Introduction
Photosynthesis is a process used by phototrophic organisms to harness chemical energy from light. Generally attributed to plants and algae, photosynthesis may occur in metazoans that establish endosymbiotic associations with algae. A particular case is that of Sacoglossa sea slugs that feed suctorially on macroalgae and maintain functional chloroplasts in their digestive glands, a process termed kleptoplasty (Greene, 1970; Greene & Muscatine, 1972; Kawaguti & Yamasu, 1965) as the animal effectively “steals” the organelle for its own use. After having pierced the algal cell wall with its radula, the animal sucks and digests all the cellular components, including the nucleus, while the chloroplasts are maintained intact and are integrated in the animal cells. In some species, the stolen chloroplasts – kleptoplasts – can continue to function for several weeks to a few months, despite the absence of algal nuclear genes necessary to encode most chloroplast proteins. The process is often considered an example of endosymbiosis, although the chloroplast itself does not constitute an organism (Dorrell & Howe, 2012).
While in some species of Sacoglossa sea slugs (e.g., Elysia timida and Plakobranchus ocellatus) kleptoplasts are mostly visible only in some body regions (e.g., the dorsal area), in other species such as E. viridis, they are distributed evenly and not concentrated in a specific part of the animal (Gallop et al., 1980). In E. viridis, the presence of ramifications of digestive tubules, throughout most of the sea slug’s body, contributes to a colour resembling that of its algal food and helps the animal to blend with the environment to escape predators (Hirose, 2005). Moreover, the presence of kleptoplasts could provide additional advantages such as the translocation of photosynthates to other animal cells that do not host kleptoplasts. Recent studies, for example, demonstrated that carbon derived from photosynthesis is translocated to the reproductive organs in two different sea slugs (i.e., Elysia timida and Elysia viridis) (Cartaxana et al., 2021; Cruz et al., 2020). The availability of “autotrophic powered cells” has multiple advantages for the animals as active photosynthesis can help in minimizing the loss of weight during food shortage, supporting the reproductive output of the sea slugs or increasing mucus production (Cartaxana et al., 2021; Donohoo et al., 2020; Evertsen & Johnsen, 2009; Lopes et al., 2022; Maeda et al., 2021; Shiroyama et al., 2020; Yamamoto et al., 2013).
Acquiring chloroplasts, however, may pose some problems to the animal cells: photosynthesis, especially under stronger light, is often associated with the production of reactive oxygen species (ROS) that inhibit the de novo synthesis of proteins (i.e., impairing the repair of photosystem II (PSII)), but also damage DNA and non-photosynthetic host cells (Murata et al., 2007). To tackle damages, photosynthetic organisms are equipped with multiple photoprotective mechanisms that shield the photosynthetic apparatus from damages after light is absorbed by the light-harvesting systems. The prevalent mechanism is the conversion and dissipation of the excess excitation energy as heat, defined as the energy-dependent component of non-photochemical quenching (NPQ), qE. This fast reversible NPQ component depends on an irradiance-dependent proton gradient across the thylakoid membrane that decrease the lumenal pH. In land plants and algae, PsbS protein serves as the sensor that detects these changes and that activates qE quenching in PSII antenna by interacting with light harvesting complexes (LHCII) and inducing conformational changes (Christa et al., 2017; Dall’Osto et al., 2005). qE is further modulated by the activation of a xanthophyll cycle (XC) (i.e., a process where violaxanthin (Vx) is reversibly converted to zeaxanthin (Zx) under high light through the intermediate conversion into antheraxanthin (Ax) by the enzymes violaxanthin de-epoxidase (VDE) and zeaxanthin epoxidase (ZEP) (Goss & Jakob, 2010; Müller et al., 2001). Apart from qE, authors hypothesized the presence of a pH-independent quenching mechanism, based on the direct binding of Zx to the periphery of antenna complexes. This NPQ component, named qZ, would appear later than qE and would use the Zx already synthesized and, as such, would be independent from lumen acidification and subsequent activation of VDE enzyme (Dall’Osto et al., 2005). A fast reversible NPQ component and functional XCs has been reported in kleptoplasts of E. timida and E. chlorotica (Cartaxana et al., 2019; Cruz et al., 2015) as they are one of the main mechanisms present in the algal donors (i.e., Acetabularia acetabulum and Vaucheria litorea, respectively). Not all the macroalgae, however, have a functional XC and most of the protoprotective mechanism in this class of organisms are currently unclear. For example, reports suggest that some members of the order Bryopsidales lack a functional XC and do not show qE-type quenching during light stress, but instead accumulate other carotenoids (e.g., all-trans-neoxanthin) as a way to shield the reaction centers or to contribute to an efficient energy transfer between photosystem components (Benson & Cobb, 1983; Giossi et al., 2020; Giossi et al., 2021; Li et al., 2023; Zuo et al., 2006).
E. viridis is a polyphagous sacoglossan sea slug (i.e., can eat a wide array of different macroalgae). In the Swedish coast, for example, it has been found foraging on multiple species such as the septate algae Cladophora sericea, Cladophora rupestris, Chaetomorpha melagonium, and Ceramium virgatum (a rhodophyte, differently to all the other mentioned taxa, that are chlorophytes), as well as the siphonaceous species Codium fragile and Bryopsis plumosa (Baumgartner & Toth, 2014). On the Portuguese coast, E. viridis can be found eating the alga C. tomentosum and this association, together with its photophysiology, has been extensively characterized (Cruz et al., 2014; Cruz et al., 2015; Rauch et al., 2018). C. tomentosum is one of the species that does not show a functional XC and, as such, E. viridis has never been reported to be able to functionally replicate such mechanism. Recently, in laboratory conditions, we could observe an active feeding behaviour of E. viridis on samples of Chaetomorpha sp. associated with the retention of functional chloroplasts. Chaetomorpha is structurally very different from Codium as it is a filamentous alga that can grow up to several centimeters in length. The thallus has a cylindrical shape and is usually unbranched, loosely entangled and stiff, made by the junction of several squared cells separated by septa (Blair et al., 1982). This characteristic affects the feeding pattern of the animals that must move and pierce every single cell to suck the cytoplasm. Chaetomorpha is typically of a bright green colour but can sometimes appear darker or even blackish depending on the growth environment. Interestingly, the toughness of the outer cell wall seems also to be influenced by the intensity of the environmental light, assuming a rigid consistence when the alga is cultured under low irradiance (Krause-Jensen et al., 1996). Moreover, Chaetomorpha is reported to have a XC cycle (although its functionality has not been tested) and grown under high irradiances accumulates lutein, showing then a pigment composition different from C. tomentosum (Bischof et al., 2006; Christa et al., 2017).
Experimental studies on polyphagous sea slugs fed with specific algal chloroplast donors show that functionality and longevity of kleptoplasts depend on plastid origin (Cartaxana et al., 2023; Curtis et al., 2015). In this work, we compared the photophysiology of the sea slug E. viridis fed with the two different algae, investigating to which extent the xanthophyll cycle of the algal donor is conserved in the animals.
Methods
Animals and algae collection and maintenance
Wild sea slug Elysia viridis (Montagu, 1804) and the macroalga Codium tomentosum Stackhouse, 1797, were collected during low tide in the intertidal rocky area of Aguda beach, Vila Nova de Gaia, Portugal (41°02′50.2″N, 8°39′15.2″W). A minimum of 100 animals were collected in several expeditions, depending on the tide and on the animal availability. The number was decided based on the dedicated space in the laboratory to ensure the best possible maintenance conditions. After collection, the animals and the algae were transported to the laboratory and maintained in 150 L recirculated life support systems (LSS) operated with artificial seawater (ASW) at 18 °C and a salinity of 35 ensured by a refrigerating system (Ultra Titan 200; HAILEA, GuangDong, China). A laboratory adaptation period of 2 weeks was chosen to ensure replicability in feeding and the light history of the animals at the beginning of the experiment. The photoperiod was set to 12 h light:12 h dark, with a photon scalar irradiance of 60–80 μmol photons m−2 s−1, at the water surface, being provided by T5 fluorescent lamps. Irradiance was measured in the water with a US-SQS Spherical Micro Quantum Sensor and a ULM-500 Universal Light Meter (Walz, Effeltrich, Germany). Chaetomorpha sp. strands were obtained from coral life support systems existing in the same laboratory. Exact origin is unknown. The alga of this study was specifically cultivated in 2 L flasks with f/2 medium (without silica) and constant aeration at 20 °C and an irradiance of 60–80 μmol photons m−2 s−1 provided by LED lamps (Valoya 35 W, spectrum NS12), for 2 weeks before time zero of the experiment and up to the final feeding moment.
70 animals chosen to be used for the following evaluations were isolated in fish maternity nets in the same LSS with the above-described light conditions to ensure homogeneity of water conditions and a high degree of monitoring. The animals chosen among the original 100 sea slugs collected were the ones visually similar in size and color. Specimens were then provided with a constant supply of food (35 fed with either C. tomentosum or Chaetomorpha sp.) for 1 month. Approximately 2 g of new algae were provided at least once every 5 days. Variables such as light distribution across the LSS and in different depths of the maternity net were considered providing that the two experimental settings were having the same characteristics. Every day, animals were monitored to ensure that no specimen was isolated in zones of the maternity net without algal food. The animals were weighed at the start and at the end of the feeding phase to estimate the daily weight increase by placing them on a nylon mesh with absorbent paper below, for gently removing the excess of water before weighing on an FH-200 laboratory scale (Waagenet AF GmbH, Berlin, Germany).
Photosynthetic measurements
Fluorescence measurements were carried out on the samples by using an Imaging-PAM fluorometer (Mini version, Heinz Walz GmbH). To efficiently perform the measures on the sea slugs avoiding movements, the animals were blocked in a 0.2% agar solution in ASW before starting the measurements. The solution was prepared by mixing the appropriate concentration of agar in ASW, boiling the mixture, and letting it cool on ice. The solution was collected in an ice-cooled Pasteur pipette, slowly poured on the animals in a petri dish and solidified on a bed of ice before taking the measurements. At the end of the experiment, the animals were carefully removed from the embedding agar by using a Pasteur pipette and moved to a container with ASW to let them recover. They took approximately 15 min to recover full mobility. Effective quantum yield of photosystem II (ΦPSII) was measured as ΔF/Fm’, where ΔF corresponds to Fm’- F (the maximum minus the minimum fluorescence of light-exposed organisms). Maximum quantum yield of PSII, Fv/Fm, was calculated as (Fm-Fo)/Fm, where Fm and Fo are, respectively, the maximum and the minimum fluorescence of dark-adapted samples. For dark acclimation, samples were incubated for at least 30 min in darkness to allow the full relaxation of photosystems. Light curves were constructed with 12 incremental steps of actinic irradiance (E; 0, 15, 37, 55, 82, 136, 176, 238, 371, 446, 538, 649 µmol photons m-2 s-1). For each step, ΦPSII was monitored every minute and electron transport rate (ETR) was calculated as E x ΦPSII x 0.84 x 0.5 (where 0.84 is the light absorptance by an average green leaf and 0.5 is the fraction of absorbed quanta available for PSII). The light response and associated parameters ETRm (maximum electron transport rate), Ek (light saturation coefficient) and alpha (photosynthetic rate in light limited region of the light curve) were characterized by fitting iteratively the model of the rETR versus E curves using MS Excel Solver (Platt et al., 1980). The fit was very good in all the cases (r>0.98). The NPQ kinetics were obtained by recording chlorophyll a fluorescence values in samples exposed to a light stress and recovery (LSR) protocol: sequential periods of 15 min dark, 20 min high light (HL, 1200 μmol photons m−2 s−1) and 40 min recovery under low light (LLRec, 40 μmol photons m−2 s−1). NPQ was calculated as (Fm-Fm’)/Fm’ where Fm is the maximum fluorescence obtained in dark adapted samples while Fm’ is the maximum fluorescence recorded in any subsequential saturating light pulse. qE, qZ (qM) and qI components of NPQ were estimated as described in Sello et al. (2019) by fitting the relaxation kinetic with a biexponential decay (y=y0+A1 e−x/t1+ A2 e−x/t2) in the SigmaPlot software. Y0, the minimum value reached by the fitting, represented the NPQ that is not relaxed after 20 min of dark recovery and thus represents an estimation of the slow qI component. A1 and A2 instead corresponded to the fastest qE and qZ (or qM) components.
Pigments analysis
Pigment analysis was performed as described by Cruz et al. (2014). Briefly, sea slugs and algae were sampled and immediately frozen in liquid nitrogen. Samples were freeze-dried, powdered by using a fine metal rod and pigments extracted in 95% cold buffered methanol (2% ammonium acetate) by adding the buffer, sonicating the samples for 2 min and then incubating them at -20°C for a minimum amount of 20 min. Sample debris were then removed by passing the samples through a 0.2 mm Fluoropore membrane filters (Millipore, Billerica, MA, USA). After filtration, the extracts were injected into a Prominence i –LC-2030C 3D Plus HPLC system (Shimadzu, Kyoto, Japan) equipped with the proprietary inbuilt photodiode array detector (PDA). Pigments were identified from absorbance spectra and retention times and concentrations were calculated in comparison with pure crystalline standards (DHI, Hørsolm, Denmark). The activity of the xanthophyll cycle and the sequential de-epoxidation of the pigments violaxanthin (Vx) to antheraxanthin (Ax) and zeaxanthin (Zx), was estimated by calculating the de-epoxidation state (DES) as: DES=([Zx]+0.5×[Ax])/([Zx]+[Ax]+[Vx]).
Softwares and statistical analysis
Raw data obtained from the ImagingWin (WALZ, chlorophyll a variable fluorescence) and from Shimadzu LabSolution softwares were exported and analysed in Microsoft Excel (Microsoft Corporation, 2018. Available at: https://office.microsoft.com/excel). The same software has been used to build the figures and to calculate statistically significant differences by using independent samples t-tests.
Results and discussion
Data underlying the results can be found on BioStudies (Morelli, 2023).
Elysia viridis mirrors the photosynthetic performance and the pigment profile of the different algal donors
Elysia viridis is a species able to feed on multiple algae, contrary to other members of the same genus such as E. timida or E. chlorotica that can feed and retain chloroplasts only from one specific algal food (Baumgartner & Toth, 2014). Among the wide range of algal food, the sea slug is predominantly found on C. tomentosum or C. fragile, two coenocytic algae whose cells lack septation facilitating ingestion of cytoplasm by the animals. Sea slugs collected in the wild on the Portuguese coast are typically associated to C. tomentosum, thus, to carry out the experiments, we maintained them either on this alga or we provided them with abundant Chaetomorpha to induce a diet switch. In sacoglossans, the radula features a single row of teeth that is adapted to the group's suctorial feeding habits. Since the algal food exhibit a wide range of characteristics, such as toxic substances or heavy calcification, polyphagous species, such as E. viridis, have a high level of plasticity in form and dimension of teeth depending on the food source (Jensen, 1993). When an animal is transferred from one alga to another, there is a learning span of at least one week, during which the morphology of the radular teeth is not distinguishable from that present with the previous food source (Jensen, 1989; Rauch et al., 2018). This learning process involves increased efficiency in grasping the food, piercing the algal cell, and sucking out the cytoplasm. Accordingly, when the animals were transferred from their natural habitat (where they mostly feed on C. tomentosum) to Chaetomorpha, the animals spent between 3 to 5 days only crawling on the algal filaments. The sea slugs became then more static between 7 and 10 days after being transferred, likely coinciding with the change of teeth and the process of learning how to pierce the cell wall, and feed properly. This plasticity corroborates previous observations (Jensen, 1989), where specimens of E. viridis found on Chaetomorpha and moved on to Codium were able to efficiently learn how to feed on the latter alga. The animals, however, required a relatively longer time to learn again how to properly handle Chaetomorpha once transferred back to the original food source (Jensen, 1989).
After one month of continuous feeding, the specimens fed on Chaetomorpha (Ev-Ch) showed a clearly different colour compared to the ones fed on C. tomentosum (Ev-Ct) (Figure 1A). Chromatographic analysis associated the different shades of green with an altered pigment profile: Ev-Ct specimens showed high levels of siphonoxanthin and β,ε-carotene, typical of Bryopsidales algae (Cruz et al., 2014; Giossi et al., 2021), while specimens fed with Chaetomorpha had no trace of the abovementioned carotenoids and accumulated instead high levels of lutein, β,β-carotene and loroxanthin (Figure 1B). Moreover, we found on both Ev-Ct and Ev-Ch an unknown carotenoid in animal samples already reported in other studies (Cruz et al., 2014) with the maximum absorption of 460 nm, with a retention time of about 23 min (Figure 1C).
Figure 1. Pigment profile of Elysia viridis and its algae food sources.
(A) Representative pictures of E. viridis specimens fed with Chaetomorpha sp. (Ev-Ch) or with C. tomentosum (Ev-Ct). The scale bar corresponds to 0.5 cm; (B) Carotenoid amount in sea slugs fed with the different algae. Data corresponds to mean and standard deviation (n=4) and values are expressed as relative to 100 µmol of Chl a in the same samples; (C) HPLC chromatograms extracted at 440 nm, representative of sea slugs (straight line) and macroalgae (dotted line) pigment profiles. Siph, siphonaxanthin; t-Neo, all- trans-neoxanthin; c-Neo, 9′-cis-neoxanthin; Vx, violaxanthin; Ax, antheraxanthin; Zx, Zeaxanthin; Lut, Lutein; Siph-do, siphonaxanthin dodecenoate; Chl b, chlorophyll b; Chl a, chlorophyll a; β,ε-Car, β,ε-carotene; β,β-car, β,β-carotene; Unkn. Car., unidentified Elysia viridis carotenoid.
While the nature of this pigment is currently unclear, it could be a compound synthesized by the animal and necessary for its own metabolism that needs a common carotenoid precursor present in C. tomentosum and in Chaetomorpha. The carotenoid biosynthetic pathway is well characterized in plants and algae, occurring mainly in the chloroplasts, but it is absent in the animals that must obtain these compounds through their diets (Maoka, 2011; Morelli & Rodriguez-Concepcion, 2023). Indeed, the use of algae-derived carotenoids as precursors for keto-carotenoids necessary for animal metabolism is not so uncommon in molluscs. Sea slugs such as Clione limacina and Paedoclione doliiformis, oxidatively metabolize dietary carotenoids and accumulate them in their gonads to protect against oxidative stress (Borodina & Zadorozhny, 2021; Maoka et al., 2014), while specimens of E. timida were hypothesized to accumulate carotenoid photoreactive pigments in the eyespots used for light perception (Rahat & Monselise, 1979).
Apart from the pigmentation, sea slugs photosynthetic performance was differently influenced by the algal food. The maximum quantum yield (Fv/Fm) of Ev-Ch specimens was significantly lower compared to the one observed in Ev-Ct animals. Interestingly, while the Fv/Fm in Ev-Ct slugs was higher than the one of C. tomentosum itself, Ev-Ch samples showed a lower value compared to the one of Chaetomorpha sp. (Figure 2A). As already reported in other works, photosynthetic performance of sea slugs tends to be better than that of algae they are fed on, likely because of an intracellular supply of respired inorganic carbon and nutrients produced by the metabolism of the host (Serôdio et al., 2014). In the case of Chaetomorpha chloroplasts, they could be functional but losing stability very fast, hindering their performance once integrated in the animal host cells. The lifespan of Chaetomorpha-derived kleptoplasts in E. viridis tissues is unknown. However, a link between the different algal food and the retention performance in this species has already been described, with sea slugs being photosynthetically competent once fed with Bryopsis hypnoides but unable to incorporate chloroplasts from Cladophora sp. (Rauch et al., 2018). When fed with the former, or with C. tomentosum, in fact, E. viridis is classified as a long-term retention (LtR) species while it does not show traces of photosynthetic activity (non-retention, NR) while fed with Cladophora sp. (Rauch et al., 2018). We can then hypothesize that the incorporation process and the subsequential kleptoplast features could have a critical impact on the stability of the kleptoplasts.
Figure 2. Photosynthetic performance of Elysia viridis and its algae food sources.
(A) Maximum quantum yield (Fv/Fm) in E. viridis fed with Chaetomorpha sp. (Ev-Ch), Chaetomorpha sp., E. viridis fed with Codium tomentosum (Ev-Ct) and C. tomentosum. Data correspond to mean and standard deviation (n=5); (B) Averaged daily weight increase estimated for feeding animals, data corresponds to mean and standard deviation (n=10) measured after 1 month of continuous feeding; (C) Light curves of sea slugs and the respective algal food. Data corresponds to mean and standard deviation (n=10); (D) alpha, ETRm and Ek parameters calculated from the LCs represented in panel C. Boxes show the values between the upper and the lower quartile, the cross represents the mean and the horizontal line the median. Whiskers (the upper and lower extremes) and circles represent single data and the ones located outside of the whiskers limit are the outliers (data with the same numerical value are visualized as a single point). Asterisks mark statistically significant differences (t-test, ** p < 0.01).
To classify the photosynthetic state of the kleptoplasts, we calculated light curves (LCs) in E. viridis specimens and in their respective algal foods (Figure 2C). Photosynthetic parameters estimated by plotting the data according to the model of Platt (Platt et al., 1980) showed a significantly higher maximum electron transport rate (ETRm) and light saturation coefficient (Ek) for Ev-Ct individuals and C. tomentosum, while the photosynthetic rate in the light-limited region of the light curve (alpha) was higher in Ev-Ch sea slugs and Chaetomorpha (Figure 2D). More importantly, the LCs obtained from the animals were similar to the ones obtained from the algal food, confirming that chloroplasts are functional in the animal cells and that their photoacclimation state is inherited by the algae and maintained in the animal, as observed in other similar studies (Cartaxana et al., 2018). Curiously, Ev-Ch sea slugs shown a higher daily weight increase compared to Ev-Ct ones (Figure 2B). We could speculate that sea slugs continuously feeding on Chaetomorpha could retain chloroplast for less time in their body (likely because of the poor photosynthetic performance) and would eat more algae when provided with unlimited food. In presence of Chaetomorpha, sea slugs could adopt a binge eating habit to have a constant caloric intake instead of focusing on the integration of intact plastids with low functionality in their body similarly to what happens in juveniles of E. timida that before establishing kleptoplasty feed continuously and digest chloroplasts to support their own body growth (Laetz & Wägele, 2017).
Elysia viridis fed with Codium tomentosum can maintain chloroplast photoprotective mechanisms, while animals fed with Chaetomorpha sp. cannot
One of the main unresolved questions when investigating kleptoplasty is how plastids can continue to function in animal cells for long periods even if they are exposed constantly to wide range of stress conditions and without the access to many fundamental algal nuclear-encoded proteins. In particular, the conservation of mechanisms to tackle light stress in these photosynthetic animals is still puzzling (Cruz & Cartaxana, 2022). Sacoglossan sea slugs are known to contribute to chloroplast shielding, either by folding their parapodia under high irradiances (i.e., to shield internal kleptoplasts while permitting filtered light energy to reach kleptoplasts on the parapodial undersides) or by simply crawling away from excessive light (Cartaxana et al., 2018; Donà et al., 2022). Furthermore, physiological mechanisms involved in chloroplast protection can be maintained when the plastids are transferred to the animal cells. Some of the algae currently used as a food by sacoglossan sea slugs, indeed, are very resilient and show robust chloroplasts able to survive in harsh conditions. For example, isolated thylakoids of V. litorea were found to be more resilient to photoinhibition of PSII than spinach thylakoids, likely because of a lower 1O2 production and higher rates of ROS detoxification (e.g., through the action of α-tocopherol and carotenoids) (Havurinne et al., 2022). In some algae, the active conversion of Vx to Zx under high irradiances (i.e., the xanthophyll cycle) has been reported as one of the main mechanisms to protect against light stress and in some animals fed with these algae (e.g., E. timida and E. chlorotica) the cycle is maintained during medium periods of starvation and actively participate in kleptoplast protection (Cartaxana et al., 2019). However, other sea slugs (i.e., E. cornigera), fed with the same A. acetabulum were reported to show very different degree of kleptoplast compatibility being unable to cope with ROS accumulation with the same efficiency as E. timida (de Vries et al., 2015). We hypothesized, thus, that the efficacy of the photoprotective mechanisms is not depending only on the physiologic characteristics of the algal donor but also on the individual compatibility of the stolen plastids with the sea slugs species.
To test our hypothesis, we evaluated the response to short term light stress in Ev-Ct and Ev-Ch specimens and in the respective food sources. Under high light (HL, 1200 μmol photons m-2 s-1), the photosynthetic yield ΦPSII of the sea slugs reached values very near 0, showing an expected photoinhibition state, regardless of the algal food (Figure 3A). At the same time NPQ level increased to be then slowly dissipated under low irradiances (LL Rec, 40 μmol photons m-2 s-1) in concomitance with a recovery of photosynthetic yield (Figures 3A, B). The relaxation and recovery kinetics followed the same pattern in sea slugs and algae and as observed in other studies, 40 min of LL incubation were not enough to recover the maximum quantum yield (Cruz et al., 2015). The slow relaxation of the NPQ in C. tomentosum could be influenced by chloroplast movement inside the algal tissue as chloroplasts can redistribute and reorientate in the cell as a response to the light direction resulting in typical patterns for light of low or high fluence rate. In this condition, plastids take a “high intensity arrangement” designed to protect the chloroplasts against excessive radiation by stacking the plastids on the cell borders and piling them to provide self-shading (Davis & Hangarter, 2012). In C. tomentosum, which has no functional XC, chloroplast movement could have a prevalent role on preventing excess energy absorption. In siphonous algae such as Halimeda distorta, the piling of chloroplasts to one side of the algae branch following prolonged exposure to very high irradiance or darkness is so intense to change the green color intensity (Drew & Abel, 1992). Moreover, the kinetic of NPQ relaxation under low light in C. tomentosum and Ev-Ct is strikingly like the one observed in A. thaliana npq4 mutants. The latter lack the PsbS protein and are unable to carry on a functional xanthophyll cycle thus rely on plastid movement to develop a slow, qE-type, energy quenching mechanism named qM (Dall’Osto et al., 2014). Accordingly, we could mathematically calculate a high contribution of qM component to the quenching by fitting the relaxation kinetic to the equation of a biexponential decay (Figure 3C). In fact, during NPQ relaxation, a pivotal role is played by the fast component qE that act in the first minutes of low light/dark exposure, but a slower component, associated with Zx binding to LHC proteins named qZ is the responsible for energy quenching after 10–15 min of relaxation (Dall’Osto et al., 2005). In organisms where this pigment is not present, such as C. tomentosum or the npq4 A. thaliana mutant, the dissipation of energy is related to chloroplast movement, hence the qM definition (Dall’Osto et al., 2012). On another hand, differently from Codium, Chaetomorpha accumulates Zx under high irradiances and its NPQ kinetic is very similar to the ones of other XC-performing algae such as V. litorea, suggesting a more marginal role for chloroplast movement-based photoprotective mechanisms over the XC. Despite this, as observed for Codium, also in Chaetomorpha the recovery of ΦPSII is not complete after 40 min in low light. However, the fast qE-quenching component in the first minutes is evident and, considering the presence of Zx, the subsequent slower recovery could be related to the qZ component. Interestingly, Ev-Ch animals showed the ability to build up NPQ up to a certain extent but were unable to relax it and show little recovery of the photosynthetic activity during LLRec (Figures 4A, B).
Figure 3. Light stress and recovery of Elysia viridis and its algae food sources.
(A) Effective quantum yield (ΦPSII) calculated in E. viridis fed with Chaetomorpha sp. (Ev-Ch), Chaetomorpha sp., E. viridis fed with Codium tomentosum (Ev-Ct) and C. tomentosum during a light stress-recovery experiment. In the chart, the different phases of the protocol are identified by the black box (15 min, previous dark acclimation), the white box (light stress, exposure to 1200 μmol photons m-2 s-1 for 20 min) and the grey box (low light recovery, 40 μmol photons m-2 s-1 for 40 min). Data corresponds to mean and standard deviation (n=5); (B) Non-photochemical quenching (NPQ) kinetics obtained in the same conditions as described for panel A; (C) Graphs representing the relaxation phase of the NPQ kinetic fitted to the equation of a bi-exponential decay in SigmaPlot. The program is used also to calculate the components of the NPQ represented in the two bar charts as part of the total NPQ level. Asterisks mark statistically significant differences (t-test, ** p < 0.01, ns: no significant differences) between the values of total NPQmax in the indicated samples.
Figure 4. Operation of the xanthophyll cycle in Elysia viridis fed with Chaetopmorpha sp. (Ev-Ch) and in the individual algae.
The top panels show the de-epoxidation state (DES) expressed as (Zx+0.5*Ax)/(Vx+Ax+Zx) in Ev-Ch sea slugs and Chaetomorpha sp. subjected to the light stress and recovery protocol represented in Figure 3; Vx, violaxanthin; Ax, antheraxanthin; Zx, zeaxanthin. The lower panel represent the levels of the single xanthophylls expressed as µmol of pigment relative to 100 µmol of Chl a observed in the same samples. Data corresponds to mean and standard deviation (n=4). Asterisks mark statistically significant differences between the high light (HL) and the recovery in low light (LL Rec) phases (t-test, ** p < 0.01, ns: no significant differences).
When investigating the functionality of the XC, we observed that dark-acclimated Chaetomorpha sp. showed no traces of Zx, accumulated it after 20 min of HL exposure, and about 75% of Zx was converted back to Vx at the end of the LL Rec (Figure 4). The cycle resulted in a significantly higher de-epoxidation state (DES) during the HL exposure compared to the LL Rec. On the other hand, Ev-Ch sea slugs showed traces of Zx already upon dark acclimation, under HL the amount of this pigment increased, but did not decrease under LL Rec, accordingly with the inability to quench the built up of NPQ. As previously observed, the photosynthetic competence of Chaetomorpha chloroplasts diminished when integrated into E. viridis. Consequently, excessive light exposure could lead to severe photoinhibition. During this state, the proton gradient across the thylakoidal membranes might be altered, preventing the recovery of the cycle back to violaxanthin due to the unavailability of a suitable environment for the responsible enzymes to function (Tjus & Andersson, 1993). In algae, this situation is usually overcome by plastid-targeted proteins encoded by nuclear genes likely lacking in E. viridis. Experimental evidence from other kleptoplastic organisms has demonstrated that kleptoplasty is supported by nucleus-encoded genes for plastid-targeted proteins, which possess specific signals for targeting these proteins to the kleptoplasts. Plastid transporters are also present to facilitate the targeting of proteins and metabolites into the kleptoplasts (Hehenberger et al., 2019; Lekieffre et al., 2018).
In certain kleptoplastic organisms, such as Ross Sea dinoflagellates (RSD), photosynthetic functions are divided between an ancestral plastid (peridinin plastid) and the kleptoplasts. During plastid sorting, electron flow from PSII to PSI is disrupted, but it is subsequently restored through proteins encoded by the dinoflagellate nucleus, which are then targeted to the kleptoplasts via a specific signal (Hehenberger et al., 2019). We hypothesize that when E. viridis consumes an alga that is not its "preferred" donor (e.g., Chaetomorpha), compatibility is only partial. Even if the kleptoplasts within animal cells can maintain certain functionalities (e.g., basal photosynthetic activity), they might struggle to manage stress due to the necessity for specific protein coding and import.
It is worth noting that transit peptide diversity across the plant kingdom is significant, and sometimes proteins encoded by one plant species cannot enter the chloroplasts of another organism without minor changes in the coding sequence (Patron & Waller, 2007). A kleptoplast-targeted protein encoded by E. viridis, but designed to enter Codium chloroplasts, may not be able to interact effectively with Chaetomorpha plastids. Consequently, fundamental functions in this chloroplast, such as repair or metabolic regulation, might be compromised, leading to rapid decay. Furthermore, the mechanism of kleptoplast integration in animal cells is a subject of debate. Kleptoplasts integrated into various sacoglossan sea slug species have been reported to exhibit diverse ultrastructures compared to their original forms within the algal donors. For example, in the LtR species E. timida, chloroplasts were found to have functional thylakoids and stroma, but no inner and outer envelopes, being surrounded only by the phagosome membrane while, in the NR form Thuridilla hopei, kleptoplasts showed the whole set of membranes (Martin et al., 2013). In E. viridis, chloroplasts derived from different algal donors could preserve different features that could impact the actual photosynthetic function of the kleptoplast and the possibility of specific proteins to enter the plastids. The association between E. viridis and Codium likely evolved specifically, resulting in the encoding of all necessary subunits of a functional translocon complex capable of importing useful proteins to maintain chloroplast functionality. However, in the case of Chaetomorpha chloroplasts, certain components may be absent or interact differently with the slug's nuclear-encoded proteins, resulting in a loss of function. To test these hypotheses, further molecular studies will be required.
Conclusions
This study assesses the photophysiology of the sea slug E. viridis fed with algae with different photoprotective and photosynthetic capabilities (C. tomentosum and Chaetomorpha sp.). In this work, we investigated which photoprotective mechanisms present in the algae are found in the animal host. Our results show that specific photoprotective mechanisms of algal chloroplasts (e.g., the xanthophyll cycle) are not necessarily maintained once the plastids are transferred to the sea slug cells and suggest that plastid functionality depends on the sea slug-alga combination. Algae chloroplasts have their individual robustness but, once part of the host animal cell, require a support that only some can provide. Thus, only in the case of specific associations, such as those between E. timida and A. acetabulum or E. chlorotica and V. litorea, it is possible for the kleptoplasts to maintain all their functionalities.
Ethics and consent
The use of E. viridis specimens was not subjected to ethical approval considering that the use of lower-level invertebrates species (e.g., brine shrimp, fruit flies, nematodes, mosquitoes, etc.) is not restricted for research purposes. After the collection, animals were maintained in optimal conditions using the LSS in controlled environment to ensure the maximum fitness. Animals were subjected to starvation only when required by the experimental setting.
