The role of sorting nexins in macropinocytosis and Salmonella invasion

Qi, Xiaying (2015). The role of sorting nexins in macropinocytosis and Salmonella invasion PhD Thesis, Institute for Molecular Bioscience, The University of Queensland. doi:10.14264/uql.2015.1022

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Author Qi, Xiaying
Thesis Title The role of sorting nexins in macropinocytosis and Salmonella invasion
Formatted title
The role of sorting nexins in macropinocytosis and Salmonella invasion
School, Centre or Institute Institute for Molecular Bioscience
Institution The University of Queensland
DOI 10.14264/uql.2015.1022
Publication date 2015-11-06
Thesis type PhD Thesis
Supervisor Rohan Teasdale
Andrea Bugarcic
Total pages 203
Language eng
Subjects 060109 Proteomics and Intermolecular Interactions (excl. Medical Proteomics)
060108 Protein Trafficking
Formatted abstract
Salmonella enterica serovar Typhimurium (S. Typhimurium) can invade non- phagocytic epithelial cells by injecting virulence factors into the host cell via a type III secretion system (T3SS) to induce macropinocytosis. However, the precise molecular processes that lead to this uptake are currently unknown. In this thesis I show that several sorting nexin (SNX) proteins, i.e. SNX18, SNX20 and SNX21, are involved in Salmonella invasion and examined their molecular action during this process.

First I demonstrated that after docking at the plasma membrane S. Typhimurium triggers rapid translocation of cytosolic SNX18, a SH3-PX-BAR domain sorting nexin protein, to the bacteria-induced membrane ruffles and to the nascent Salmonella-containing vacuole (SCV). SNX18 recruitment required the inositol- phosphatase activity of the Salmonella T3SS effector SopB and an intact phosphoinositide-binding site within the PX domain of SNX18, but occurred independently of Rho-GTPases Rac1 and Cdc42 activation. I also demonstrate that SNX18 promotes formation of the SCV from the plasma membrane by acting as a scaffold to recruit Dynamin-2 and N-WASP in a process dependent on the SH3 domain of SNX18. Quantification of bacteria uptake revealed that overexpression of the full-length SNX18 increased the efficiency of bacteria internalization, whereas a decrease was detected in cells overexpressing the phosphoinositide-binding mutant R303Q, the ΔSH3 mutant, and in cells where endogenous levels of SNX18 were knocked-down by shRNA. This study identifies SNX18 as a novel target of SopB and suggests a mechanism where S. Typhimurium engages host factors via local manipulation of phosphoinositide composition at the site of invasion to orchestrate the internalization process.

Secondly, I investigated the molecular details of SNX18 recruitment to the plasma membrane during the Salmonella invasion process. As we identified a significant cytosolic pool of SNX18 which can translocate to the site of S. Typhimurium invasion, we hypothesized that cytosolic SNX18 represents a closed auto-inhibited form where the N-terminal SH3 domain and adjacent low complexity (LC) region fold back onto the C-terminal PX-BAR domains. The cytosolic SNX18 required a conformational change into an open form, exposing the phosphoinositide-binding site for interaction with membrane. We also show that the bacteria-induced translocation of SNX18 is necessary but not sufficient for transient SNX18 phosphorylation. The LC domain of SNX18 functions in maintenance of the cytosol/membrane equilibrium of the protein and contains a not yet specified kinase binding motif and/or phosphosite(s). Screen for novel SNX18-specific interaction partners identified α- actinin-4 (ACTN4), a potential regulator for macropinocytosis and pathogen invasion as well. Though ACTN4 is recruited to the Salmonella induced ruffles, its recruitment is independent from SNX18 recruitment. And Akt translocation and phosphorylation induced by Salmonella invasion does not rely on SNX18 or ACTN4. Above all, this chapter provides an insight into the role of SNX18 as a scaffolding protein involved in plasma membrane remodeling and into manipulation of this process by bacterial pathogen.

Finally, I commenced characterization of another SNX subfamily that contains SNX20 and SNX21 as potential regulators of Salmonella invasion. The study found that SNX20 and SNX21 localized to early endosomes in mammalian cells and the intact phosphoinositide-binding site in the PX domain is necessary for the localisation. S. Typhimurium could also recruit both SNX20 and SNX21 to the newly formed SCVs. However, live cell imaging demonstrated that the association between SNX20 or SNX21 with endosomes or SCVs is very transient. This suggested a role of SNX20 and SNX21 in early time points of endocytic process and pathogen internalization and vacuole maturation.
Keyword Macropinocytosis
Sorting nexin (SNX)
S. Typhimurium

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Created: Thu, 22 Oct 2015, 20:50:41 EST by Xiaying Qi on behalf of Scholarly Communication and Digitisation Service