Inclusion bodies are a site of ebolavirus replication

Thomas Hoenen, Reed S. Shabman, Allison Groseth, Astrid Herwig, Michaela Weber, Gordian Schudt, Olga Dolnik, Christopher F. Basler, Stephan Becker, Heinz Feldmann

Research output: Contribution to journalArticlepeer-review

135 Scopus citations

Abstract

Inclusion bodies are a characteristic feature of ebolavirus infections in cells. They contain large numbers of preformed nucleocapsids,but their biological significance has been debated, and they have been suggested to be aggregates of viral proteins without any further biological function. However, recent data for otherviruses that produce similar structures have suggested that inclusion bodies might be involved in genome replication and transcription. In order to study filovirus inclusion bodies,we fused mCherry to the ebolavirus polymerase L, which is found in inclusion bodies. The resulting L-mCherry fusion protein was functional in minigenomeassays and incorporated into virus-like particles. Importantly, L-mCherry fluorescence in transfected cells was readily detectable and distributed in a punctate pattern characteristic for inclusion bodies. A recombinant ebolavirus encoding L-mCherry instead of L was rescued and showed virtually identical growth kinetics and endpoint titers to those for wild-type virus. Using this virus, we showed that the onset of inclusion body formation corresponds to the onset of viral genome replication, but that viral transcription occurs prior to inclusion body formation. Live-cell imaging further showed that inclusion bodies are highly dynamic structures andthat they can undergo dramatic reorganization during cell division. Finally, by labeling nascent RNAs using click technology we showed that inclusion bodies are indeed the site of viral RNA synthesis. Based on these data we conclude that, rather than being inert aggregates of nucleocapsids, ebolavirus inclusion bodies are in fact complex and dynamic structures and an important site at which viral RNA replication takes place.

Original languageEnglish
Pages (from-to)11779-11788
Number of pages10
JournalJournal of Virology
Volume86
Issue number21
DOIs
StatePublished - Nov 2012

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