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RtsA and RtsB coordinately regulate expression of the invasion and flagellar genes in Salmonella enterica serovar Typhimurium
Journal article   Open access   Peer reviewed

RtsA and RtsB coordinately regulate expression of the invasion and flagellar genes in Salmonella enterica serovar Typhimurium

Craig D Ellermeier and James M Slauch
Journal of bacteriology, Vol.185(17), pp.5096-5108
09/2003
DOI: 10.1128/JB.185.17.5096-5108.2003
PMCID: PMC181000
PMID: 12923082
url
https://doi.org/10.1128/JB.185.17.5096-5108.2003View
Published (Version of record) Open Access

Abstract

Salmonella enterica serovar Typhimurium encounters numerous host environments and defense mechanisms during the infection process. The bacterium responds by tightly regulating the expression of virulence genes. We identified two regulatory proteins, termed RtsA and RtsB, which are encoded in an operon located on an island integrated at tRNA(PheU) in S. enterica serovar Typhimurium. RtsA belongs to the AraC/XylS family of regulators, and RtsB is a helix-turn-helix DNA binding protein. In a random screen, we identified five RtsA-regulated fusions, all belonging to the Salmonella pathogenicity island 1 (SPI1) regulon, which encodes a type III secretion system (TTSS) required for invasion of epithelial cells. We show that RtsA increases expression of the invasion genes by inducing hilA expression. RtsA also induces expression of hilD, hilC, and the invF operon. However, induction of hilA is independent of HilC and HilD and is mediated by direct binding of RtsA to the hilA promoter. The phenotype of an rtsA null mutation is similar to the phenotype of a hilC mutation, both of which decrease expression of SPI1 genes approximately twofold. We also show that RtsA can induce expression of a SPI1 TTSS effector, slrP, independent of any SPI1 regulatory protein. RtsB represses expression of the flagellar genes by binding to the flhDC promoter region. Repression of the positive activators flhDC decreases expression of the entire flagellar regulon. We propose that RtsA and RtsB coordinate induction of invasion and repression of motility in the small intestine.
Promoter Regions, Genetic Salmonella typhimurium - genetics Salmonella typhimurium - pathogenicity Salmonella typhimurium - growth & development Humans Virulence Bacterial Proteins - genetics Repressor Proteins - genetics Helix-Loop-Helix Motifs Transcription Factors - genetics DNA-Binding Proteins - genetics AraC Transcription Factor Salmonella typhimurium - metabolism DNA-Binding Proteins - metabolism Transcription Factors - metabolism Flagella - metabolism Trans-Activators - genetics Bacterial Proteins - metabolism Trans-Activators - metabolism Flagella - genetics Gene Expression Regulation, Bacterial Repressor Proteins - metabolism

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