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Differential requirements for VirB1 and VirB2 during Brucella abortus infection.


ABSTRACT: The Brucella abortus virB operon, encoding a type IV secretion system (T4SS), is required for intracellular replication and persistent infection in the mouse model. The products of the first two genes of the virB operon, virB1 and virB2, are predicted to be localized at the bacterial surface, where they could potentially interact with host cells. Studies to date have focused on characterization of transposon mutations in these genes, which are expected to exert polar effects on downstream genes in the operon. In order to determine whether VirB1 and VirB2 are required for the function of the T4SS apparatus, we constructed and characterized nonpolar deletion mutations of virB1 and virB2. Both mutants were shown to be nonpolar, as demonstrated by their ability to express the downstream gene virB5 during stationary phase of growth in vitro. Both VirB1 and VirB2 were essential for intracellular replication in J774 macrophages. The nonpolar virB2 mutant was unable to cause persistent infection in the mouse model, demonstrating the essential role of VirB2 in the function of the T4SS apparatus during infection. In contrast, the nonpolar virB1 mutant persisted at wild-type levels, showing that the function of VirB1 is dispensable in the mouse model of persistent infection.

SUBMITTER: den Hartigh AB 

PROVIDER: S-EPMC517456 | biostudies-literature | 2004 Sep

REPOSITORIES: biostudies-literature

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Differential requirements for VirB1 and VirB2 during Brucella abortus infection.

den Hartigh Andreas B AB   Sun Yao-Hui YH   Sondervan David D   Heuvelmans Niki N   Reinders Marjolein O MO   Ficht Thomas A TA   Tsolis Renée M RM  

Infection and immunity 20040901 9


The Brucella abortus virB operon, encoding a type IV secretion system (T4SS), is required for intracellular replication and persistent infection in the mouse model. The products of the first two genes of the virB operon, virB1 and virB2, are predicted to be localized at the bacterial surface, where they could potentially interact with host cells. Studies to date have focused on characterization of transposon mutations in these genes, which are expected to exert polar effects on downstream genes  ...[more]

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