Anion homeostasis is important for non-lytic release of BK polyomavirus from infected cells

Open Biol. 2015 Aug;5(8):150041. doi: 10.1098/rsob.150041.

Abstract

BK polyomavirus (BKPyV) is a member of a family of potentially oncogenic viruses, whose reactivation can cause severe pathological conditions in transplant patients, leading to graft rejection. As with many non-enveloped viruses, it is assumed that virus release occurs through lysis of the host cell. We now show the first evidence for a non-lytic release pathway for BKPyV and that this pathway can be blocked by the anion channel inhibitor DIDS. Our data show a dose-dependent effect of DIDS on the release of BKPyV virions. We also observed an accumulation of viral capsids in large LAMP-1-positive acidic organelles within the cytoplasm of cells upon DIDS treatment, suggesting potential late endosome or lysosome-related compartments are involved in non-lytic BKPyV release. These data highlight a novel mechanism by which polyomaviruses can be released from infected cells in an active and non-lytic manner, and that anion homeostasis regulation is important in this pathway.

Keywords: BKPyV; DIDS; anion homeostasis; polyomavirus; virus release.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid / pharmacology
  • Anions / metabolism*
  • BK Virus / physiology*
  • Biological Transport
  • Cell Line
  • Homeostasis*
  • Humans
  • Vacuoles / metabolism
  • Virus Release / drug effects
  • Virus Replication
  • Voltage-Dependent Anion Channels / antagonists & inhibitors

Substances

  • Anions
  • Voltage-Dependent Anion Channels
  • 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid