The acquisition of thermally tolerant algal symbionts by corals has been proposed as a natural or assisted mechanism of increasing coral reef resilience to anthropogenic climate change, but the cell-level processes determining the performance of new symbiotic associations are poorly understood. We used liquid chromatography–mass spectrometry to investigate the effects of an experimentally induced symbiosis on the host proteome of the model sea anemone Exaiptasia pallida. Aposymbiotic specimens were colonised by either the homologous dinoflagellate symbiont (Breviolum minutum) or a thermally tolerant, ecologically invasive heterologous symbiont (Durusdinium trenchii). Anemones containing D. trenchii exhibited minimal expression of Niemann-Pick C2 proteins, which have predicted biochemical roles in sterol transport and cell recognition, and glutamine synthetases, which are thought to be involved in nitrogen assimilation and recycling between partners. D. trenchii-colonised anemones had higher expression of methionine-synthesising betaine–homocysteine S-methyltransferases and proteins with predicted oxidative stress response functions. Multiple lysosome-associated proteins were less abundant in both symbiotic treatments compared with the aposymbiotic treatment. The differentially abundant proteins are predicted to represent pathways that may be involved in nutrient transport or resource allocation between partners. These results provide targets for specific experiments to elucidate the mechanisms underpinning compensatory physiology in the coral–dinoflagellate symbiosis.
The cnidarian–dinoflagellate symbiosis allows biodiverse coral reef ecosystems to thrive within nutrient-limited oceans . A range of cnidarian taxa, such as corals, sea anemones, and jellyfish, are obligate hosts of dinoflagellate algal symbionts from the family Symbiodiniaceae, which support their hosts through the exchange of photosynthetic products . Genetic diversity within the Symbiodiniaceae is extensive, and this family has been recently reclassified into seven genera containing a rapidly increasing number of formally described species [3,4,5]. Symbiodiniaceae exhibit variation in their physiologies, with a range of thermal tolerances and host specificities [6, 7]. Some Symbiodiniaceae can form symbioses with a diversity of hosts, whereas many hosts only associate with a single dominant symbiont species [8, 9]. The underlying mechanisms of host–symbiont specificity remain only partially described but include cellular recognition and nutrient exchange between the partners [2, 10, 11]. Symbiotic interactions between cnidarians and Symbiodiniaceae are thought to exist on a continuum from mutualism to parasitism [12, 13]. Symbionts can exhibit less beneficial qualities such as impairing host metabolism and reproduction, reducing the proportion of photosynthate translocated to the host, or increasing nitrogen assimilation at the expense of the host, particularly at elevated temperatures [13,14,15]. Symbiont genotypes that are found naturally in a given host species are considered to be homologous, while symbioses with heterologous symbionts can occur due to perturbation of the symbiosis by environmental stress, geographic invasion, or experimental manipulation [16, 17]. Some heterologous symbionts have been demonstrated to translocate lower amounts of photosynthetically fixed carbon to their hosts compared with homologous symbionts [16, 17].
Coral reefs worldwide are threatened by warming oceans inducing the breakdown of the coral–dinoflagellate symbiosis, also called coral bleaching [18,19,20]. Unless a symbiont population can be re-established quickly, coral bleaching may lead to host mortality . Some Symbiodiniaceae are particularly tolerant of higher temperatures, both while free living and in symbiosis, potentially providing greater resistance to host bleaching [22,23,24]. These thermally-tolerant algae can act as opportunists, replacing the previously dominant symbiont genotype if its population declines, as occurs in a bleaching event [25, 26]. It has been proposed that corals may be able to adapt to climate change by ‘shuffling’ or ‘switching’ their symbiont assemblages, resulting in a more thermally tolerant symbiont species as the dominant partner, and a more thermally robust holobiont of coral, symbiont and associated microbes [7, 27,28,29]. Durusdinium trenchii (formerly Symbiodinium trenchii) is endemic to the Indo-Pacific, where it exists in mutualisms with multiple scleractinian coral genera, often in warm-water environments, and has been recently introduced into the Caribbean [16, 23, 30, 31]. In many Caribbean coral species, it exists as a background population that becomes temporarily dominant after bleaching, an example of shuffling [32, 33]; however, it is unknown if heterologous symbionts are capable of supplanting the homologous symbiont species and establishing a lasting true mutualism that increases host fitness and persists over multiple host generations. Given that D. trenchii has no coevolutionary history with Caribbean cnidarians but has become established, if at very low cell densities, in a wide diversity of Caribbean corals, it is an ideal genotype in which to test the effects of heterologous symbiont colonisation on a naive host.
In the anemone Exaiptasia pallida, a model for corals commonly known as Aiptasia [2, 34,35,36], colonisation by heterologous symbionts results in poorly understood differences in host phenotype [11, 17, 37]. Reduced, poorly regulated, or inefficient nutrient or metabolite exchange might reduce growth and fitness of either or both partners, resulting in a less mutualistic symbiosis. Additionally, heterologous symbionts may be less tolerated by host immune functions and consequently limited to a lower maximum density within host tissues, further restricting their potential contribution to the symbiosis. We hypothesise that nutrient transport and resource allocation between partners, as well as host immune tolerance of intracellular symbionts, is more optimal in established symbioses and that novel heterologous symbioses will exhibit deficiencies in these functions. Therefore, proteins predicted to be involved in host immune responses, nutrient regulation of symbionts, or transporting specific metabolites between partners are primary candidates for determining symbiosis success, and we anticipate differences in their abundances between symbioses.
To test these hypotheses, we compared the effects of colonisation with a heterologous symbiont (D. trenchii ), with those of colonisation with a homologous symbiont (Breviolum minutum, formerly Symbiodinium minutum ) on the Aiptasia host proteome. Aiptasia experimentally colonised by D. trenchii have been demonstrated to show greatly reduced growth and asexual reproductive output, despite displaying similar photosynthetic rates and symbiont densities to Aiptasia colonised by the homologous symbiont . Furthermore, combined transcriptomic and metabolomic analyses of the D. trenchii–Aiptasia symbiosis showed an increased host catabolism of storage compounds and a differential expression of signalling and reactive oxygen species pathways, indicating a suboptimal symbiosis . Here, we performed a proteomic characterisation of cnidarians hosting homologous and heterologous symbionts to clarify what cell-level changes are associated with the presence of different symbiont partners. This comparative approach was undertaken for its ability to identify for further study candidate proteins and functions that contribute to the successful establishment and persistence of the cnidarian–dinoflagellate symbiosis and to better understand the implications of symbioses with non-endemic dinoflagellate symbionts.
Materials and methods
Individuals of the symbiotic sea anemone Aiptasia were collected from a clonal laboratory stock, strain NZ1. Anemones were rendered aposymbiotic (i.e., symbiont-free) using the menthol treatment method  and maintained in 0.22 µm-filtered seawater (FSW). Approximately 750 aposymbiotic individuals were divided amongst 18 containers and placed into 25 °C water baths designated for the three treatment groups: B. minutum-colonised, D. trenchii-colonised, and aposymbiotic anemones. Light was provided by fluorescent lamps at ~ 95 µmol photons m−2s −1 on a 12 h:12 h light:dark cycle. Dinoflagellate cultures were grown in f/2 medium at 25 °C under 100 µmol photons m−2 s−1 on a 12 h:12 h light:dark cycle for 6 weeks prior to inoculation. The B. minutum culture (strain ‘FLAp2’) was originally isolated from Exaiptasia pallida, while the D. trenchii culture (strain ‘Ap2’) was originally isolated from an unknown anemone in Okinawa. The genetic identity of each culture was verified by direct sequencing of ITS2 rDNA and cp23S .
Inoculation of Aiptasia
Anemones were inoculated during the midpoint of the light cycle by applying dinoflagellate cultures at a cell density of ~3 × 106 mL−1, combined with a dilute suspension of Artemia sp. nauplii to induce phagocytosis. This process was repeated weekly for three weeks (four weeks total). Full details of the inoculation procedure are provided in the Supplemental Materials.
Five weeks after initial colonisation, anemones were flash frozen in liquid nitrogen five hours into the photoperiod and stored at −80 °C. Each biological replicate (n = 6) was composed of a pool of 20 individual anemones. Each biological replicate was thawed, mechanically homogenised, and an aliquot removed for symbiont cell density estimates. Symbiont cell densities were analysed as per Matthews et al. . Protein content was quantified using the Bradford assay . Low-speed centrifugation (2500 × g) was used to pellet the algae and the host fractions were lyophilised at –105 °C for 18 h. The genetic identity of dinoflagellates in each anemone sample was verified by ITS2 and cp23S sequencing as before . 30 mg of lyophilised host material was extracted with methanol for a parallel metabolite study  before storage at –20 °C. These host samples were then solubilised, alkylated, digested with trypsin and desalted using the methods of Oakley et al. , which are fully detailed in the Supplemental Materials.
Identification of proteins using LC-ESI-MS/MS
Peptides were analysed by liquid chromatography–electrospray ionisation–tandem mass spectrometry (LC-ESI-MS/MS) using the instrumentation, settings and software described in . The resulting spectra were searched against a custom Aiptasia database constructed primarily from the Aiptasia genome  and a contaminant database  using the Sequest algorithm in Proteome Discoverer (v2.1, Thermo Scientific). The X! Tandem algorithm in Scaffold (v4.4.8, Proteome Software, Inc.) was used to validate MS/MS-based peptide and protein identifications. Peptide and protein identifications required >99% probability by the Scaffold Local false discovery rate algorithm and a minimum of two peptides. Proteins sharing significant peptide evidence were grouped into protein clusters. Each biological replicate was analysed twice as technical replicates, and protein abundance calculated as the simple mean between technical replicates at the protein cluster level. To confirm that contaminating symbiont proteins were not present, all spectra were searched as above against a Symbiodinium microadriaticum protein sequence database . This analysis identified minimal algal proteins (mean of 14 per sample), most of which are highly conserved among eukaryotes (data not shown). Full details are available in the Supplemental Materials. Mass spectrometry data are publically available at the PRIDE repository with the dataset identifier PXD009253.
Tests for significant differences in symbiont cell density between algal species were performed with SPSS (v. 20, IBM Corporation). Non-normal or heteroscedastic data were log10-transformed prior to analysis with Student’s t-tests (p < 0.05). Protein clusters were quantified by precursor intensity in Scaffold and statistical analyses were conducted in R v. 3.3.1 (www.r-project.org). To identify proteins with significantly different abundances between treatments, a custom R script for multivariate analysis with post hoc identifications and protein load normalisation was used, as described in Oakley et al. . A linear model with treatment effects was fitted and compared against an intercept-only null model using an analysis of deviance χ2 test, where α = 0.05. This script is available online at https://zenodo.org/record/1327230#.W2Y-0FD-iUk. Protein clusters with significantly different concentrations between treatments were identified with the false discovery rate correction method of Benjamini and Hochberg , at a q-threshold of 0.05.
Proteins that were significantly different between treatments were searched against the UniProtKB database using BLAST in Geneious v10.0.2 (Biomatters Ltd, Auckland, New Zealand). The top manually-reviewed SwissProt match for each protein with an E-value ≤ 1 × 10−5 was used to assign an annotation, and any without a match were designated as hypothetical proteins. If the only match with an E-value ≤ 1 × 10−5 was an unannotated UniprotKB Nematostella vectensis sequence, that sequence identifier is listed. Principal component analysis (PCA) and heatmap plots were generated by ClustVis, using ln(x) transformed protein abundance values, Pearson’s correlations for row and column clustering, and average distances for row and column linkage . Singular value decomposition with imputation was used to calculate principal components.
Comparison of transcript and protein data
A parallel study, using different biological samples, used RNASeq-based transcriptomics to assess changes in gene expression in B. minutum- and D. trenchii-colonised Aiptasia . We attempted to assess the concordance of this dataset with the results of the proteomic analysis; full methods are available in the Supplemental Material. Briefly, transcripts from the original dataset (n = 80,703) were matched against the proteins identified (as above) using blastx with a threshold of 98% identity and an E-value of less than 1 × 10−20. Pearson’s correlation coefficient was calculated to test if the relationship between treatments was conserved between datasets by comparing the magnitude and direction of gene expression in protein abundances and mRNA counts of each matched gene.
Results and discussion
Examination of anemones in the aposymbiotic control treatment revealed no re-establishment of background symbionts at the end of the experiment. Genotyping confirmed that symbionts at the end of the experiments were the same as those originally used for inoculation. Symbiont cell densities in anemones colonised by B. minutum (average of 1.12 × 107 ± 1.16 × 106 std. error) were 1.5-fold higher (p = 0.040) than those in anemones colonised by D. trenchii (average of 7.29 × 106 ± 1.19), which is in agreement with past studies [11, 17, 48]. D. trenchii cells are approximately 1.9-fold greater in volume than B. minutum cells, however, indicating similar total symbiont biomass density .
Proteins affected by symbiont presence and species
A total of 1608 proteins were identified among all treatments; 31 decoy (known false match) sequences were discarded, and 276 sequences were not analysed further due to their being detected in fewer than 25% of samples. Overall, 142 proteins were significantly differentially abundant between the three treatments (aposymbiotic, B. minutum and D. trenchii-colonised animals, q < 0.05). Of these, 129 sequences were annotated using sequence similarities from the SwissProt database (E-value ≤ 1 × 10−5), and the remaining 13 were categorised as hypothetical proteins; five of these 13 were homologues of predicted proteins in Nematostella vectensis. Between the B. minutum-colonised and aposymbiotic samples, 105 proteins were differentially expressed (Fig. S1, Tables S1, S2); 22 proteins were differentially expressed between B. minutum-colonised and D. trenchii-colonised anemones (Table S3), and 108 proteins were differentially expressed between D. trenchii-colonised and aposymbiotic anemones (Tables S1, S4). Anemones colonised by B. minutum and those colonised by D. trenchii shared 74 differentially expressed proteins when compared with aposymbiotic anemones (Table S1).
A principal component analysis of all detected proteins (Fig. 1a) and the differentially abundant proteins (Fig. 1b) showed that aposymbiotic Aiptasia were clearly distinguished from those colonised by either of the symbiont species. Anemones colonised by B. minutum or D. trenchii demonstrated overlap in their differentially expressed proteins, relative to the aposymbiotic anemones (Fig. 1b). Cluster analysis illustrated that the protein abundances of aposymbiotic anemones were separate from those of anemones colonised by B. minutum or D. trenchii (Fig. 1c). When compared to a previous transcriptomic analysis of the same symbioses , we found no consistent correlation between abundances of transcripts and proteins detected in both experiments (details in the Supplemental Materials). These data represent snapshots of independent experiments; thus, any correlation or lack thereof should be interpreted cautiously. Furthermore, correlations between transcript and protein abundances have been demonstrated to be low in other organisms , demonstrating the value of additional methodologies to complement transcript-based gene expression studies.
Symbiont presence, regardless of species, was associated with changes in a suite of Aiptasia proteins (summarised in Table 1), which we interpret as primarily representing changes to host cell physiology in accommodating symbiont cells and the gain of photosynthetic capability via symbiosis. These proteins have predicted functions in inorganic carbon acquisition, host immune processes, and catabolism of fatty acids, carbohydrates, and proteins (see below). The homologous and heterologous symbiont associations displayed differences in their abundances of proteins with predicted lipid transport, methionine metabolism, and immune regulation functions (Table 2). These reflect host cell-level differences in response to the nature of the symbiosis. The potential roles of these proteins and their relevance to the physiological performance of the different symbioses, based on known homologue functions, are discussed below.
Dissolved inorganic carbon (DIC) transport
Two carbonic anhydrase homologues were found to be highly upregulated (4-fold) in both symbiotic associations when compared with the aposymbiotic state (q < 1.3 × 10−2, Tables 1, 2). Carbonic anhydrase is an integral part of the carbon concentrating mechanism used by symbiotic cnidarians to facilitate the interconversion of DIC species, which, in turn, makes the transport of DIC from seawater to symbiont plastids for carbon fixation more efficient [50,51,52]. The significantly higher abundance of carbonic anhydrase homologues suggests that DIC transport functions are induced in both homologous and heterologous symbiont associations. When comparing the physiology of multiple Symbiodiniaceae in the coral Orbicella spp., Pettay et al.  noted that D. trenchii-colonised hosts had similar rates of photosynthetic oxygen evolution but much lower rates of host calcification, indicating that algal DIC acquisition was uninhibited but that the host was not benefiting substantially from the produced photosynthate. Photosynthetic activity alters DIC and pH within host tissues ; however, whether the apparent carbonic anhydrase expression in hosts containing symbionts is a homeostatic response to regulate these parameters or is induced by recognition of the symbionts is unknown.
Of the 74 shared proteins differentially expressed between anemones colonised by either of the symbiont species and aposymbiotic anemones (Fig. S1), many are homologues of proteins typically localised to the lysosome (Table 1). Most of these differentially expressed and presumably endolysosomal proteins were less abundant in either of the symbiotic associations relative to the aposymbiotic state. The symbiosome membrane, which surrounds intracellular symbiont cells, is an arrested endosomal membrane that avoids lysosomal fusion [2, 54].
The protein that most significantly differentiates Aiptasia hosting the homologous B. minutum is Niemann-Pick 2 (NPC2); two homologues of NPC2 were detected exclusively in anemones colonised by B. minutum, and they were undetectable in aposymbiotic anemones or those hosting D. trenchii (q < 2 × 10−8, Table 2). In the broader UniProtKB database, these proteins were most similar to the NPC2-d protein of Anemonia viridis . Although a third NPC2 protein, most similar to NPC2-a, was detected at low levels in aposymbiotic anemones, it was significantly more abundant following colonisation with B. minutum (q = 1.9 × 10−2, Table 2). None of the NPC2 homologues had significantly different abundances between aposymbiotic and D. trenchii-colonised anemones. Four NPC2 genes have been found in the symbiotic sea anemone Anemonia viridis, where NPC2-d is localised to the symbiosome compartment [55, 56], and six NPC2 genes have been identified in the Aiptasia genome . In mammals, NPC2 is a soluble lysosomal protein that rapidly binds and shuttles cholesterol to the membrane-bound NPC1 protein for transfer and export across the lysosomal membrane [57, 58]. The cnidarian NPC2 protein may act in symbiont recognition and persistence, based on its role in the immune signalling pathways of other invertebrates [55, 59], and it has been proposed that NPC2 participates in the transport of sterols between partners [43, 55, 56, 60, 61], but this hypothesised function requires further investigation. Homologues of acid ceramidase and peroxiredoxin, both of which have predicted lysosomal lipid degradation functions [62, 63], were also upregulated in both symbioses (Table 1).
A successful intracellular mutualism requires host recognition of potential symbiont cells, tolerating their presence while regulating their growth, and this process begins with the formation of the symbiosome . To persist, the symbiosome must then avoid host lysosomal fusion, which may be a potential mechanism for symbiont population regulation . A homologue of the Ras-related protein Rab2, a signalling protein that is required for the fusion of late endosomes and lysosomes in Drosophila , was more abundant in anemones colonised by either B. minutum or D. trenchii when compared with aposymbiotic anemones (q = 1.4 × 10−2, Table 1). We detected differential abundances of several proteins with predicted immune-related protease functions depending on symbiotic state and symbiont species, including homologues of legumain, neurolysin, and several cathepsins. A legumain homologue was 4.7-fold more abundant in anemones colonised by B. minutum versus D. trenchii (q < 3 × 10−3, Table 2), while anemones hosting either B. minutum or D. trenchii expressed much lower abundances of homologues of cathepsins L, Z, and the lysosomal dipeptidyl peptidase 2 than did aposymbiotic anemones (q < 2 × 10−2, Tables 1, 2). Legumain is primarily localised to acidic compartments of the endolysosomal system . It is has a role in antigen processing and Toll-like receptor (TLR) signalling via the highly-specific cleavage of TLR receptors . TLR signalling is thought to be a primary means of immune regulation in the cnidarian innate immune system . A homologue of the peptidase neurolysin was also upregulated (3.0-fold, q = 1.2 × 10−2) in B. minutum versus D. trenchii-colonised anemones. Like legumain, the cathepsins are cysteine proteases of the endolysosomal system that play roles in TLR signalling and immunity; they also have protein catabolic functions in autophagic and endosomal vacuoles . Legumain and neurolysin are unlike the other peptidases in that their homologues were upregulated in the B. minutum symbiosis relative to the D. trenchii symbiosis (Table 2), and this may be a result of host immune responses that differ in the presence of different symbiont species. Furthermore, both cathepsin L and Z homologues exhibited much lower expression when Aiptasia hosted either algal species than when the anemones were devoid of symbionts (Table 1). Interestingly, cathepsin L deficiency in mice results in the generation of large, long-lived autophagolysosomes . As a hypothesis, a potential role of cathepsins in symbiosome maturation merits further study.
Potential immune responses to symbiont presence
The role of the coral immune response in symbiont specificity is an area of active research . Compared with aposymbiotic anemones, a homologue of the 40 S ribosomal protein S19 was elevated 4-fold and 7.6-fold in anemones colonised by B. minutum and D. trenchii, respectively (q < 1.7 × 10−2, Table 1). As this pattern was not found for other ribosomal protein homologues, we considered the possibility that cnidarian S19 has roles in regulation of the symbiosis. In addition to its ribosomal functions, S19 attenuates the activity of the pro-inflammatory cytokine macrophage migration inhibitory factor (MIF) in vertebrates . Apicomplexans, a sister taxon to the dinoflagellates, appear to exploit this to facilitate parasitic infection of vertebrates [72, 73], and MIF is also involved in regulating parasite populations in other invertebrates . Given the increased abundance of an S19 homologue in anemones colonised by dinoflagellates, especially D. trenchii, S19 and its potential role in the cnidarian host immune response to dinoflagellate colonisation should be a topic for further targeted study. A homologue of the circumsporozoite protein (CSP) was highly upregulated (4.5-fold) in B. minutum-colonised anemones compared with D. trenchii-colonised or aposymbiotic anemones (q < 2.1 × 10−2, Table 2). CSP is the primary surface antigen produced by the apicomplexan Plasmodium, and it plays a role in the invasion of host cells by receptor-mediated binding to the host plasma membrane . A potential role of the CSP homologue in the cnidarian–dinoflagellate symbiosis as a host surface ligand is interesting given the close evolutionary relationship between apicomplexans and dinoflagellates, but more directed investigation is needed to determine both the function and localisation of this protein.
Nitrogen and methionine metabolism
Nitrogen exchange between partners is central to the cnidarian–dinoflagellate symbiosis, particularly in oligotrophic reef waters, and glutamine synthetase is thought to be the primary enzyme responsible for inorganic nitrogen assimilation in both host and symbiont [76,77,78]. Two glutamine synthetase homologues were more abundant in B. minutum- versus D. trenchii-colonised anemones (q < 1.2 × 10−3, Table 2). Increased glutamine synthetase activity has previously been reported to be characteristic of symbiotic Aiptasia and other cnidarians [60, 76, 79]. Ammonium can be assimilated by both the host and symbiont through the glutamine synthetase/glutamine oxoglutarate aminotransferase cycle , which is used to catalyse the conversion of ammonia and glutamate into the amino acid glutamine . Parallel metabolomic analysis of the Aiptasia specimens used in this study measured greater abundances of labelled glutamine in D. trenchii-colonised hosts relative to B. minutum-colonised hosts , suggesting either an increased demand or a reduced synthesis of glutamine in anemones hosting B. minutum. When combined, the glutamine synthetase protein and glutamine metabolite data seem to be consistent with, but cannot confirm, simultaneous increased host glutamine synthesis and consumption when hosting homologous symbionts. This may simply be a direct result of the higher density of B. minutum cells than D. trenchii; alternately, an enhanced abundance of glutamine synthetase may serve as a mechanism for avoiding nitrogen limitation of the holobiont.
Given the importance of nitrogen and amino acid exchange in a productive coral–algal symbiosis, the observed differential expression of homologues of the methionine-synthesising enzyme betaine–homocysteine S-methyltransferase (BHMT) between symbiont species is also notable. BHMT synthesises methionine from homocysteine and betaine and acts as a central enzyme in the methionine cycle responsible for molecular methylation [81, 82]. The expression levels of two and three different BHMT protein homologues, respectively, were lower in anemones colonised by B. minutum and in those hosting D. trenchii, relative to aposymbiotic anemones (q < 3.3 × 10−2, Table 2). Aposymbiotic Aiptasia have previously been demonstrated to both synthesise methionine and exhibit high abundances of BHMT compared with Aiptasia colonised by homologous symbionts [60, 83, 84]. There is evidence that, in symbiotic corals, half of the methionine pathway enzymes are expressed by the host while the other half are expressed by the symbiont, suggesting that partner coordination may be important for the proper functioning of this pathway . The observed changes in BHMT homologue abundances suggest a change in either the methionine demand by the host or its supply by the symbiont. In a parallel study, metabolomic analysis detected doubled concentrations of methionine in Aiptasia colonised by D. trenchii rather than B. minutum . One hypothesis consistent with these data is that although aposymbiotic Aiptasia are capable of de novo methionine synthesis via the BHMT pathway, they may receive sufficient methionine (or methionine precursors) from homologous B. minutum, but not heterologous D. trenchii, thus necessitating an upregulation of BHMT in D. trenchii-colonised anemones; this topic requires further research.
Besides being required for protein synthesis, methionine is a substrate for synthesis of the methyl donor s-adenosylmethionine and the antioxidants dimethylsulfoniopropionate (DMSP) and glutathione. DMSP is a strong reactive oxygen species scavenger, and its impact on mediating coral bleaching is of interest given that DMSP concentrations in coral tissues are greatly elevated during acute thermal stress concurrent with photoinhibition and reactive oxygen species generation , as well as being dependent on symbiont genotype . Increased BHMT transcript expression corresponded with increased DMSP concentrations in Acropora under osmotic stress . A persulfide dioxygenase homologue was much less abundant in symbiosis, regardless of symbiont species (q < 2.8 × 10−6, Table 1). This enzyme catabolizes toxic hydrogen sulphide, which is generated from the interconversion of homocysteine to cysteine, to glutathione . The upregulation of BHMT homologues and of other proteins with predicted functions in oxidative stress responses in anemones hosting D. trenchii, together with previously reported methionine accumulation, suggest that symbioses may differ in their redox state. Direct measurements of host reactive oxygen species concentrations, and studies of the metabolic origins of antioxidants in the host, are needed to test whether hosts harbouring heterologous symbionts suffer elevated oxidative stress.
ER and oxidative stress
Among the proteins that were more abundantly expressed in the D. trenchii-colonised Aiptasia, two have predicted functions which suggest changes in protein assembly or endoplasmic reticulum (ER) performance. A homologue of the neurotropic factor protein Armet was upregulated 3.3-fold in these anemones relative to those hosting B. minutum (q < 1.8 × 10−2, Table 2). Armet is secreted in response to misfolded protein accumulation in the ER, protecting cells against stress-induced cell death . Additionally, BiP, a 78 kDa glucose-regulating protein that also plays a role in the ER protein folding stress-response , was previously found to be both constitutively abundant and upregulated in Aiptasia during heat shock . Here, a homologue of BiP was more abundant in D. trenchii-colonised than in B. minutum-colonised anemones (q < 4.2 × 10−3). The upregulation of BiP and Armet homologues suggests an elevated Aiptasia host stress response when colonised by D. trenchii, as supported by previously reported gene transcript and metabolite data .
Pirin is a highly conserved, redox-sensitive regulator of the transcription factor NF-κB that is upregulated in response to oxidative stress . A pirin homologue was significantly more abundant in aposymbiotic anemones than in those colonised by either B. minutum or D. trenchii (q < 3.9 × 10−3) and was also more abundant in B. minutum- than in D. trenchii-colonised anemones (q < 3.8 × 10−2, Table 2). In its oxidised form, pirin is proposed to bind and activate NF-κB , which is highly conserved, moderates immune function, and has been shown to be suppressed by dinoflagellate colonisation in Aiptasia .
This study identified proteins (summarised in Fig. 2) that differed in abundance between Aiptasia hosting different dinoflagellate symbiont species, and the predicted functions of these proteins give rise to hypotheses regarding the establishment and regulation of effective cnidarian–dinoflagellate symbioses. A NPC2-d homologue distinguished the homologous symbiosis and expression of a glutamine synthetase homologue varied between symbioses. Anemones colonised by the homologous B. minutum exhibited elevated levels of proteins with predicted nitrogen and lipid metabolism functions, whereas those colonised by the heterologous D. trenchii had greater abundances of proteins with predicted methionine pathway and oxidative stress functions. Homologues of carbonic anhydrases were expressed in both symbioses, emphasising the importance of DIC availability and photosynthetic performance for the symbiont. Only those anemones colonised by B. minutum expressed detectable levels of a homologue for NPC2-d protein, for which there is increasing evidence of a role in successful cnidarian–dinoflagellate associations [55, 56]. If this finding is confirmed in corals, it may offer a potential mechanism to explain why D. trenchii rarely dominates cnidarian hosts in its invasive range despite its ubiquity and thermal resilience . Even in hosts in which it is homologous, D. trenchii is known to trade fitness for thermal tolerance . D. trenchii colonisation also increases the methionine concentration  and BHMT homologue abundance in Aiptasia. These data identify new targets for investigating the cell biology of the cnidarian–dinoflagellate symbiosis as well as host metabolic processes that may be affected by symbiosis with heterologous symbionts. If consistent among novel cnidarian–dinoflagellate pairings, these responses may serve as physiological barriers to the establishment of successful, ecologically fit coral symbioses unless they are mutable over timescales relevant to the increasing frequency of coral bleaching events.
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Financial support for this research was provided by the Marsden Fund of the Royal Society Te Apārangi, grant number 1202, to SKD, VMW and ARG. The authors thank S. Wilkinson for the script and the three anonymous reviewers for their comments.
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The authors declare that they have no conflict of interest.
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Sproles, A.E., Oakley, C.A., Matthews, J.L. et al. Proteomics quantifies protein expression changes in a model cnidarian colonised by a thermally tolerant but suboptimal symbiont. ISME J 13, 2334–2345 (2019). https://doi.org/10.1038/s41396-019-0437-5
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