Single-Molecule FISH Reveals Non-selective Packaging of Rift Valley Fever Virus Genome Segments

The bunyavirus genome comprises a small (S), medium (M), and large (L) RNA segment of negative polarity. Although genome segmentation confers evolutionary advantages by enabling genome reassortment events with related viruses, genome segmentation also complicates genome replication and packaging. Ac...

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Veröffentlicht in:PLoS pathogens 2016-08, Vol.12 (8), p.e1005800-e1005800
Hauptverfasser: Wichgers Schreur, Paul J, Kortekaas, Jeroen
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description The bunyavirus genome comprises a small (S), medium (M), and large (L) RNA segment of negative polarity. Although genome segmentation confers evolutionary advantages by enabling genome reassortment events with related viruses, genome segmentation also complicates genome replication and packaging. Accumulating evidence suggests that genomes of viruses with eight or more genome segments are incorporated into virions by highly selective processes. Remarkably, little is known about the genome packaging process of the tri-segmented bunyaviruses. Here, we evaluated, by single-molecule RNA fluorescence in situ hybridization (FISH), the intracellular spatio-temporal distribution and replication kinetics of the Rift Valley fever virus (RVFV) genome and determined the segment composition of mature virions. The results reveal that the RVFV genome segments start to replicate near the site of infection before spreading and replicating throughout the cytoplasm followed by translocation to the virion assembly site at the Golgi network. Despite the average intracellular S, M and L genome segments approached a 1:1:1 ratio, major differences in genome segment ratios were observed among cells. We also observed a significant amount of cells lacking evidence of M-segment replication. Analysis of two-segmented replicons and four-segmented viruses subsequently confirmed the previous notion that Golgi recruitment is mediated by the Gn glycoprotein. The absence of colocalization of the different segments in the cytoplasm and the successful rescue of a tri-segmented variant with a codon shuffled M-segment suggested that inter-segment interactions are unlikely to drive the copackaging of the different segments into a single virion. The latter was confirmed by direct visualization of RNPs inside mature virions which showed that the majority of virions lack one or more genome segments. Altogether, this study suggests that RVFV genome packaging is a non-selective process.
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Although genome segmentation confers evolutionary advantages by enabling genome reassortment events with related viruses, genome segmentation also complicates genome replication and packaging. Accumulating evidence suggests that genomes of viruses with eight or more genome segments are incorporated into virions by highly selective processes. Remarkably, little is known about the genome packaging process of the tri-segmented bunyaviruses. Here, we evaluated, by single-molecule RNA fluorescence in situ hybridization (FISH), the intracellular spatio-temporal distribution and replication kinetics of the Rift Valley fever virus (RVFV) genome and determined the segment composition of mature virions. The results reveal that the RVFV genome segments start to replicate near the site of infection before spreading and replicating throughout the cytoplasm followed by translocation to the virion assembly site at the Golgi network. 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subjects Biology and life sciences
Bunyavirus
Bunyaviruses
Cell Line
CVI Virologie
CVI Virology
Experiments
Fever
Fluorescence in situ hybridization
Genes
Genetic aspects
Genome, Viral - physiology
Genomes
Genotypes
Health aspects
Humans
Identification and classification
In Situ Hybridization, Fluorescence
Medicine and health sciences
Methods
Proteins
Research and Analysis Methods
Rift Valley Fever - metabolism
Rift Valley fever virus
Rift Valley fever virus - physiology
RNA polymerase
Virologie
Virology
Virulence (Microbiology)
Virus Assembly - physiology
Viruses
title Single-Molecule FISH Reveals Non-selective Packaging of Rift Valley Fever Virus Genome Segments
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