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Journal of Clinical Microbiology, May 1998, p. 1180-1184, Vol. 36, No. 5
State Hygienic Laboratory, University of
Iowa, Iowa City, Iowa 52242,1 and
Foodborne and Diarrheal Diseases Branch, Division of
Bacterial and Mycotic Diseases, National Center for Infectious
Diseases, Centers for Disease Control and Prevention, Atlanta,
Georgia 303332
Received 6 November 1997/Returned for modification 19 December
1997/Accepted 3 February 1998
An Escherichia coli O157:H7 subtyping method based on
PCR amplification of variable DNA sequences between the repetitive
element IS3 was developed. Template DNA was prepared by
boiling cells in Chelex. Two separate IS3 PCR
amplifications were performed for each isolate: one with a single
primer (primer IS3A) and one with two primers (primers IS3A and IS3B).
The IS3 PCR subtyping method was applied to 35 epidemiologically related and unrelated E. coli O157:H7
isolates that had been previously characterized by pulsed-field gel
electrophoresis (PFGE). PFGE identified 25 different subtypes
(difference of one or more bands). PCR with single primer IS3A and
primer pair IS3A-IS3B identified 6 and 14 different subtypes,
respectively. By combining the results of the two PCR amplifications,
15 different IS3 PCR subtypes were identified. While not as
sensitive as PFGE, IS3 PCR subtyping grouped all
outbreak-related isolates. IS3 PCR banding patterns were
reproducible between amplifications and between subcultures. IS3 PCR could serve as a simple, rapid screening method for
the identification of unrelated E. coli O157:H7 isolates.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Insertion Element IS3-Based PCR Method
for Subtyping Escherichia coli O157:H7
*
Corresponding author. Mailing address: State Hygienic
Laboratory, University of Iowa, 102 Oakdale Campus, Iowa City, IA
52242. Phone: (319) 335-4500. Fax: (319) 335-4555. E-mail:
michael-loeffelholz{at}uiowa.edu.
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