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Status: Bibliographieeintrag

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Verfasst von:Reichert, Isabelle [VerfasserIn]   i
 Lee, Ji-Young [VerfasserIn]   i
 Weber, Laura [VerfasserIn]   i
 Fuh, Marceline M. [VerfasserIn]   i
 Schlaeger, Lina [VerfasserIn]   i
 Rößler, Stefanie [VerfasserIn]   i
 Kinast, Volker [VerfasserIn]   i
 Schlienkamp, Sarah [VerfasserIn]   i
 Conradi, Janina [VerfasserIn]   i
 Vondran, Florian W. R. [VerfasserIn]   i
 Pfaender, Stephanie [VerfasserIn]   i
 Scaturro, Pietro [VerfasserIn]   i
 Steinmann, Eike [VerfasserIn]   i
 Bartenschlager, Ralf [VerfasserIn]   i
 Pietschmann, Thomas [VerfasserIn]   i
 Heeren, Joerg [VerfasserIn]   i
 Lauber, Chris [VerfasserIn]   i
 Vieyres, Gabrielle [VerfasserIn]   i
Titel:The triglyceride-synthesizing enzyme diacylglycerol acyltransferase 2 modulates the formation of the hepatitis C virus replication organelle
Verf.angabe:Isabelle Reichert, Ji-Young Lee, Laura Weber, Marceline M. Fuh, Lina Schlaeger, Stefanie Rößler, Volker Kinast, Sarah Schlienkamp, Janina Conradi, Florian W.R. Vondran, Stephanie Pfaender, Pietro Scaturro, Eike Steinmann, Ralf Bartenschlager, Thomas Pietschmann, Joerg Heeren, Chris Lauber, Gabrielle Vieyres
E-Jahr:2024
Jahr:September 6, 2024
Umfang:37 S.
Illustrationen:Illustrationen
Fussnoten:Gesehen am 10.03.2025
Titel Quelle:Enthalten in: Public Library of SciencePLoS pathogens
Ort Quelle:Lawrence, Kan. : PLoS, 2005
Jahr Quelle:2024
Band/Heft Quelle:20(2024), 9, Artikel-ID e1012509, Seite 1-37
ISSN Quelle:1553-7374
Abstract:The replication organelle of hepatitis C virus (HCV), called membranous web, is derived from the endoplasmic reticulum (ER) and mainly comprises double membrane vesicles (DMVs) that concentrate the viral replication complexes. It also tightly associates with lipid droplets (LDs), which are essential for virion morphogenesis. In particular acyl-CoA:diacylglycerol acyltransferase 1 (DGAT1), a rate-limiting enzyme in triglyceride synthesis, promotes early steps of virus assembly. The close proximity between ER membranes, DMVs and LDs therefore permits the efficient coordination of the HCV replication cycle. Here, we demonstrate that exaggerated LD accumulation due to the excessive expression of the DGAT1 isozyme, DGAT2, dramatically impairs the formation of the HCV membranous web. This effect depended on the enzymatic activity and ER association of DGAT2, whereas the mere LD accumulation was not sufficient to hamper HCV RNA replication. Our lipidomics data indicate that both HCV infection and DGAT2 overexpression induced membrane lipid biogenesis and markedly increased phospholipids with long chain polyunsaturated fatty acids, suggesting a dual use of these lipids and their possible competition for LD and DMV biogenesis. On the other hand, overexpression of DGAT2 depleted specific phospholipids, particularly oleyl fatty acyl chain-containing phosphatidylcholines, which, in contrast, are increased in HCV-infected cells and likely essential for viral infection. In conclusion, our results indicate that lipid exchanges occurring during LD biogenesis regulate the composition of intracellular membranes and thereby affect the formation of the HCV replication organelle. The potent antiviral effect observed in our DGAT2 overexpression system unveils lipid flux that may be relevant in the context of steatohepatitis, a hallmark of HCV infection, but also in physiological conditions, locally in specific subdomains of the ER membrane. Thus, LD formation mediated by DGAT1 and DGAT2 might participate in the spatial compartmentalization of HCV replication and assembly factories within the membranous web.
DOI:doi:10.1371/journal.ppat.1012509
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.1371/journal.ppat.1012509
 kostenfrei: Volltext: https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1012509
 DOI: https://doi.org/10.1371/journal.ppat.1012509
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Biosynthesis
 Cellular structures and organelles
 Hepatitis C virus
 Lipid analysis
 Lipids
 Luciferase
 Transfection
 Viral replication
K10plus-PPN:191940158X
Verknüpfungen:→ Zeitschrift

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