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Infect Immun, April 1998, p. 1735-1739, Vol. 66, No. 4
Department of Biochemistry, Fralin Center for
Biotechnology, Virginia Polytechnic Institute and State University,
Blacksburg, Virginia 24061-0346
Received 22 October 1997/Returned for modification 21 November
1997/Accepted 3 January 1998
Enterotoxigenic strains of Bacteroides fragilis produce
an extracellular metalloprotease toxin (termed fragilysin) which is cytopathic to intestinal epithelial cells and induces fluid secretion and tissue damage in ligated intestinal loops. We report here that the
fragilysin gene is contained within a small genetic element termed the
fragilysin pathogenicity islet. The pathogenicity islet of B. fragilis VPI 13784 was defined as 6,033 bp in length and contained nearly perfect 12-bp direct repeats near its ends. Sequencing across the ends of the pathogenicity islet from two additional enterotoxigenic strains, along with PCR analysis of 20 additional enterotoxigenic strains, revealed that the islet is inserted at a
specific site on the B. fragilis chromosome. The site of
integration in three nontoxigenic strains contained a 17-bp GC-rich
sequence which was not present in toxigenic strains and may represent a target sequence for chromosomal integration. In addition to the fragilysin gene, we identified an open reading frame encoding a
predicted protein with a size and structural features similar to those
of fragilysin. The deduced amino acid sequence was 28.5% identical and
56.3% similar to fragilysin and contained a nearly identical
zinc-binding motif and methionine-turn region.
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Molecular Characterization of the Fragilysin
Pathogenicity Islet of Enterotoxigenic Bacteroides
fragilis
*
Corresponding author. Mailing address: Department of
Biochemistry, Fralin Center for Biotechnology, Virginia Polytechnic
Institute and State University, Blacksburg, VA 24061-0346. Phone: (540) 231-5094. Fax: (540) 231-7126. E-mail: jmoncrie{at}vt.edu.
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