Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.682052
Title: The ubiquitin pathway in host-parasite interactions during infection by Trichinella spiralis
Author: White, Rhiannon Rose
ISNI:       0000 0004 5922 6776
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2014
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Abstract:
These studies present the identification of the first parasite secreted ubiquitin pathway enzyme, and report a system for the characterisation of the role of Trichinella spiralis secreted proteins in the context of mammalian muscle cell re-programming. T. spiralis invade terminally differentiated myofibres, secreting proteins (SP) into the host cell and inducing dedifferentiation and cell cycle re-entry. Since myogenic differentiation and the cell cycle are heavily influenced by the ubiquitin pathway, this study used T. spiralis as a model to investigate the extent to which parasites specifically manipulate the ubiquitin pathway during infection. Ubiquitin is ligated to protein substrates by E1, E2 and E3 enzymes, and removed by deubiquitinating enzymes (DUBs). This ubiquitin 'tag' regulates the fate and function of the substrate protein. A DUB expressed by T. spiralis, TsUCH37, was characterised as a conserved proteasome interaction partner, however no evidence was found of the presence of this, or any other T. spiralis DUB in the muscle larvae SP. Upon further investigation an E2 enzyme, TsUBE2L3, was identified. The ubiquitin conjugation activity of T. spiralis SP was confirmed, and was only possible in the presence of human E1 and E3 enzyme partners. The effect of TsUBE2L3 on mammalian muscle cells was investigated by expressing the T. spiralis protein in a mouse muscle cell line. Although no significant effect on the cell cycle or differentiation state of the muscle cells was observed, TsUBE2L3 expression led to a significant reduction of the tumour suppressor protein, p53 that was confirmed to occur at the protein level. T. spiralis strikes a delicate balance between host cell modulation and host protection. This thesis builds on the proposal that the host-targeted muscle cell modulators of T. spiralis may inspire the development of parasite-derived therapeutics for the treatment of disease.
Supervisor: Artavanis-Tsakonas, Katerina ; Gounaris, Niki Sponsor: Medical Research Council
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.682052  DOI: Not available
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