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Infection and Immunity, July 2008, p. 3086-3092, Vol. 76, No. 7
0019-9567/08/$08.00+0     doi:10.1128/IAI.00363-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Francisella tularensis subsp. tularensis Schu S4 Disulfide Bond Formation Protein B, but Not an RND-Type Efflux Pump, Is Required for Virulence{triangledown}

Aiping Qin,1 David W. Scott,1 and Barbara J. Mann1,2*

Department of Medicine,1 Department of Microbiology, University of Virginia, Charlottesville, Virginia 229082

Received 20 March 2008/ Returned for modification 22 April 2008/ Accepted 25 April 2008

Francisella tularensis subsp. tularensis is a highly virulent bacterium that is a CDC select agent. Despite advancements in the understanding of its biology, details pertaining to virulence are poorly understood. In previous work, we identified a transposon insertion mutant in the FTT0107c locus that was defective in intracellular survival in HepG2 and J77A.1 cells. Here, we report that this mutant was also highly attenuated in vivo. The FTT0107c locus is predicted to encode an ortholog of the disulfide bond formation B protein (DsbB). This designation was confirmed by complementation of an Escherichia coli dsbB mutant. This dsbB mutant of Schu S4 was highly attenuated in mice, but unlike what has been reported for Francisella novicida, intranasal immunization with a sublethal dose did not induce protection against wild-type challenge. dsbB was found to be transcribed in an operon with acrA and acrB, which encode an RND-type efflux pump. However, this pump did not make a significant contribution to virulence because strains with nonpolar deletions in acrA and acrB behaved like wild-type strain Schu S4 with respect to intracellular growth and in vivo virulence. This result is in contrast to a report that an acrB mutant of a live vaccine strain of F. tularensis has decreased virulence in mice. Overall, these results demonstrate key differences between the virulence requirements of Schu S4 and less virulent subspecies of Francisella. We have shown that DsbB is a key participant in intracellular growth and virulence, and our results suggest that there are critical virulence factors that contain disulfide bonds.


* Corresponding author. Mailing address: University of Virginia Health System, P.O. Box 801364, Charlottesville, VA 22908. Phone: (434) 924-9666. Fax: (434) 924-0075. E-mail: bjm2r{at}virginia.edu

{triangledown} Published ahead of print on 5 May 2008.

Editor: A. J. Bäumler


Infection and Immunity, July 2008, p. 3086-3092, Vol. 76, No. 7
0019-9567/08/$08.00+0     doi:10.1128/IAI.00363-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







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