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Reovirus Low-Density Particles Package Cellular RNA.

Timothy W Thoner1, Xiang Ye1, John Karijolich1

  • 1Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

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Summary
This summary is machine-generated.

Mammalian orthoreovirus (reovirus) virions selectively package only viral double-stranded RNA. In contrast, reovirus top component particles incorporate host RNAs, suggesting differential selectivity in viral RNA packaging mechanisms.

Keywords:
ReoviridaedsRNApackagingreovirussegmentedtop component

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Area of Science:

  • Virology
  • Molecular Biology
  • Genomics

Background:

  • Packaging of segmented viral RNA genomes requires precise coordination between viral proteins and RNA segments.
  • Mammalian orthoreovirus (reovirus) is known to package either all or none of its ten double-stranded RNA genome segments, excluding host RNA.
  • Reovirus produces both genome-containing virions and
  • genomeless
  • top component particles, but the RNA content of these particles, particularly regarding host RNA, remains uncharacterized.

Purpose of the Study:

  • To investigate the RNA content of reovirus particles to understand reovirus packaging potential and mechanisms.
  • To determine whether reovirus virions or top component particles package host RNA.

Main Methods:

  • Utilized next-generation RNA sequencing to comprehensively analyze the RNA content of enriched reovirus particles.
  • Compared RNA composition between reovirus virions and top component particles.

Main Results:

  • Reovirus virions exclusively packaged viral double-stranded RNA, demonstrating highly selective genome packaging.
  • Reovirus top component particles contained reduced amounts of viral double-stranded RNA and were significantly enriched for various host RNA species, particularly short, non-polyadenylated transcripts.
  • Host RNA selection was independent of cellular RNA abundance and varied between reovirus strains, indicating a selective, non-random incorporation mechanism not solely dependent on the viral RNA polymerase.

Conclusions:

  • Reovirus genome packaging into virions is exquisitely selective.
  • Host RNA incorporation into top component particles is differentially selective and may be linked to inefficient viral RNA packaging processes.
  • These findings provide critical insights into the distinct mechanisms governing RNA packaging in reovirus virions versus top component particles.