Ebola virus inclusion body formation and RNA synthesis are controlled by a novel domain of NP interacting with VP35
T. Miyake, C. Farley, B. E. Neubauer, T. Beddow, T. Hoenen, D. A. Engel
Abstract
Ebola virus (EBOV) inclusion bodies (IBs) are cytoplasmic sites of nucleocapsid formation and RNA replication, housing key steps in the virus life cycle that warrant further investigation. During infection IBs display dynamic properties regarding their size and location. Also, the contents of IBs must transition prior to further viral maturation, assembly and release, implying additional steps in IB function. Interestingly, expression of the viral nucleoprotein (NP) alone is sufficient for generation of IBs, indicating that it plays an important role in IB formation during infection. In addition to NP, other components of the nucleocapsid localize to IBs, including VP35, VP24, VP30 and the RNA polymerase L. Previously we defined and solved the crystal structure of the C-terminal domain of NP (NP-Ct), but its role in virus replication remained unclear. Here we show that NP-Ct is absolutely required for IB formation when NP is expressed alone. Interestingly, we find that NP-Ct is also required for production of infectious virus-like particles and retention of viral RNA within these particles. Furthermore, co-expression of the nucleocapsid component VP35 overcomes deletion of NP-Ct in triggering IB formation, demonstrating a functional interaction between the two proteins. Of all the EBOV proteins only VP35 is able to overcome the defect in IB formation caused by deletion of NP-Ct. This effect is mediated by a novel protein-protein interaction between VP35 and NP that controls both regulation of IB formation and RNA replication itself, and which is mediated by a newly identified domain of NP, the "central domain" (CD). ImportanceInclusion bodies (IBs) are cytoplasmic sites of RNA synthesis for a variety of negative sense RNA viruses including Ebola virus. In addition to housing important steps in the viral life cycle, IBs protect new viral RNA from innate immune attack and contain specific host proteins whose function is under study. A key viral factor in Ebola virus IB formation is the nucleoprotein, NP, which also is important in RNA encapsidation and synthesis. In this study, we have identified two domains of NP that control inclusion body formation. One of these, the central domain (CD), interacts with viral protein VP35 to control both inclusion body formation and RNA synthesis. The other is the NP C-terminal domain (NP-Ct), whose function has not previously been reported. These findings contribute to a model in which NP and its interactions with VP35 link the establishment of IBs to the synthesis of viral RNA.
02 /Specification & Classification
Click any tag to browse matching papersReproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Impact of Ebola virus nucleoprotein on VP40 virus-like particle production: a computational approach
Xiao Liu, Robert Virgil Stahelin, Elsje Pienaar·Communications BiologyPeer-reviewed·May 25, 2024
- Intracellular Ebola Virus nucleocapsid assembly revealed by in situ cryo-electron tomography.
Reika Watanabe, Dawid S. Zyla, … Erica Ollmann Saphire·CellPeer-reviewed·Sep 17, 2024
- Ebola virus VP35 NNLNS motif modulates viral RNA synthesis and MIB2-mediated signaling
Grace Uwase, Priya Luthra, … Gaya K. Amarasinghe·Proceedings of the National Academy of SciencesPeer-reviewed·Sep 22, 2025
- Structure of the Ebola virus nucleoprotein - RNA complex
R. N. Kirchdoerfer, E. O. Saphire, A. B. Ward·bioRxiv·Feb 13, 2019
- Structural basis of Ebola virus nucleocapsid assembly and functions
Yoko Fujita, Shangfan Hu, … Takeshi Noda·Nature CommunicationsPeer-reviewed·Mar 10, 2025
- Ebola Virus Sequesters IRF3 in Viral Inclusion Bodies to Evade Host Antiviral Immunity