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Journal of Bacteriology, February 1999, p. 998-1004, Vol. 181, No. 3
Department of Molecular Microbiology, Howard
Hughes Medical Institute, Washington University School of Medicine,
St. Louis, Missouri 63110
Received 9 October 1998/Accepted 12 November 1998
Pathogenicity islands are chromosomal clusters of pathogen-specific
virulence genes often found at tRNA loci. We have determined the
molecular genetic structure of SPI-3, a 17-kb pathogenicity island
located at the selC tRNA locus of Salmonella
enterica serovar Typhimurium. The G+C content of SPI-3 (47.5%)
differs from that of the Salmonella genome (52%),
consistent with the notion that these sequences have been horizontally
acquired. SPI-3 harbors 10 open reading frames organized in six
transcriptional units, which include the previously described
mgtCB operon encoding the macrophage survival protein MgtC
and the Mg2+ transporter MgtB. Among the newly identified
open reading frames, one exhibits sequence similarity to the ToxR
regulatory protein of Vibrio cholerae and one is similar to
the AIDA-I adhesin of enteropathogenic Escherichia coli.
The distribution of SPI-3 sequences varies among the salmonellae: the
right end of the island, which harbors the virulence gene
mgtC, is present in all eight subspecies of
Salmonella; however, a four-gene cluster at the center of
SPI-3 is found in only some of the subspecies and is bracketed by
remnants of insertion sequences, suggesting a multistep process in the evolution of SPI-3 sequences.
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
The SPI-3 Pathogenicity Island of
Salmonella enterica
*
Corresponding author. Mailing address: Howard Hughes
Medical Institute, Washington University School of Medicine, Department of Molecular Microbiology, 660 South Euclid Ave., Campus Box 8230, St.
Louis, MO 63110. Phone: (314) 362-3692. Fax: (314) 362-1232. E-mail:
groisman{at}borcim.wustl.edu.
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