Interrogating Host-virus Interactions and Elemental Transfer Using NanoSIMS

Alexis Pasulka, California Institute of Technology, Geology and Planetary Sciences, Pasadena, CA, United States, Kimberlee Thamatrakoln, Rutgers University, New Brunswick, NJ, United States, Bonnie Poulos, University of Arizona, Ecology and Evolutionary Biology, AZ, United States, Kay D Bidle, Rutgers University, Marine and Coastal Sciences, New Brunswick, NJ, United States, Matthew B Sullivan, Ohio State University and Victoria J Orphan, California Institute of Technology, Pasadena, CA, United States
Abstract:
Marine viruses (bacteriophage and eukaryotic viruses) impact microbial food webs by influencing microbial community structure, carbon and nutrient flow, and serving as agents of gene transfer. While the collective impact of viral activity has become more apparent over the last decade, there is a growing need for single-cell and single-virus level measurements of the associated carbon and nitrogen transfer, which ultimately shape the biogeochemical impact of viruses in the upper ocean. Stable isotopes have been used extensively for understanding trophic relationships and elemental cycling in marine food webs. While single-cell isotope approaches such as nanoscale secondary ion mass spectrometry (nanoSIMS) have been more readily used to study trophic interactions between microorganisms, isotopic enrichment in viruses has not been described. Here we used nanoSIMS to quantify the transfer of stable isotopes (13C and 15N) from host to individual viral particles in two distinct unicellular algal-virus model systems. These model systems represent a eukaryotic phytoplankton (Emiliania huxleyi strain CCMP374) and its ~200nm coccolithovirus (EhV207), as well as a cyanobacterial phytoplankton (Synechococcus WH8101) and its ~80nm virus (Syn1). Host cells were grown on labeled media for multiple generations, subjected to viral infection, and then viruses were harvested after lysis. In both cases, nanoSIMS measurements were able to detect 13C and 15N in the resulting viral particles significantly above the background noise. The isotopic enrichment in the viral particles mirrored that of the host. Through use of these laboratory model systems, we quantified the sensitivity (ion counts), spatial resolution, and reproducibility, including sources of methodological and biological variability, in stable isotope incorporation into viral particles. Our findings suggest that nanoSIMS can be successfully employed to directly probe virus-host interactions at the resolution of individual viral particles and quantify the amount of carbon and nitrogen transferred into viruses during infection of autotrophic phytoplankton.