» Articles » PMID: 38206964

Revisiting the Origins of the Sobemovirus Genus: A Case for Ancient Origins of Plant Viruses

Overview
Journal PLoS Pathog
Specialty Microbiology
Date 2024 Jan 11
PMID 38206964
Authors
Affiliations
Soon will be listed here.
Abstract

The discrepancy between short- and long-term rate estimates, known as the time-dependent rate phenomenon (TDRP), poses a challenge to extrapolating evolutionary rates over time and reconstructing evolutionary history of viruses. The TDRP reveals a decline in evolutionary rate estimates with the measurement timescale, explained empirically by a power-law rate decay, notably observed in animal and human viruses. A mechanistic evolutionary model, the Prisoner of War (PoW) model, has been proposed to address TDRP in viruses. Although TDRP has been studied in animal viruses, its impact on plant virus evolutionary history remains largely unexplored. Here, we investigated the consequences of TDRP in plant viruses by applying the PoW model to reconstruct the evolutionary history of sobemoviruses, plant pathogens with significant importance due to their impact on agriculture and plant health. Our analysis showed that the Sobemovirus genus dates back over four million years, indicating an ancient origin. We found evidence that supports deep host jumps to Poaceae, Fabaceae, and Solanaceae occurring between tens to hundreds of thousand years ago, followed by specialization. Remarkably, the TDRP-corrected evolutionary history of sobemoviruses was extended far beyond previous estimates that had suggested their emergence nearly 9,000 years ago, a time coinciding with the Neolithic period in the Near East. By incorporating sequences collected through metagenomic analyses, the resulting phylogenetic tree showcases increased genetic diversity, reflecting a deep history of sobemovirus species. We identified major radiation events beginning between 4,600 to 2,000 years ago, which aligns with the Neolithic period in various regions, suggesting a period of rapid diversification from then to the present. Our findings make a case for the possibility of deep evolutionary origins of plant viruses.

Citing Articles

Genomic characterization of novel viruses associated with Olea europaea L. in South Africa.

Read D, Pietersen G, Slippers B, Steenkamp E Arch Virol. 2024; 169(10):210.

PMID: 39327328 PMC: 11427506. DOI: 10.1007/s00705-024-06132-1.

References
1.
Issaka S, Traore O, Longue R, Pinel-Galzi A, Gill M, Dellicour S . Rivers and landscape ecology of a plant virus, Rice yellow mottle virus along the Niger Valley. Virus Evol. 2023; 7(2):veab072. PMC: 9927878. DOI: 10.1093/ve/veab072. View

2.
Ghafari M, du Plessis L, Raghwani J, Bhatt S, Xu B, Pybus O . Purifying Selection Determines the Short-Term Time Dependency of Evolutionary Rates in SARS-CoV-2 and pH1N1 Influenza. Mol Biol Evol. 2022; 39(2). PMC: 8826518. DOI: 10.1093/molbev/msac009. View

3.
Fargette D, Pinel A, Rakotomalala M, Sangu E, Traore O, Sereme D . Rice yellow mottle virus, an RNA plant virus, evolves as rapidly as most RNA animal viruses. J Virol. 2008; 82(7):3584-9. PMC: 2268501. DOI: 10.1128/JVI.02506-07. View

4.
Duchene S, Holmes E, Ho S . Analyses of evolutionary dynamics in viruses are hindered by a time-dependent bias in rate estimates. Proc Biol Sci. 2014; 281(1786). PMC: 4046420. DOI: 10.1098/rspb.2014.0732. View

5.
Simmonds P, Aiewsakun P, Katzourakis A . Prisoners of war - host adaptation and its constraints on virus evolution. Nat Rev Microbiol. 2018; 17(5):321-328. PMC: 7097816. DOI: 10.1038/s41579-018-0120-2. View