Key result
Rotavirus transcripts selectively partition into viral ribonucleoprotein condensates, a process dependent on the viral RNA chaperone NSP2 and segment-specific untranslated regions.
Why the study?
Understanding mechanisms of viroplasm assembly and RNA enrichment is crucial to gaining insight into their function and stoichiometric assortment of rotavirus transcripts.
No immediate clinical impact; leaves open NSP2 as antiviral target in rotavirus replication.
Rotaviruses transcribe eleven distinct protein-coding RNAs that must be stoichiometrically co-packaged prior to their replication to make an infectious virion. During infection, rotavirus transcripts accumulate in cytoplasmic ribonucleoprotein (RNP) condensates, termed viroplasms. Understanding the mechanisms of viroplasm assembly and RNA enrichment within is crucial to gaining greater insight into their function and stoichiometric assortment of individual transcripts. We analysed the subcellular distribution of individual RV transcripts and viroplasm transcriptome by combining multiplexed DNA-barcoded single-molecule RNA FISH of infected cells. Using DNA-PAINT microscopy, we provide evidence of the early onset of viral transcript oligomerisation that occurs prior to the formation of viroplasms. We demonstrate that viral sequences lacking the conserved terminal regions fail to undergo enrichment in rotavirus RNP condensates. We show that individual viral transcripts exhibit variable propensities to partition into viroplasms, irrespective of their absolute numbers in cells, suggesting a selective RNA enrichment mechanism distinct from other known cellular RNP granules. We suggest that rotavirus replication factories represent unique RNP condensates enriched in eleven types of cognate transcripts that may facilitate the assembly of a multi-segmented RNA genome.
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Strauss et al. (2021) studied Rotavirus infection. Rotavirus infection and NSP2 knockdown vs. Mock-infected cells and scrambled shRNA was evaluated on RNA recruitment and viroplasm assembly. Rotavirus transcripts selectively partition into viral ribonucleoprotein condensates, a process dependent on the viral RNA chaperone NSP2 and segment-specific untranslated regions.
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