SORA

Advancing, promoting and sharing knowledge of health through excellence in teaching, clinical practice and research into the prevention and treatment of illness

Classical swine fever virus Npro antagonises IRF3 to prevent IFN-independent TLR3 and RIG-I-mediated apoptosis

Hardy, S; Jackson, B; Goodbourn, SE; Seago, J (2021) Classical swine fever virus Npro antagonises IRF3 to prevent IFN-independent TLR3 and RIG-I-mediated apoptosis. JOURNAL OF VIROLOGY, 95 (5). e01136-20. ISSN 0022-538X https://doi.org/10.1128/JVI.01136-20
SGUL Authors: Goodbourn, Stephen Edward

[img]
Preview
PDF Accepted Version
Available under License Creative Commons Attribution.

Download (2MB) | Preview

Abstract

Classical swine fever virus (CSFV) is the causative agent of classical swine fever,a notifiable disease of economic importance that causes severe leukopenia, fever and haemorrhagic disease in domesticated pigs and wild boar across the globe. CSFV has been shown to antagonise the induction of type I IFN, partly through a function of its N-terminal protease (Npro) which binds IRF3 and targets it for proteasomal degradation. Additionally, Npro has been shown to antagonise apoptosis triggered by the dsRNA-homologpoly (I:C), however the exact mechanism by which this is achieved has not been fully elucidated. In this study we confirm the ability of Npro to inhibit dsRNA-mediated apoptosis and show that Npro is also able to antagonise Sendai virus-mediated apoptosis in PK-15 cells. Gene editedPK-15 cell lines were used to show the dsRNA-sensing pathogen recognition receptors (PRRs) TLR3 and RIG-I specifically respond to poly(I:C) and SeV respectively, subsequently triggering apoptosis through pathways that convergeon IRF3 and culminate in the cleavage of caspase-3.Importantly, this IRF3-mediated apoptosis was found to be dependent on transcription-independent functions of IRF3 and also on Bax, a pro-apoptotic Bcl-2 family protein, through a direct interaction between the two proteins. Deletion of IRF3, stable expression of Npro and infection with wild-type CSFV were found to antagonise the mitochondrial localisation of Bax, a key hallmark of the intrinsic, mitochondrial pathway of apoptosis. Together, these findings show that Npro’s putative interaction with IRF3 is involved not only in its antagonism of type I IFN, but also dsRNA-mediated mitochondrial apoptosis.

Item Type: Article
Additional Information: Copyright © 2020 Hardy et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/).
Keywords: Virology, 06 Biological Sciences, 07 Agricultural and Veterinary Sciences, 11 Medical and Health Sciences
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: JOURNAL OF VIROLOGY
ISSN: 0022-538X
Dates:
DateEvent
March 2021Published
16 December 2020Published Online
22 November 2020Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
BBS/E/I/00007032Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
BBS/E/I/00007037Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
URI: https://openaccess.sgul.ac.uk/id/eprint/112631
Publisher's version: https://doi.org/10.1128/JVI.01136-20

Actions (login required)

Edit Item Edit Item