ApiATs are broadly-distributed in apicomplexan parasites

To identify ApiAT-family proteins in the apicomplexan parasites T. gondii, Neospora caninum, Eimeria tenella, P. falciparum, P. berghei, Theileria annulata, Babesia bovis and Cryptosporidium parvum, we undertook Basic Local Alignment Search Tool (BLAST) searches using each of the five P. falciparum ApiATs as initial query sequences (www.eupathdb.org; [14]) We also undertook BLAST searches of the genomes from the chromerids Chromera velia and Vitrella brassicaformis, which are close free-living relatives of apicomplexans [15] (www.eupathdb.org, www.blast.ncbi.nlm.nih.gov; [14, 16]). In addition to the previously described five Plasmodium ApiAT family proteins, we identified sixteen ApiAT family proteins in both T. gondii and N. caninum, eight in E. tenella, nine in T. annulata, six in B. bovis, and one in C. parvum (S1 Fig; S1 Table). Using this search strategy, we were unable to identify ApiAT family proteins in chromerids. Using PbNPT1 as a search query in profile hidden Markov Model searches, we identified the LAT3 and LAT4 proteins from humans (http://hmmer.org; [17]; S2 Fig). LAT3 and LAT4 are members of the SLC43 family of the major facilitator superfamily of transporters, and mediate the transport of branched chain and other large neutral amino acids [18].

To determine the phylogenetic relationships between ApiAT family proteins, we constructed a multiple sequence alignment (S1 Fig). This revealed the presence of a major facilitator superfamily (MFS) signature sequence between transmembrane domains 2 and 3 of most ApiAT family protein (S2 Fig; [19, 20]). Most ApiAT proteins were predicted to be polytopic membrane proteins containing 12 transmembrane domains (www.cbs.dtu.dk/services/TMHMM/; [21]), and exhibited highest sequence similarity in the regions encompassing these transmembrane domains (S1 Fig). These analyses are consistent with previous studies and protein database annotations placing members of the ApiAT family into the major facilitator superfamily of transporters [9, 10].

We next performed a maximum likelihood phylogenetic analysis. This revealed the presence of multiple ApiAT subfamilies, which we defined as groupings that had greater than 75% bootstrap support (Fig 1). Orthologs of the ApiAT2 subfamily were present in all organisms in the study with the exception of Cryptosporidium parvum, although the only C. parvum ApiAT protein that we identified grouped with the ApiAT2 subfamily with weak support (Fig 1). Members of the ApiAT1, ApiAT3, ApiAT5, ApiAT6 and ApiAT7 subfamilies were restricted to coccidians (a group of apicomplexans that includes T. gondii and N. caninum), the ApiAT4, ApiAT8, ApiAT9 and ApiAT10 subfamilies were restricted to the Plasmodium genus, and the ApiAT11 family was restricted to the piroplasms T. annulata and B. bovis (Fig 1). The ApiAT8 family includes the previously described cationic transporter PbNPT1 [9], here annotated as PbApiAT8. Although similar in function to the T. gondii arginine transporter TgApiAT1 (previously TgNPT1), PbApiAT8 and TgApiAT1 appear not to be orthologous.

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Fig 1. Phylogenetic analysis of ApiAT family proteins.

Consensus maximum likelihood tree of ApiAT family proteins. The tree was generated from a multiple sequence alignment of 66 putative ApiAT proteins from a range of apicomplexans, with 464 residues used in the analysis. Bootstrap values are depicted by black circles (>90% support), blue circles (>75–90% support), or white circles (55–75% support). The tree is unrooted. Abbreviations: Bb, Babesia bovis; Cp, Cryptosporidium parvum; Et, Eimeria tenella; Nc, Neospora caninum; Pb. Plasmodium berghei; Pf, Plasmodium falciparum; Tg, Toxoplasma gondii; Ta, Theileria annulate; ug, ungrouped.

https://doi.org/10.1371/journal.ppat.1007577.g001

T. gondii ApiATs localize to the parasite periphery

Previous studies demonstrated that the P. berghei ApiAT8 protein (previously PbNPT1) localized to the periphery of the parasite (likely to the plasma membrane), and that the T. gondii ApiAT1 protein (previously TgNPT1) localized to the plasma membrane [9, 11]. To determine the expression pattern and localization of ApiAT family proteins in T. gondii, we introduced a hemagglutinin (HA) tag into the 3’ end of the open reading frame of the remaining fifteen ApiAT genes (S3A and S3B Fig).

Western blotting indicated that TgApiAT2, TgApiAT3-1, TgApiAT3-2, TgApiAT3-3, TgApiAT5-3, TgApiAT6-1, TgApiAT6-2, TgApiAT6-3, and TgApiAT7-2 proteins were expressed in tachyzoite stage parasites (Fig 2A–2E). We were unable to detect expression of TgApiAT5-1, TgApiAT5-2, TgApiAT5-4, TgApiAT5-5, TgApiAT5-6 and TgApiAT7-1. Of the ApiATs that were expressed in T. gondii tachyzoites, most exhibited a lower mass than predicted (S1 Table). Although we cannot rule out the possibility of N-terminal processing in these proteins, we note that hydrophobic membrane proteins commonly run faster than predicted on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE; [22]). Immunofluorescence assays (IFAs) demonstrated that TgApiAT2, TgApiAT3-1, TgApiAT3-2, TgApiAT3-3, TgApiAT5-3, TgApiAT6-1 (as reported previously; [23]), and TgApiAT6-3 localized to parasite periphery, overlapping with the plasma membrane marker P30 (Fig 2F–2I). TgApiAT3-3 showed additional localization to the trans-Golgi network (Fig 2G). Although detectable by western blotting (Fig 2D and 2E), we could not detect TgApiAT6-2 or TgApiAT7-2 by IFA, possibly because the level of expression of these proteins was below the detection limits of IFAs.

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Fig 2. Expression and localization analysis of T. gondii ApiAT family proteins.

(A-E) Western blots with anti-HA antibodies to measure the expression and molecular mass of tagged TgApiAT proteins in tachyzoites stages of the parasite. Western blots with antibodies against GRA8 and Tom40 were used to test for the presence of protein in samples where the HA-tagged TgApiAT protein was not detected. (F-I) Immunofluorescence assays with anti-HA antibodies to determine the localisation of HA-tagged TgApiAT proteins (green in merge). Samples were co-labelled with antibodies against the plasma membrane marker P30 (red in merge). TgApiAT3-3-HA-expressing parasites were co-transfected with the trans-Golgi network (TGN) marker Stx6-GFP [63], and labelled with anti-HA (red in merge), anti-P30 (plasma membrane, PM; blue in merge) and anti-GFP (green in merge) antibodies. All scale bars are 2 μm.

https://doi.org/10.1371/journal.ppat.1007577.g002

T. gondii, like many apicomplexans, contains a series of flattened membrane sacs termed alveolae that contribute to the inner membrane complex (IMC) that localizes just beneath the plasma membrane of these parasites [24]. The IMC first appears as the ‘buds’ of daughter parasites within the parent cell just before cytokinesis. To compare the localization of an ApiAT protein with the IMC, we co-labelled TgApiAT5-3-HA parasites with anti-HA and anti-IMC antibodies. We found that TgApiAT5-3-HA did not localize to daughter buds (S4A Fig). TgApiAT5-3-HA localization extended along the cell periphery at the apical and basal ends of the parasite, regions from which the IMC marker was absent (S4A and S4B Fig, arrows). Taken together, these data indicate that TgApiAT5-3 is localized primarily to the plasma membrane, although in the absence of higher resolution microscopy approaches, we cannot rule out that some could also be located in IMC.

We conclude that ten of the sixteen TgApiAT proteins are expressed in the tachyzoite stage of T. gondii, and that those with detectable expression by IFA all localize to the periphery of the parasite, most likely to the parasite plasma membrane.

CRISPR/Cas9-mediated disruption of ApiAT-encoding genes identifies three family members that are important for parasite growth

To determine the importance of TgApiATs for parasite growth, we attempted to genetically disrupt all sixteen T. gondii ApiATs using a CRISPR/Cas9-based approach [25]. With this strategy, we were able to disrupt fifteen of the sixteen TgApiAT genes (S2 Table). The mutant parasites all had frameshift mutations that will lead to the production of truncated (and likely non-functional) proteins. We refer to each of these mutants on the basis of which amino acids will be absent from the final protein (e.g. TgApiAT5-3 encodes a protein of 504 amino acids; the TgApiAT5-3 mutant is truncated from residue 188 and is referred to as apiAT5-3^Δ188–504). TgApiAT1 could only be disrupted when parasites were grown in excess arginine, as described previously [9]. We were unable to generate frameshift mutations in TgApiAT6-1 after screening 12 clones from three separate transfections of a guide RNA targeting the TgApiAT6-1 locus. Of these clones, two had a 3 bp insertion and one had a 3 bp deletion, indicating that the guide RNA was capable of targeting the TgApiAT6-1 locus (S2 Table).

To determine which TgApiATs were important for parasite growth, we performed plaque assays on each of the genetically disrupted TgApiAT lines grown in human foreskin fibroblasts (HFFs) and cultured in Dulbecco’s modified Eagle’s medium (DMEM). Compared to parental wild type (WT) controls, we observed greatly reduced plaque sizes in the apiAT2^Δ138–588 and apiAT5-3^Δ188–504 strains (Fig 3). No plaques were observed in the apiAT1^Δ54–534 strain grown in DMEM (containing 400 μM L-arginine) but normal growth of this strain was observed when grown in Roswell Park Memorial Institute 1640 (RPMI) medium (containing 1.15 mM L-Arg; Fig 3A), mirroring previous results with TgApiAT1 knockouts [9]. By contrast, the remaining 12 mutant apiAT lines exhibited plaques that were similar in size to those observed in WT controls (Fig 3).

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Fig 3. Genetic disruption of T. gondii ApiAT family proteins reveals the importance of TgApiAT2 and TgApiAT5-3 for parasite growth in vitro.

(A-F) Plaque assays depicting growth of disrupted TgApiAT strains and their corresponding parental WT strain. 150 parasites were added to wells of a 6-well plate and cultured for 9 days in DMEM. (A) WT (RHΔhxpgrt) and apiAT1^Δ54–534 parasites grown in DMEM (left) or RPMI (right). (B) WT (TATi/Tomato), apiAT2^Δ138–588 and apiAT2^Δ138–588 parasites complemented with a constitutively expressed TgApiAT2 (apiAT2^Δ138-588/cTgApiAT2). (C) WT (TATi) and apiAT3 sub-family mutants. (D) WT (TATi/Tomato) and apiAT5 sub-family mutants. (E) WT (TATi/Tomato) and apiAT6 sub-family mutants. (F) apiAT7 sub-family mutants. Note that the TATi/Tomato strain served as WT strain for the apiAT2, apiAT5, apiAT6, and apiAT7 sub-family mutants, and the identical image of the TATi/Tomato plaque assay is shown in B, D and E to facilitate interpretation of the data. All images are from the same experiment, and are representative of three independent experiments.

https://doi.org/10.1371/journal.ppat.1007577.g003

Our previous data indicated that some ApiAT family proteins transport amino acids [9]. We tested each of the mutant apiAT strains for whether growth defects were altered in medium containing reduced amino acid concentrations (Minimal Amino Acid Medium, MAAM). The growth defects in the apiAT2^Δ138–588 and apiAT5-3^Δ188–504 strains were exacerbated in MAAM (S5 Fig), implicating these ApiATs in the uptake of amino acids. By contrast, the apiAT1^Δ54–534 strain grew better in MAAM than in DMEM (S5 Fig). Our previous study of the arginine transporter TgApiAT1 found that parasites lacking this transporter could grow in medium containing a high Arg:Lys ratio [9]. In this context, we note that MAAM contains proportionally more L-Arg than L-Lys (3:1 Arg:Lys; S3 Table) than DMEM (1:2 Arg:Lys). We observed no major growth differences between minimal amino acid and complete growth media for any of the other mutants (S5 Fig).

To test whether the growth defect in the apiAT2^Δ138–588 strain was due specifically to disruption of the TgApiAT2 locus, we complemented apiAT2^Δ138–588 with constitutively expressed TgApiAT2. This restored parasite growth (Fig 3B).

Together, these results indicate that TgApiAT1, TgApiAT2 and TgApiAT5-3 are required for normal intracellular growth of T. gondii in standard in vitro culture conditions.

TgApiAT5-3 is important for amino acid homeostasis in T. gondii

TgApiAT proteins that are important for parasite growth are likely to have critical roles in nutrient acquisition. In the remainder of this manuscript, we focus on one such protein, TgApiAT5-3. Our previous study of TgApiAT1 and PbApiAT8-1 indicated a key role for these transporters in cationic amino acid uptake [9], and we hypothesized that TgApiAT5-3 could also function as an amino acid transporter. To investigate this possibility, we incubated WT and apiAT5-3^Δ188–504 parasites in medium containing a mixture of [¹³C]-labelled amino acids for 15 mins. Polar metabolites were extracted from parasite lysates and analyzed by GC-MS. These analyses were used to quantitate the levels of intracellular amino acids and determine the extent of labeling with exogenous amino acids based on [¹³C]-enrichment in each of the two strains. Strikingly, both the abundance and fractional labelling of [¹³C]-L-tyrosine (L-Tyr) was reduced significantly in the apiAT5-3^Δ188–504 strain (Fig 4). Abundance and fractional labeling of a number of other [¹³C]-amino acids were altered significantly in the apiAT5-3^Δ188–504 strain, although none to the same extent as L-Tyr (Fig 4). The levels of several other amino acids were reduced in the apiAT5-3^Δ188–504 mutant, although the differences were not statistically significant (Fig 4A), possibly reflecting differences in the growth rate and physiological state of the two lines. In support of this notion, the rate of turnover of these amino acids, as indicated by rate of ¹³C-enrichment in intracellular pools was unchanged (Fig 4B). These data indicate that TgApiAT5-3 is important for amino acid homeostasis, playing a key role in the uptake of L-Tyr into the parasite.

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Fig 4. Analysis of [¹³C] amino acid uptake into WT and apiAT5-3^Δ188–504 parasites reveals a role for TgApiAT5-3 in amino acid homeostasis.

(A-B) Extracellular WT (TATi/Tomato) or apiAT5-3^Δ188–504 tachyzoites were incubated in medium containing [¹³C]-L-amino acids for 15 min. Polar metabolites were extracted and amino acid abundance (A) and levels of [¹³C]-amino acid enrichment (B) in WT (black) and apiAT5-3^Δ188–504 (red) tachyzoites determined by GC-MS. Only L-amino acids that could be detected in all experiments are shown. The data are averaged from three independent experiments and error bars represent ± s.e.m. (*, P < 0.05; **, P < 0.01; ***, P < 0.001, ****, P < 0.0001; Student’s t test. Where significance values are not shown, the differences were not significant; P > 0.05).

https://doi.org/10.1371/journal.ppat.1007577.g004

TgApiAT5-3 is an aromatic and large neutral amino acid uniporter with exchange activity

To characterize the substrate specificity of TgApiAT5-3 further, we expressed HA-tagged TgApiAT5-3 in Xenopus laevis oocytes, and confirmed its expression and plasma membrane localization by western blotting (S6A Fig). Given the GC-MS data implicating TgApiAT5-3 in L-Tyr uptake (Fig 4), we hypothesised that TgApiAT5-3 transports L-Tyr. We compared the uptake of radiolabelled [¹⁴C]-tyrosine ([¹⁴C]Tyr) into oocytes expressing TgApiAT5-3 relative to uninjected oocytes. Under the conditions of the experiment, there was a significant, 7-fold increase in the initial uptake rate of [¹⁴C]Tyr into oocytes expressing TgApiAT5-3 compared to uninjected control oocytes (Fig 5A).

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Fig 5. TgApiAT5-3 is an L-tyrosine transporter that is stimulated by the presence of L-tyrosine on the trans side of the membrane.

(A) Timecourse for the uptake of L-Tyr into X. laevis oocytes expressing TgApiAT5-3 (squares) or into uninjected oocytes (circles). Uptake was measured in the presence of 1 mM L-Tyr containing 0.5 μCi/ml [¹⁴C]Tyr. Each data point represents the mean uptake in 10 oocytes from a single experiment ± standard deviation, and the data are representative of 3 independent experiments. A first order rate equation was fitted to each timecourse (R² = 0.97 for TgApiAT5-3-expressing oocytes and R² = 0.77 for uninjected controls). Both the rate constant for L-Tyr uptake and the maximal L-Tyr uptake measured in TgApiAT5-3-expressing oocytes were significantly higher than those measured in uninjected oocytes (P < 0.01, Student’s t tests). (B) TgApiAT5-3-expressing oocytes (squares) and uninjected oocytes (circles) were preloaded (P.L.) with L-Tyr by incubation in 2.5 mM unlabelled L-Tyr (filled symbols) for 32 or 72 hr, respectively, or not preloaded (open symbols). Following the preincubation period, uptake of L-Tyr was measured in a solution of 1 mM L-Tyr containing 0.5 μCi/ml [¹⁴C]Tyr. Data show the mean uptake in 10 oocytes from a single experiment ± standard deviation, and are representative of 3 independent experiments. First order rate equations were fitted to the uptake timecourses for the preloaded and non-preloaded TgApiAT5-3-injected oocytes (R² = 0.98 for preloaded, and R² = 0.95 for non-preloaded oocytes). Both the first order rate constants for L-Tyr uptake and the maximal L-Tyr uptake were significantly higher in preloaded compared to non-preloaded TgApiAT5-3-expressing oocytes (P < 0.01, Student’s t tests). (C) TgApiAT5-3-expressing oocytes were preloaded by incubation in 1 mM L-Tyr containing 0.5 μCi/ml [¹⁴C]Tyr for 32 hr. Subsequent efflux (filled symbols) and retention (open symbols) of the preloaded substrate was measured over the timecourse indicated, in the presence of an extracellular medium containing 2.5 mM L-Tyr (squares) or extracellular medium lacking of L-Tyr (circles). Data show the mean efflux and retention ± standard deviation in 3 replicates (measuring efflux/retention from 5 oocytes each) from a single experiment, and are representative of 3 independent experiments. (D) Trans-stimulated initial rate kinetic analysis of L-Tyr transport by TgApiAT5-3. The rate of L-Tyr uptake was measured at a range of [L-Tyr] concentrations in the external medium (i.e. [L-Tyr]_cis) in TgApiAT5-3-expressing oocytes preloaded with 0 mM to 2.5 mM L-Tyr (i.e. [L-Tyr]_trans). The TgApiAT5-3-mediated uptake (calculated by subtracting the uptake in uninjected oocytes from the uptake in TgApiAT5-3-expressing oocytes) at each [L-Tyr]_trans condition tested conformed to a Michaelis-Menten kinetic model (R² > 0.90 for all non-linear regressions). The data were fitted to a Scatchard linear regression (0.89 ≤ R² ≤ 0.98 for all linear regressions). Data show the mean uptake rate ± standard deviation in 10 oocytes from a single experiment, and are representative of 2 independent experiments.

https://doi.org/10.1371/journal.ppat.1007577.g005

To investigate the possibility that TgApiAT5-3 has exchange activity, we tested whether the uptake of [¹⁴C]Tyr was stimulated by the presence of amino acids on the trans side of the membrane (i.e. inside the oocyte). Following preliminary experiments to optimise the preloading of L-Tyr into oocytes, we measured [¹⁴C]Tyr uptake over 2 hr at an extracellular concentration of 1 mM L-Tyr in TgApiAT5-3 cRNA-injected or uninjected oocytes that had been pre-loaded in medium containing 2.5 mM unlabelled L-Tyr. The initial rate of [¹⁴C]Tyr uptake in TgApiAT5-3-expressing oocytes preloaded with L-Tyr was 3-fold higher than in TgApiAT5-3-expressed oocytes that were not pre-loaded (Fig 5B), indicating that L-Tyr uptake into TgApiAT5-3-expressing oocytes was stimulated by L-Tyr on the trans side of the membrane.

We next tested whether L-Tyr efflux was also trans-stimulated. We preloaded TgApiAT5-3-expressing and uninjected oocytes with radiolabelled L-Tyr and measured the efflux and retention of the radiolabel upon the addition of 2.5 mM unlabelled L-Tyr to the external medium. [¹⁴C]Tyr efflux was increased, and [¹⁴C]Tyr retention reduced, in TgApiAT5-3-expressing oocytes exposed to 2.5 mM L-Tyr compared to those in external medium lacking L-Tyr (Fig 5C). Nevertheless, there was some [¹⁴C]Tyr efflux over time in the absence of trans-substrate (Fig 5C), indicating that TgApiAT5-3 can mediate unidirectional flux of L-Tyr. We observed no differences in [¹⁴C]Tyr efflux or retention in control uninjected oocytes upon incubation of oocytes in 2.5 mM L-Tyr compared to incubation in buffer lacking L-Tyr (S6B Fig). These data indicate that the transporter operates more effectively under ‘exchange conditions’ than under conditions in which it is mediating a unidirectional flux.

To examine the exchange activity of TgApiAT5-3 further, we investigated the kinetic properties of L-Tyr transport in more detail. Steady-state kinetic parameters for exchangers must be conducted at different trans- and cis-substrate concentrations to determine accurate K_0.5 values [26]. We examined the kinetics for the uptake of [¹⁴C]Tyr following the preloading of oocytes with different L-Tyr concentrations (note that this, and all subsequent, uptake measurements were conducted over 10 min, which falls within the initial, approximately linear, phase of the influx timecourse; Fig 5B). Both Michaelis-Menten analysis (Table 1) and Scatchard linear regressions (Fig 5D) demonstrated that the apparent K_0.5 values for L-Tyr uptake into oocytes was unaffected by the cytosolic L-Tyr concentration. The gradients of fitted Scatchard plots are negative reciprocals of the apparent K_0.5 and, therefore, equivalent slopes reflect similar apparent substrate affinities. K_0.5 values were consistent for both Scatchard and Michaelis-Menten plots derived from the same data, ranging from 0.25 to 0.40 μM (Table 1). As expected for trans-stimulated uptake, maximum rate (V_max) values increased in proportion to the concentration of preloaded L-Tyr (Fig 5D; Table 1).

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Table 1. Michaelis-Menten kinetic parameters for the initial rate of L-Tyr uptake by TgApiAT5-3^a.

https://doi.org/10.1371/journal.ppat.1007577.t001

To assess whether TgApiAT5-3 might function as an ion:amino acid co-transporter, we conducted systematic ion-replacement uptake experiments as described previously [9]. We observed no significant change in [¹⁴C]Tyr uptake under any ion-replacement conditions, suggesting that the transporter does not co-transport any of the ions tested (S6C Fig). To determine whether TgApiAT5-3 is an electrogenic transporter (as is the case for TgApiAT1; [9]), we perfused oocytes expressing TgApiAT5-3 with L-Tyr and measured the electrical current across the oocyte plasma membrane using a two-electrode voltage clamp configuration. We observed no net current under any of the conditions tested, including those in which the membrane potential and pH gradient across the membrane were altered (S6D Fig). Together, these data indicate that L-Tyr transport by TgApiAT5-3 does not co-transport any charged species.

Incubation of WT and apiAT5-3^Δ188–504 parasites in a [¹³C]-amino acid mix resulted in significant increases or decreases in the ¹³C-labelling of several amino acids (Fig 4), suggesting that TgApiAT5-3 may transport a range of amino acids. To investigate the substrate specificity of TgApiAT5-3 further, we measured the uptake of 500 μM [¹⁴C]Tyr in oocytes expressing TgApiAT5-3 in the presence of equimolar amounts of unlabelled L-amino acids on the cis side of the membrane. Only unlabelled L-tryptophan (L-Trp) caused a significant reduction of L-Tyr uptake under the conditions tested (S7A Fig). To examine the trans-stimulated influx specificity of TgApiAT5-3, we pre-injected mixtures of L-amino acids and other metabolites into oocytes expressing TgApiAT5-3, then measured uptake of [¹⁴C]Tyr. TgApiAT5-3-mediated [¹⁴C]Tyr uptake was trans-stimulated by pre-injected mixtures of L-amino acids, but not amino acid derivatives, D-amino acids, nucleotides, nitrogenous bases, or sugars (S7B Fig; S4 Table). To identify which amino acids might be responsible for this trans-stimulation, we pre-injected oocytes expressing TgApiAT5-3 with 19 of the 20 proteinogenic amino acids, each to a final concentration of 5 mM. The one exception was L-Tyr which, in light of its low solubility, was preloaded to equilibrium instead of being injected. After pre-injecting or preloading of the amino acids, we measured the trans-stimulated uptake of [¹⁴C]Tyr. We found that aromatic and large neutral amino acids, but not smaller or charged amino acids, trans-stimulated [¹⁴C]Tyr uptake (Fig 6A).

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Fig 6. TgApiAT5-3 is an exchanger for aromatic and large neutral amino acids.

(A) TgApiAT5-3-expressing oocytes were pre-injected with a range of L-amino acids at a calculated oocyte cytosolic concentration of 5 mM (with the exception of L-Tyr (§) which was preloaded into oocytes via incubation in 2.5 mM L-Tyr for 32 hr), or were not pre-injected (ND96 condition). Subsequent uptake of 1 mM L-amino acids containing 0.5 or 1 μCi/ml [¹⁴C]-labelled amino acid (cis-Substrate) was measured over 10 minutes and normalised to uptake per minute. Each box in the heat map shows the mean uptake in 10 oocytes from a single experiment, representative of 3 independent experiments. The statistical analyses compare pre-injected/pre-loaded oocytes to ND96 controls for each substrate tested (*, P < 0.05, one-way ANOVA, Dunnet’s post-hoc test. Where significance values are not shown, the differences are not significant, P > 0.05). (B) TgApiAT5-3-expressing oocytes were preloaded with a range of L-amino acids containing 0.5 or 1 μCi/ml [¹⁴C] radiolabelled amino acids (calculated final concentrations shown beneath each substrate), and efflux of these substrates was measured over 5 min in the absence of external amino acids (ND96) or in the presence of 5 mM external amino acids (with the exception of L-Tyr (§), which was present at a concentration of 2.5 mM), and normalised to efflux per minute. Each box in the heat map shows the mean rate of efflux from 3 replicates (each comprised of 5 oocytes) from a single experiment, representative of 3 independent experiments. Statistical analyses compare trans substrates to ND96 controls for each efflux substrate tested (*, P < 0.05, one-way ANOVA, Dunnet’s post-hoc test. Where significance values are not shown, the differences are not significant, P > 0.05).

https://doi.org/10.1371/journal.ppat.1007577.g006

We tested the uptake of a range of [¹⁴C]-labelled aromatic and large neutral amino acids, including L-Trp, L-histidine (L-His), L-phenylalanine (L-Phe), L-leucine (L-Leu) and L-isoleucine (L-Ile), into oocytes expressing TgApiAT5-3. In the absence of a trans substrate, the rates of uptake of aromatic and large neutral amino acids were significantly increased compared to uninjected oocytes (1.7-fold increase for L-Trp, 3.1-fold increase for L-His, 5.5-fold increase for L-Phe, 2.2-fold increase for L-Leu, and 2.4-fold increase for L-Ile; S7C Fig). The uptake of the cationic amino acid L-Arg did not differ between TgApiAT5-3 injected and uninjected oocytes (S7C Fig). As was seen for L-Tyr, uptake of the aromatic and large neutral amino acids tested were trans-stimulated by aromatic and large neutral amino acids, and not by smaller or charged L-amino acids (Fig 6A). The uptake of L-Arg was not trans-stimulated by any of the amino acids tested (Fig 6A). We next measured efflux of preloaded [¹⁴C]-labelled L-Tyr, L-Trp, L-His, L-Phe and L-Leu in the presence of all 20 proteinogenic amino acids in the extracellular medium. We observed the same substrate specificity, with aromatic and large neutral L-amino acids stimulating the efflux of the [¹⁴C]-labelled substrates tested (Fig 6B).

From the experiments conducted in this section, we conclude that TgApiAT5-3 mediates the transport of aromatic and large neutral amino acids. The transporter can function as a uniporter, but has a strong propensity for exchange, implying a role for TgApiAT5-3 in the homeostasis of a range of aromatic and large neutral amino acids.

TgApiAT5-3 is important for tyrosine uptake into parasites

The [¹³C] amino acid uptake data and oocyte experiments indicate a role for TgApiAT5-3 in L-Tyr uptake into the parasite (Fig 4; Fig 5). We set out to test the importance of TgApiAT5-3 for the uptake of L-Tyr and other amino acids and, subsequently, its importance for parasite growth and virulence. Preliminary experiments indicated that the parental strain used to make the original apiAT5-3^Δ188–504 strain was avirulent in mice, precluding its use for virulence studies. We therefore remade the apiAT5-3^Δ188–504 mutant in virulent RHΔhxgprt/Tomato strain parasites (S2 Table; [27]), and performed all subsequent experiments with this strain.

To test the importance of TgApiAT5-3 for L-Tyr uptake in T. gondii, we measured the kinetics of [¹⁴C]Tyr uptake in WT (RHΔhxgprt/Tomato) and apiAT5-3^Δ188–504 parasites. The initial rate of [¹⁴C]Tyr uptake in apiAT5-3^Δ188–504 parasites was decreased by 4.7-fold compared to that in WT parasites (Fig 7A; S8A Fig). Both [¹⁴C]Tyr uptake and parasite growth were restored upon complementation of the apiAT5-3^Δ188–504 mutant with a constitutively expressed copy of TgApiAT5-3 (apiAT5-3^Δ188-504/cTgApiAT5-3; Fig 7A; S9 Fig).

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Fig 7. TgApiAT5-3 mediates the uptake of L-tyrosine and L-phenylalanine into T. gondii.

Initial rate of uptake of (A) [¹⁴C]Tyr, (B) [¹⁴C]Phe, and (C) [¹⁴C]Arg, in WT (RHΔhxgprt/Tomato), apiAT5-3^Δ188–504, and apiAT5-3^Δ188-504/cTgApiAT5-3 strain parasites. Uptake was measured in PBS-glucose containing either 60 μM unlabelled L-Tyr and 0.1 μCi/ml [¹⁴C]Tyr (A), 15 μM unlabelled L-Phe and 0.1 μCi/ml [¹⁴C]Phe (B), or 100 μM unlabelled L-Arg and 0.1 μCi/ml [¹⁴C]Arg (C). The initial rates of transport for each substrate were computed from the initial slopes of the fitted single-order exponential curves (S8 Fig), and represent the mean ± SEM from three independent experiments (* P<0.05; ** P<0.01; n.s. = not significant; Student’s t test).

https://doi.org/10.1371/journal.ppat.1007577.g007

Our previous data indicated that TgApiAT5-3 can transport aromatic amino acids other than L-Tyr (Fig 6, S7A Fig). We measured uptake of [¹⁴C]Phe in WT and apiAT5-3^Δ188–504 parasites. We observed a significant, 2.8-fold decrease in the initial rate of [¹⁴C]Phe uptake in parasites lacking TgApiAT5-3, and this was restored upon TgApiAT5-3 complementation (Fig 7B; S8B Fig). We were unable to detect robust levels of uptake of [¹⁴C]Trp in either WT or apiAT5-3^Δ188–504 parasites, precluding analysis of the role of TgApiAT5-3 in uptake of this amino acid into parasites. As a control, we measured uptake of [¹⁴C]Arg, which is not transported by TgApiAT5-3 (Fig 6; S7A Fig), in WT, apiAT5-3^Δ188–504 and apiAT5-3^Δ188-504/cTgApiAT5-3 strain parasites. The rate of [¹⁴C]Arg uptake did not differ significantly between these parasite lines (Fig 7C; S8C Fig), indicating that the defect we observed in the uptake of aromatic amino acids is specific to this class of amino acids, and does not represent a general defect in amino acid uptake.

Growth of parasites lacking TgApiAT5-3 is modulated by the concentrations of aromatic amino acids in the growth medium

We next investigated the dependence of the growth of apiAT5-3^Δ188–504 parasites on the concentration of L-Tyr in the culture medium. WT, apiAT5-3^Δ188–504 and complemented (apiAT5-3^Δ188-504/cTgApiAT5-3) parasites were grown in DMEM containing 0–2.5 mM L-Tyr. Growth of all three parasite strains in the absence of L-Tyr was significantly impaired (S10A Fig), consistent with a previous study that indicated T. gondii parasites are auxotrophic for this amino acid [28]. WT and complemented parasites grew normally in [L-Tyr] as low as 39 μM (Fig 8A). By comparison, growth of apiAT5-3^Δ188–504 parasites was negligible at [L-Tyr] of 156 μM and below, and severely impaired at concentrations below 1 mM (Fig 8A). We also measured growth of WT, apiAT5-3^Δ188–504 and complemented parasites grown in DMEM vs DMEM containing 2.5 mM L-Tyr, by plaque assay. Both WT and complemented parasites grew normally in both media (S9 Fig). Consistent with the results of the fluorescence growth assays, the growth of apiAT5-3^Δ188–504 parasites was restored to wild type levels by growth in 2.5 mM L-Tyr (S9 Fig).

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Fig 8. In vitro growth of parasites lacking TgApiAT5-3 is modulated by the concentration of aromatic amino acids in the growth medium, and TgApiAT5-3 is important for parasite virulence.

(A-C) Fluorescence growth assay for WT (RHΔhxgprt/Tomato, black), apiAT5-3^Δ188–504 (red) and apiAT5-3^Δ188-504/cTgApiAT5-3 strain parasites cultured for 5 days in DMEM containing a range of L-Tyr (A), L-Phe (B), or L-Trp (C) concentrations. Growth is expressed as a percentage of maximum growth measured on day 5 for each parasite strain. Sigmoidal curves were fitted to the data in (A). All data shown are averaged from three biological replicates (mean ± SEM). (D) Balb/c mice were infected intraperitoneally with 1,000 WT (black), apiAT5-3^Δ188–504 (red), or apiAT5-3^Δ188-504/cTgApiAT5-3 (blue) strain parasites and monitored for symptoms of toxoplasmosis. Data for WT and apiAT5-3^Δ188–504 parasites are derived from 2 biological replicates consisting of 5 mice each, whereas data for apiAT5-3^Δ188-504/cTgApiAT5-3 parasites is derived from a single experiment consisting of 5 mice.

https://doi.org/10.1371/journal.ppat.1007577.g008

These data indicate that uptake of L-Tyr via TgApiAT5-3 is important for the growth of T. gondii parasites in standard in vitro conditions. They also point to the existence of an alternative L-Tyr uptake pathway that can mediate sufficient L-Tyr uptake to rescue growth of apiAT5-3^Δ188–504 parasites if the culture medium contains ≥ 1 mM L-Tyr.

To assess the physiological importance of TgApiAT5-3-mediated L-Phe uptake for parasite growth, WT, apiAT5-3^Δ188–504 and complemented parasites were cultivated in medium containing 0 to 10 mM L-Phe (at a constant [L-Tyr] of 2.5 mM). Both WT and complemented parasites showed minimal growth in the absence of L-Phe (S10B Fig), indicating that T. gondii is auxotrophic for this amino acid, but both lines grew normally at [L-Phe] of 39 μM and above (Fig 8B). By contrast, growth of apiAT5-3^Δ188–504 parasites was impaired at 39 μM [L-Phe] (Fig 8B). apiAT5-3^Δ188–504 parasites grew optimally at [L-Phe] between 78 μM and 625 μM, but parasite growth decreased at [L-Phe] of 1.25 mM and above (Fig 8B). These data indicate that TgApiAT5-3 is required for parasite growth at both low and high exogenous concentrations of L-Phe, but not at intermediate concentrations. This points to the existence of other L-Phe uptake pathways in the parasite.

We next measured the growth of WT, apiAT5-3^Δ188–504 and complemented parasites in medium containing 0–2 mM L-Trp (and a constant [L-Tyr] of 2.5 mM). WT and complemented parasites exhibited minimal growth in the absence of L-Trp (S10C Fig), consistent with a previous study that indicated T. gondii is auxotrophic for this amino acid [29]. WT and complemented parasites grew optimally at [L-Trp] above approximately 0.5 mM, and exhibited decreased growth in [L-Trp] below 0.5 mM (Fig 8C). By contrast, apiAT5-3^Δ188–504 parasites grew optimally at 31–125 μM L-Trp (Fig 8C). Growth of apiAT5-3^Δ188–504 parasites was negligible below 8 μM L-Trp, and decreased in [L-Trp] of 250 μM and above (Fig 8C). Together, these data reveal that TgApiAT5-3 is required for parasite growth at high exogenous L-Phe and L-Trp concentrations, consistent with high concentrations of L-Phe or L-Trp competitively inhibiting uptake of L-Tyr via an alternative, non-TgApiAT5-3 L-Tyr uptake pathway(s). This is considered further in the Discussion.

TgApiAT5-3 is important for parasite virulence

Standard media formulations used to culture parasite in vitro do not necessarily reflect the amino acid concentrations that parasites encounter in vivo. Since the importance of TgApiAT5-3 for parasite growth in vitro varied with the concentrations of aromatic amino acids in the growth medium (Fig 8A–8C), we investigated the importance of TgApiAT5-3 for parasite virulence in a mouse infection model. We infected BALB/c mice intraperitoneally with 10³ WT (RHΔhxgprt/Tomato), apiAT5-3^Δ188–504 or complemented (apiAT5-3^Δ188-504/cTgApiAT5-3) parasites and monitored disease progression. Mice infected with WT and complemented parasites exhibited symptoms of toxoplasmosis and were euthanized 5–7 days post-infection (Fig 8D). By contrast, mice infected with apiAT5-3^Δ188–504 parasites exhibited no symptoms of toxoplasmosis across the entire 45 days of the experiments (Fig 8D), indicating that TgApiAT5-3 is essential for parasite virulence.

Phylogenetic analysis of the ApiAT protein family

We sought to identify orthologues of the five previously identified Plasmodium falciparum NPT proteins [10] in the proteomes of the apicomplexans Plasmodium berghei, Toxoplasma gondii, Cryptosporidium parvum, Eimeria tenella, Neospora caninum, Babesia bovis and Theileria annulata, and the chromerids Chromera velia and Vitrella brassicaformis. First we performed Protein BLAST searches using each P. falciparum NPT protein against each target species (www.eupathdb.org). We examined all ‘hits’ with an E value of <10. Candidates that had <8 or >15 transmembrane domains were excluded from further analysis, since this would be inconsistent with them being MFS transporters, which typically have 12 transmembrane domains [20]. We also excluded any candidates annotated as proteins that were not transporters, or proteins already identified as members of other transporter families. Each remaining candidate was used as the query sequence for BLAST searches against the P. falciparum proteome, and we only accepted candidates for which the top match in the reciprocal BLAST search was to one of the five P. falciparum NPTs. We next undertook BLAST searches with the candidate ApiAT against all organisms (using the NCBI BLAST search tool, excluding proteins in its own genus), and accepted only those candidates where the top hit was to proteins from other apicomplexans/chromerids. Of those, we included only candidate ApiATs where the top hit in members of the other target species was to proteins that had met all of the previous criteria (i.e. were already included as candidates on the list of potential ApiATs). This would theoretically exclude proteins that were not descended from the common ancestor of ApiATs. None of the candidate chromerid proteins met these latter criteria (all had top ‘hits’ in the NCBI BLAST search to proteins outside apicomplexans), and so were excluded from the subsequent phylogenetic analyses. We identified 66 proteins that met all the criteria. The gene IDs and nomenclature of these are listed in S1 Table.

The 66 ApiAT protein sequences were aligned using Clustal Omega Version 1.2.2 [40, 41]. The multiple sequence alignment was edited in Jalview (www.jalview.org) to remove poorly aligned blocks. After sequence editing, 464 residues were left for subsequent phylogenetic analysis using PHYLIP v3.69 (evolution.genetics.washington.edu/phylip/getme.html) as described previously [42]. Briefly, a consensus maximum likelihood tree and bootstrap values were generated by running the alignment file through the ‘seqboot’ program, which was used to generate 300 pseudosamples of the alignment. Next, multiple phylogenetic trees were generated from the pseudosamples using the ‘proml’ tree algorithm, using a randomised order of entry and three jumbles. Finally, the multiple phylogenetic trees were converted to a consensus tree with bootstrap values using the program ‘consense’.

Trees were viewed using the program FigTree (http://tree.bio.ed.ac.uk/software/figtree/) and annotated using Inkscape (https://inkscape.org/en). For visual representation of the alignment, shading for sequence identity was carried out using the TeXshade package for LaTex [43], using similarity mode with the ‘\fingerprint’ command (https://ctan.org/pkg/texshade?lang=en) and a texshade.sty file kindly provided by Dr Eric Beitz (Uni. Kiel).

Parasite culture

Parasites were maintained in human foreskin fibroblasts (HFFs; a kind gift from Holger Schülter, Peter MacCallum Cancer Centre) cultured at 37°C in a humidified 5% CO₂ incubator. Unless otherwise noted, parasites were cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 1% (v/v) fetal calf serum and antibiotics. All fluorescence growth assay experiments were conducted in medium containing dialyzed serum. ‘Homemade’ media were generated as described previously [9], with amino acids at the concentrations found in DMEM, or modified as specified in the text. Amino acid concentrations in the Minimal Amino Acid Medium (MAAM) are specified in S3 Table. apiAT5-3^Δ188–504 parasites were grown continuously in DMEM supplemented with 2.5 mM L-Tyr. TATi [44], TATi/Tomato, TATi/Δku80 [45], and RHΔhxgprt/Tomato [27] parasites were used as parental strains for the genetically modified parasites generated in this study.

Generation of genetically modified T. gondii parasites

Guide RNA (gRNA)-encoding sequences specific to target genes were introduced into the vector pSAG1::Cas9-U6::sgUPRT (Addgene plasmid # 54467; [25]) using Q5 site-directed mutagenesis (New England Biolabs) as described previously [25]. A list of the forward primers used to generate gRNA-expressing vectors for introducing frame-shift mutations are described in S5 Table. In each instance, the reverse primer 5’-AACTTGACATCCCCATTTAC was used. For generating frameshift mutations in TgApiAT genes, gRNAs were designed to target the open reading frames of TgApiAT genes, and transfected into parasites on a vector that also expressed Cas9-GFP. Transfections were performed as described previously [46]. GFP positive parasites were selected and cloned using flow cytometry 2–3 days following transfection using a FACSAria I or FACSAria II cell sorter (BD Biosciences). The region of the candidate genes targeted by the gRNAs were sequenced in clonal parasites, and clones in which the target gene had been disrupted by a frameshift mutation or insertion of a premature stop codon (i.e. where the open reading frame was disrupted) were selected for subsequent analyses. For 3’ replacements, gRNAs were selected to target a region near the stop codon of the gene of interest, using the primers listed in S6 Table. In addition, a donor DNA sequence encoding a 3x HA tag was amplified by PCR to contain 50 bp of flanking sequences homologous to the target gene either side of the stop codon. Template DNA encoding the 3x HA tag was generated as a gBlock (Integrated DNA Technologies), with the sequence listed in S7 Table. Forward and reverse primers used to amplify the HA tag for each target gene are also listed in S7 Table. gRNA-expressing vectors, which simultaneously encode Cas9 fused to GFP, were co-transfected into T. gondii parasites with the donor DNA sequence. 2–3 days after transfection, GFP-Cas9-expressing parasites were selected and cloned into wells of a 96-well plate by flow cytometry as described above.

3’ replacement plasmids were created to epitope tag TgApiAT2, TgApiAT3-2, TgApiAT3-3, TgApiAT5-3, TgApiAT6-1, TgApiAT6-2 and TgApiAT7-1 using conventional crossover recombination methods as described previously [47]. Regions of DNA homologous to the 3’ ends of the genes were amplified by PCR using primers described in S8 Table, and ligated into the BglII and AvrII sites of the vector pgCH [9] or the PacI and AvrII sites of pLIC-HA₃-DHFR [47]. Resulting plasmids were linearized in the flanking sequence using restriction enzymes (S8 Table), then transfected into TATi/Δku80 parasites. Parasites were selected on chloramphenicol or pyrimethamine as described [46]. In cases where we were unable to subsequently detect a protein of approximately the expected molecular mass by western blotting, we confirmed correct integration of the HA tag by sequencing of CRISPR-modified 3’ ends (TgApiATs 5–1, 5–2, 5–4, 5–5 and 5–6), or by PCR screening (TgApiAT7-1). For assessing HA integration into the TgApiAT7-1 locus, DNA was extracted from TgApiAT7-1-HA parasite clones, and used as template in a PCR with the primers 5’-GGCGAAGAGAAGGCGTTG and 5’-GTCATCCCTTTTCTTCGATAA, with the presence of a 2.5 kb band indicative of successful integration (S3C Fig).

To complement the apiAT2^Δ138–588 mutant with a constitutively-expressed copy of TgApiAT2, we amplified the open reading frame of TgApiAT2 from genomic DNA with the primers 5’-GATCGGATCCAAAATGGCGGCTGCTCAG and 5’-GATCCCTAGGCACAGCGACCTCTGGACTCGGT. We digested the resultant PCR product with BamHI and AvrII and ligated this into the BglII and AvrII sites of the pUgCTH₃ vector [9]. The resultant vector was linearised with MfeI, transfected into apiAT2^Δ138–588 parasites and selected on chloramphenicol. To complement the apiAT5-3^Δ188–504 mutant with a constitutively-expressed copy of TgApiAT5-3, we amplified the open reading frame of TgApiAT5-3 with the primers 5’-GATCGGATCCAAAATGGAGTCGACCGAGGCGACTAT and 5’-GATCCCTAGGCAGCACCTTCGGGACTTTTCTCTTC, using the TgApiAT5-3-expressing oocyte vector (described below) as template. We digested the resultant PCR product with BamHI and AvrII and ligated this into the BglII and AvrII sites of the pUgCTH₃ vector. The resultant vector was linearised with MfeI, transfected into apiAT5-3^Δ188–504 parasites and selected on chloramphenicol.

Immunofluorescence assays and western blotting

Immunofluorescence assays and western blotting were performed as described previously [9]. For western blotting, membranes were probed with rat anti-HA antibodies (clone 3F10, Sigma) at dilutions between 1:1,000 to 1:3,000, mouse anti-GRA8 (a kind gift from Gary Ward, U. Vermont, [48]) at a dilution of 1:80,000, or rabbit anti-TgTom40 antibodies [49] at 1:2,000 dilution, and horseradish peroxidase (HRP)-conjugated goat anti-rat (sc-2006, Santa Cruz Biotechnology), HRP-conjugated goat anti-mouse (sc-2005, Santa Cruz Biotechnology), or HRP-conjugated goat anti-rabbit (sc-2004, Santa Cruz Biotechnology) antibodies at dilutions of 1:5,000 to 1:10,000.

For immunofluorescence assays, samples were probed with the following primary antibodies: rat anti-HA (clone 3F10, Sigma) at a 1:200 dilution, mouse anti-P30 (clone TP3, Abcam) at a 1:2,000 dilution, rabbit anti-P30 (a kind gift from John Boothroyd, Stanford U) at dilutions between 1:25,000 and 1:90,000, rabbit anti-GFP (a kind gift from Alex Maier, ANU) at a 1:200 dilution, or mouse anti-IMC (a kind gift from Gary Ward, U. Vermont) at a 1:500 dilution. Samples were next probed with the following secondary antibodies: CF488A-conjugated goat anti-rat (SAB4600046, Sigma) at a dilution of 1:500, AlexaFluor 488-conjugated goat anti-rat (4416, Cell Signaling Technology) at dilution of 1:250, AlexFluor488-conjugated goat anti-rabbit (A11008, Life Technologies) at a dilution of 1:500, AlexFluor546-conjugated goat anti-rabbit (A11035, Life Technologies) at a dilution of 1:500, AlexFluor546-conjugated goat anti-mouse (A11030, Life Technologies) at a dilution of 1:500, or AlexFluor647-conjugated goat anti-mouse (A21236, Life Technologies) at a dilution of 1:500.

Fluorescence microscopy was performed on a DeltaVision Elite system (GE Healthcare) using an Olympus IX71 inverted microscope with a 100X UPlanSApo objective lens (NA 1.40). Images were recorded using a CoolSNAP HQ2 camera. Images were deconvolved using SoftWoRx Suite 2.0 software, and images were linearly adjusted for contrast and brightness.

Parasite growth and virulence assays

To measure parasite growth by plaque assays, either 150 parasites were added to wells of a 6-well plate containing confluent HFFs, or 500–1,000 parasites were added to confluent HFFs in 25 cm² tissue culture flasks. Parasites were grown for 8 to 9 days before fixation and staining with crystal violet as described previously [46].

Fluorescence growth assays were performed as described previously [50, 51], with slight modifications. Briefly, wells of an optical bottom 96-well plate containing confluent HFFs were washed twice in medium lacking L-Tyr, L-Phe or L-Trp. Wells were filled with medium containing a range of L-Tyr, L-Phe or L-Trp concentrations. 2,000 parasites were inoculated into each of these wells, and plates were incubated at 37°C in a 5% CO₂ incubator. Well fluorescence was measured 5 days post-inoculation in a FluoStar Optima fluorescence plate reader (BMG Labtech), a time point at which WT parasites were in mid-logarithmic stage of growth. Relative growth was expressed as a percentage of the well fluorescence in the optimum amino acid concentration for WT, apiAT5-3^Δ188–504 or apiAT5-3^Δ188-504/cTgApiAT5-3 parasites at this time point.

To measure parasite virulence, freshly egressed WT (RHΔhxgprt/Tomato), apiAT5-3^Δ188–504 or apiAT5-3^Δ188-504/cTgApiAT5-3 parasites were filtered through a 3 μm polycarbonate filter, washed once in phosphate-buffered saline (PBS), then were diluted to 10⁴ parasites/ml in PBS. 10³ parasites were injected intraperitoneally into 7-week-old, female Balb/c mice using a 26-gauge needle. Mice were weighed regularly, and monitored for symptoms of toxoplasmosis (weight loss, ruffled fur, lethargy and hunched posture). Mice exhibiting terminal symptoms of toxoplasmosis were euthanized in accordance with protocols approved by the Australian National University Animal Experimentation Ethics Committee (protocol number A2016/42).

[¹³C]Amino acid labelling and detection

Freshly egressed WT (TATi/Tomato) or apiAT5-3^Δ188–504 tachyzoites (10⁸ parasites each sample) were incubated in 500 μl of amino acid-free Roswell Park Memorial Institute 1640 medium supplemented with 2 mg/ml algal [¹³C]amino acid mix (Cambridge Isotope Laboratories) for 15 minutes at 37°C in a 5% CO₂ incubator. [¹³C]amino acid labelling was terminated by rapid dilution in 14 ml of ice cold PBS. Parasite metabolites were extracted in chloroform:methanol:water (1:3:1 v/v/v) containing 1 nmol scyllo-inositol (Sigma). The aqueous phase metabolites were dried in a heated speedvac concentrator, methoxymated by treatment with 20 mg/ml methoxyamine in pyridine overnight, then trimethylsilylated by treatment with N,O-bis(trimethylsilyl)trifluoroacetamide containing 1% trimethylsilyl for 1 hr at room temperature. Samples were analyzed using GC-MS as described previously [52]. The fractional labelling of all detected amino acids was estimated as the fraction of the metabolite pool containing one or more ¹³C-atoms after correction for natural abundance using the program DExSI, as described previously [53]. Total metabolite counts were normalized to scyllo-inositol as an internal standard.

Xenopus laevis oocyte preparation and TgApiAT5-3 expression

The open reading frame of TgApiAT5-3 was amplified from RHΔhxgprt strain cDNA template using the primers 5’- GATCACCGGTCCACCATGGAGTCGACCGAGGCGACTAT and 5’- GATCCCTAGGCAGCACCTTCGGGACTTTTCTCTTC. The resultant product was digested with AgeI and AvrII, and ligated into the XmaI and AvrII sites of the vector pGHJ-HA [9]. The plasmid was linearised by incubation in NotI overnight, and complementary RNA (cRNA) encoding HA-tagged TgApiAT5-3 was prepared for injection into oocytes as previously described [54–56]. Xenopus laevis oocytes were surgically removed and prepared for cRNA injection as described [55]. For all transporter assays in oocytes, 15 ng of TgApiAT5-3 cRNA was micro-injected into stage 5 or 6 oocytes using a Micro4 micro-syringe pump controller and A203XVY nanoliter injector (World Precision Instruments).

Oocyte surface biotinylation and whole membrane preparation

Oocyte surface biotinylation and whole membrane preparations were performed as described previously [55, 57]. Briefly, for surface biotinylation, 15 oocytes were selected 3–6 days post cRNA injection, washed thrice in ice-cold PBS (pH 8.0), incubated for 45 mins at room temperature in 0.5 mg/ml of EZ-Link Sulfo-NHS-LC-Biotin (Thermo Fisher Scientific), and then washed thrice more in ice-cold PBS. Oocytes were subsequently solubilised in oocyte lysis buffer (20 mM Tris-HCl pH 7.6, 150 mM NaCl, 1% v/v Triton X-100) for 2 hr on ice. Samples were centrifuged at 16,000 g, and the supernatant was mixed with 50 μl of streptavidin-coated agarose beads (Thermo Fisher Scientific). The mixture was incubated at 4°C on slow rotation overnight. Beads were washed 4 times with oocyte lysis buffer before elution in SDS-PAGE sample buffer. For whole membrane preparation, 10–25 oocytes were homogenised by trituration in homogenisation buffer (50 mM Tris-HCl pH 7.4, 100 mM NaCl, 1 mM EDTA, protease inhibitors). Homogenised oocytes were centrifuged at 2,000 g for 10 min at 4°C and the resulting supernatant further centrifuged for 30 min at 140,000 g at 4°C. The resulting pellet was washed with homogenisation buffer and solubilised in homogenisation buffer containing 4% (w/v) SDS, and then in SDS-PAGE sample buffer. Protein samples from surface biotinylation and whole membrane preparations were separated by SDS-PAGE then detected by western blotting as described above.

Oocyte assays: Uptake, efflux and electrophysiology

For uptake experiments in either non-preloaded, preloaded, or pre-injected oocytes, batches of 10 oocytes were washed 4 times in ND96 buffer (96 mM NaCl, 2 mM KCl, 1 mM MgCl₂, 1.8 mM CaCl₂, 5 mM HEPES, pH 7.4) at RT, and then incubated in the desired concentration of radiolabelled substrates as indicated in figure legends. For all substrate screening measurements, uptake was measured over 10 mins. For kinetic experiments, parallel batches of oocytes were preloaded with 0–1.78 mM L-Tyr, and uptake of [¹⁴C]Tyr at a range of L-Tyr concentrations was measured over 10 mins. For other uptake experiments, uptake was measured for the timecourse indicated in the figures. Uptake was quenched by washing oocyte batches four times in ice-cold ND96.

For efflux experiments, batches of 5 oocytes/substrate were preloaded with [¹⁴C]L-amino acids as described below. Following preloading, oocytes were washed 4 times in ND96 and incubated in trans-stimulating substrates at concentrations described in the figure legends. To measure efflux, the 5 oocytes were incubated in 500 μl aliquots of the extracellular solution, of which 100 μl was removed for each time point and the efflux immediately quenched by washing the oocytes four times in ice-cold ND96. Retention of radiolabel within the oocytes was measured by removing the oocytes following quenching of efflux. For the substrate efflux screen depicted in Fig 6B, the extracellular solution was sampled at 5 min, which fell within the initial, approximately linear phase of the uptake timecourse. For efflux experiments depicted in Fig 5C, efflux was measured for the timecourse indicated in the figure.

All oocyte uptake and efflux experiments were performed in solutions containing both [¹⁴C]-labelled and unlabelled isotopes of the amino acid being studied, with the total substrate concentrations and concentration of [¹⁴C]-labelled amino acids specified in the relevant figure legend.

Following the relevant incubation periods, oocytes or aliquots were distributed into OptiPlate96-well plates (Perkin-Elmer) and oocytes were lysed overnight in 10% (w/v) SDS. 150 μl/well of Microscint-40 scintillation fluid (Perkin-Elmer) was added to the samples, and plates covered and shaken for 5 min before radioactivity was counted on a Perkin-Elmer MicroBeta² 2450 microplate scintillation counter.

All steady-state electrical recordings were made with an Axon GeneClamp 500B amplifier (Axon Instruments) in a two-voltage clamp configuration as previously described [57, 58]. Voltage clamp was set to −50 mV or 0 mV and data were sampled at 3 Hz using pClamp 8.2 software (Axon Instruments). Boron silicate microelectrodes capillaries (World Precision Instruments) with a tip resistance of: 1.5 ≥ R_e ≥ 0.5 MΩ were pulled by a P-97 Flaming/Brown micropipette puller (Sutter Instruments) and filled with 3 M KCl. Silver microelectrodes were coated using a 5 M NaCl single-chamber galvanic cell to form AgCl₂ electrodes. The membrane potential was adjusted digitally in voltage-clamp mode between 0 and −50 mV. Oocytes were chosen for recording when they had a resting membrane potential −25 mV < E_m < −45 mV. ND96 (pH 7.4) was used as the control solution for all electrophysiological recordings. Assay buffer pH was varied by mixing different ratios of acidic ND96 (pH 3.6) (5 mM MES instead of HEPES) with basic ND96 (pH 10) (5 mM Tris instead of HEPES).

Preloading of oocytes with substrates

For uptake experiments measuring trans-stimulation by a range of amino acids and other metabolites (Fig 6A and S7B Fig), all L-amino acids substrates and metabolite mixes, except for L-Tyr, were pre-injected at 25 nl/oocyte using a Micro4 micro-syringe pump controller and A203XVY nanoliter injector (World Precision Instruments). All pre-injected oocytes were incubated on ice for 30 mins prior to uptake experiments to allow time for recovery from the injection. Stock solutions containing 100 mM L-amino acids in ND96 were pre-injected to give a calculated cytosolic concentration of 5 mM, based on an assumed free aqueous volume of 500 nl/oocyte. Stage 5 or 6 oocytes diameters vary from 1−1.3 mm and free aqueous oocyte volumes measured from 368 to > 500 nl [59, 60]. Therefore, calculations of cytosolic concentrations from pre-injection should be treated as approximations only. For the experiments giving rise to S7B Fig, different metabolite groups were pre-injected to give estimated final concentrations of each metabolite as indicated in S4 Table. The low solubility of L-Tyr in aqueous solutions (0.453 g/L at 25°C, pH 7.4; [61]) necessitated preloading of this amino acid by incubation, rather than injection. L-Tyr solutions were prepared by dissolving L-Tyr in ND96 to a final concentration of 2.5 mM and performing dilutions in ND96 to the required concentrations. Pre-loading of L-Tyr in TgApiAT5-3-injected oocytes was optimized by monitoring the time-dependent uptake of radiolabelled L-Tyr by oocytes in media containing either 2.5 or 1 mM L-Tyr. In TgApiAT5-3-expressing oocytes, L-Tyr equilibrium was reached after 10 to 12 hr, while uninjected oocytes reached a similar cytosolic concentration after incubation of approximately 68–72 hr. As a consequence, L-Tyr was preloaded for 32 hr in TgApiAT5-3 injected oocytes and for 72 hr in uninjected oocytes for all trans-stimulation experiments.

All efflux substrate screening with [¹⁴C]labelled amino acids (Fig 6B) were conducted by preloading L-amino acids for 3 hr prior to uptake. L-Tyr containing 0.5 μCi/ml [¹⁴C]Tyr was preloaded at a concentration of 2.5 mM, while the other L-amino acids (containing 0.5–1 μCi/ml [¹⁴C]-labelled substrate) were preloaded at a concentration of 5 mM. Calculation of the pre-loaded [¹⁴C]labelled L-amino acids concentrations were conducted using a control set of oocytes for each substrate, pre-loaded in parallel to those used for efflux trans-stimulation. Calculations were made assuming a cytosolic volume of 500 nl/oocyte (see above).

Oocyte data analysis and statistics

All oocyte data were analyzed using OriginPro (2015). All data displayed in figures represent the mean ± S.D. except where otherwise indicated. Unless uptake data from uninjected oocytes is included in figures, uptake in uninjected oocytes was subtracted from uptake in TgApiAT5-3-injected oocytes to give the ‘TgApiAT5-3-mediated uptake’. All data sets were analysed for Gaussian normalcy by first running a Shapiro-Wilk test prior to analysis and used only if passing the normalcy test at the P < 0.05 level. Multi-variant experiments with 3 or more experimental conditions were subjected to a one-way ANOVA with Dunnet’s post-hoc test and significance tested at the P < 0.05 level.

Timecourse analysis of uptake and oocyte retention data of L-Tyr in TgApiAT5-3-injected oocytes were fitter to 1^st order integrated rate equations: (1)

Or: (2)

Eq 2 being the Box Lucas 1 model with zero offset [62], where S_t, and S₀, and are the amount of substrate (S) at variable time (t), or when t = 0, S_max is the vertical asymptote of substrate amount, and k is the 1^st order rate constant.

Steady-state kinetic data collected under initial rate conditions were fitted to both the Michaelis-Menten equation: (3)

And a Scatchard linear regression equation: (4)

In the Scatchard regression, the apparent Michaelis constant (K_0.5) is derived from the slope (1/−K_0.5) and the maximal rate (V_max) from the ordinate intercept (V_max/K_0.5).

All curve fittings were evaluated using adjusted R² values as indicated in the text and figure legends. All non-linear fitting was conducted using the Levenburg-Marquardt algorithm, with iteration numbers varying from 4 to 11 before convergence was attained.

Amino acid uptake assays in T. gondii parasites

Amino acid uptake assays were carried out as described previously [9], with slight modifications. Briefly, extracellular parasites were washed twice in Dulbecco’s PBS pH 7.4 (Sigma) supplemented with 10 mM glucose (PBS-glucose). Parasites were incubated in PBS-glucose containing radiolabelled amino acids, and 200 μl aliquots removed at regular time points. Parasite samples were centrifuged through an oil mix to separate parasites from unincorporated radiolabel as described previously [9]. L-Arg uptake was measured by incubation in 0.1 μCi/ml [¹⁴C]Arg and 100 μM L-Arg, L-Tyr uptake was measured by incubation in 0.25 μCi/ml [¹⁴C]Tyr and 60 μM L-Tyr, and L-Phe uptake was measured by incubation in 0.1 μCi/ml [¹⁴C]Phe and 15 μM L-Phe. The timecourses of radiolabel uptake in each amino acid tested were fitted by a single exponential function and the initial rate of transport was estimated from the initial slope of the fitted line.

Ethics statement

All animal research was conducted in accordance with the National Health and Medical Research Council’s Australian Code for the Care and Use of Animals for Scientific Purposes, and the Australian Capital Territory Animal Welfare Act 1992. Mice were maintained and handled in accordance with protocols approved by the Australian National University Animal Experimentation Ethics Committee (protocol number A2016/42). Maintenance of Xenopus laevis and preparation of oocytes was approved by the Australian National University Animal Experimentation Ethics Committee (protocol number A2014/20).