Regulatory Role of Phospholipids in Hepatitis C Virus Replication and Protein Function

被引:1
|
作者
Bulankina, Anna V. [1 ,2 ]
Richter, Rebecca M. [1 ,2 ]
Welsch, Christoph [1 ,2 ]
机构
[1] Goethe Univ Hosp Frankfurt, Dept Internal Med 1, D-60590 Frankfurt, Germany
[2] Res Grp Mol Evolut & Adaptat, D-60590 Frankfurt, Germany
来源
PATHOGENS | 2022年 / 11卷 / 01期
关键词
RNA virus; hepatitis C virus; phospholipid; viral replication; membrane remodeling; interactions; NS5A; OXYSTEROL-BINDING PROTEIN; FATTY-ACID SYNTHASE; NS5A PROTEIN; RNA REPLICATION; PHOSPHATIDYLINOSITOL; 4-PHOSPHATE; CRYSTAL-STRUCTURE; LIPID KINASE; DOMAIN; MEMBRANE; HCV;
D O I
10.3390/pathogens11010102
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Positive-strand RNA viruses such as hepatitis C virus (HCV) hijack key factors of lipid metabolism of infected cells and extensively modify intracellular membranes to support the viral lifecycle. While lipid metabolism plays key roles in viral particle assembly and maturation, viral RNA synthesis is closely linked to the remodeling of intracellular membranes. The formation of viral replication factories requires a number of interactions between virus proteins and host factors including lipids. The structure-function relationship of those proteins is influenced by their lipid environments and lipids that selectively modulate protein function. Here, we review our current understanding on the roles of phospholipids in HCV replication and of lipid-protein interactions in the structure-function relationship of the NS5A protein. NS5A is a key factor in membrane remodeling in HCV-infected cells and is known to recruit phosphatidylinositol 4-kinase III alpha to generate phosphatidylinositol 4-phosphate at the sites of replication. The dynamic interplay between lipids and viral proteins within intracellular membranes is likely key towards understanding basic mechanisms in the pathobiology of virus diseases, the mode of action of specific antiviral agents and related drug resistance mechanisms.
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页数:15
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