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

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...

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Main Authors: Tian Xia, Xin Wu, Eunjin Hong, Kyle Jung, Chih-Jen Lai, Mi-Jeong Kwak, Hogyu Seo, Stephanie Kim, Zhongyi Jiang, Inho Cha, Jae U Jung
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-03-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1011232
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author Tian Xia
Xin Wu
Eunjin Hong
Kyle Jung
Chih-Jen Lai
Mi-Jeong Kwak
Hogyu Seo
Stephanie Kim
Zhongyi Jiang
Inho Cha
Jae U Jung
author_facet Tian Xia
Xin Wu
Eunjin Hong
Kyle Jung
Chih-Jen Lai
Mi-Jeong Kwak
Hogyu Seo
Stephanie Kim
Zhongyi Jiang
Inho Cha
Jae U Jung
author_sort Tian Xia
collection DOAJ
description 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.
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spelling doaj.art-5881408929ae41b6bb272edd694383422023-07-04T05:31:43ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742023-03-01193e101123210.1371/journal.ppat.1011232Glucosylceramide is essential for Heartland and Dabie bandavirus glycoprotein-induced membrane fusion.Tian XiaXin WuEunjin HongKyle JungChih-Jen LaiMi-Jeong KwakHogyu SeoStephanie KimZhongyi JiangInho ChaJae U JungDue 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.https://doi.org/10.1371/journal.ppat.1011232
spellingShingle Tian Xia
Xin Wu
Eunjin Hong
Kyle Jung
Chih-Jen Lai
Mi-Jeong Kwak
Hogyu Seo
Stephanie Kim
Zhongyi Jiang
Inho Cha
Jae U Jung
Glucosylceramide is essential for Heartland and Dabie bandavirus glycoprotein-induced membrane fusion.
PLoS Pathogens
title Glucosylceramide is essential for Heartland and Dabie bandavirus glycoprotein-induced membrane fusion.
title_full Glucosylceramide is essential for Heartland and Dabie bandavirus glycoprotein-induced membrane fusion.
title_fullStr Glucosylceramide is essential for Heartland and Dabie bandavirus glycoprotein-induced membrane fusion.
title_full_unstemmed Glucosylceramide is essential for Heartland and Dabie bandavirus glycoprotein-induced membrane fusion.
title_short Glucosylceramide is essential for Heartland and Dabie bandavirus glycoprotein-induced membrane fusion.
title_sort glucosylceramide is essential for heartland and dabie bandavirus glycoprotein induced membrane fusion
url https://doi.org/10.1371/journal.ppat.1011232
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