SteC is a Salmonella kinase required for SPI-2-dependent F-actin remodelling

Autor: Mei Liu, Ad Spanos, David W. Holden, Paul S. Freemont, Charlotte Odendall, John Poh, Cliona Boyle
Přispěvatelé: Medical Research Council (MRC)
Rok vydání: 2007
Předmět:
Salmonella typhimurium
animal diseases
Mutant
Vacuole
Mice
1108 Medical Microbiology
III SECRETION SYSTEM
0303 health sciences
biology
Virulence
Kinase
Effector
ENTERICA SEROVAR TYPHIMURIUM
Transfection
ESCHERICHIA-COLI
Salmonella enterica
EFFECTORS
RHO-KINASE
Life Sciences & Biomedicine
Sequence Analysis
0605 Microbiology
CHROMOSOMAL GENES
Immunology
Microbiology
Cell Line
03 medical and health sciences
Virology
Animals
Humans
Point Mutation
Secretion
Kinase activity
VACUOLAR MEMBRANE
030304 developmental biology
Science & Technology
Sequence Homology
Amino Acid

030306 microbiology
Macrophages
Epithelial Cells
Cell Biology
STRESS FIBERS
Intracellular Membranes
Original Articles
PROTEIN-KINASE
biochemical phenomena
metabolism
and nutrition

biology.organism_classification
bacterial infections and mycoses
Actins
Mutagenesis
Insertional

Vacuoles
bacteria
Protein Kinases
Gene Deletion
Zdroj: Cellular Microbiology
ISSN: 1462-5822
Popis: Salmonella enterica serovar Typhimurium (S. Typhimurium) replicates inside mammalian cells within membrane‐bound compartments called Salmonella‐containing vacuoles. Intracellular replication is dependent on the activities of several effector proteins translocated across the vacuolar membrane by the Salmonella pathogenicity island 2 (SPI‐2)‐type III secretion system (T3SS). This is accompanied by the formation in the vicinity of bacterial vacuoles of an F‐actin meshwork, thought to be involved in maintaining the integrity of vacuolar membranes. In this study, we investigated the function of the SPI‐2 T3SS effector SteC. An steC mutant strain was not defective for intracellular replication or attenuated for virulence in mice. However, the steC mutant was defective for SPI‐2‐dependent F‐actin meshwork formation in host cells, although the vacuolar membranes surrounding mutant bacteria appeared to be normal. Expression of SteC in fibroblast cells following transfection caused extensive rearrangements of the F‐actin cytoskeleton. Sequence analysis identified amino acid similarity between SteC and the human kinase Raf‐1. A His‐tagged SteC fusion protein had kinase activity in vitro and a point mutant lacking kinase activity was unable to induce F‐actin rearrangements in vivo. We conclude that SPI‐2‐dependent F‐actin meshwork formation depends on the kinase activity of SteC, which resembles more closely eukaryotic than prokaryotic kinases.
Databáze: OpenAIRE