2013
DOI: 10.1016/j.resmic.2013.03.019
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Structural basis of eukaryotic cell targeting by type III secretion system (T3SS) effectors

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Cited by 24 publications
(20 citation statements)
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“…However, various studies have shown that some type III effectors from plant-and animal-pathogenic bacteria would exert similar functions in eukaryotic host cells (5). These functions would include the manipulation of Rho GTPases and the ubiquitination cascade, proteolysis, and acetylation of host proteins as well as the disruption of the target membrane or phosphorylation/dephosphorylation of cellular targets, among others (6).…”
mentioning
confidence: 99%
“…However, various studies have shown that some type III effectors from plant-and animal-pathogenic bacteria would exert similar functions in eukaryotic host cells (5). These functions would include the manipulation of Rho GTPases and the ubiquitination cascade, proteolysis, and acetylation of host proteins as well as the disruption of the target membrane or phosphorylation/dephosphorylation of cellular targets, among others (6).…”
mentioning
confidence: 99%
“…15,45 Invasive pathogens (e.g., Salmonella spp., Shigella spp, and enterohemorrhagic or enteroinvasive Escherichia coli) use their needle-like type III secretion systems to inject effector proteins into epithelial cells, and subsequently manipulate the host cytoskeletal actins for anchorage and entry. 50 In contrast to pathogens with specialized machinery to invade cells, the lipid raft/caveolae-mediated pathway was utilized by noninvasive mucosal bacteria to penetrate cells by hijacking the host endocytic machinery. These studies pinpointed the location of the portal as lipid rafts on apical membrane invaginations, but have left open the question of how bacteria pass through the BB and gain access to the base of the intermicrovillous cleft.…”
Section: Mechanisms Of Intestinal Bacterial Endocytosis By Epithelialmentioning
confidence: 99%
“…A key component of the T3S system is the needle-like structure that spans both bacterial membranes and through which effectors are delivered directly into the cytosol of host cells (1,3,4). The needle is formed by the polymerization of single proteins: YscF in Yersinia spp., PrgI and SsaG (Salmonella pathogenicity island 1 (SPI-1) and Salmonella pathogenicity island 2 (SPI-2), respectively) in Salmonella enterica serovar Typhimurium, PscF in Pseudomonas spp., and MxiH in Shigella flexneri (3)(4)(5)(6)(7)(8).…”
mentioning
confidence: 99%
“…The needle is formed by the polymerization of single proteins: YscF in Yersinia spp., PrgI and SsaG (Salmonella pathogenicity island 1 (SPI-1) and Salmonella pathogenicity island 2 (SPI-2), respectively) in Salmonella enterica serovar Typhimurium, PscF in Pseudomonas spp., and MxiH in Shigella flexneri (3)(4)(5)(6)(7)(8). X-ray crystallography and nuclear magnetic resonance (NMR) have been utilized to analyze structures of several needle proteins: MxiH from Shigella (9), BsaL from Burkholderia pseudomallei (10), and PrgI from Salmonella Typhimurium (11).…”
mentioning
confidence: 99%
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