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Journal of Bacteriology, July 2007, p. 4708-4717, Vol. 189, No. 13
0021-9193/07/$08.00+0 doi:10.1128/JB.00299-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Elena Y. Enioutina,2
Raymond A. Daynes,2
Robert L. Sinsheimer,1 and
Michael J. Mahan1*
Department of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, California 93106,1 Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah 841322
Received 27 February 2007/ Accepted 18 April 2007
Salmonella enterica serovar Typhimurium that lacks the DNA adenine methylase (Dam) ectopically expresses multiple genes that are preferentially expressed during infection, is attenuated for virulence, and confers heightened immunity in vaccinated hosts. The safety of dam mutant Salmonella vaccines was evaluated by screening within infected mice for isolates that have an increased capacity to cause disease relative to the attenuated parental strain. Since dam mutant strains are sensitive to the DNA base analog 2-aminopurine (2-AP), we screened for 2-AP-resistant (2-APr) isolates in systemic tissues of mice infected with dam mutant Salmonella. Such 2-APr derivatives were isolated following intraperitoneal but not oral administration and were shown to be competent for infectivity via intraperitoneal but not oral infection of naïve mice. These 2-APr derivatives were deficient in methyl-directed mismatch repair and were resistant to nitric oxide, yet they retained the bile-sensitive phenotype of the parental dam mutant strain. Additionally, introduction of a mutH null mutation into dam mutant cells suppressed the inherent defects in intraperitoneal infectivity and nitric oxide resistance, as well as overexpression of SpvB, an actin cytotoxin required for Salmonella systemic survival. These data suggest that restoration of intraperitoneal virulence of dam mutant strains is associated with deficiencies in methyl-directed mismatch repair that correlate with the production of systemically related virulence functions.
Published ahead of print on 27 April 2007.
Present address: Department of Biology, Westmont College, 955 La Paz Rd., Santa Barbara, CA 93108.
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