Cellular v-ATPase is required for virion assembly compartment formation in human cytomegalovirus infection

Open Biol. 2017 Nov;7(11):160298. doi: 10.1098/rsob.160298.

Abstract

Successful generation of virions from infected cells is a complex process requiring orchestrated regulation of host and viral genes. Cells infected with human cytomegalovirus (HCMV) undergo a dramatic reorganization of membrane organelles resulting in the formation of the virion assembly compartment, a process that is not fully understood. Here we show that acidification of vacuoles by the cellular v-ATPase is a crucial step in the formation of the virion assembly compartment and disruption of acidification results in mis-localization of virion components and a profound reduction in infectious virus levels. In addition, knockdown of ATP6V0C blocks the increase in nuclear size, normally associated with HCMV infection. Inhibition of the v-ATPase does not affect intracellular levels of viral DNA synthesis or gene expression, consistent with a defect in assembly and egress. These studies identify a novel host factor involved in virion production and a potential target for antiviral therapy.

Keywords: assembly and egress; herpesvirus; host virus interaction; human cytomegalovirus; v-ATPase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Cytomegalovirus / metabolism
  • Cytomegalovirus / pathogenicity
  • Cytomegalovirus / physiology*
  • Fibroblasts / virology
  • Humans
  • Vacuolar Proton-Translocating ATPases / genetics
  • Vacuolar Proton-Translocating ATPases / metabolism*
  • Vacuoles / virology
  • Virion / metabolism*
  • Virus Assembly*
  • Virus Release

Substances

  • Vacuolar Proton-Translocating ATPases