Clinical and Diagnostic Laboratory Immunology, July 2001, p. 711-717, Vol. 8, No. 4
1071-412X/01/$04.00+0 DOI: 10.1128/CDLI.8.4.711-717.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Division of Microbiological Studies, Food and Drug Administration, Washington, D.C. 20204,1 and Department of Bacteriology, The Kitasato Institute,2 and Department of Infectious Diseases Research, National Children's Medical Research Center,3 Tokyo, Japan.
Received 20 November 2000/Returned for modification 13 March 2001/Accepted 28 March 2001
An Escherichia coli O157:H7 strain isolated from a
patient with hemorrhagic colitis was found to exhibit two slightly
different colony morphology types on differential medium. Each
morphological type, designated TT12A and TT12B, was isolated, and
serological testing using various assays confirmed that both strains
carried the O157 and the H7 antigens. Biochemical testing showed that the strains had identical profiles on AP120E analysis and, like typical
O157:H7 strains, did not ferment sorbitol or exhibit
-glucuronidase activity. Analysis with a multiplex PCR assay showed that TT12B did not
carry the gene for either Shiga toxin 1 (Stx1) or Stx2, whereas these
genes were present in TT12A and the toxins were produced. Apart from
that, both strains carried the +93 gusA mutation, the
cluster I ehxA gene for enterohemolysin, and the
eae gene for
-intimin, which are all characteristics of
the O157:H7 serotype. Phenotypic assays confirmed that both strains
exhibited enterohemolysin activity and the attachment and effacing
lesion on HeLa cells. Multilocus enzyme electrophoresis analysis showed
that the strains are closely related genetically and belong in the same
clonal group. Pulsed-field gel electrophoresis (PFGE) typing of
XbaI-digested genomic DNA revealed that the two strains
differed by two bands but shared 90% similarity and clustered in the
same clade. All other non-Stx-producing O157:H7 strains examined
clustered in a major clade that was distinct from that of Stx-producing
O157:H7 strains. The findings that TT12B was identical to TT12A, except for Stx production, and its PFGE profile is also more closely related
to that of Stx-producing O157:H7 strains suggest that TT12B was derived
from TT12A by the loss of both stx genes.
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