Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.597592
Title: Rotavirus inclusion bodies ('viroplasms') are structurally and functionally associated with lipid droplet components
Author: Cheung, W. K. S.
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 2011
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Abstract:
Rotaviruses are a leading cause of acute gastroenteritis in infants and young children worldwide and possess a genome of 11 double-stranded (ds) RNA segments. Early morphogenesis of RV particles and viral RNA replication occur in cytoplasmic inclusion bodies called ‘viroplasms’, of which the viral non-structural proteins NSP2 and NSP5 are essential components. Using confocal microscopy (CM), we demonstrated association of viroplasms with lipids and lipid droplet (LD)-associated proteins (perilipin A, ADRP). LD-associated proteins were found to co-localise with viroplasm-like structures (VLS) in cells co-transfected with NSP2- and NSP5- expressing plasmids in the absence of rotavirus infection, as well as viroplasms containing NSP5-EGFP. Close spatial proximity between NSP5-EGFP and perilipin A was demonstrated by Fluorescence Resonance Energy Transfer (FRET). Time course CM studies showed increasing recruitment of perilipin A to viroplasms during the progression of rotavirus infection. Separation of RV-infected cell extracts on iodixanol gradients demonstrated co-localisation of rotavirus dsRNA, NSP5 and perilipin A in low density fractions. Chemical compounds interfering with LD formation or homeostasis (isoproterenol + IBMX, triacsin C, C75) decreased the number and size of viroplasms in rotavirus-infected cells, dsRNA replication and the production of infectious progeny virus, whilst significantly protecting cells from cytopathicity caused by rotavirus infection. These data contribute to a novel understanding of the role of LDs in rotavirus replication. Using a cell line stably expressing NSP5-EGFP, the dynamics of viroplasm formation in relation to dsRNA replication and production of infectious virus was investigated.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.597592  DOI: Not available
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