Non-axenic A. anophagefferens CCMP1984 cultures were grown at 19°C, on a 14:10 light dark cycle at 100 μmol photons m^–2 s^–1 in modified ASP₁₂A growth medium (Gann, 2016). Cultures were acclimated to four different NO3- concentrations (1.47, 0.735, 0.147, 0.0147 mM) (Table 1) by at least three successive transfers at each NO3- concentration prior to experimentation. Preliminary efforts demonstrated that A. anophagefferens would not grow at concentrations less than 0.0147 mM so it was chosen as our lowest condition. Previous studies have demonstrated that culturing A. anophagefferens in higher concentrations of a sole nitrogen source (0.030 mM NH₄⁺) cause physiologically and transcriptional differences compared to replete conditions (Frischkorn et al., 2014). To prevent nutrient carry over, cultures were pelleted (2,000 × g, 5 min), and resuspended in fresh ASP₁₂A with the respective NO3- concentration. The AaV lysate used to infect cultures was concentrated 50-fold from freshly lysed cultures using a Lab-scale Tangential Flow Filtration System (Fisher Scientific, Waltham, MA, United States) equipped with a Durapore^TM 30 kDa Pellicon XL Filter (MilliporeSigma, Burlington, MA, United States). To deplete lysates of nitrate, the concentrate was diluted 20-fold with ASP₁₂A without added nitrate, and then viruses re-concentrated, before being passed through a 0.45-μm pore-size syringe filter (Millex-HV PVDF, Millipore Sigma, Burlington, NJ, United States). Less than 0.5 mL of the re-concentrated lysate was added to cultures (20 mL) for each experiment.

Before enumerating concentrations, 1 mL of cultures were either directly fixed in 0.5% glutaraldehyde (for A. anophagefferens enumeration) or first passed through a 0.45-μm pore-size syringe filter (Millex-HV 0.45 μm nominal pore-size PVDF, Millipore Sigma, Burlington, NJ, United States) before fixation (for AaV enumeration). Although filtering cultures for enumeration of viruses reduced the concentration of viruses (∼43%) (Supplementary Figure 1), we wanted to reduce clumping or adsorption of viruses to cellular material. Fixed samples were stored at 4°C for at least 30 min before being measured on a FACSClibur flow cytometer (Becton, Dickinson and Company, Franklin Lakes, NJ, United States). A. anophagefferens populations were gated on red chlorophyll a fluorescence and forward scatter (Moniruzzaman et al., 2018). Mean forward scatter (FSC-H), side scatter (SSC-H), and red fluorescence (FL3-H) for each gated A. anophagefferens populations was also recorded. These act as proxies for cell size, cellular granularity, and chlorophyll a autofluorescence, respectively.

AaV was enumerated as described previously (Brussaard, 2004; Brown and Bidle, 2014). Briefly, the fixed AaV samples were diluted 100-fold in ASP₁₂A and then inoculated with a 10,000-fold diluted SYBR Green DNA stain (Lonza, Basel, Switzerland), before being incubated at 80°C for 10 min. AaV populations were gated on SYBR green emission (excitation: 520 nm) and side scatter (Supplementary Figure 2). To determine host and virus concentrations a known concentration of diluted FluoSphere Carboxylate-Modified Microspheres, 1.0 μm, yellow-green fluorescent (505/515) (Invitrogen, Waltham, MA, United States) was added to each sample before being ran for one minute.

To determine the influence of nitrate concentration acclimation, A. anophagefferens cultures in late logarithmic growth and pre-acclimated to the four different nitrate concentrations (Table 1) were collected by centrifugation (2,000 × g, 5 min). Cell pellets were resuspended in media containing the respective NO3- concentration and replicates pooled to concentrate cell densities ∼50-fold. To observe the entire growth curve, four 20 mL biological replicates were inoculated to a final cell density between 5 × 10⁴ and 1 × 10⁵ mL^–1. To assess differences in the physiological state of the cells due to the different NO3- concentrations, the mean of various flow cytometry parameters (FSC-H, SSC-H, and FL3-H) of the gated A. anophagefferens cells was averaged on 2 days during the middle of logarithmic growth (days 6 and 7). Doubling time of the cultures was calculated using the following equation, with days three and eight as time_N and time_N0, respectively:

To determine the influence of acclimation to different nitrate concentration on the AaV infection cycle, multiple cultures at late logarithmic growth that were acclimated to the four different nitrate concentrations (Table 1) were first pelleted by centrifugation (2,000 × g, 5 min). Cell pellets were resuspended in media containing the respective NO3- concentration and pooled to concentrate the cultures ∼50-fold. Five biological replicates (20 mL) were inoculated to a final cell density at 10⁶ cells mL^–1 and a multiplicity of infection (m.o.i) ∼100 particles per cell. Uninfected controls were also done in five biological replicates. A high multiplicity of infection was used as only a small fraction of AaV are infectious and infecting cultures with m.o.i’s between ∼20 and 100 allows for lysis of the majority of cells (>99%) within 3 days (Gann et al., 2020). Cultures were infected at the start of the light cycle. We collected samples immediately upon infection, and then every 4 h for 24 h, and 48 and 72 h post infection. Sampling throughout the first 24 h allowed for the adsorption rate of AaV to be determined as described previously (Cottrell and Suttle, 1995) using the following formula:

where a is the slope of the linear regression of the natural log of free viruses over the course of the first 24 h and N is equal to the concentration of A. anophagefferens. The number of viruses produced per cell lyses, or burst size, was calculated using the following formula:

The host and virus concentrations at time N₀ is when free viruses did not decline further: 24 h for 1.47, 0.735, and 0.147 mM NO3- cultures, and 48 h for the 0.0147 mM NO3- cultures. Time N was the end of the experiment, 72 h. Changes in basic cellular physiology during the infection cycle were determined through various flow cytometry parameters of the gated A. anophagefferens cells including forward scatter (FSC-H), side scatter (SSC-H), and red fluorescence (FL3-H).

To determine the influence of external nitrate concentration on the AaV infection cycle, multiple 1.47 mM NO3- acclimated cultures at late logarithmic growth were first pelleted by centrifugation (2,000 × g, 5 min). Cell pellets were resuspended in ASP₁₂A with no added nitrate and pooled to concentrate the cultures ∼50-fold. Immediately before infection, NO3- was added to the cultures (final cell density = 1 × 10⁶ mL^–1) at three different concentrations (1.47 mM, 0.0147 mM, and no added NO3-). Five biological replicates were infected at a m.o.i ∼20 particles per cell in 20 mL, where five uninfected controls were brought up to 20 mL with ASP₁₂A with no nitrate. Samples were collected each day for 4 days. Burst sizes were calculated as described above, using time points of 1 and 4 days for times N and N_o, respectively.

Statistical analyses were performed using Prism 7.03 (GraphPad, San Diego, CA, United States). To compare differences between treatments a one-way ANOVA was used followed by Tukey’s HSD post hoc testing.

Cultures were acclimated to four different NO3- concentrations (1.47, 0.735, 0.147, and 0.0147 mM), with a constant PO43- concentration (0.12 mM), producing environments with decreasing N:P ratios (Table 1). There was a difference in the length of the logarithmic phase of growth as well as the final abundance of cells reached between the 0.0147 mM acclimated cultures and the other treatments. For the 1.47, 0.735, and 0.147 mM NO3- acclimated cultures, the length of the logarithmic phase of growth was 9–10 days (Figure 1A), and there was no significant difference in end point abundances which were: 1.7 × 10⁷ cells mL^–1 (SD = 9.7 × 10⁵), 1.9 × 10⁷ cells mL^–1 (SD = 8.7 × 10⁵), 1.6 × 10⁷ cells mL^–1 (SD = 1.4 × 10⁵), respectively (Supplementary Table 1). The 0.0147 mM NO3- acclimated culture had a final cell abundance of half (8.5 × 10⁶ cells mL^–1, SD = 9.7 × 10⁵) the three higher acclimation concentration cultures at the end of the 14-day experiment, with the logarithmic phase being 1–2 days shorter (Figure 1A). The four different acclimating NO3- concentrations did not greatly influence the doubling time of the cultures, with all cultures having doubling times between 0.99 and 1.09 days (Figure 1B and Supplementary Table 2). To further understand how decreasing N:P ratios influences A. anophagefferens cells, we used parameters measured during flow cytometry (Figure 1B). The relative values of forward scatter (FSC-H), side scatter (SSC-H), and chlorophyll a autofluorescence (FL3-H) of all cells gated as A. anophagefferens were averaged during two consecutive days in mid-logarithmic growth (Figure 1C). The 0.735 and 0.147 mM NO3- acclimated cultures had FSC-H, SSC-H, and FL3-H values that were not significantly different from one another (Supplementary Table 3). Cultures acclimated to 1.47 mM NO3- had a slight, but significant increase for FSC-H and SSC-H, whereas there was statistically no difference with FL3-H compared to the 0.735 and 0.147 mM NO3- acclimated cultures (Supplementary Table 3). There was a significant decrease in all three parameters for the 0.0147 mM NO3- acclimated cultures compared to the other three (Supplementary Table 3).

When we infected cultures acclimated to the four NO3- concentrations with AaV at an m.o.i of ∼100, only the 0.0147 mM NO3- acclimated cultures showed differences in infection dynamics. The 1.47, 0.735, and 0.147 mM NO3- acclimated cultures all had similar trends as previously reported (Rowe et al., 2008; Brown and Bidle, 2014), where new viruses were produced and cells lysed after 24 h (Figures 2A,B), while cell lysis and virus production was delayed 1 day for the 0.0147 mM acclimated culture. The burst sizes for the 1.47 mM (465.8 ± 32.2 viruses produced cell lysed^–1), 0.735 mM (427.1 ± 93.7 viruses produced cell lysed^–1), and 0.147 mM (465.8 ± 32.2 viruses produced cell lysed^–1) NO3- acclimated cultures were not significantly different from one another. These treatments however, had a burst size ∼3× greater than the 0.0147 mM NO3- acclimated cultures (142.6 ± 40.4 viruses produced cell lysed^–1, Figure 2C and Supplementary Table 4). There were no differences in the adsorption rates due to NO3- concentration (Figure 2D and Supplementary Table 5). We used parameters measured during flow cytometry to look at changes between infected and uninfected cells over the first day 24 h of the infection cycle (Supplementary Figure 3). All uninfected populations increased in FSC-H, and FL3-H, while all but the 0.0147 mM NO3- acclimated culture increased in SSC-H. The FSC-H and SSC-H of infected cells either remained the same or decreased slightly (<5%) (Supplementary Figures 3A,B). The FL3-H values remained the same for the first twelve hours of the infection cycle but then decreased between 6.8 and 9.5% for all the NO3- concentrations (Supplementary Figure 3C).

To determine whether the external nitrate concentration altered viral production, we collected A. anophagefferens cells grown at 1.47 mM, infected cultures at an m.o.i ∼20, then added back variable NO3- concentrations (1.47, 0.0147 or 0 mM) (Figure 3). In controls, the end point abundance after the 4 days significantly decreased with reduced NO3- concentrations (Supplementary Table 6). The final cell abundances were 6.2 × 10⁶ cells mL^–1 (SD = 3.9 × 10⁵), 5.0 × 10⁶ cells mL^–1 (SD = 5.9 × 10⁵), and 3.4 × 10⁶ cells mL^–1 (SD = 3.1 × 10⁵), for cultures that had 1.47, 0.0147, and 0 mM NO3- added back, respectively. There was also a decrease in FL3-H for the control 0 and 0.0147 mM cultures compared to the 1.47 mM cultures (Supplementary Figure 4). Although there was a hindrance to the growth of control cultures, infecting cultures with decreasing NO3-concentrations added back did not change the length of time for cells to lyse (Figure 3A) or new viruses to be produced (Figure 3B) or decrease the burst size (Figure 3C and Supplementary Table 7).

The effect of acclimation of A. anophagefferens cultures to decreasing NO3- concentrations, was only seen in the lowest concentration (0.0147 mM), where there was a decreased biomass accumulation and end point cell abundance. These acclimated cultures appeared to be physiologically different from the other cultures as there was a reduction in forward scatter, side scatter, and red fluorescence, as detected by flow cytometry. Our observations suggest that the cells in the lowest NO3- concentrations are smaller (based on forward scatter) and have less chlorophyll a per cell (based on red fluorescence). In previous studies of various A. anophagefferens strains the maximum efficiency of photosystem II (F_v/F_m) is reduced in lower or limiting nitrogen concentrations (Berg et al., 2008; Dong et al., 2014; Frischkorn et al., 2014), and in vivo fluorescence per cell is also reduced (Dong et al., 2014). Experimental data is also supported by transcriptomes of A. anophagefferens CCMP1850 in low nitrogen environments, where there is a down regulation of light harvesting complexes and an increase in proteases and peptidases (Frischkorn et al., 2014). The reduction of red fluorescence or chlorophyll a per cell has been seen in other species of algae as well, leading to a reduced F_v/F_m (Berges and Falkowski, 1998; Maat et al., 2016a; Maat and Brussaard, 2016), and was hypothesized that this reduction in chlorophyll a content decreases the nitrogen requirement within the cell (Maat and Brussaard, 2016).

Similar, to the growth kinetics of cultures, only infections of the 0.0147 mM NO3- acclimated cultures were influenced negatively by the nitrate concentration, with a reduction in burst size and a prolonged production of new viruses. A prolonged infection cycle has been seen in multiple systems due to growth in lower nitrogen concentrations (Bratbak et al., 1998; Maat and Brussaard, 2016), as has the reduced burst size (Bratbak et al., 1998; Cheng et al., 2015; Maat and Brussaard, 2016). We sampled multiple times throughout the first 24 h of the experiment to detect differences in infected populations by flow cytometry and determined the adsorption rates. There was no difference in adsorption rates between any of the acclimated NO3- concentration treatments. The average adsorption rate determined in this study (5.9 × 10^–10 mL min^–1) agrees with that previously reported in this system (5.8 × 10^–10 mL min^–1) (Brown and Bidle, 2014). The Chlorella variabilis NC64A infecting Paramecium bursaria Chlorella Virus, PBCV-1, adsorption rate was also not influenced by altered less than optimum C:P ratios (Clasen and Elser, 2007), suggesting that although algal cells differ physiologically under non-optimal nutrient conditions, viruses are able to adsorb with the same efficiency.

Forward scatter and side scatter remain constant over the course of the infection cycle, while red fluorescence begins to decrease around 12 h post-infection. A reduction in red fluorescence has been detected in other virus-host systems (Lawrence et al., 2006; Lonborg et al., 2013) at specific points in the infection cycle, depending on the virus (Lawrence et al., 2006). This correlates with a reduction in chlorophyll a and F_v/F_m over the course of the infection cycle (Schatz et al., 2014). Measurements for F_v/F_m have not been collected during the Aureococcus infection cycle, but daily measurements for control and infected cultures have shown an initial increase compared to control cultures then a drastic decrease (Gobler et al., 2007). In both natural populations and lab cultures, when many viruses are present in the cells there is either no chloroplast or it appears to be much smaller than uninfected cells (Sieburth et al., 1988; Gastrich et al., 2004; Rowe et al., 2008). More work is needed to determine whether this reduction in chloroplast size corresponds to the decrease in red fluorescence beginning around twelve hours post infection.

It was hypothesized that the differences in burst sizes in cells grown in low nitrogen environments were caused by the resources available within the host (Cheng et al., 2015), due to a decreased nitrogen quota within cells grown in low nitrogen (Cheng et al., 2015; Maat and Brussaard, 2016). Altered internal quota has also been hypothesized to cause a reduced burst size in cells grown at altered C:P ratios (Clasen and Elser, 2007). In Thalassiosira weissflogii, Dunaliella tertiolecta (Berges and Falkowski, 1998), and Chlorella variabilis NC64A (Cheng et al., 2015), as cells became more limited of nitrogen, their internal C:N ratio increased, hypothetically due to the reduction of nitrogen stores or non-essential proteins (Berges and Falkowski, 1998). This reduced chlorophyll a content within the cells and decreased F_v/F_m as discussed above may prevent viruses from acquiring all of the energy or nitrogen required to produce the large number of viruses per cell. Algae also have increased starch and lipid production (Cheng et al., 2015), and protease activity (Berges and Falkowski, 1998; Frischkorn et al., 2014) under nitrogen stress which may reduce the ability of a successful infection from occurring. More work is needed to understand how stresses influence nutrient and metabolite pools of virocells.

The dependence on the external nutrient pools is variable depending on the system and the nutrient. Transitioning Escherichia coli grown in a nutrient rich broth to minimal media without various components greatly reduced the T2 phage produced, and the effects of specific nutrient(s) added back partially restored viral production showed the external supplies are required for maximum production of phage (Fowler and Cohen, 1948). Also, adding back various organic phosphorous to phosphorus-starved Micromonas pusilla did not decrease the length of time to produce new viruses but did significantly increase the number of viruses produced (Maat et al., 2016b). In contrast, for three marine bacterium-phage systems the majority of the phage genomes were constructed from recycled materials of host origin (Wikner et al., 1993). Moreover, the majority of the nitrogen within the cyanophage S-SM1 was derived from its host, Synechococcus WH8102, although amount varied depending on light availability (Waldbauer et al., 2019). To test this in our system, cultures acclimated to a high external NO3- concentration were shifted to environments with decreasing concentrations of external NO3- concentrations post infection. There was no delay in virus production, or a decrease in burst size when cells were moved from a high NO3- external concentration (1.47 mM) to media where there was little (0.0147 mM) or no NO3- added back compared to cultures moved back into the same NO3- external concentration (1.47 mM). We acknowledge using this method, may cause some carry-over of nutrients, but we do believe this method allowed for us to see differences caused by external NO3- concentrations. This can be seen in the control cultures as decreasing external NO3- concentrations caused a significantly reduced end point cell abundance, and a decrease in FL3-H which acts as a proxy for chlorophyll a per cell. Cultures with no added NO3- only achieved a final cell abundance 55% that of the cultures with 1.47 mM NO3- added back. This is worth noting as acclimating cultures to even 0.147 mM NO3- (10% that of normal ASP₁₂A), had no effect on growth or the infection cycle.

One caveat of this work is that the A. anophagefferens cultures are non-axenic. Although there are reports of axenic cultures and methods for their production (Berg et al., 2002), we have been unable to remove the heterotrophic bacteria when cultured on a defined growth medium, suggesting there is the production of a compound required by A. anophagefferens not present in ASP₁₂A. The use of a defined medium despite the requirement of bacteria, did allow us to know the concentration of NO3- added, and any variability that would exist in a medium with a natural seawater base would not be present. Previous estimates of the number of heterotrophic bacteria in our cultures during late logarithmic growth of A. anophagefferens are between 1.8 and 8.1 × 10⁵ colony forming units mL^–1. The amount of nitrogen found within the heterotrophic community in the cultures therefore could reduce the amount of NO3- A. anophagefferens has access to. Using the estimates of nitrogen found within cells in natural and cultural studies (1.6–100 fg cell^–1) (Fagerbakke et al., 1996), allows for the estimate of amount of nitrogen found within these cells in our cultures (2.88 × 10⁵ to 8.1 × 10⁸ fg of nitrogen). This would account for 1.4 × 10^–4 to 0.4% of the nitrogen found within the 0.0147 mM NO3- acclimated cultures. Although this is a small amount of the total external nitrogen available, heterotrophic bacteria can be influencing the growth of A. anophagefferens in other ways. More work is needed to understand the interactions between A. anophagefferens and heterotrophic bacteria, as well as if these bacteria influence the infection cycle in any way.

From the experiments performed in this study, the data support the hypothesis that there is enough nitrogen present within an A. anophagefferens cell for the infection cycle to proceed and does not utilize external nitrogen pools. To further support this hypothesis, we performed theoretical calculations from available data about A. anophagefferens nutrient pools, C:N:P amounts within the algal virus, PBCV-1, and burst size ranges to assess whether enough nitrogen exists in an infected cell (Table 2).

The amount of carbon and nitrogen in an A. anophagefferens cell has been calculated to be 2.2 × 10³ fg cell^–1 and 3.4 × 10² fg cell^–1, respectively. The phosphorus concentration has been estimated to be 2.1 × 10¹ fg cell^–1 based on estimates using the Redfield ratio (Gobler et al., 1997). The amount of carbon, nitrogen, and phosphorus within an AaV particle are unknown, but these values have been calculated for PBCV-1. We believe this was a good model for AaV as they have a diameter of 1900Å (AaV: data not shown, PBCV-1; Fang et al., 2019), have similar genome sizes [AaV: ∼371 kbp (Moniruzzaman et al., 2014) vs. PBCV-1: ∼331 kbp (Dunigan et al., 2012)], both contain internal membranes (Rowe et al., 2008; Milrot et al., 2017), and have similar capsid structures (AaV: data not shown; PBCV-1; Fang et al., 2019). The C:N:P ratio for PBCV-1 was calculated to be 17:5:1. The ratio was calculated by totaling the C, N, and P found in each macromolecule in the particle, as the percentage of lipids, proteins, and nucleic acids had been previously determined (Clasen and Elser, 2007). As the weight of a single particle is known to be ∼1 × 10⁹ Da (Van Etten et al., 1983), the amount of C, N, and P per particle was calculated.

The burst size of AaV has been shown to be dependent on multiplicity of infection where larger multiplicities of infection produce less viruses per cell (Brown and Bidle, 2014). This is not unique, as it has been shown in other systems (i.e., Van Etten et al., 1982). In this study, two multiplicities of infection were used (∼20 and ∼100 viruses cell^–1). Using the burst sizes determined with the 1.47 mM NO3- acclimated cultures in both experiments, our results add further evidence that multiplicity of infection influences burst size, as the low multiplicity of infection produced a burst size 5.2 times greater than that of the high multiplicity of infection. The calculated burst sizes in this study are greater than those determined previously by flow cytometry, as Brown and Bidle determined the burst size of AaV to be 191 viruses per cell (2.4–12.6 times less than this study) (Brown and Bidle, 2014). Although the same strain of A. anophagefferens and AaV were used, the growth medium used were different. The previous study utilized f/2 media which has a natural sea water base, and different nutrients and metals added to it than ASP₁₂A. It is therefore possible this could account for some of the differences. Burst sizes determined in this study are similar to those determined by qPCR in laboratory studies using ASP₁₂A (Gann et al., 2020). Differences caused by culturing in different growth media on the infection cycle should be determined. For our calculations we used the average burst size calculated from a high multiplicity of infection of 1.47 mM NO3- cultures (466 viruses per cell), and the average burst size calculated from the low multiplicity of infection of 1.47 mM NO3- cultures (2,415 viruses per cell). These estimates are less than the theoretical maximum number of viruses that could be produced in an A. anophagefferens cell. A. anophagefferens is between 2 and 3 μm (Gobler and Sunda, 2012), so its volume assuming 2.5 μm is 8.19 × 10⁹ nm³, and the volume of an icosahedral with a diameter of 190 nm is 2.17 × 10⁶ nm³. Therefore, the theoretical maximum number of particles that can be produced is 3,767 particles per cell. Using these values, around one quarter of carbon and one half of nitrogen within an Aureococcus cell would be required to produce a burst size of 466 particles, while over 150% of the phosphorus within the cells would be required. At a high burst size, the quotas of C, N, and P within the cell would not be enough to produce the number of particles (Table 2). These numbers do not consider any virally encoded proteins that are required for production of new progeny but are not packaged. The PBCV-1 genome for instance, encodes for 416 proteins, yet only 148 of them are packaged (Dunigan et al., 2012). Also, not considered in these calculations are if cellular machinery required for the infection needs to continue to be synthesized.

Although, these numbers are crude estimates, it does suggest that the virocell has a strong requirement for external phosphorus, that is not required for nitrogen, to produce a burst size that is similar to those determined in this study. Using the previously published transcriptome of the infected A. anophagefferens culture, transporters in the host were evaluated (Moniruzzaman et al., 2018). There were no NO3- transporters over expressed at any point sampled compared to the uninfected controls, and most sugar transporters were either under expressed or did not change (Supplementary Figure 5). In contrast, several inorganic phosphate transporters were over expressed late in the infection cycle, as previously has been reported (Moniruzzaman et al., 2018). These transporters have previously been shown to be upregulated in phosphorus stressed cultures (Wurch et al., 2011).

Differences in uptake of external nitrogen pools in eukaryotic algae seem to depend on the evolution the host virus pair evolved from, and not necessarily on their laboratory growth rate as previously hypothesized (Fowler and Cohen, 1948; Waldbauer et al., 2019). Both Ostreococcus tauri and A. anophagefferens have similar growth rates when grown on nitrate (Figure 1C; Worden et al., 2004), but the virocell’s reliance on the external environment for nitrogen appears to be different. The lack of change in infection cycle dynamics due to external nitrogen concentration (Figure 3), and the virus-encoded nucleotide recycling genes (Brown and Bidle, 2014; Moniruzzaman et al., 2014), suggest AaV evolved to utilize the internal stores within A. anophagefferens. This is further supported by the lack of virally encoded nitrogen or phosphorus transporters. In contrast viruses that infect O. tauri encode their own nitrogen transporters which aids the overexpressed host transporters to uptake more external nitrogen than uninfected cells, suggesting this system evolved to utilize external sources (Monier et al., 2017).

Many harmful algal blooms are terminated by lysis of viruses globally (Brussaard et al., 2005; Vardi et al., 2012), playing important roles in nutrient cycling. The interplay between nutrient availability for the hosts and maximized virus production is not well characterized, and seems to depend on the specific virus-host system (Maat and Brussaard, 2016). Here we have contributed to the growing data about the influence of nitrogen on the infection cycle for an ecologically important virus-host system. Acclimation of cultures to NO3- concentrations that negatively influence growth caused a decreased efficiency of the AaV infection cycle. Our observation suggests that nitrogen-pollution in the early stages of the bloom may influence natural virus-mediated constraints on the bloom but once infection has begun, then nitrogen-loading would have no influence on this control (but may enhance bloom growth). Determining how the infection cycle of AaV responds to the many other nitrogenous species (Berg et al., 2008) may provide further insight into how the host’s metabolism shapes the outcome of interactions with this viral giant.