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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.

Isogenic Strain of Escherichia coli O157:H7 That Has Lost both Shiga Toxin 1 and 2 Genes

Peter Feng,1,* Manashi Dey,1 Akio Abe,2 and Tae Takeda3

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 beta -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 gamma -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.


* Corresponding author. Mailing address: HFS-516, FDA, 200 C St. SW, Washington, DC 20204. Phone:(202) 205-4518. Fax:(202) 401-7740. E-mail: pfeng{at}cfsan.fda.gov.


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.






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Copyright © 2001 by the American Society for Microbiology. All rights reserved.