Complete nucleotide sequence of the prophage VT2-Sakai carrying the verotoxin 2 genes of the enterohemorrhagic Escherichia coli O157:H7 derived from the Sakai outbreak.

Kozo Makino(Osaka University), Katsushi Yokoyama(Osaka University), Yoshino Kubota(Osaka University), Chikako H. Yutsudo(Osaka University), S Kimura(Osaka University), Ken Kurokawa(Osaka University), Kazuo Ishii(Kitasato University), Masahiro Hattori(The University of Tokyo), Ichiro Tatsuno(The University of Tokyo), Hiroyuki Abé(The University of Tokyo), Tetsuya Iida(Osaka University), Koichiro Yamamoto(Osaka University), Makoto Onishi(Shinshu University), Tetsuya Hayashi(Shinshu University), Teruo Yasunaga(Osaka University), Takeshi Honda(Osaka University), Chihiro Sasakawa(The University of Tokyo), Hideo Shinagawa(Osaka University)
Genes & Genetic Systems
January 1, 1999
Cited by 136Open Access
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Abstract

The enterohemorrhagic Escherichia coli (EHEC) O157:H7 strain RIMD 0509952, derived from an outbreak in Sakai city, Japan, in 1996, produces two kinds of verotoxins, VT1 and VT2, encoded by the stx1 and stx2 genes. In the EHEC strains, as well as in other VT-producing E. coli strains, the toxins are encoded by lysogenic bacteriophages. The EHEC O157:H7 strain RIMD 0509952 did not produce plaque-forming phage particles upon inducing treatments. We have determined the complete nucleotide sequence of a prophage, VT2-Sakai, carrying the stx2A and stx2B genes on the chromosome, and presumed the putative functions of the encoded proteins and the cis-acting DNA elements based on sequence homology data. To our surprise, the sequences in the regions of VT2-Sakai corresponding to the early gene regulators and replication proteins, and the DNA sequences recognized by the regulators share very limited homology to those of the VT2-encoding 933W phage carried by the EHEC O157:H7 strain EDL933 reported by Plunkett et al. (J. Bacteriol., p1767-1778, 181, 1999), although the sequences corresponding to the structural components are almost identical. These data suggest that these two phages were derived from a common ancestral phage and that either or both of them underwent multiple genetic rearrangements. An IS629 insertion was found downstream of the stx2B gene and upstream of the lysis gene S, and this might be responsible for the absence of plaque-forming activity in the lysate obtained after inducing treatments.


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