Integrating global regulatory input into the Salmonella pathogenicity island 1 type III secretion system

Genetics. 2012 Jan;190(1):79-90. doi: 10.1534/genetics.111.132779. Epub 2011 Oct 20.

Abstract

Salmonella enterica serovar Typhimurium uses the Salmonella pathogenicity island 1 (SPI1) type III secretion system to induce inflammatory diarrhea and bacterial uptake into intestinal epithelial cells. The expression of hilA, encoding the transcriptional activator of the SPI1 structural genes, is directly controlled by three AraC-like regulators, HilD, HilC, and RtsA, each of which can activate the hilD, hilC, rtsA, and hilA genes, forming a complex feed-forward regulatory loop. A large number of factors and environmental signals have been implicated in SPI1 regulation. We have developed a series of genetic tests that allows us to determine where these factors feed into the SPI1 regulatory circuit. Using this approach, we have grouped 21 of the known SPI1 regulators and environmental signals into distinct classes on the basis of observed regulatory patterns, anchored by those few systems where the mechanism of regulation is best understood. Many of these factors are shown to work post-transcriptionally at the level of HilD, while others act at the hilA promoter or affect all SPI1 promoters. Analysis of the published transcriptomic data reveals apparent coregulation of the SPI1 and flagellar genes in various conditions. However, we show that in most cases, the factors that affect both systems control SPI1 independently of the flagellar protein FliZ, despite its role as an important SPI1 regulator and coordinator of the two systems. These results provide a comprehensive model for SPI1 regulation that serves as a framework for future molecular analyses of this complex regulatory network.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Bacterial Secretion Systems / genetics*
  • Gene Expression Regulation, Bacterial*
  • Genomic Islands*
  • Peptide Chain Initiation, Translational
  • Promoter Regions, Genetic
  • Protein Processing, Post-Translational
  • RNA Stability
  • RNA, Messenger / metabolism
  • Salmonella typhimurium / genetics*
  • Salmonella typhimurium / metabolism*
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Bacterial Proteins
  • Bacterial Secretion Systems
  • HilA protein, Salmonella
  • HilD protein, Salmonella typhimurium
  • RNA, Messenger
  • Spi1 protein, Salmonella
  • Trans-Activators
  • Transcription Factors