Genes encoding putative effector proteins of the type III secretion system of <i>Salmonella</i> pathogenicity island 2 are required for bacterial virulence and proliferation in macrophages

TLDR

The SPI‑2 type III secretion system is essential for systemic infection in mice, and its sseB, sseC, and sseD genes encode proteins homologous to known T3SS effectors EspA, EspD, and EspB. Mutagenesis of sseA, sseB, and sseC abolishes virulence and macrophage proliferation, while mutations in sseE, sseF, and sseG have little effect, indicating SPI‑2 promotes intracellular bacterial growth.

Abstract

The type III secretion system of Salmonella pathogenicity island 2 (SPI‐2) is required for systemic infection of this pathogen in mice. Cloning and sequencing of a central region of SPI‐2 revealed the presence of genes encoding putative chaperones and effector proteins of the secretion system. The predicted products of the sseB , sseC and sseD genes display weak but significant similarity to amino acid sequences of EspA, EspD and EspB, which are secreted by the type III secretion system encoded by the locus of enterocyte effacement of enteropathogenic Escherichia coli . The transcriptional activity of an sseA :: luc fusion gene was shown to be dependent on ssrA , which is required for the expression of genes encoding components of the secretion system apparatus. Strains carrying non‐polar mutations in sseA , sseB or sseC were severely attenuated in virulence, strains carrying mutations in sseF or sseG were weakly attenuated, and a strain with a mutation in sseE had no detectable virulence defect. These phenotypes were reflected in the ability of mutant strains to grow within a variety of macrophage cell types: strains carrying mutations in sseA , sseB or sseC failed to accumulate, whereas the growth rates of strains carrying mutations in sseE , sseF or sseG were only modestly reduced. These data suggest that, in vivo , one of the functions of the SPI‐2 secretion system is to enable intracellular bacterial proliferation.