The inner tegument promotes herpes simplex virus capsid motility along microtubules in vitro

André Wolfstein, Claus Henning Nagel, Kerstin Radtke, Katinka Döhner, Victoria J. Allan, Beate Sodeik

    Research output: Contribution to journalArticlepeer-review

    Abstract

    After viral fusion, capsids of the neurotropic herpes simplex virus are transported along microtubules (MT) to the nuclear pores for viral genome uncoating, nuclear transcription and replication. After assembly and egress from the nucleus, cytosolic capsids are transported to host membranes for secondary envelopment or to the axon terminal for further viral spread. Using GFP-tagged capsids, Cy3-labelled MT and cytosol, we have econstituted viral capsid transport in vitro. In the presence of ATP, capsids moved along MT up to 30 μm. Blocking the function of dynactin, a cofactor of dynein and kinesin-2, inhibited the transport. Removing outer tegument proteins from the capsids increased in vitro motility. In contrast, capsids isolated from infected nuclei that were devoid of inner as well as outer tegument proteins showed little interaction with dynein and its cofactor dynactin. Our data suggest that the inner tegument of alphaherpesviruses contains viral receptors for MT motors. © Blackwell Munksgaard, 2005.
    Original languageEnglish
    Pages (from-to)227-237
    Number of pages10
    JournalTraffic (Malden): the international journal of intracellular transport
    Volume7
    Issue number2
    DOIs
    Publication statusPublished - Feb 2006

    Keywords

    • Cytoplasmic dynein
    • Digital time-lapse microscopy
    • Dynactin
    • Herpes simplex virus
    • In vitro MT transport

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