Interrogating marine virus‐host interactions and elemental transfer with BONCAT and nanoSIMS‐based methods

• Published in: Environmental microbiology 2018-02, Vol.20 (2), p.671-692
• Main Authors: Pasulka, Alexis L., Thamatrakoln, Kimberlee, Kopf, Sebastian H., Guan, Yunbin, Poulos, Bonnie, Moradian, Annie, Sweredoski, Michael J., Hess, Sonja, Sullivan, Mathew B., Bidle, Kay D., Orphan, Victoria J.
• Format: Article
• Language: English
• Subjects: Amino acids; Amino Acids - analysis; Biogeochemistry; Conversion factors; Dynamics; E coli; Fluorescence; Haptophyta; Host Microbial Interactions; Interactions; Isotope Labeling; Labeling; Mass spectrometry; Mass spectroscopy; Microscopy; Mineral nutrients; Nitrogen enrichment; Nutrient cycles; Nutrient dynamics; Proteins; Secondary ion mass spectrometry; Spectrometry, Mass, Secondary Ion; Stable isotopes; Substrates; Synechococcus; Tracers; Virus Physiological Phenomena; Viruses; Water Microbiology
• ISSN: 1462-2912; 1462-2920
• DOI: 10.1111/1462-2920.13996

Summary While the collective impact of marine viruses has become more apparent over the last decade, a deeper understanding of virus‐host dynamics and the role of viruses in nutrient cycling would benefit from direct observations at the single‐virus level. We describe two new complementary approaches – stable isotope probing coupled with nanoscale secondary ion mass spectrometry (nanoSIMS) and fluorescence‐based biorthogonal non‐canonical amino acid tagging (BONCAT) – for studying the activity and biogeochemical influence of marine viruses. These tools were developed and tested using several ecologically relevant model systems (Emiliania huxleyi/EhV207, Synechococcus sp. WH8101/Syn1 and Escherichia coli/T7). By resolving carbon and nitrogen enrichment in viral particles, we demonstrate the power of nanoSIMS tracer experiments in obtaining quantitative estimates for the total number of viruses produced directly from a particular production pathway (by isotopically labelling host substrates). Additionally, we show through laboratory experiments and a pilot field study that BONCAT can be used to directly quantify viral production (via epifluorescence microscopy) with minor sample manipulation and no dependency on conversion factors. This technique can also be used to detect newly synthesized viral proteins. Together these tools will help fill critical gaps in our understanding of the biogeochemical impact of viruses in the ocean.