Selective Packaging of Rotavirus Double-Layered Particles into Host Microvesicles
Abstract
Rotavirus is a non-enveloped RNA virus traditionally thought to exit host cells through lytic or conventional vesicular pathways, but recent evidence shows that it also exploits host microvesicles for non-lytic transmission. To characterize this transmission pathway, we combined high-resolution microscopy (TEM, confocal microscopy, immunogold labeling) with biochemical and infectivity assays. Our work revealed that rotavirus infection robustly increased microvesicle production, and individual vesicles frequently contained multiple viral particles. Quantitative analysis revealed striking differential partitioning of particle types. Mature triple-layered particles predominated within infected cells, whereas extracellular microvesicles were strongly enriched for immature double-layered particles. Although free double-layered particles lack the outer capsid required for classical receptor-mediated entry, microvesicle-associated particles initiated productive infections, whereas disruption of the vesicular membrane abolished infectivity. These findings suggest an evolutionarily advantageous dual transmission strategy. By using host-derived membranes to transmit otherwise non-infectious intermediates, rotavirus can bypass outer-capsid-dependent entry, potentially reducing the energetic cost of producing fully mature infectious particles while enabling collective transmission. Maintaining a free-virus pathway may nevertheless be important because transmission by individual mature virions imposes population bottlenecks that limit the propagation of defective or cheating genomes and preserve high-fitness genotypes. Thus, partitioning viral progeny between vesicle-associated double-layered particles and free triple-layered particles may balance the immediate benefits of collective spread with long-term genetic quality control. Whether double-layered particle enrichment arises from active sorting or spatial coupling between viral assembly and microvesicle biogenesis remains unresolved.
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BibTeX
@misc{islam2026selective,
title = {{Selective Packaging of Rotavirus Double-Layered Particles into Host Microvesicles}},
author = {Z. M. Islam and J. Luo and A. Castillo and A. Sokol and E. Chen and I. S. Maisha and K. Nguyen and J. J. Dennehy},
howpublished = {bioRxiv},
year = {2026},
month = sep,
doi = {10.64898/2026.09.16.752160},
url = {https://www.biorxiv.org/content/10.64898/2026.09.16.752160v1},
note = {CC BY-NC-ND},
}
RIS
TY - UNPB
TI - Selective Packaging of Rotavirus Double-Layered Particles into Host Microvesicles
AU - Z. M. Islam
AU - J. Luo
AU - A. Castillo
AU - A. Sokol
AU - E. Chen
AU - I. S. Maisha
AU - K. Nguyen
AU - J. J. Dennehy
PY - 2026
DA - 2026/09/16
PB - bioRxiv
DO - 10.64898/2026.09.16.752160
UR - https://www.biorxiv.org/content/10.64898/2026.09.16.752160v1
AB - Rotavirus is a non-enveloped RNA virus traditionally thought to exit host cells through lytic or conventional vesicular pathways, but recent evidence shows that it also exploits host microvesicles for non-lytic transmission. To characterize this transmission pathway, we combined high-resolution microscopy (TEM, confocal microscopy, immunogold labeling) with biochemical and infectivity assays. Our work revealed that rotavirus infection robustly increased microvesicle production, and individual vesicles frequently contained multiple viral particles. Quantitative analysis revealed striking differential partitioning of particle types. Mature triple-layered particles predominated within infected cells, whereas extracellular microvesicles were strongly enriched for immature double-layered particles. Although free double-layered particles lack the outer capsid required for classical receptor-mediated entry, microvesicle-associated particles initiated productive infections, whereas disruption of the vesicular membrane abolished infectivity. These findings suggest an evolutionarily advantageous dual transmission strategy. By using host-derived membranes to transmit otherwise non-infectious intermediates, rotavirus can bypass outer-capsid-dependent entry, potentially reducing the energetic cost of producing fully mature infectious particles while enabling collective transmission. Maintaining a free-virus pathway may nevertheless be important because transmission by individual mature virions imposes population bottlenecks that limit the propagation of defective or cheating genomes and preserve high-fitness genotypes. Thus, partitioning viral progeny between vesicle-associated double-layered particles and free triple-layered particles may balance the immediate benefits of collective spread with long-term genetic quality control. Whether double-layered particle enrichment arises from active sorting or spatial coupling between viral assembly and microvesicle biogenesis remains unresolved.
ER -