Glucose-Regulated Protein 78 Interacts with Zika Virus Envelope Protein and Contributes to a Productive Infection

• Published in: Viruses 2020-05, Vol.12 (5), p.524
• Main Authors: Royle, Jamie, Ramírez-Santana, Carolina, Akpunarlieva, Snezhana, Donald, Claire L, Gestuveo, Rommel J, Anaya, Juan-Manuel, Merits, Andres, Burchmore, Richard, Kohl, Alain, Varjak, Margus
• Format: Article
• Language: English
• Subjects: Analysis; Diagnosis; Endoplasmic reticulum; Endoplasmic Reticulum - metabolism; Endoplasmic Reticulum - virology; Fetuses; Flaviviridae; Gene expression; Genomes; GRP78; Guillain-Barre syndrome; Heat-Shock Proteins - genetics; Heat-Shock Proteins - metabolism; Host-Pathogen Interactions; Humans; Infections; Infectivity; Life cycles; Mass spectroscopy; Molecular chaperones; Protein Binding; Protein biosynthesis; Proteins; Proteomics; Replication; siRNA; Transcription; Viral envelope proteins; Viral Envelope Proteins - genetics; Viral Envelope Proteins - metabolism; Virus Replication; virus–cell interactions; Zika virus; Zika Virus - genetics; Zika Virus - metabolism; Zika virus infection; Zika Virus Infection - genetics; Zika Virus Infection - metabolism; Zika Virus Infection - virology
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v12050524

Zika virus (ZIKV; Flaviviridae) is a mosquito-borne flavivirus shown to cause fetal abnormalities collectively known as congenital Zika syndrome and Guillain-Barré syndrome in recent outbreaks. Currently, there is no specific treatment or vaccine available, and more effort is needed to identify cellular factors in the viral life cycle. Here, we investigated interactors of ZIKV envelope (E) protein by combining protein pull-down with mass spectrometry. We found that E interacts with the endoplasmic reticulum (ER) resident chaperone, glucose regulated protein 78 (GRP78). Although other flaviviruses are known to co-opt ER resident proteins, including GRP78, to enhance viral infectivity, the role ER proteins play during the ZIKV life cycle is yet to be elucidated. We showed that GRP78 levels increased during ZIKV infection and localised to sites coincident with ZIKV E staining. Depletion of GRP78 using specific siRNAs significantly reduced reporter-virus luciferase readings, viral protein synthesis, and viral titres. Additionally, GRP78 depletion reduced the ability of ZIKV to disrupt host cell translation and altered the localisation of viral replication factories, though there was no effect on viral RNA synthesis. In summary, we showed GRP78 is a vital host-factor during ZIKV infection, which may be involved in the coordination of viral replication factories.