Complementary activities of SseJ and SifA regulate dynamics of the Salmonella typhimurium vacuolar membrane

• Published in: Molecular microbiology 2002-05, Vol.44 (3), p.645-661
• Main Authors: Ruiz‐Albert, Javier, Yu, Xiu‐Jun, Beuzón, Carmen R., Blakey, Abigail N., Galyov, Edouard E., Holden, David W.
• Format: Article
• Language: English
• Subjects: Animals; Bacterial Proteins - genetics; Bacterial Proteins - physiology; Base Sequence; Cell Division; Female; Glycoproteins - genetics; Glycoproteins - physiology; HeLa Cells - microbiology; HeLa Cells - ultrastructure; Humans; Intracellular Membranes - metabolism; Lipase - genetics; Lipase - physiology; Macrophages, Peritoneal - microbiology; Macrophages, Peritoneal - ultrastructure; Membrane Lipids - metabolism; Membrane Proteins - metabolism; Mice; Mice, Inbred BALB C; Molecular Sequence Data; Recombinant Fusion Proteins - metabolism; Salmonella Infections, Animal - microbiology; Salmonella Infections, Animal - pathology; Salmonella typhimurium; Salmonella typhimurium - genetics; Salmonella typhimurium - growth & development; Salmonella typhimurium - metabolism; Salmonella typhimurium - pathogenicity; SifA protein; sifB gene; srfJ gene; sseI gene; sseJ gene; SseJ protein; Vacuoles - metabolism; Vacuoles - microbiology; Virulence
• ISSN: 0950-382X; 1365-2958
• DOI: 10.1046/j.1365-2958.2002.02912.x

Summary The Salmonella pathogenicity island 2 (SPI‐2) type III secretion system (TTSS) of Salmonella typhimurium is required for bacterial replication within host cells. It acts by translocating effector proteins across the membrane of the Salmonella‐containing vacuole (SCV). The SifA effector is required to maintain the integrity of the SCV membrane, and for the formation in epithelial cells of Salmonella‐induced filaments (Sifs), which are tubular extensions of SCVs. We have investigated the role in S. typhimurium virulence of the putative SPI‐2 effector genes sifB, srfJ, sseJ and sseI. An S. typhimurium strain carrying a mutation in sseJ was mildly attenuated for systemic virulence in mice, but strains carrying mutations in either srfJ, sseI or sifB had very little or no detectable virulence defect after intraperitoneal inoculation. Expression of SseJ in HeLa cells resulted in the formation of globular membranous compartments (GMCs), the composition of which appears to be similar to that of SCV membranes and Sifs. The formation of GMCs was dependent on the serine residue of the predicted acyltransferase/lipase active site of SseJ. Transiently expressed SseJ also inhibited Sif formation by wild‐type bacteria, and was found to associate with Sifs, SCV membranes and simultaneously expressed SifA. Intracellular vacuoles containing sseJ mutant bacteria appeared normal but, in contrast to a sifA mutant, a sifA sseJ double mutant strain did not lose its vacuolar membrane, indicating that loss of vacuolar membrane around sifA mutant bacteria requires the action of SseJ. Collectively, these results suggest that the combined action of SseJ and SifA regulate dynamics of the SCV membrane in infected cells.