Infection and Immunity, November 2002, p. 6365-6372, Vol. 70, No. 11
0019-9567/02/$04.00+0 DOI: 10.1128/IAI.70.11.6365-6372.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Genetic Structure and Distribution of Four Pathogenicity Islands (PAI I536 to PAI IV536) of Uropathogenic Escherichia coli Strain 536
Ulrich Dobrindt,1 Gabriele Blum-Oehler,1 Gabor Nagy,1,2 György Schneider,1 André Johann,3 Gerhard Gottschalk,3 and Jörg Hacker1*
Institut für Molekulare Infektionsbiologie, Universität Würzburg, D-97070 Würzburg,1
Institut für Mikrobiologie und Genetik, Labor für Genomanalysen, Universität Göttingen, 37077 Göttingen, Germany,3
Department of Medical Microbiology and Immunology, University Medical School, Pécs, Hungary2
Received 29 May 2002/
Returned for modification 8 July 2002/
Accepted 29 July 2002
For the uropathogenic Escherichia coli strain 536 (O6:K15:H31), the DNA sequences of three pathogenicity islands (PAIs) (PAI I536 to PAI III536) and their flanking regions (about 270 kb) were determined to further characterize the virulence potential of this strain. PAI I536 to PAI III536 exhibit features typical of PAIs, such as (i) association with tRNA-encoding genes; (ii) G+C content differing from that of the host genome; (iii) flanking repeat structures; (iv) a mosaic-like structure comprising a multitude of functional, truncated, and nonfunctional putative open reading frames (ORFs) with known or unknown functions; and (v) the presence of many fragments of mobile genetic elements. PAI I536 to PAI III536 range between 68 and 102 kb in size. Although these islands contain several ORFs and known virulence determinants described for PAIs of other extraintestinal pathogenic E. coli (ExPEC) isolates, they also consist of as-yet-unidentified ORFs encoding putative virulence factors. The genetic structure of PAI IV536, which represents the core element of the so-called high-pathogenicity island encoding a siderophore system initially identified in pathogenic yersiniae, was further characterized by sample sequencing. For the first time, multiple PAI sequences (PAI I536 to PAI IV536) in uropathogenic E. coli were studied and their presence in several wild-type E. coli isolates was extensively investigated. The results obtained suggest that these PAIs or at least large fragments thereof are detectable in other pathogenic E. coli isolates. These results support our view that the acquisition of large DNA regions, such as PAIs, by horizontal gene transfer is an important factor for the evolution of bacterial pathogens.
* Corresponding author. Mailing address: Institut für Molekulare Infektionsbiologie, Röntgenring 11, D-97070 Würzburg, Germany. Phone: 49 (0)931 312575. Fax: 49 (0)931 312578. E-mail: j.hacker{at}mail.uni-wuerzburg.de.
Editor: J. T. Barbieri
Infection and Immunity, November 2002, p. 6365-6372, Vol. 70, No. 11
0019-9567/02/$04.00+0 DOI: 10.1128/IAI.70.11.6365-6372.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
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Copyright © 2002 by the American Society for Microbiology. All rights reserved.