AI Article Synopsis

  • Type III protein secretion is crucial for the virulence of Gram-negative bacteria, particularly in Salmonella enterica serotype Typhimurium (S. Typhimurium), with its genetic components found in pathogenicity islands or virulence plasmids.
  • Analysis of the Type III secretion system from Salmonella Pathogenicity Island 2 (SPI2) revealed its essential role in causing systemic disease in mice, despite challenges in studying low abundance proteins directly through proteomics.
  • Recombinant expression and two-dimensional electrophoresis were employed to create a protein map of SPI2, and pulse labeling was vital for identifying growth phase-regulated proteins that are typically difficult to detect.

Article Abstract

Type III protein secretion is a common virulence determinant in Gram-negative bacteria and the genetic information is often clustered in pathogenicity islands or on virulence plasmids. We have analyzed the type III secretion system encoded by Salmonella Pathogenicity Island 2 (SPI2) that is indispensable for systemic disease of Salmonella enterica serotype Typhimurium (S. Typhimurium) in mice. Since the low abundance of this secretion system restricted direct analysis by proteomic approaches, several putative proteins were expressed as recombinant products and analyzed by two-dimensional electrophoresis. The map obtained for SPI2 encoded proteins was correlated to the expression pattern of S. Typhimurium. The latter was compared to the proteins induced by SsrAB, the two-component system regulating SPI2 gene expression. Our results exemplify that recombinant expression is a complementary tool for analysis of low abundant proteins or membrane proteins. This approach contributes to the characterization of these proteins by subcellular fractionation. Furthermore, we show that pulse labeling was necessary to analyze growth phase regulated SPI2 proteins that might not be otherwise detectable.

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http://dx.doi.org/10.1002/1615-9861(200206)2:6<792::AID-PROT792>3.0.CO;2-VDOI Listing

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