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Nature reviews Microbiology January 2008. Salmonella sp. Gram-negative Enterobacteria D iameter 0.7 - 1.5 µm S. enterica serovar Typhimurium serovar Typhi. Diseases range from mild diarrhoea to severe typhoid fever. WHO : typhoid fever 16 million cases of per year
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Nature reviews Microbiology January 2008
Salmonella sp. Gram-negative Enterobacteria Diameter0.7 - 1.5 µm S. enterica serovar Typhimurium serovar Typhi Diseases range from mild diarrhoea to severe typhoid fever WHO: typhoid fever 16 million cases of per year 600 000 fatal cases Ways of acquirement: - Contaminated food and water - Exposure to reptiles and amphibians Daniel Elmer Salmon Theobald Smith
Salmonellae preferably enter microfold (M) cellsin the small intestine Severe acute necrotizing enteritis Normal Peyer’s patches and ileum Non typhoid strain infection is limited to intestine Some Salmonella serotypes can cause systemic illness
Virulence-associated type III secretion system (T3SS) • mediates the transfer of bacterial proteins into the host cell • found only in Gram-negative, mostly inpathogenic bacteria • evolutionary related to flagellar system T3SS Flagellum
Needle complex (NC) 9 KDa T3S proteins 100-150 subunits Length: 60-80 nm Width:8 nm Inner diameter: 3 nm Proteins – effectors: N-terminal secretion signal Binding site for chaperone Chaperones can act as transcription factors
Two distinct T3SSs are encoded within Salmonella pathogenecity islands (SPI)
Salmonella SPI1 encoded type III secretion system and it’s effectors
SPI 1 T3SS Activation of the Rho GTPases Actin cytoskeleton rearrangement Bacterial-mediated endocytosis
Salmonella SPI1 encoded type III secretion system and it’s effectors
SPI 1 T3SS Tight junctions destabilization Transepithelial migration Intestinal inflammatory responses Normal structure regainment Salmonellae might be evolving towards parasitism or commensalism
Effectors of the Salmonella SPI2 encoded type III secretion system
Salmonella containing vesicles (SCV) and SPI 2 T3SS SCV – unique phagosome, can persist intracellularly up to several days Associated with early, late endosomal as well as lysosomal markers Moves to perinuclear position, associated with Golgi SCV is believed to be a niche for Salmonellae replication
Effectors of the Salmonella SPI2 encoded type III secretion system
Formation of the Salmonella induced filaments (Sifs) Sifs - originate from the SCV and extend throughout the cell Possible mechanism - vesicle budding from SCV Requires microtubules, kinesin, dynein, Salmonella SifA and PipB2 effectors • The importance of the Sif formation is currently not understood • promotes bacterial replication via increasing the size of the SCV • redirects nutrient-rich organellas to the SCV
Sensing and response to the vacuole 919 genes in S. typhimurium are upregulated in phagosome Antimicrobial peptides: PhoQ sensor and surface remodelling Decreasing length of the O antigen Alterations in lipid A Oxygen and nitrogen radicals: Cu,Zn superoxid dismutases LPS
Summary • Salmonellae encode two virulence-associated T3SS: • SPI 1 T3SS translocates effectors across the plasma membrane • - rearrangement of the actin cytoskeleton • destabilization of the tight junctions • - entry into non-phagocytic cells by bacterial-mediated endocytosis • - partial blocking of the NF-kB activity • SPI 2 T3SS translocates effectors across the vacuolar membrane • Sif formation • SCV movement to perinuclear position • rearrangement of the cell organells • transport of metabolic molecules into the SCV • promotes bacterial replication within host cell • Salmonellae can sense phagosomal environment and are able to induce various systems to promote intracellular survival