Early Events in Foamy Virus-Host Interaction and Intracellular Trafficking

被引:16
作者
Berka, Ursula [1 ,2 ]
Hamann, Martin Volker [1 ,2 ]
Lindemann, Dirk [1 ,2 ]
机构
[1] Tech Univ Dresden, Med Fac Carl Gustav Cams, Inst Virol, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Ctr Biotechnol, DFG Ctr Regenerat Therapies Dresden CRTD Cluster, D-01307 Dresden, Germany
来源
VIRUSES-BASEL | 2013年 / 5卷 / 04期
关键词
foamy virus; entry; trafficking; ENVELOPE GLYCOPROTEIN; NUCLEAR-LOCALIZATION; HEPARAN-SULFATE; GAG PROTEINS; IN-VITRO; BINDING; RECEPTOR; RETROVIRUS; REPLICATION; RESTRICTION;
D O I
10.3390/v5041055
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Here we review viral and cellular requirements for entry and intracellular trafficking of foamy viruses (FVs) resulting in integration of viral sequences into the host cell genome. The virus encoded glycoprotein harbors all essential viral determinants, which are involved in absorption to the host membrane and triggering the uptake of virus particles. However, only recently light was shed on some details of FV's interaction with its host cell receptor(s). Latest studies indicate glycosaminoglycans of cellular proteoglycans, particularly heparan sulfate, to be of utmost importance. In a species-specific manner FVs encounter endogenous machineries of the target cell, which are in some cases exploited for fusion and further egress into the cytosol. Mostly triggered by pH-dependent endocytosis, viral and cellular membranes fuse and release naked FV capsids into the cytoplasm. Intact FV capsids are then shuttled along microtubules and are found to accumulate nearby the centrosome where they can remain in a latent state for extended time periods. Depending on the host cell cycle status, FV capsids finally disassemble and, by still poorly characterized mechanisms, the preintegration complex gets access to the host cell chromatin. Host cell mitosis finally allows for viral genome integration, ultimately starting a new round of viral replication.
引用
收藏
页码:1055 / 1074
页数:20
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