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Infection and Immunity, March 1999, p. 1415-1423, Vol. 67, No. 3
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
The Virulence Plasmid-Encoded impCAB Operon Enhances
Survival and Induced Mutagenesis in Shigella flexneri
after Exposure to UV Radiation
Laura J.
Runyen-Janecky,
Mei
Hong,
and
Shelley M.
Payne*
Department of Microbiology and Institute for
Cellular and Molecular Biology, University of Texas at Austin,
Austin, Texas 78712-1095
Received 7 October 1998/Returned for modification 16 November
1998/Accepted 21 December 1998
Upon exposure to UV radiation, Shigella flexneri SA100
displayed survival and mutation frequencies comparable to those of Escherichia coli AB1157, which contains a functional UmuDC
error-prone DNA repair system. Survival of SA100 after UV
irradiation was associated with the presence of the 220-kb virulence
plasmid, pVP. This plasmid encodes homologues of ImpA and ImpB, which
comprise an error-prone DNA repair system encoded on plasmid TP110 that was initially identified in Salmonella typhimurium, and
ImpC, encoded upstream of ImpA and ImpB. Although the impB
gene was present in representatives of all four species of
Shigella, not all isolates tested contained the gene.
Shigella isolates that lacked impB were more
sensitive to UV radiation than isolates that contained
impB. The nucleotide sequence of a 2.4-kb DNA fragment containing the imp operon from S. flexneri SA100 pVP was 96% identical to the imp
operon from the plasmid TP110. An SA100 derivative with a
mutation in the impB gene had reduced survival following UV
irradiation and less UV-induced mutagenesis relative to the parental
strain. We also found that S. flexneri contained a
chromosomally encoded umuDC operon; however, the
umuDC promoter was not induced by exposure to UV radiation.
This suggests that the imp operon but not the
umuDC operon contributes to survival and induced
mutagenesis in S. flexneri following exposure to UV radiation.
*
Corresponding author. Mailing address: Department of
Microbiology and Institute for Cellular and Molecular Biology,
University of Texas at Austin, Austin, TX 78712-1095. Phone: (512)
471-9258. Fax: (512) 471-7088. E-mail:
payne{at}mail.utexas.edu.

Present address: Chiron Corporation, Emeryville, CA 94608-2916.
Infection and Immunity, March 1999, p. 1415-1423, Vol. 67, No. 3
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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