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The role of non-structural protein NS3 in the African horse sickness virus infection cycle in mammalian and insect cells

Thesis (PhD)--University of Pretoria, 2020.

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Other Authors: Van Staden, Vida
Format: Thesis
Language:English
Published: University of Pretoria 2020
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access_status_str Open Access
author2 Van Staden, Vida
author_browse Van Staden, Vida
author_facet Van Staden, Vida
collection Thesis
dc_rights_str_mv © 2019 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Thesis (PhD)--University of Pretoria, 2020.
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institution University of Pretoria (South Africa)
language English
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license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2020
publishDateRange 2020
publishDateSort 2020
publisher University of Pretoria
publisherStr University of Pretoria
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source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/75834 The role of non-structural protein NS3 in the African horse sickness virus infection cycle in mammalian and insect cells Van Staden, Vida linda.ferreira2707@gmail.com Theron, Jacques Ferreira-Venter, Linda Genetics Reverse Genetics Animal health UCTD Thesis (PhD)--University of Pretoria, 2020. African horse sickness is an economically important equid disease caused by African horse sickness virus (AHSV). Upon infection, the virus produces seven structural proteins that constitute the virus particle, and four non-structural proteins with various supportive roles during replication. This study focused on the pleiotropic non-structural protein NS3 and its isoform, NS3A. Arthropod-borne viruses are uniquely equipped to replicate in multiple species, often with significant infection cycle differences. Notably, while AHSV infection is highly pathogenic to the mammalian host, the insect vector exhibits no detrimental effect. One potential contributing factor to these observed differences is the viral release mechanism, with NS3/A playing an essential role in mediating these final infection cycle stages. Multiple conserved protein domains have been identified for NS3/A. This study aimed to address questions regarding the way in which these domains contribute to the protein’s function, in mammalian and insect cells, respectively. The initial phase of this study involved augmenting a panel of reverse genetics-derived AHSV NS3mutants. As these viruses each express a modified version of the NS3/A protein, an in-depth investigation into the function of the different conserved domains was possible. Consequently, a comparative analysis of the wild-type and mutant virus strains was conducted in both mammalian and insect cells, using biochemical, virological and microscopy techniques. In mammalian cells, the results indicated a variable contribution of the different NS3/A domains to the cytopathic effect and in ensuring effective virus trafficking and release. The transmembrane (TM) domains were identified as essential mediators of NS3/A intracellular distribution, as the abnormal processing of the TM mutant proteins resulted in their nuclear localisation and unique interaction with another viral protein, NS1. Additionally, the TM domain disruptions resulted in cytosolic virus particle accumulation. A similar mutant phenotype was observed when the C-terminus of NS3/A was deleted, with an apparent lack of efficient virus trafficking and release. Disruption of the NS3/A late domain (LD) resulted in abnormal tethering of virions to the plasma membrane, suggesting that AHSV utilises the cellular ESCRT (Endosomal Sorting Complex Required for Transport) pathway for non-lytic release events within mammalian cells. Comparatively, while some of the NS3/A domains appear to have similar functions within insect cells, key differences were also observed. Most notably, within insect cells, NS3/A localised to the periphery of unique large cytoplasmic vesicle-like structures, likely facilitating non-lytic release. Interestingly, disruption of the TM domains of NS3/A resulted in the degradation of these mutant proteins as they could not be detected within infected cells. Correspondingly, this apparent absence of NS3/A resulted in diminished release, with most of the virus particles remaining cell-associated throughout the course of infection. Notwithstanding normal NS3/A protein localisation, deletion of the C-terminus of NS3/A also prevented proper virus egress. Disruption of the LD did not have any significant effect within insect cells, with no abnormal virus particle localisation and efficient virus release observed. Consequently, in insect cells, virus particle trafficking and release appears independent of characteristic cellular membrane trafficking systems utilised in mammalian cells. National Research Foundation (NRF) Poliomyelitis Research Foundation University of Pretoria Institutional Research Theme Genetics PhD Unrestricted 2020-08-21T08:24:06Z 2020-08-21T08:24:06Z 2020-09-30 2020-04-02 Thesis Ferreira-Venter, L 2020, The role of non-structural protein NS3 in the African horse sickness virus infection cycle in mammalian and insect cells, PhD Thesis, University of Pretoria, Pretoria, viewed yymmdd <http://hdl.handle.net/2263/75834> S2020 http://hdl.handle.net/2263/75834 en © 2019 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle Genetics
Reverse Genetics
Animal health
UCTD
The role of non-structural protein NS3 in the African horse sickness virus infection cycle in mammalian and insect cells
title The role of non-structural protein NS3 in the African horse sickness virus infection cycle in mammalian and insect cells
title_full The role of non-structural protein NS3 in the African horse sickness virus infection cycle in mammalian and insect cells
title_fullStr The role of non-structural protein NS3 in the African horse sickness virus infection cycle in mammalian and insect cells
title_full_unstemmed The role of non-structural protein NS3 in the African horse sickness virus infection cycle in mammalian and insect cells
title_short The role of non-structural protein NS3 in the African horse sickness virus infection cycle in mammalian and insect cells
title_sort role of non structural protein ns3 in the african horse sickness virus infection cycle in mammalian and insect cells
topic Genetics
Reverse Genetics
Animal health
UCTD
url http://hdl.handle.net/2263/75834