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Journal of Bacteriology, July 2008, p. 4427-4436, Vol. 190, No. 13
0021-9193/08/$08.00+0     doi:10.1128/JB.00406-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

VirB3 to VirB6 and VirB8 to VirB11, but Not VirB7, Are Essential for Mediating Persistence of Brucella in the Reticuloendothelial System{triangledown}

Andreas B. den Hartigh, Hortensia G. Rolán, Maarten F. de Jong, and Renée M. Tsolis*

University of California, Davis, Department of Medical Microbiology and Immunology, Davis, California 95616

Received 21 March 2008/ Accepted 28 April 2008

The Brucella abortus virB locus contains 12 open reading frames, termed virB1 through virB12, which encode a type IV secretion system. Polar mutations in the virB locus markedly reduce the ability of B. abortus to survive in cultured macrophages or to persist in organs of mice. While a nonpolar deletion of the virB2 gene reduces survival in cultured macrophages and in organs of mice, a nonpolar deletion of virB1 only reduces survival in macrophages, whereas virB12 is dispensable for either virulence trait. Here we investigated the role of the remaining genes in the virB locus during survival in macrophages and virulence in mice. Mutants carrying nonpolar deletions of the virB3, virB4, virB5, virB6, virB7, virB8, virB9, virB10, or virB11 gene were constructed and characterized. All mutations reduced the ability of B. abortus to survive in J774A.1 mouse macrophage-like cells to a degree similar to that caused by a deletion of the entire virB locus. Deletion of virB3, virB4, virB5, virB6, virB8, virB9, virB10, or virB11 markedly reduced the ability of B. abortus to persist in the spleens of mice at 8 weeks after infection. Interestingly, deletion of virB7 did not reduce the ability of B. abortus to persist in spleens of mice. We conclude that virB2, virB3, virB4, virB5, virB6, virB8, virB9, virB10, and virB11 are essential for virulence of B. abortus in mice, while functions encoded by the virB1, virB7, and virB12 genes are not required for persistence in organs with this animal model.

* Corresponding author. Mailing address: University of California, Davis, Department of Medical Microbiology and Immunology, Davis, CA 95616. Phone: (530) 754-8497. Fax: (530) 754-7240. E-mail: rmtsolis{at}ucdavis.edu

{triangledown} Published ahead of print on 9 May 2008.

Journal of Bacteriology, July 2008, p. 4427-4436, Vol. 190, No. 13
0021-9193/08/$08.00+0     doi:10.1128/JB.00406-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.





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