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Impact of dynamin 2 on adenovirus nuclear entry

  • Ji Sun Lee
  • , Ashrafali M. Ismail
  • , Jeong Yoon Lee
  • , Xiaohong Zhou
  • , Emma C. Materne
  • , James Chodosh
  • , Jaya Rajaiya*
  • *Corresponding author for this work
  • Harvard Medical School

Research output: Contribution to journalJournal articlepeer-review

Abstract

The large GTPase dynamin 2 controls both endosomal fission and microtubule acetylation. Here we report that dynamin 2 alters microtubules and regulates the trafficking of human adenovirus type 37. Dynamin 2 knockdown by siRNA in infected cells resulted in accumulation of acetylated tubulin, repositioning of microtubule organizing centers (MTOCs) closer to cell nuclei, increased virus in the cytosol (with a compensatory decrease in endosomal virus), reduced proinflammatory cytokine induction, and increased binding of virus to the nucleoporin, Nup358. These events led to increased viral DNA nuclear entry and viral replication. Overexpression of dynamin 2 generated opposite effects. Therefore, dynamin 2 inhibits adenovirus replication and promotes innate immune responses by the infected cell. MTOC transposition in dynamin 2 knockdown promotes a closer association with nuclear pore complexes to facilitate viral DNA delivery. Dynamin 2 plays a key role in adenoviral trafficking and influences host responses to infection.

Original languageEnglish
Pages (from-to)43-56
Number of pages14
JournalVirology
Volume529
DOIs
StatePublished - 2019.03

Keywords

  • Adenovirus
  • Cytokines
  • Dynamin 2
  • Microtubule organizing center
  • Microtubules
  • Nucleoporin
  • Viral trafficking

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