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Rotavirus assembly is a complex process that involves the stepwise acquisition of protein layers in distinct intracellular locations to form the fully assembled particle. Understanding and visualization of the assembly process has been hampered by the inaccessibility of unstable intermediates. We characterize the assembly pathway of group A rotaviruses observed in situ within cryo-preserved infected cells through the use of cryoelectron tomography of cellular lamellae. Our findings demonstrate that the viral polymerase VP1 recruits viral genomes during particle assembly, as revealed by infecting with a conditionally lethal mutant. Additionally, pharmacological inhibition to arrest the transiently enveloped stage uncovered a unique conformation of the VP4 spike. Subtomogram averaging provided atomic models of four intermediate states, including a pre-packaging single-layered intermediate, the double-layered particle, the transiently enveloped double-layered particle, and the fully assembled triple-layered virus particle. In summary, these complementary approaches enable us to elucidate the discrete steps involved in forming an intracellular rotavirus particle.

Original publication

DOI

10.1016/j.chom.2023.03.004

Type

Journal article

Journal

Cell Host Microbe

Publication Date

12/04/2023

Volume

31

Pages

604 - 615.e4

Keywords

Reoviridae, cellular structural biology, cryoelectron tomography, dsRNA viruses, electron microscopy, in situ, rotavirus, subtomogram averaging, virus assembly, virus structure, Rotavirus, Tomography, Virus Assembly