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Flexibility of the Rotavirus NSP2 C-Terminal Region Supports Factory Formation via Liquid-Liquid Phase Separation

Sarah L. Nichols, Emil M. Nilsson, Heather M. Brown, Leslie E. W. LaConte, Julia Acker, Alexander Borodavka, Sarah McDonald Esstman

2023Journal of Virology25 citationsDOIOpen Access PDF

Abstract

Viruses often condense the materials needed for their replication into discrete intracellular factories. For rotaviruses, agents of severe gastroenteritis in children, factory formation is mediated in part by an octameric protein called NSP2. A flexible C-terminal region of NSP2 has been proposed to link several NSP2 octamers together, a feature that might be important for factory formation. Here, we created a change in NSP2 that reduced C-terminal flexibility and analyzed the impact on rotavirus factories. We found that the change caused the formation of smaller and more numerous factories that could not readily fuse together like those of the wild-type virus. The altered NSP2 protein also had a reduced capacity to form factory-like condensates in a test tube. Together, these results add to our growing understanding of how NSP2 supports rotavirus factory formation-a key step of viral replication.

Topics & Concepts

BiologyIntracellularFactory (object-oriented programming)VirologyFlexibility (engineering)Replication (statistics)RotavirusPhase (matter)Cell biologyMaterials scienceVirusPhysicsComputer scienceMathematicsStatisticsProgramming languageQuantum mechanicsViral gastroenteritis research and epidemiologyViral Infections and Immunology ResearchAnimal Virus Infections Studies
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