Journal Article

Glucosylceramide is essential for Heartland and Dabie bandavirus glycoprotein-induced membrane fusion

Hong, Eunjin, Lai, Chih-Jen, Seo, Hogyu, Cha, Inho, Jiang, Zhongyi, Kim, Stephanie, Wu, Xin, Xia, Tian, Kwak, Mi-Jeong, Jung, Jae U., Jung, Kyle

2023

Overview

Due to climate changes, there has been a large expansion of emerging tick-borne zoonotic viruses, including Heartland bandavirus (HRTV) and Dabie bandavirus (DBV). As etiologic agents of hemorrhagic fever with high fatality, HRTV and DBV have been recognized as dangerous viral pathogens that likely cause future wide epidemics. Despite serious health concerns, the mechanisms underlying viral infection are largely unknown. HRTV and DBV Gn and Gc are viral surface glycoproteins required for early entry events during infection. Glycosphingolipids, including galactosylceramide (GalCer), glucosylceramide (GlcCer) and lactosylceramide (LacCer), are a class of membrane lipids that play essential roles in membrane structure and viral lifecycle. Here, our genome-wide CRISPR/Cas9 knockout screen identifies that glycosphingolipid biosynthesis pathway is essential for HRTV and DBV infection. The deficiency of UDP-glucose ceramide glucosyltransferase (UGCG) that produces GlcCer resulted in the loss of infectivity of recombinant viruses pseudotyped with HRTV or DBV Gn/Gc glycoproteins. Conversely, exogenous supplement of GlcCer, but not GalCer or LacCer, recovered viral entry of UGCG-deficient cells in a dose-dependent manner. Biophysical analyses showed that GlcCer targeted the lipid-head-group binding pocket of Gc to form a stable protein-lipid complex, which allowed the insertion of Gc protein into host lysosomal membrane lipid bilayers for viral fusion. Mutagenesis showed that D841 residue at the Gc lipid binding pocket was critical for GlcCer interaction and thereby, viral entry. These findings reveal detailed mechanism of GlcCer glycosphingolipid in HRTV and DBV Gc-mediated membrane fusion and provide a potential therapeutic target for tickborne virus infection.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: Analysis / Arachnids / Binding / Biology and Life Sciences / Biosynthesis / Care and treatment / Causes of / Ceramide / Ceramide glucosyltransferase / Climate change / CRISPR / Drug dosages / Epidemics / Fever / Galactosylceramide / Gangliosides / Genes / Genomes / Genomics / Glucosylceramides - metabolism / Glucosyltransferase / Glycoproteins / Glycoproteins - chemistry / Glycosphingolipids / Health aspects / Hemorrhage / Hemorrhagic fever / Infection / Infections / Infectivity / Lactosylceramides / Life cycle analysis / Lipid bilayers / Lipids / Membrane Fusion / Membrane lipids / Membrane proteins / Membrane structure / Membrane structures / Membranes / Mutagenesis / Phospholipids / Physiological aspects / Prevention / Proteins / Research and analysis methods / Risk factors / RNA polymerase / RNA Viruses - metabolism / Therapeutic targets / Thrombocytopenia / Tick-borne diseases / Viruses / Zoonoses