Chewing the Fat: The Conserved Ability of DNA Viruses to Hijack Cellular Lipid Metabolism

被引:37
作者
Lange, Philip T. [1 ]
Lagunoff, Michael [2 ,3 ]
Tarakanova, Vera L. [1 ,4 ]
机构
[1] Med Coll Wisconsin, Dept Microbiol & Immunol, Milwaukee, WI 53226 USA
[2] Univ Washington, Dept Microbiol, Seattle, WA 98101 USA
[3] Univ Washington, Mol & Cellular Biol Program, Seattle, WA 98101 USA
[4] Med Coll Wisconsin, Canc Ctr, Milwaukee, WI 53226 USA
来源
VIRUSES-BASEL | 2019年 / 11卷 / 02期
关键词
DNA virus; lipids; fatty acids; cholesterol; herpesvirus; MHV68; HERPES-SIMPLEX-VIRUS; HUMAN CYTOMEGALOVIRUS-INFECTION; RECEPTOR-RELATED PROTEIN-1; LOW-DENSITY-LIPOPROTEIN; HOST RESTRICTION FACTOR; VARICELLA-ZOSTER-VIRUS; CHOLESTEROL; 25-HYDROXYLASE; NUCLEAR RECEPTOR; ACID SYNTHESIS; 3-HYDROXY-3-METHYLGLUTARYL-COA REDUCTASE;
D O I
10.3390/v11020119
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Viruses manipulate numerous host factors and cellular pathways to facilitate the replication of viral genomes and the production of infectious progeny. One way in which viruses interact with cells is through the utilization and exploitation of the host lipid metabolism. While it is likely that mostif not allviruses require lipids or intermediates of lipid synthesis to replicate, many viruses also actively induce lipid metabolic pathways to sustain a favorable replication environment. From the formation of membranous replication compartments, to the generation of ATP or protein modifications, viruses exhibit differing requirements for host lipids. Thus, while the exploitation of lipid metabolism is a common replication strategy, diverse viruses employ a plethora of mechanisms to co-opt these critical cellular pathways. Here, we review recent literature regarding the exploitation of host lipids and lipid metabolism specifically by DNA viruses. Importantly, furthering the understanding of the viral requirements for host lipids may offer new targets for antiviral therapeutics and provide opportunities to repurpose the numerous FDA-approved compounds targeting lipid metabolic pathways as antiviral agents.
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页数:19
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