Studies into the effects of the vaccinia virus protein A46R on Interleukin-1/Toll-Like receptor signalling pathways

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Trinity College (Dublin, Ireland). School of Biochemistry and Immunology

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Julianne Stack, 'Studies into the effects of the vaccinia virus protein A46R on Interleukin-1/Toll-Like receptor signalling pathways', [thesis], Trinity College (Dublin, Ireland). School of Biochemistry and Immunology, 2005, pp 330

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Poxviruses circumvent the host immune response by encoding proteins that can antagonise host defence mechanisms. The vaccinia virus (VV) protein, A46R, was identified based on sequence similarity to the Toll/Interleukin-1/Resistance homology (TIR) domain, the cytosolic signalling domain of the interleukin-1 receptor (IL-IR ) and Toll-like receptors (TLRs). TLRs play a crucial role in host defence against invading micro-organisms by mediating pro-inflammatory signalling cascades, mainly through their cytoplasmic TIR domains. A46R is the only viral protein so far identified to have a TIR domain. Initial studies revealed that A46R could inhibit IL-1, but not tumour necrosis factor (TNF) a-induced NFkB activation (Bowie et al, 2000), suggesting a role for the protein in immune evasion. This study shows that A46R also blocked multiple signals em anating from TLR4, suggesting that it was acting on a molecule close to the receptor complex that was also required for IL-1 signalling. Immunoprecipitation and GST-pulldown experiments revealed that A46R targeted MyD88, a TIR adaptor molecule used by both IL-1 and TLR4, while further studies showed A46R blocked MyD88-dependent pathways in murine macrophages. This is the first example of a viral protein targeting MyD88.

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Qualification name: Doctor of Philosophy (Ph.D.)
Publisher: Trinity College (Dublin, Ireland). School of Biochemistry and Immunology
Type of material: thesis