Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/98693
Type: Theses
Title: Polarity and secretion of Shigella flexneri IcsA: a classical autotransporter
Author: Doyle, Matthew Thomas
Issue Date: 2015
School/Discipline: School of Biological Sciences
Abstract: The classical autotransporter IcsA is an essential virulence factor for the enteropathogen Shigella flexneri as it provides adherence properties and allows intra- and intercellular spreading in the colonic mucosa. IcsA is an outer membrane surface protein that specifically hijacks host-cell actin recruiting and polymerising complexes allowing actin polymerisation as a form of actin-based motility (ABM). Importantly, since IcsA is localised specifically at one end of the bacterium (the pole), the resulting ABM is unidirectional which is a requirement for efficient S. flexneri dissemination. However, the molecular mechanisms that generate IcsA polarity remain poorly understood. Furthermore, IcsA is a member of the autotransporter family of secreted virulence factors (Type Va). Although many steps in the autotransporter pathway have been elucidated, it is still poorly understood how these diverse proteins are efficiently translocated to the bacterial cell surface. As such, this thesis investigates the two arms of IcsA biogenesis: (1) polar targeting and (2) autotransport. Regarding IcsA polarity, it was identified here that the IcsA-specific outer membrane protease IcsP localises to the septa of dividing S. flexneri and to the opposing pole relative IcsA. The concentration of IcsP was higher at the septum than the pole showing a life cycle dependent distribution of IcsP. This provides the basis of a model where IcsP is important during division of S. flexneri for setting up (and the continued maintenance of) IcsA polarity by the proteolysis of misdirected IcsA. Further, multiple previous reports have suggested that the S. flexneri lipopolysaccharide O-antigen surface structure can influence IcsA polarity by augmenting membrane fluidity or by asymmetric masking of IcsA surface exposure. These notions were tested here resulting in data that clearly refutes these models and agues simply that IcsA exposure is masked symmetrically over the bacterial cell surface. Finally, IcsA itself contains polar targeting (PT) regions that direct it to the pole by an, as yet, unclear mechanism. Examination of these regions revealed that the central PT (cPT) is most important in polarity augmentation and contains critical polarity targeting function residues. Regarding IcsA autotransport, a highly conserved but uncharacterised autotransporter motif was scrutinized for potential biogenesis functions and was designated in this work as the passenger-associated transport repeat (PATR). It was found that the PATR plays a critical role in the efficient secretion of IcsA to the cell surface. Strikingly, bioinformatics analyses revealed that the PATR delineates an important separate autotransporter sub-type with unique functions, composition, and architecture.
Advisor: Morona, Renato
Dissertation Note: Thesis (Ph.D.) (Research by Publication) -- University of Adelaide, School of Biological Sciences, 2015.
Keywords: Shigella flexneri
intracellular spread
dysentery
IcsA
Provenance: This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals
Appears in Collections:Research Theses

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