Dynamic genome evolution and complex virocell metabolism of globally-distributed giant viruses

Mohammad Moniruzzaman, Carolina A. Martínez-Gutiérrez, Alaina Weinheimer, Frank O. Aylward

Nature Communications · 2020 · 245 citations · 66 references

DOIFull text

Open access

TL;DR

The discovery of eukaryotic giant viruses has transformed our understanding of viral complexity, yet the extent of their encoded metabolic diversity remains unclear. The study aims to generate 501 metagenome‑assembled genomes of Nucleo‑Cytoplasmic Large DNA Viruses from global environments and analyze their encoded functional capacity. The authors assembled 501 NCLDV genomes from metagenomic data worldwide, annotated their metabolic genes, and performed phylogenetic clustering against cellular homologs. The analysis revealed a remarkable diversity of metabolic genes—including nutrient uptake, light harvesting, nitrogen metabolism, glycolysis, and TCA cycle components—clustered into virus‑specific divergent clades, indicating that giant viruses encode complex metabolic capabilities with evolutionary histories largely independent of cellular life and thus act as important drivers of global biogeochemical cycles.

Abstract

Abstract The discovery of eukaryotic giant viruses has transformed our understanding of the limits of viral complexity, but the extent of their encoded metabolic diversity remains unclear. Here we generate 501 metagenome-assembled genomes of Nucleo-Cytoplasmic Large DNA Viruses (NCLDV) from environments around the globe, and analyze their encoded functional capacity. We report a remarkable diversity of metabolic genes in widespread giant viruses, including many involved in nutrient uptake, light harvesting, and nitrogen metabolism. Surprisingly, numerous NCLDV encode the components of glycolysis and the TCA cycle, suggesting that they can re-program fundamental aspects of their host’s central carbon metabolism. Our phylogenetic analysis of NCLDV metabolic genes and their cellular homologs reveals distinct clustering of viral sequences into divergent clades, indicating that these genes are virus-specific and were acquired in the distant past. Overall our findings reveal that giant viruses encode complex metabolic capabilities with evolutionary histories largely independent of cellular life, strongly implicating them as important drivers of global biogeochemical cycles.

References

66