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Structural and Proteomic Studies of the Aureococcus anophagefferens Virus Demonstrate a Global Distribution of Virus-Encoded Carbohydrate Processing

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...

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Autores principales: Gann, Eric R., Xian, Yuejiao, Abraham, Paul E., Hettich, Robert L., Reynolds, Todd B., Xiao, Chuan, Wilhelm, Steven W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507832/
https://www.ncbi.nlm.nih.gov/pubmed/33013751
http://dx.doi.org/10.3389/fmicb.2020.02047
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author Gann, Eric R.
Xian, Yuejiao
Abraham, Paul E.
Hettich, Robert L.
Reynolds, Todd B.
Xiao, Chuan
Wilhelm, Steven W.
author_facet Gann, Eric R.
Xian, Yuejiao
Abraham, Paul E.
Hettich, Robert L.
Reynolds, Todd B.
Xiao, Chuan
Wilhelm, Steven W.
author_sort Gann, Eric R.
collection PubMed
description 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.
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spelling pubmed-75078322020-10-02 Structural and Proteomic Studies of the Aureococcus anophagefferens Virus Demonstrate a Global Distribution of Virus-Encoded Carbohydrate Processing Gann, Eric R. Xian, Yuejiao Abraham, Paul E. Hettich, Robert L. Reynolds, Todd B. Xiao, Chuan Wilhelm, Steven W. Front Microbiol Microbiology 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. Frontiers Media S.A. 2020-09-08 /pmc/articles/PMC7507832/ /pubmed/33013751 http://dx.doi.org/10.3389/fmicb.2020.02047 Text en Copyright © 2020 Gann, Xian, Abraham, Hettich, Reynolds, Xiao and Wilhelm. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Gann, Eric R.
Xian, Yuejiao
Abraham, Paul E.
Hettich, Robert L.
Reynolds, Todd B.
Xiao, Chuan
Wilhelm, Steven W.
Structural and Proteomic Studies of the Aureococcus anophagefferens Virus Demonstrate a Global Distribution of Virus-Encoded Carbohydrate Processing
title Structural and Proteomic Studies of the Aureococcus anophagefferens Virus Demonstrate a Global Distribution of Virus-Encoded Carbohydrate Processing
title_full Structural and Proteomic Studies of the Aureococcus anophagefferens Virus Demonstrate a Global Distribution of Virus-Encoded Carbohydrate Processing
title_fullStr Structural and Proteomic Studies of the Aureococcus anophagefferens Virus Demonstrate a Global Distribution of Virus-Encoded Carbohydrate Processing
title_full_unstemmed Structural and Proteomic Studies of the Aureococcus anophagefferens Virus Demonstrate a Global Distribution of Virus-Encoded Carbohydrate Processing
title_short Structural and Proteomic Studies of the Aureococcus anophagefferens Virus Demonstrate a Global Distribution of Virus-Encoded Carbohydrate Processing
title_sort structural and proteomic studies of the aureococcus anophagefferens virus demonstrate a global distribution of virus-encoded carbohydrate processing
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507832/
https://www.ncbi.nlm.nih.gov/pubmed/33013751
http://dx.doi.org/10.3389/fmicb.2020.02047
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