Abstract

BackgroundEncephalomyocarditis virus (EMCV) can infect a variety of animal species and humans. Although the EMCV infection is known to induce autophagy to promote its replication in host cells, the viral proteins that are responsible for inducing autophagy are unknown.MethodsThe recombinant plasmids that were expressing the EMCV proteins were constructed to analyze the role of each protein in the induction of autophagy. Autophagy inductions by the EMCV proteins in BHK-21 cells were investigated by confocal microscopy, Western blotting and transmission electron microscopy. ER stress in BHK-21 cells was examined by detecting the marker molecules using western blotting and luciferase assays.ResultsThis study presents the first demonstration that the nonstructural proteins 2C or 3D of EMCV were involved in inducing autophagy in BHK-21 cells that were expressing 2C or 3D, and we found that inhibiting Beclin1 expression influenced this autophagy induction process. Next, 2C and 3D were shown to be involved in inducing autophagy by activating the ER stress pathway. Finally, EMCV 2C or 3D were demonstrated to regulate the proteins associated with PERK and ATF6alpha pathway.ConclusionsOur findings indicate that 2C and 3D are involved in EMCV-induced autophagy by activating ER stress molecules and regulating the proteins expression associated with UPR pathway, helping to better understand the EMCV-induced autophagy process.Electronic supplementary materialThe online version of this article (doi:10.1186/1743-422X-11-156) contains supplementary material, which is available to authorized users.

Highlights

  • Encephalomyocarditis virus (EMCV) can infect a variety of animal species and humans

  • Puncta accumulated in the BHK-21 cells that were co-transfected with the EMCV protein-expressing plasmid and pEGFP-light chain 3 (LC3) The LC3 is a specific marker protein for monitoring autophagic vesicle formation through its vesicle formation and lipidation reaction [26]

  • The green fluorescent pattern exhibited puncta morphology upon EMCV infection, resembling the pattern of autophagosome-like vesicles, which suggests that the BHK-21 cells that were transfected and were expressing green fluorescent protein-tagged LC3 plasmid (GFP-LC3) were suitable for studying autophagy (Figure 1A)

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Summary

Introduction

Encephalomyocarditis virus (EMCV) can infect a variety of animal species and humans. the EMCV infection is known to induce autophagy to promote its replication in host cells, the viral proteins that are responsible for inducing autophagy are unknown. Encephalomyocarditis virus (EMCV) belongs to the Cardiovirus genus of the Picornaviridae family [1]. This virus has a wide host-range among domestic and wild animals [2,3,4]. The genome is approximately 7.8-kb long with a single open reading frame (ORF) that is translated into a polyprotein precursor [7] This precursor is proteolytically processed into structural proteins (VP1, VP2, VP3 and VP4), primarily forming the viral nucleocapsid and nonstructural proteins (2A, 2B, 2C, 3A, 3B, 3C and 3D) along with several protein intermediates that are needed for viral replication [8]. The roles of EMCV proteins have been widely investigated, a further exploration of the virus-host interaction and important cellular components in the EMCV life cycle is essential to determine a control strategy for EMCV infection

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