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Media type:
E-Article
Title:
COPII Vesicle Transport Is Required for Rotavirus NSP4 Interaction with the Autophagy Protein LC3 II and Trafficking to Viroplasms
Contributor:
Crawford, Sue E.;
Criglar, Jeanette M.;
Liu, Zheng;
Broughman, James R.;
Estes, Mary K.
Published:
American Society for Microbiology, 2019
Published in:
Journal of Virology, 94 (2019) 1
Language:
English
DOI:
10.1128/jvi.01341-19
ISSN:
0022-538X;
1098-5514
Origination:
Footnote:
Description:
In a morphogenic step that is exceedingly rare for nonenveloped viruses, immature rotavirus particles assemble in replication centers called viroplasms, and bud through cytoplasmic cellular membranes to acquire the outer capsid proteins for infectious particle assembly. Historically, the intracellular membranes used for particle budding were thought to be endoplasmic reticulum (ER) because the rotavirus nonstructural protein NSP4, which interacts with the immature particles to trigger budding, is synthesized as an ER transmembrane protein. This present study shows that NSP4 exits the ER in COPII vesicles and that the NSP4-containing COPII vesicles are hijacked by the cellular autophagy machinery, which mediates the trafficking of NSP4 to viroplasms. Changing the paradigm for rotavirus maturation, we propose that the cellular membranes required for immature rotavirus particle budding are not an extension of the ER but are COPII-derived autophagy isolation membranes.