4.6 Article

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

Journal

OPEN BIOLOGY
Volume 5, Issue 8, Pages -

Publisher

ROYAL SOC
DOI: 10.1098/rsob.150041

Keywords

polyomavirus; BKPyV; DIDS; anion homeostasis; virus release

Funding

  1. Isaac Newton Trust
  2. Wellcome Trust
  3. Medical Research Council
  4. Royal Society [UF090010]
  5. Medical Research Council [1498984] Funding Source: researchfish

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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.

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