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Updated: Jun 5, 2025

Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
Published on: April 4, 2019
Structural and molecular properties of mumps virus inclusion bodies
Hiroshi Katoh1, Ryuichi Kimura2,3, Tsuyoshi Sekizuka4
1Department of Microbiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Tokyo 113-0033, Japan.
Abstract:
Viral RNA synthesis of mononegaviruses occurs in cytoplasmic membraneless organelles called inclusion bodies (IBs). Here, we report that IBs of mumps virus (MuV), which is the causative agent of mumps and belongs to the family Paramyxoviridae, displayed liquid organelle properties formed by liquid-liquid phase separation. Super-resolution microscopic analysis of MuV IBs demonstrated that nucleocapsid and phospho (P)-proteins formed a cage-like structure and that the viral polymerase adopted a reticular pattern and colocalized with viral RNAs. In addition, we characterized host RNAs localized in MuV IBs by a spatial transcriptome analysis, and found that RNAs containing G-quadruplex motif sequences (G4-RNAs) were concentrated. An in vitro phase separation assay showed that the G4-RNAs interacted with the P protein and enhanced condensation in P droplets. Together, our data show that MuV generates IBs with a characteristic cage-like structure and host G4-RNAs play an important role in forming MuV IBs.
Insights
Mumps virus inclusion bodies (IBs) form liquid organelles through phase separation. Host G-quadruplex RNAs (G4-RNAs) interact with viral proteins, playing a key role in forming these essential viral structures.
Area of Science:
- Virology
- Molecular Biology
- Cell Biology
Background:
- Mononegaviruses synthesize viral RNA within cytoplasmic inclusion bodies (IBs).
- Mumps virus (MuV), a Paramyxoviridae member, causes mumps and relies on IBs for replication.
Purpose of the Study:
- To investigate the structural properties and formation mechanism of MuV inclusion bodies (IBs).
- To identify host factors involved in MuV IB assembly.
Main Methods:
- Super-resolution microscopy to analyze MuV IB structure.
- Spatial transcriptome analysis to identify host RNAs in IBs.
- In vitro phase separation assays to study protein-RNA interactions.
Main Results:
- MuV IBs exhibit liquid organelle properties, driven by liquid-liquid phase separation.
- Nucleocapsid and phospho (P)-proteins form a cage-like structure, with viral polymerase and RNA localized within.
- Host G-quadruplex RNAs (G4-RNAs) are concentrated in MuV IBs and enhance P-protein condensation.
Conclusions:
- MuV IBs possess a distinct cage-like structure indicative of liquid organelle behavior.
- Host G4-RNAs are crucial components that facilitate the formation and condensation of MuV IBs.
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