Host Coenzyme Q Redox State Is an Early Biomarker of Thermal Stress in the Coral Acropora millepora

Bleaching episodes caused by increasing seawater temperatures may induce mass coral mortality and are regarded as one of the biggest threats to coral reef ecosystems worldwide. The current consensus is that this phenomenon results from enhanced production of harmful reactive oxygen species (ROS) that disrupt the symbiosis between corals and their endosymbiotic dinoflagellates, Symbiodinium. Here, the responses of two important antioxidant defence components, the host coenzyme Q (CoQ) and symbiont plastoquinone (PQ) pools, are investigated for the first time in colonies of the scleractinian coral, Acropora millepora, during experimentally-induced bleaching under ecologically relevant conditions. Liquid chromatography-mass spectrometry (LC-MS) was used to quantify the states of these two pools, together with physiological parameters assessing the general state of the symbiosis (including photosystem II photochemical efficiency, chlorophyll concentration and Symbiodinium cell densities). The results show that the responses of the two antioxidant systems occur on different timescales: (i) the redox state of the Symbiodinium PQ pool remained stable until twelve days into the experiment, after which there was an abrupt oxidative shift; (ii) by contrast, an oxidative shift of approximately 10% had occurred in the host CoQ pool after 6 days of thermal stress, prior to significant changes in any other physiological parameter measured. Host CoQ pool oxidation is thus an early biomarker of thermal stress in corals, and this antioxidant pool is likely to play a key role in quenching thermally-induced ROS in the coral-algal symbiosis. This study adds to a growing body of work that indicates host cellular responses may precede the bleaching process and symbiont dysfunction.

Introduction photochemical efficiency, chlorophyll concentration and Symbiodinium density estimates were used to follow the effects of thermal stress on the state of the symbiosis over time.

Ethics Statement
All necessary permits were obtained for the described field studies. Specimens for this study were collected under permit number G09/30237.1, issued by the Australian Government's Great Barrier Reef Marine Park Authority. The locations of sample collection are not privatelyowned, and no endangered or protected species were collected.

Experimental design
Twelve A. millepora colonies roughly 50 cm in diameter containing type C2 Symbiodinium (ITS1 terminology, see below) were collected from Pelorus Island, Great Barrier Reef, Australia (18°33' S/146°29' E) in May 2010. Colonies were transferred to the Australian Institute of Marine Science (Townsville) and divided into a total of 24 fragments, each comprising approximately 25 branches. Fragments were arranged in eight indoor tanks in a balanced randomised block design, resulting in the allocation of twelve coral fragments (three per tank) to each of the control and thermal stress temperature treatments (27°C and 32°C, respectively). All tanks were continuously supplied with fresh, 1 μm filtered seawater at a rate of 1.5 L min −1 from 500 L reservoirs in a temperature-controlled room maintained at 27 ± 0.5°C (two reservoirs per treatment). Each reservoir was heated with two titanium heaters (3 kW) controlled by a CR1000 datalogger (Campbell Scientific) and a temperature sensor in the treatment tanks. All tanks were fitted with a small power head pump to maintain water movement and an air stone and pump to provide aeration. UV-filtered 400 W metal halide lights (BLV, Germany) were mounted above each tank and provided an average underwater light intensity of 350μmol photons m −2 s −1 (12:12 h light:dark cycle). The UV-filters were used to minimise UV-radiationinduced bleaching [39].
The colony fragments were acclimated for two weeks prior to starting the experiment, then seawater temperatures in four tanks were ramped at a constant rate (0.7°C d -1 ) to 32 ± 0.5°C over seven days; the remaining four control tanks were maintained at 27°C for the entire duration of the experiment (Fig 1). The heat stress temperature was chosen to represent an ecologically relevant 1°C above the estimated local bleaching threshold of approximately 31°C for nearby Orpheus Island, Great Barrier Reef (18°35' S/146°29' E;~31°C: [40]). Coral branches were sampled at four time points during the experiment: at the end of the acclimation period (t = 0 d), upon reaching the 32°C target temperature in the hyperthermal stress treatment (t = 7 d), and after five (t = 12 d) and ten days (t = 17 d) at 32°C. At each time point, coral nubbins (approximately 50 mm in length) were collected from each coral fragment after six hours of light (n = 12 in control and heat treatment, respectively) and from a subset of fragments after six hours of darkness (n = 9 in control and heat treatment, respectively). Samples were immediately snap-frozen in liquid nitrogen at time of collection to quench the PQ and CoQ pool redox states. Total sample size was optimised to ensure all samples could be processed in less than four weeks after sampling to ascertain the redox stability of the extracts.

Photosystem II photochemical efficiency
Photosystem II (PSII) photochemical efficiency, expressed as maximum quantum yield ((F M − F O )/F M = F V /F M ) was measured daily with a Diving-PAM (Walz Gmbh, Germany) from three randomly chosen branches per coral fragment two hours before the start of the light cycle [41]. A 6 mm fibre optic probe was placed perpendicular to the surface at least 20 mm from the tip of the branch and 3 mm from the coral tissue surface (controlled via a rubber spacer) to obtain the measurements. Minimum fluorescence (F O ) was measured using a weak pulsed measuring light (< 0.15 μmol photons m −2 s −1 ; gain = 3) and maximum fluorescence (F M ) was measured upon application of a saturating pulse of light (> 4000 μmol photons m −2 s −1 ).

Prenylquinone quantification
Coral nubbins for prenylquinone extraction were stored in liquid nitrogen for a maximum of 48 hours. Nubbins were extracted using a 1:1 mixture of isopropanol and ethyl acetate containing 0.1 μM CoQ 9 (internal standard). Coral CoQ 10 and Symbiodinium PQ 9 pools were quantified by LC-MS using a slightly modified method of Lutz et al. [25]. In brief: prenylquinones were resolved using a Phenomenex Kinetex C18 column (150 mm × 4.6 mm, 2.6 μm particle size) on an Agilent 1100 series HPLC (Agilent, USA) coupled to a Bruker Esquire 3000 (Bruker Daltonics, USA). Absolute quantities of the prenylquinones were calculated from calibration plots obtained from standard compounds containing 0.1 μM CoQ 9 (internal standard). CoQ and PQ redox states (%PQH 2 and %CoQH 2 ) were expressed as the proportion of reduced to total (oxidised + reduced) prenylquinone. Coral CoQ data could potentially be biased by CoQ of Symbiodinium; however, symbiont CoQ was not detected with the method applied here, either because Symbiodinium type C2 contains a different isoform than the host CoQ 10 or because concentrations are below the detection limit [37].

Symbiodinium densities
For Symbiodinium densities, one coral nubbin per coral fragment and time point was immediately processed at midday (n = 12 in control and heat treatment, respectively). Coral nubbins were airbrushed in individual plastic bags in 4 mL of 0.2 μm filtered seawater. The slurry was homogenised using a Turrax disperser (IKA, Germany) to break down aggregates and was centrifuged at 3000 g. The supernatant was removed and the pellet resuspended in 1 mL of 10% formalin in phosphate buffer saline (PBS). Symbiodinium cells were counted under a light microscope (eight technical replicates per sample) using a haemocytometer (depth 0.1 mm).

Calculation of surface area and chlorophyll concentrations
Tissue remaining on the coral nubbins was removed by soaking in diluted commercial bleach (0.5% NaClO) overnight. Surface areas of the coral nubbins were determined using a wax dipping technique [42]. Chlorophyll concentrations (a and c 2 ) were measured from aliquots of the prenylquinone extracts on a microplate reader (Powerwave, Bio-Tek Instruments, USA) [43] and determined using the equations presented in Ritchie et al. [44].

Symbiodinium genotyping
The Symbiodinium genotypes were identified based on sequence differences in the nuclear ribosomal DNA internal transcribed spacer 1 (ITS1) region using single-strand conformation polymorphism (SSCP) analysis as described by van Oppen et al. [45]. Total coral and Symbiodinium DNA was extracted using a modified protocol [46] and the Symbiodinium ITS1 region amplified with fluorescently labelled Sym ITS1 PCR primers for SSCP analysis on non-denaturing polyacrylamide gels. The symbiont genotype was determined by comparison of manually scored gel images of known reference standards run in parallel with the samples [47]. SSCP profiles from all colonies were single bands identical to type C2 Symbiodinium (GenBank Accession AF380552) sensu van Oppen et al. [45].

Transmission electron microscopy (TEM)
At each time point, one coral branch was sampled in four coral fragments per treatment, transferred directly into fixative (1.25% glutaraldehyde + 0.5% paraformaldehyde in 0.2 μm filtered seawater) and stored at 4°C until required. Fixed coral nubbins were decalcified in a formic acid:fixative mixture (1:3), with the solution changed every 12 h until complete dissolution of the skeleton. Three individual polyps per sample were postfixed in osmium and subsequently dehydrated with increasing concentrations of ethanol followed by dry acetone. Dehydrated samples were infiltrated in increasing concentrations of Araldite resin before being cured for 24 h at 60°C. Longitudinal sections, 90-nm thick, were collected on copper grids and imaged at 120 kV in a JEOL 2100 TEM.

Statistical analysis
Linear mixed models [51,52] were applied to assess treatment effects using time (sampling day), treatment (control vs. heated) and the interaction as fixed effects and a random intercept for each coral fragment to account for repeated measures of the same colonies. F V /F M , %PQH 2 and %CoQH 2 data were power transformed; PQ concentration was log transformed. Model comparison was conducted using Akaike's information criterion (AIC). Tank effects were nonsignificant (fixed) and redundant (random), and thus discarded to avoid overfitting in all models. First order autocorrelation covariate structure was determined as best model fit in all models. Multiple pairwise comparisons were corrected using the false discovery rate following Hochberg and Benjamini [53]. All statistical analyses were conducted using SPSS version 17.0.

Results
A. millepora colony fragments exposed to hyperthermal stress (32°C) showed clear symptoms of bleaching, when compared to ambient (27°C) treatment controls (Fig 2A-2D). In the thermal stress treatment group, Symbiodinium cell densities were reduced by 25.7% after five days and by 82.4% at the end of the experiment (Fig 2E). No significant changes were observed in cellular chlorophyll concentrations (a and c 2 ) during the experiment (mean = 29.6 ± 4.5 pg cell −1 ; p = 0.46). Mortality was low; of the 24 colony fragments used, only two of the 12 exposed to thermal stress showed signs of necrosis, patchy tissue sloughing and algal overgrowth. No further data were collected for these fragments after day 13 and 15, respectively, when symptoms of mortality were first observed. PSII photochemical efficiency (F V /F M ± 95% confidence interval (CI)) remained stable in control colonies (mean = 0.68 ± 0.1) but declined markedly in the 32°C treatment group concomitant with the loss of Symbiodinium cells after day 9 ( Fig 2F; p < 0.001; Table 1). The declining trend of F V /F M was observable from the third day after heating commenced; however, F V /F M did not differ significantly from control samples until day five (t-test; F 1,278 = 10.683; p = 0.0012). TEM images showed no impact on the Symbiodinium thylakoid membrane or cell wall structure in the first seven days of the experiment; however, disintegrated internal organelles were observed in 7% of the cells examined (total 1502). After five days exposure to 32°C (t = 12 d), all of the remaining Symbiodinium cells exhibited both structurally compromised thylakoid membranes and widespread disintegration of organelles in the cytoplasm (Fig 3). While damage to internal structures was apparent, cell walls appeared intact and no fragmented symbiont cells were observed.
The Symbiodinium PQ pool was predominantly reduced at the start of the experiment, and remained approximately constant during the first twelve days of heat stress (from t = 0 h to 12 d: mean = 90.8 ± 1.4% in light and 87.3 ± 4.2 in dark); note that the PQ redox state (%PQH 2 ± 95% CI) did not differ significantly between the light and dark periods (Fig 2G;  Table 1). However, the heat stressed colonies exhibited a highly significant 12% (light) and 11% (dark) decline in PQH 2 at the end of the experiment (at t = 17 d, mean = 78.9 ± 3.5% and 76.2 ± 5.1%; respectively; p < 0.002). When normalised per Symbiodinium cell, this decline in PQH 2 coincided with an apparent five-fold increase in total PQ concentration (PQ + PQH 2 ) from 1.49 ± 0.23 pmol cell −1 (mean, t = 0 d to 12 d) to 5.11 ± 2.06 pmol cell −1 at t = 17 d (Fig 2I; p = 0.008) in the heat treatment.
Whereas the redox state of the PQ pool remained essentially stable for 12 days, the coral CoQ pool (%CoQH 2 ± 95% CI) became oxidised more rapidly in response to the hyperthermal stress. CoQH 2 declined from 89.4 ± 1.0% to 80.9 ± 2.6 in the light, and from 89.7 ± 1.1% to 82.3 ± 3.3% in the dark, within the first seven days of the experiment (i.e. at the end of the heating phase from 27°C to 32°C; Fig 2H; p < 0.002). In the 32°C treatment group, %CoQH 2 continued to decline steadily over the next ten days to 77.3 ± 2.9% (light) and 75.4 ± 7.9% (dark). As in the case of the plastoquine pool, light and dark estimates of %CoQH 2 did not differ significantly. Likewise, total CoQ (CoQ + CoQH 2 ; normalised per coral surface area) did not differ between control and heat stress, remaining stable throughout the experiment (Fig 2J; Light: mean = 0.41 ± 0.03 nmol cm −2 ; p = 0.36; Dark: mean = 0.40 ± 0.03 nmol cm −2 ; p = 0.21).

Coenzyme Q pool redox state
The results presented here demonstrate that the A. millepora host CoQ redox state is sensitive to hyperthermal stress, exhibiting an overall 13% decline of CoQH 2 in response to the stressor (Fig 2H). This oxidative shift was not caused by an increase of de novo synthesised CoQ, as the total CoQ concentration (CoQ + CoQH 2 ) did not increase during the heat stress. Oxidation of the CoQ pool occurred early in the thermal stress treatment, upon reaching 32°C (after seven days with a daily temperature increase of approximately 0.7°C per day) and prior to any measurable loss of Symbiodinium cells from the host tissue. Oxidation of the CoQ pool occurred before a major decline in PSII photochemical efficiency was observed, i.e., while the effects of the hyperthermal stress on the Symbiodinium photosynthesis apparatus were still limited (F V / F M > 0.65). Moderate irradiance levels (350 μmol photons m −2 s −1 ) were used in order to avoid major light stress concomitantly with the applied hyperthermal stress [2,54,55]. Maximum daily irradiance at 1-3 m depths regularly exceeds 1000 μmol photons m −2 s −1 for nearby (< 25 km), equally turbid Great Palm Island waters [56]. The results therefore indicate that the A. millepora CoQ pool is oxidised significantly in response to hyperthermal stress in the absence of strong light exacerbating ROS leakage from the symbiont [57,58]. Although a contribution of photosynthetically derived ROS to the observed CoQ pool oxidation cannot be discounted, the results presented here add to a growing body of work that indicates host cellular responses may precede the bleaching process and symbiont dysfunction [5,[17][18][19][20]59]. In Fig 2. Effects of thermal stress on physiological parameters of the scleractinian coral Acropora millepora. Images of representative coral nubbins demonstrating the visual difference in Symbiodinium cell densities within A. millepora tissues under control (27°C) (A-B) and thermal stress (32°C) (C-D) conditions at day 17 (end of experiment). Scale bars = 1 mm. Thermal stress effects on (E) Symbiodinium density; (F) photosystem II photochemical efficiency; (G) plastoquinone (%PQH 2 ) and (H) coenzyme Q (%CoQH 2 ) pool redox states; (I) total plastoquinone concentration (PQ + PQH 2 ) per Symbiodinium cell and (J) total coenzyme Q concentration (CoQ + CoQH 2 ) per coral surface area over the course of the experiment. All data points are means ± 95% CI; * indicate significant differences between control and treatment at p < 0.05; n = 6-12 (see Table 1  addition, other thermal stress-related responses such as transcriptional and physiological changes that were not measured here are expected to occur in both coral symbiosis partners prior to host CoQ pool oxidation. For example, other reported early changes include a reduction in epithelial tissue, signs of increased apoptosis in the gastrodermis, and changes to the transcriptome, which have been associated with an upregulation of chaperone and antioxidant defence genes alongside transcriptional changes that, by analogy to vertebrate models, are assumed to be linked to apoptosis [18,25,26,[60][61][62][63]. It should also be noted that the heat/light sensitivity of the photosynthetic apparatus varies among different symbiont types and that this affects host sensitivity to bleaching [64][65][66]; however, bleaching susceptibility differs widely among different coral genera despite often hosting the same Symbiodinium types [67][68][69]. Considering this, the results presented here require confirmation in other symbiont-host associations prior to postulation of a generalized physiological response during the bleaching cascade. Nonetheless, the oxidative shift in the CoQ redox state observed here is among the earliest known metabolic changes in the coral partner in response to a realistic temperature level. Coenzyme Q pool redox state regulation. CoQ/CoQH 2 is present (in varying quantities) in all intracellular membranes of every animal with the highest concentrations found in the mitochondrial membranes at the primary site of ROS production [32,70]. In eukaryotes, CoQ redox processes are relatively complex (Fig 4; for relevant enzymes identified in Acropora sp. see S1 Table). Within mitochondrial membranes, CoQH 2 is continuously regenerated by the respiratory chain (complex I, II and alternative NAD(P)H dehydrogenases) [71] and other mitochondrial enzymes (glycerol-3-phosphate dehydrogenase, electron-transferring flavoprotein dehydrogenase, dihydroorotate dehydrogenase; [72]). In other membranes, several enzymes catalyse CoQ reduction including a NADH-cytochrome b 5 reductase [73] and a distinct, unresolved NADPH-CoQ reductase [74]. Interestingly, a cytosolic NAD(P)H:quinone Respiratory "linear" electron flows (black arrows) proceed from NADH in the mitochondrial matrix to H 2 O via the CoQ pool and the enzyme complexes I, II, III, and IV, forming ubiquinol (CoQH 2 ) as an intermediary product. The electron flows via complexes I, III and IV occur (mostly) via tunnelling or micro-diffusion of CoQ/CoQH 2 in I-II-IV supercomplexes rather than via the larger mobile CoQ pool [72]. "Non-linear" electron flows (dark blue arrows) proceed from electron donors (e.g. NAD(P)H) via several quinone dehydrogenases to the CoQ pool, and to H 2 O from CoQH 2 via AOX. Plasma membrane electron transport occurs from NAD(P)H to H 2 O via one or more type of NAD(P)H-CoQ reductases, the plasma membrane CoQ pool and Ecto-NOX. CoQH 2 ROS scavenging occurs continuously in O 2 metabolism primarily via chain breaking of lipid peroxidation (LPO) caused by O 2 •− and H 2 O 2 . Abbreviations: AOX, alternative oxidase; cyt-c, cytochrome c; DHAP, dihydroxyacetone phosphate; DHO, dihydroorotate; DHODH, dihydroorotate dehydrogenase; Ecto-NOX, external quinone oxidase; ETF red/ox , reduced/oxidised electron-transferring-flavoprotein; ETFDH, electron-transferringflavoprotein dehydrogenase reduced/oxidised; Ecto-NOX, external quinone oxidase; GPDH, glycerol-3-phosphate dehydrogenase; G-3-P, glycerol-3-phosphate; H 2 O 2 , hydrogen peroxide ; LPO, lipid peroxidation; pmNDH/mNDH, plasma membrane/mitochondrial NAD(P)H dehydrogenases; OA, orotate; O 2 •− , superoxide.
doi:10.1371/journal.pone.0139290.g004 reductase (NQO1; formerly DT-diaphorase) [75]-the most studied CoQ reducing enzymeappears to be absent in cnidarians along with other NQO genes [76]. In contrast to the reduction of the CoQ pool, CoQH 2 is oxidised by direct interaction with ROS, in particular lipid peroxyl radicals and the lipid peroxidation initiating perferryl radicals (Fe 3 O 2 •− ) found in all membranes [28], by complex III and alternative oxidases (AOX) of the mitochondrial ETC [77], and by the external oxidases of the plasma membrane electron transport (Ecto-NOX; [78]). Considering the known CoQ pool redox mechanisms of other animals, the oxidative shift in the CoQ redox state in A. millepora can therefore be attributed to: (1) an increase in ROS scavenging by CoQH 2 ; (2) a decline in net CoQ reduction by the mitochondrial ETC; (3) extra-mitochondrial pathways; or 4) any combination of these processes.
Coenzyme Q pool reactive oxygen species scavenging in corals. Attributing the thermal stress-induced oxidative shift in CoQ redox state of A. millepora to a specific physiological mechanism is difficult, primarily because current understanding of CoQ functions in the coral-Symbiodinium symbiosis is very limited and existing methods cannot distinguish between functionally and spatially different CoQ pools present in different organelles [79]. Theoretically, a net decline in CoQ reduction caused by the mitochondrial ETC or extra-mitochondrial pathways are conceivable by postulating a decline in CoQ reducing or an increase in CoQH 2 oxidising enzyme activities; however, no such direct impact of thermal stress on the CoQ pool has been demonstrated so far. In particular, the emerging consensus that the complexes I-III-IV occur mostly as supercomplexes further complicates attributing shifts in the CoQ redox state to a specific location in the mitochondrial ETC as electron transfer in these supercomplexes appears to occur via tunnelling or microdiffusion of CoQ/CoQH 2 rather than via a mobile CoQ pool in mitochondrial membranes [72].
Short term heat stress in the bleaching model Aiptasia has been reported to cause the degradation of host mitochondria prior to symbiont impairment and to lead to the downregulation of genes associated with ATP production and electron transport at the site of, and downstream from, cytochrome c [19]. However, the report did not include any genes upstream of complex III (Fig 4), thus there is no indication that the CoQ pool reducing side of the mitochondrial ETC was affected. A recent transcriptional analysis provided further evidence of the thermal stability of complex III gene expression in A. millepora [80] but analyses at the enzyme activity level in cnidarians remain outstanding. The visible, pre-bleaching mitochondrial damage in Aiptasia [19] would be expected to incapacitate the mitochondrial ETC and potentially lead to CoQ oxidation due to a decline in electron flux to the pool; however, there is currently no data available to lend support to such a model. On the other hand, an inefficient mitochondrial ETC is likely leading to the increased formation of ROS [8,59,81], in particular during daytime hyperoxia [24,82]. Thus, even though it is possible that any components of the CoQ pool redox mechanisms are affected by thermal stress, attributing the oxidative shift in the CoQ redox state to increased CoQH 2 ROS scavenging in response to hyperthermal stress currently provides the most parsimonious explanation.
In mammals, oxidative shifts in the CoQ pool redox state have been observed in a variety of pathological conditions that are associated with oxidative stress [35,36,83]. These oxidative shifts are understood to result from an increasingly challenged antioxidant defence [28]. In cnidarian-Symbiodinium symbioses, it has been repeatedly demonstrated that the cnidarian host reacts to thermal stress and high light by increasing its antioxidant activities, which indicates an increased requirement to detoxify ROS in the host tissues [7,38,54,[84][85][86]. ROS formation also occurs in aposymbiotic cnidarians upon exposure to light and elevated temperatures, although in symbiosis, the hyperoxia caused by algal photosynthesis aggravates the coral's innate ROS formation because it increases relative to oxygen concentration [24,59,[87][88][89][90][91]. Bleaching in symbiotic cnidarians can also be triggered in the absence of photosynthetically produced ROS by thermal stress in darkness [21]. It is not yet understood what role nonphotosynthetically produced ROS play in this dark-bleaching; however, mitochondria would appear to be the most likely origin for these ROS. Mitochondria (the primary source of ROS in animals) are the location of the highest cellular CoQ/CoQH 2 concentration in eukaryotes [28,78]. Here, superoxide (O 2

•−
) and other ROS are generated by enzymes involved in the ETC, particularly the NADH dehydrogenase of complex I, and the interface between the CoQ pool and complex III [91,92]. The co-localisation of the ROS producing respiratory ETC and the CoQ pool within mitochondrial membranes is likely an important factor in the high antioxidant effectiveness of CoQH 2 [28,93]. In addition to ROS generation by the coral, ROS leakage from Symbiodinium probably exceeds the host's innate ROS generation [24,57,58]. Moreover, impaired or damaged photosynthetic ETC may further increase ROS formation and, ultimately, ROS leaking into the host [7,8,94]. The expulsion of Symbiodinium cells by the coral host has therefore been regarded as a protective mechanism: the coral prevents further ROS leakage from Symbiodinium into host cells by removing the primary source of ROS production and also by reducing tissue hyperoxia during daylight exposure [95,96]. The CoQ pool likely provides an early line of antioxidant defence because ROS leaking from Symbiodinium cells would need to cross the host-derived symbiosomal membrane, which like all animal membranes is expected to contain CoQ/CoQH 2 [32,70]. Nonetheless, it would be expected that an increase in Symbiodinium cellular ROS concentrations to a point where leakage into the host occurs would manifest as a distinct decline in PSII photochemical efficiency. However, a major decline in F V /F M was only observed here after significant CoQ pool oxidation had already occurred (Fig 2F and 2H). This suggests that ROS leakage is unlikely to be a major contributing factor to the initial oxidation of the CoQ pool, although this cannot be ruled out in the later stages where a major decline in F V /F M was observed.

Plastoquinone pool redox state
In contrast to the host CoQ pool redox state, the Symbiodinium PQ redox state remained stable until the point at which PSII photochemical efficiency was severely impaired and coral nubbins were distinctly bleached (Fig 2C and 2D). The observed initial stability of the PQ redox state, despite hyperthermal stress, is consistent with short-term acute heat stress results [37]. By analogy with high light stress [29,97], the oxidative shift due to hyperthermal stress could be caused by increased ROS scavenging of PQH 2 within Symbiodinium chloroplasts or changes in photosynthetic ETC such as increased plastid terminal oxidase activity. PQH 2 is a highly effective quencher of 1 O 2 [33,34] and, like CoQ, acts as a lipid peroxidation chain breaker either directly or via the regeneration of α-tocopherol [30,31]. Even though irradiance was maintained at a moderate level during the experiment described here, the applied temperature stress caused chronic photoinhibition of PSII, which is commonly reported in coral bleaching experiments (e.g. [14,15,98]) and a known indicator of ROS formation within the photosynthetic ETC [99].
A five-fold increase in PQ pool concentrations was recorded concomitantly with the observed PQ pool oxidation (Fig 2I). Newly synthesized PQ is predominantly in the reduced form (PQH 2 , not PQ) [97], thus the observed oxidative shift in the PQ pool at this stage should be the result of increased non-enzymatic formation of PQ from PQH 2 after its interaction with ROS, which are increasingly generated by a thermally damaged photosynthetic ETC [7,14,81,94]. In plants and algae, a considerable proportion of the PQ pool is associated with the chloroplast plastoglobuli which are thought to act as PQH 2 reservoirs [100,101]. Consequently, the size of the PQ pool increases when plants and algae are exposed to conditions that induce the formation of 1 O 2 , such as high light exposure [29,33,97]. Accordingly, the increase in the total PQ pool observed here could be seen as a cellular protective mechanism against the oxidative stress caused by the increasingly impaired photosynthetic ETC. The lack of compromised cell walls in the TEM images (Fig 3) implies that this increase is unlikely to be the result of a normalisation artefact: i.e. loss of structurally compromised cells during the extraction procedure, thus underestimating cell counts. Nonetheless, the concomitant loss of internal cellular structure and the highly compromised state of thylakoid membranes at this time point indicate a need for further experimental work before a definitive protective mechanism can be attributed to de novo synthesised (reduced) PQ during bleaching.

Conclusions
This study demonstrated that hyperthermal stress in A. millepora was associated with oxidation of the coral host CoQ pool redox state. This oxidation occurred prior to any measurable loss of Symbiodinium cells from the host and major decline in PSII photochemical efficiency. Thus the oxidation of CoQ pool redox state is among the earliest known impacts of hyperthermal stress on the cellular chemistry of the coral host and adds to a growing body of work that indicates host cellular responses may precede the bleaching process and symbiont dysfunction. Furthermore, the Symbiodinium PQ pool redox state remained unaffected by hyperthermal stress until PSII photochemical efficiency was severely impaired. At this stage, the PQ pool exhibited a five-fold increase in concentration and a distinct oxidative shift.
Supporting Information S1 Table. Enzymes involved in coenzyme Q pool redox reactions identified in the Acropora digitifera genome a , the Acropora millepora transcriptome b and the EST sequences deposited at GenBank c . (PDF)