Mammalian orthoreoviruses exhibit rare genotype variability in genome constellations

Diller, Julia R.; Thoner, Timothy W.; Ogden, Kristen M.

doi:10.1016/j.meegid.2023.105421

Cited by 2 publications

(1 citation statement)

References 71 publications

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“…Consistent with past literature, the S1 gene was the most divergent ( 51 ); for example, the T1E1 and T3D PL S1 genes were only 40.61% and 25.23% identical at the nucleotide and amino acid levels, respectively. The other genes consistently had >70% nucleotide and >80%–90% amino acid identities, congruent with a recent study ( 52 ). Taken together, the four natural Edmonton reovirus isolates are genetically distinct from prototypic strains, any known reovirus isolates, and even from each other despite their geographic closeness.…”

Section: Resultssupporting

confidence: 90%

Reovirus genomic diversity confers plasticity for protease utility during adaptation to intracellular uncoating

Lin,

Wong,

Eaton

et al. 2023

J Virol

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Mammalian orthoreoviruses (reoviruses) infect many mammals and provide a safe model to study enteric viruses. Knowledge of reoviruses is derived from prototypic lab strains, notably T1L and T3D. Based on these prototypic strains, reoviruses can efficiently utilize gut or lysosomal proteases for uncoating and penetration into host cytoplasm. To discover natural reovirus characteristics, we isolated four genetically diverse wastewater reovirus samples and compared their genetic and phenotypic characteristics to those of T1L/T3D. On L929 cells, the most commonly used model for reovirus studies, naturally derived reoviruses displayed lower fitness than T1L/T3D, evident from smaller plaques and higher relative particle-to-PFU ratios. In contrast to T1L/T3D, which are uncoated efficiently by lysosomal-mediated proteolysis, naturally derived reoviruses displayed poor uncoating kinetics. Exposure of naturally derived reoviruses to gut proteases led to rapid extracellular uncoating and significantly improved infectivity relative to T1L/T3D, indicating that wild reoviruses depended more on extracellular gut proteases. To discover if reovirus can adapt to new host proteases, naturally derived samples were passaged on L929 cells, and large and small plaque-forming isolates were evaluated. Larger plaque sizes correlate with faster intracellular uncoating. Whole-genome sequencing identified the outer capsid σ3 protein as the determinant of uncoating proficiency between wild reoviruses. Interestingly, mutations that permitted intracellular uncoating were found in 0.01% of the parental quasispecies, suggesting that variants with altered protease sensitivity were rapidly selected for during cell culture propagation. Altogether, these findings indicate that naturally circulating reoviruses are more reliant on gut proteases, but the genetic diversity of reovirus quasispecies bestows tremendous plasticity toward protease utility. IMPORTANCE Reoviruses infect many mammals and are widely studied as a model system for enteric viruses. However, most of our reovirus knowledge comes from laboratory strains maintained on immortalized L929 cells. Herein, we asked whether naturally circulating reoviruses possess the same genetic and phenotypic characteristics as laboratory strains. Naturally circulating reoviruses obtained from sewage were extremely diverse genetically. Moreover, sewage reoviruses exhibited poor fitness on L929 cells and relied heavily on gut proteases for viral uncoating and productive infection compared to laboratory strains. We then examined how naturally circulating reoviruses might adapt to cell culture conditions. Within three passages, virus isolates from the parental sewage population were selected, displaying improved fitness and intracellular uncoating in L929 cells. Remarkably, selected progeny clones were present at 0.01% of the parental population. Altogether, using reovirus as a model, our study demonstrates how the high genetic diversity of naturally circulating viruses results in rapid adaptation to new environments.

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Section: Resultssupporting

confidence: 90%