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Appl. Environ. Microbiol., Mar 1996, 791-797, Vol 62, No. 3
M Datz, C Janetzki-Mittmann, S Franke, F Gunzer, H Schmidt and H Karch
In this study, we determined the nucleotide sequence of the p gene
contained within a 5-kb EcoRI restriction fragment cloned from Shiga- like
toxin II (SLT-II)-converting phage 933W of Escherichia coli O157:H7 strain
EDL933. The p gene was 702 bp long and had 95.3% sequence similarity to the
p gene of phage lambda. Multiple hybridization patterns were obtained when
genomic DNA fragments were hybridized with both p and slt-I, slt-II, or
slt-IIc sequences. All O157 isolates also possessed an analog of lambda
gene p which was not linked with either slt-I or slt-II. Restriction
fragment length polymorphism comparisons of clinical O157 isolates and
derivates undergoing genotype turnover during infection were made, and loss
of large DNA fragments that hybridized with slt-II and p sequences was
observed. To further analyze the DNA region containing the p and slt genes,
we amplified fragments by using a PCR with one primer complementary to p
and the other complementary to either the slt-I or the slt-II gene. PCR
analysis with enterohemorrhagic E. coli O157 and non-O157 strains yielded
PCR products that varied in size between 5.1 and 7.8 kb. These results
suggest that even within O157 isolates, the genomes of SLT-converting
phages differ. The methods described here may assist in further
investigation of SLT-encoding phages and their role in the epidemiology of
infection with enterohemorrhagic E. coli.
Copyright © 1996, American Society for Microbiology
Analysis of the enterohemorrhagic Escherichia coli O157 DNA region containing lambdoid phage gene p and Shiga-like toxin structural genes
Institut fur Hygiene und Mikrobiologie der Universitat Wurzburg, Germany.
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