Abstract

Viruses modulate the function(s) of environmentally relevant microbial populations, yet considerations of the metabolic capabilities of individual virus particles themselves are rare. We used shotgun proteomics to quantitatively identify 43 virus-encoded proteins packaged within purified Aureococcus anophagefferens Virus (AaV) particles, normalizing data to the per-virion level using a 9.5-Å-resolution molecular reconstruction of the 1900-Å (AaV) particle that we generated with cryogenic electron microscopy. This packaged proteome was used to determine similarities and differences between members of different giant virus families. We noted that proteins involved in sugar degradation and binding (e.g., carbohydrate lyases) were unique to AaV among characterized giant viruses. To determine the extent to which this virally encoded metabolic capability was ecologically relevant, we examined the TARA Oceans dataset and identified genes and transcripts of viral origin. Our analyses demonstrated that putative giant virus carbohydrate lyases represented up to 17% of the marine pool for this function. In total, our observations suggest that the AaV particle has potential prepackaged metabolic capabilities and that these may be found in other giant viruses that are widespread and abundant in global oceans.

Highlights

  • The most biologically complex virus particles may be the “giants” that belong to the Nucleocytoplasmic Large dsDNA Virus (NCLDV) group

  • Due to a limited number of images, a fivefold-only reconstruction could not be performed to confidently determine whether there is a unique vertex of anophagefferens Virus (AaV) as seen in PBCV-1 and Mimivirus (Cherrier et al, 2009; Xiao et al, 2009)

  • To normalize the data to individual particle complements, we coupled this work with a cryo-electron microscopy reconstruction of the virus particle to determine the protein distribution per particle of a significant marker protein

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Summary

Introduction

The most biologically complex virus particles may be the “giants” that belong to the Nucleocytoplasmic Large dsDNA Virus (NCLDV) group These viruses have genomes and particle sizes that can rival bacteria in size (Wilhelm et al, 2017). Given the abundance of these viruses in nature yet paucity of NCLDV model systems and information on their physiological ecology, complete characterization of lab models to infer environmental function is a necessity. This is true for the virus particle and its potential to have biochemical activity at the onset of the interaction with the host, as well as once released into the environment

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