observations reveal that disease-associated and bovine-associated STEC bacteria differ in their basal and inducible Stx production characteristics.


* Corresponding author. Mailing address: Division of Geographic Medicine and Infectious Diseases, Tufts-New England Medical Center, 750 Washington St., Boston, MA 02111. Phone: (617) 636-4134. Fax: (617) 636-5292. E-mail: jritchie1{at}lifespan.org.


Applied and Environmental Microbiology, February 2003, p. 1059-1066, Vol. 69, No. 2
0099-2240/03/$08.00+0     DOI: 10.1128/AEM.69.2.1059-1066.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




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