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Evolution of clitellate phaosomes from rhabdomeric photoreceptor cells of polychaetes – a study in the leech Helobdella robusta (Annelida, Sedentaria, Clitellata)
Frontiers in Zoology volume 10, Article number: 52 (2013)
In Annelida two types of photoreceptor cells (PRCs) are regarded as generally present, rhabdomeric and ciliary PRCs. In certain taxa, however, an additional type of PRC may occur, the so called phaosomal PRC. Whereas the former two types of PRCs are always organized as an epithelium with their sensory processes projecting into an extracellular cavity formed by the PRCs and (pigmented) supportive cells, phaosomes are seemingly intracellular vacuoles housing the sensory processes. Phaosomal PRCs are the only type of PRC found in one major annelid group, Clitellata. Several hypotheses have been put forward explaining the evolutionary origin of the clitellate phaosomes. To elucidate the evolution of clitellate PRC and eyes the leech Helobdella robusta, for which a sequenced genome is available, was chosen.
TEM observations showed that extraocular and ocular PRCs are structurally identical. Bioinformatic analyses revealed predictions for four opsin genes, three of which could be amplified. All belong to the rhabdomeric opsin family and phylogenetic analyses showed them in a derived position within annelid opsins. Gene expression studies showed two of them expressed in the eye and in the extraocular PRCs. Polychaete eye-typic key enzymes for ommochromme and pterin shading pigments synthesis are not expressed in leech eyes.
By comparative gene-expression studies we herein provide strong evidence that the phaosomal PRCs typical of Clitellata are derived from the rhabdomeric PRCs characteristic for polychaete adult eyes. Thus, they represent a highly derived type of PRC that evolved in the stem lineage of Clitellata rather than another, primitive type of PRC in Metazoa. Evolution of these PRCs in Clitellata is related to a loss of the primary eyes and most of their photoreceptive elements except for the rhabdomeric PRCs. Most likely this happened while changing to an endobenthic mode of life. This hypothesis of PRC evolution is in accordance with a recently published phylogeny of Annelida based on phylogenomic data. The data provide a nice example how morphologically highly divergent light sensitive structures emerged from a standard type of photoreceptor cell.
A functional eye requires two fundamental building blocks: photoreceptors and shading pigment [1, 2]. These functions may occur together in one cell type or they are separated and exhibited in two or more different cell types , commonly referred to as photoreceptor cells (PRCs) and pigmented supportive cells (PSCs) (see , for terminology). In Metazoa generally two types of PRCs can be recognized; rhabdomeric and ciliary PRCs [1, 4–6]. For photoreception these cells use either microvilli or cilia. These cell types can be distinguished not only morphologically, but also by cell-type-specific sets of molecular markers, their so-called molecular fingerprint. These characters also enable clarifying their evolutionary history and diversification [2, 5, 7–12].
In Annelida these two types of PRCs are considered to be generally present, but in certain taxa an additional type of PRC may occur, the so-called phaosomal PRC . The former two types of PRCs are always organized as an epithelium with their sensory processes – cilia or microvilli - projecting into an extracellular cavity formed by PRCs and supportive cells. Phaosomes, however, are seemingly intracellular vacuoles housing the sensory processes which may be cilia or microvilli as well [13, 14]. Phaosomal PRCs are rare in polychaetes, but are typical for Clitellata and constitute their only known type of photoreceptor cell [15, 16]. In Clitellata these phaosomal PRCs primarily occur extraocular and are present within or outside the brain [16–21].
Whereas phaosomal PRCs are widespread or even ubiquitous in Clitellata, pigmented eyes occur only exceptionally and are restricted to species of Naidinae, Pristinae and Hirudinea [15, 16, 22]. In contrast to their soil-dwelling relatives, species of these groups are characterized by inhabiting the littoral zone of various freshwater habitats (certain leeches may even be termed terrestrial). The eyes in these taxa are not as closely related to the brain as is the case in polychaetes. Although in Naidinae they are prostomial, they may not represent cerebral eyes . They are segmental in leeches, occurring from segment II onward posteriorly in one or several pairs [22–24]. These eyes are composed of PRCs and PSCs [16, 17, 22–24]. They exclusively employ phaosomal PRCs as well, indicating an evolutionary origin independent from that of the pigmented eyes present in polychaetes, which use rhabdomeric PRCs [13, 16].
Several hypotheses have been put forward explaining the evolutionary origin of the clitellate phaosomes. These cover a wide range of scenarios from either being comparatively primitive PRCs or having newly evolved in the stem lineage of clitellates [15, 16]. Whether these PRCs really represent a cell type completely evolved de novo and independently from both ciliary and rhabdomeric PRCs or whether they may have been derived from one of these cell types may only be evaluated by tracing the molecular fingerprints of phaosomal PRCs. The investigations of Ukhanov and Walz  on phototransduction in leech eyes give some indication for a relationship to rhabdomeric PRCs. In this study we addressed this question by investigating gene expression patterns in the phaosomes of a leech, Helobdella robusta Shankland et al., 1991. This species was chosen for several reasons: it is an example of a clitellate with both extraocular and ocular phaosomes, a sequenced genome is available, the species can easily be cultured in the lab, and in situ protocols are available. Although TEM investigations are available for another Helobdella species, H. stagnalis (Linnaeus, 1758) ; we complemented the ultrastructural data for the eyes in H. robusta. In addition we described the extraocular phaosomes and also looked for the presence of putative ciliary PRCs. The data on opsin expression and phylogenetic analysis of opsin sequences as well as the presence of a gq protein in the phaosomal PRCs are indicative for polychaete adult eye PRCs. These data provide strong evidence that the clitellate PRCs evolved from the rhabdomeric PRCs present in these eyes. Due to the absence of expression of either tryptophane-2,3-dioxygenase and sepiapterine reductase in leech pigmented supportive cells (PSCs), genes which are typical for the pigment synthesis pathway in polychaete eyes, the PSCs in leeches most likely have no counterparts in the eyes of polychaetes.
In H. robusta only one pair of pigmented eyes is present. It is situated in the region of the anterior sucker on the third annulus and deeply embedded in the connective tissue below the epidermis (Figures 1A and 2A); in the juvenile specimens studied, this area is about 50 μm behind the anterior tip of the animals.
Electron microscopic observations
In H. robusta the eyes generally have the same structure as described by Clark  for Helobdella stagnalis (Linnaeus, 1758). The eyes are of the pigment cup type  opening to left anterior in the left eye and to right anterior in the right eye (Figures 1A and 2A). In the juvenile specimens investigated each eye comprises 10–15 phaosomal PRCs covering an area of about 8 by 16 μm on cross sections. In the pigmented eye the PRCs are close together and not separated by ECM (Figures 1C and 2A). The cell bodies of the PRCs are located at the opening of the eye cup. The phaosomes are somewhat staggered in the eye cup so that usually no more than 10 phaosomes are visible on a given section. The phaosomes are completely occupied by densely packed sensory microvilli, leaving no central space inside the cavity (Figure 1B).
The pigmented supportive cells (PSCs) form a comparatively thin sheath of about 0.7-1.5 μm around the PRCs, providing space for at least 2–7 layers of membrane-bounded pigment granules. At certain areas there is some overlap of pigment cells (Figure 1A, B). The PSCs border directly on one another but are separated by an ECM (0.1 μm wide) from the PRCs (Figures 1B and 2A). Their nuclei are situated on the convex side of the pigment cup (Figures 1B and 2A).
Several extraocular phaosomal PRCs occur in groups of always 2–3 cells in front of and behind the pigmented eyes (Figure 1D, E). These extraocular phaosomal PRCs are invisible in living animals. In juveniles these PRCs primarily form a pair of bands situated in the outer quarter of the animals (Figure 1D). The PRCs are located in the connective tissue underneath the epidermis (Figure 1D). In the juveniles studied with TEM up to seven phaosomes have been counted on a given cross section. The total number of extraocular PRCs has not been determined and appears to be related to the age of the individuals.
The extraocular PRCs are separated from one another by a thin layer of ECM (0.1-0.3 μm thick; Figures 1E and 2B). Thus, they are never in direct contact with one another. Each PRC houses a single, slightly ovoid phaosome approximately 6 by 6–8 μm in cross section and up to 10 μm in length (Figures 1E and 2B). The phaosome is located eccentrically in the cell body of each PRC (Figure 1E). The cell body contains plentiful mitochondria which are evenly distributed throughout the cell. Except for the region housing the nucleus, the cells form a thin cytoplasmic sheath of 0.3-0.6 μm around the phaosome (Figures 1E and 2B). The nuclei are somewhat flattened (2 × 5 × 5 μm) and contain a remarkably low amount of heterochromatin (Figure 1E). The phaosome is completely filled with densely packed sensory microvilli (Figure 1E). In most regions of the phaosome the microvilli are oriented strictly parallel; only in certain regions are the microvilli sectioned in different directions (Figure 1E, F). The microvilli are 2.5-3 μm long, have a diameter of 20–40 nm and are separated by a 10-nm-wide gap. Each microvillus contains a prominent bundle of thin filaments (Figure 1F).
Analyses of serial TEM sections through the brain region in H. robusta did not give any indication for the existence of ciliated sensory cells in the CNS.
Bioinformatic analyses and amplification of genes
Bioinformatic analyses of the published genome of H. robusta resulted in sequence predictions of four opsins (in the following called opsin A, B, C, and D), two G αq -subunits of guanine nucleotide-binding proteins, one tryptophane-2,3-dioxygenase and one sepiapterine reductase. Despite thorough additional searches by means of a newly developed algorithm specifically for searches of opsin sequences, no additional opsins could be found. Based on these predictions, specific primers were designed and used for both H. robusta strains.
Opsins A, B and C were amplified from cDNA of both strains. The predicted fourth opsin D could neither be amplified from cDNA nor from genomic DNA of either strain. The experimentally obtained sequences closely match the predictions and there are only insignificant differences on the nucleotide levels between the opsins of the two populations H. robusta CA and H. robusta TX. The phylogenetic tree in Figure 3 shows this as the opsins cluster according to their subtype A, B and C, and not according to the respective Helobdella strain. The phylogenetic analysis shows that all obtained opsins fall into the rhabdomeric opsin sub-tree and therein group together with the other known annelid rhabdomeric opsins. Within this cluster the opsins of H. robusta form one distinct and highly supported group (Figure 3). In this analysis the rhabdomeric opsin of Capitella teleta is sister to those of H. robusta.
All four predicted opsins show the typical SHP amino acid motif following the seventh transmembrane domain, clearly identifying them as rhabdomeric opsins  (Figure 4). The alignment shows the seven transmembrane domains typical for G-Protein coupled receptors the protein family opsins belong to. The highly conserved Lysine residue (K296 in the bovine opsin) in the seventh transmembrane domain is essential for the Schiff-base linkage of the chromophore and identifies functional opsins. Another essential amino acid is the counter-ion Glutamate (E) in non-vertebrates at position 181 [11, 26].
The specific primers for the G αq subunits only worked for the strain H. robusta CA. Not even degenerate primers helped to amplify G αq subunits for H. robusta TX. The genes tryptophane-2,3-dioxygenase and sepiapterine reductase were amplified from H. robusta TX in order to identify whether the pigments known to be employed in the eyes in other annelids are active in H. robusta as well .
Gene expression analyses
Expression analyses of the G αq subunits, the opsins as well as tryptophane-2,3-dioxygenase and sepiapterine reductase were carried out by WMISH and additionally for the opsins by in situ hybridization of paraffin sections.
Expression of opsin A in the pigmented eyes and in unpigmented single phaosomal PRCs could be shown in paraffin sections (Figure 6C, D). In whole mounts only the extraocular phaosomal PRCs are detectable (Figure 5D). As to be expected , in adults there is a strong ring-shaped expression in the region of the anterior and the posterior sucker due to the presence of phaosomal PRCs (Figure 7A). At higher magnification it is evident that it is caused by numerous single cells which are not arranged in a strictly bilateral symmetric pattern. In the anterior sucker there are at least 40 cells on each side of the body, which is by far exceeded in the posterior sucker (Figure 7B). Opsin B could be detected in the PRCs on sections and additionally in whole mounts, whereas the supportive pigment cells (PSCs) remained unstained (Figures 5A, C-G and 6F-G). Even after complete bleaching of the shading pigment there is no signal in the PSCs whereas there is a strong signal in the cell bodies of PRCs (Figure 6G). At higher magnification it becomes obvious that the staining is weaker in the centre of the PRC (Figure 5F). The LSM reflection shows that the messenger RNA of opsin B is located only in the cell body and not in the microvilli themselves (Figure 5G). That this region in fact represents the phaosomal cavity and not the unstained nucleus is shown in Figure 5E through an additional DAPI staining. The 3D projection of the LSM scans shows the blue-stained nucleus located next to the unstained phaosomal cavity (Figure 5E). Thus, the messenger is not stored in the microvilli themselves. This is in accordance with the appearance of the phaosomal PRCs in the TEM, clearly showing the phaosome surrounded by a sheath of cytoplasm and the nucleus being situated in a lateral extension of the cell body in the case of extraocular phaosomal receptor cells (Figures 1E and 5H). The same can be observed from the expression pattern in the extraocular phaosomes in the head region of adults (Figure 7B). The expression site of opsin C remains unknown as no in situ experiment showed positive results (data not shown).
Most likely SPCs do not express the pigment genes investigated: neither tryptophane-2,3-dioxygenase nor sepiapterine reductase expression was found to occur in either PSCs or PRCs. However, WMISH showed a segmental expression pattern in the epidermis demonstrating that the experimental protocol worked, at least in a subset of tissues (Figure 8A-B). This expression pattern observed is related to the developmental stages: in juveniles older than stage 11 (data on stage 11 not shown; staging according to ) the expression of both genes could no longer be detected. For the time being the pigment present in the PSCs remains unknown.
Evolutionary origin of phaosomal PRCs
The main objective of the present investigation was to clarify the evolutionary origin of the phaosomal PRC typical of Clitellata. The overall uniformity in clitellate PRC structure is in contrast to the situation found in the other annelids, which exhibit a remarkable diversity in PRCs and eyes [13–15, 29, 30]. Whereas Jamieson [15, 29] regarded the phaosomal PRCs as plesiomorphic mainly by inferring that simple equals primitive, Purschke  reached an opposite conclusion. He regarded these PRCs as being highly derived structures developed after the PRCs and eyes usually present in annelids had been lost, supposedly in connection with a change of life style in the stem lineage of Clitellata. It remained unresolved whether the third type of PRCs, the phaosomal PRC, evolved independently from rhabdomeric and ciliary PRCs or from one of the latter two [13, 16].
The ultrastructure of clitellate phaosomes reveals that they primarily comprise microvilli (e. g., [17, 20, 31]). Together with similarities in the phototransduction mechanism  this seems to indicate a relationship to rhabdomeric PRCs. An origin from rhabdomeric annelid PRCs would raise the question whether the clitellate PRCs have evolved from larval or adult eyes, since a pair of pigmented larval eyes and at least one pair of adult eyes belong to the ground pattern of Annelida, and both of these employ rhabdomeric PRCs [2, 13, 32–34]. Moreover, the rhabdomeric PRCs present in the adult eye of Capitella spp. structurally resemble the phaosomal PRCs present in certain oligochaete clitellates such as Stylaria lacustris (Linnaeus, 1767) and Eisenia fetida (Savigny, 1826). In these annelid species these PRCs are still situated in the epithelial continuity of the epidermis and their phaosomes show a connection to the subcuticular extracellular space [16, 18, 35]. Such structural peculiarities are unknown in other polychaetes. Thus, likelihood appears to be greatest that Helobdella phaosomes are derived from adult rhabdomeric PRCs. These observations are in concordance with a recently published phylogeny of Annelida based on phylogenomic demonstration of Clitellata in a highly derived position [34, 36].
Molecular and gene expression data
From our genomic studies it is evident that the opsins present in H. robusta belong to the rhabdomeric type. Although opsin sequences are currently available only from a few annelids, the phylogenetic analyses show that the opsins from H. robusta form one distinct and highly supported cluster within the annelid r-opsins, which in turn cluster as a single well supported group within protostomian r-opsins. Moreover, the in situ experiments show that two of the r-opsins are expressed in the phaosomal PRCs. Thus, phaosomes are derived from annelid rhabdomeric PRCs with a high degree of probability. The hypothesis that they represent a plesiomorphic type of PRC clearly has to be rejected [15, 16, 29]. The position of the Helobdella opsins in the phylogenetic tree suggests that their diversification most likely occurred after separation of Clitellata from the remaining annelids.
Whereas two out of four opsins in H. robusta are clearly related to photoreception, the function and expression site of the other two remain unclear. Among these, opsin D could not be cloned from cDNA and might therefore be expressed at another life history stage. Opsin C was cloned from cDNA but in situ expression analysis remained unsuccessful. The unusual large insert between the 5th and 6th transmembrane domain may indicate a divergent function for this opsin.
Whether the phaosomal PRCs evolved from larval or adult eyes cannot be answered from the opsins alone, since both types of eyes use the same set of r-opsins in Platynereis dumerilii (Audouin & Milne-Edwards, 1834). In P. dumerilii larval and adult eye PRCs may either be distinguished by their neurotransmitters, acetylcholine or glutamate, respectively, or by the presence of Gq-alpha in the PRCs of adult eyes [32, 37]. Unfortunately, neurotransmitters have not been studied in H. robusta but the phaosomal PRCs express a Gq protein which is characteristic for annelid adult eye PRCs.
Evolutionary scenario of clitellate PRC evolution
Presuming that phaosomal PRCs originated from rhabdomeric PRCs, the question arises how and why phaosomes evolved. First, the development is direct inside a cocoon, so that the trochophore larva typical of annelids was probably lost [38–40]. Since this is one autapomorphic character of Clitellata, this loss must have happened in the clitellate stem lineage. With loss of the larva very likely its entire sensory equipment got lost as well.
Second, clitellates usually are infaunal, inhabiting various types of sediments and soils (e.g. ). In such environments vision is of minor importance and numerous examples for reductions of pigmented eyes exist throughout various metazoan lineages. Therefore, it seems conceivable that eyes typical of non-clitellate annelids were lost during invasion of deeper sediment zones.
This scenario applies for the PSCs but probably not for the rhabdomeric PRCs. The primary function of such PRCs might have been triggering the endogenous clock as well as basic detection of light resulting in light-avoiding reactions . In other annelids the former functions are usually related to the cilary PRCs [7, 8] which in Clitellata were lost as well, as indicated by the obvious lack of any c-opsin in the genome of H. robusta.
Cytological and structural constraints
Structurally photoreception is typically related to the apical membrane domain of epithelialized cells, i.e. to either cilia or microvilli projecting into an extracellular space. To provide as much membrane surface as possible for housing a high number of such cell processes only two possibilities exist: out-folding or infolding of the apical plasma membrane. The former usually is realized in most annelid eyes and this requires supporting cells to seal the extracellular space from the opposite side [13, 14, 33].
If supportive cells are absent, the only alternative for forming such an extracellular space is by infolding of the apical plasma membrane of the PRC and finally closure of this space, resulting in a seemingly intracellular vacuole, the phaosome. Interestingly, in the clitellates Stylaria lacustris, Lumbriculus variegatus and Eisenia fetida the phaosomes structurally represent such an intermediate stage in phaosome formation [16, 18, 21]. Completely closed phaosomal cavities are typical of leeches where the respective sensory cells are usually deeply embedded in the body tissues [22, 31]. However, this feature is not restricted to this group and has been reported for the phaosomes of e.g. Lumbricus terrestris as well, indicating convergent events [19, 20].
Evolution of clitellate eyes
Eyes as generally present in leeches and their PSCs very likely evolved de novo in Clitellata. From the present results there are several indications for this hypothesis: (1) different pigment genes are involved in pigment formation in leech PSCs, (2) the PSCs are structurally separated by the ECM from the PRCs, and (3) within Clitellata pigmented eyes are only present in taxa having a comparatively derived phylogenetic position.
In Platynereis dumerilii both cell types forming the pigmented eye, PSCs and PRCs, express genes involved in the pathways of Pterin and Ommochrome synthesis [27, 35, 42]. We could not detect any signal of these pathways in either the eyes or the phaosomal PRCs in H. robusta although the genes are expressed in the trunk, which might serve as an indication for a lack of expression in the eyes. Loss of expression of these genes in older stages is consistent with observations in other animals.
As mentioned above, in Clitellata pigmented eyes are restricted to three taxa: Naidinae, Pristinae and Hirudinea. Both of these form high end terminals in the respective branches in the phylogenetic trees published [43–46]. This is indicative not only for an independent origin in Clitellata but likewise for a convergent evolution in the two groups as well; this most likely occurred together with an independent change to an epibenthic life style in the two groups .
Leech PRC diversity
Leech eyes and extraocular phaosomes are well known from light microscopic observations since the end of the 19th century [23, 24, 47]. Extraocular phaosomes have thus far been reported mainly from the region around the eyes, from segmental sensillae and from the posterior sucker where they in certain cases may even form simple eyes [23, 24, 47]. Electron microscopic observations have been carried out in Helobdella stagnalis, Helobdella triserialis (Blanchard, 1849), Haementeria depressa Ringuelet, 1972, Mooreobdella microstoma (Moore, 1901) as well as in Hirudo medicinalis Linnaeus, 1758 (see [17, 22, 31, 48]). In contrast to oligochaete clitellates leech phaosomes generally show little variation between species [19–21]. However, so far no ultrastructural data on extraocular phaosomes in leeches have been reported. From the present investigation it is obvious that in general the phaosomal PRCs show no differences, regardless of whether they are situated within or outside the eyes. In the eyes of all leech species studied the pigment cup is separated from their PRCs by a thin but conspicuous ECM. This feature at least seems to indicate that their precursor cells have been separated quite early in development and may even belong to different germ layers, i.e. ectoderm and mesoderm.
Unlike many other annelids ciliary PRC-like cells could not be detected either by screening series of ultrathin sections through the anterior region including the brain, or by screening the genome for a ciliary opsin. No ultrastructural data on ciliary PRCs have been reported elsewhere. This appears to be a good indication for the entire absence of such PRCs in Hirudinea. However, TEM investigations revealed a type of ciliary sense organ with presumed ciliary PRCs in certain microdrile oligochaetes [49–52]. Whether these ciliary sensors represent ciliary PRCs remains still to be proven. Several attempts failed to amplify and clone c-opsins with degenerated primers from the naidids Pristina longiseta (Ehrenberg, 1828), Nais communis (Piguet, 1906), Tubifex tubifex (Müller, 1774) as well as Limnodrilus hoffmeisteri Claparède, 1862. Thus, for the time being it can be assumed that in Clitellata PRCs are present only in the form of phaosomal rhabdomeric PRCs.
The phaosomal PRCs in Clitellata very likely evolved from a precursor cell representing a rhabdomeric PRC as is present in pigmented eyes of various polychaetous annelids. Moreover, there is strong evidence that these PRCs represent the remnants of the adult polychaete eyes. Thus, phaosomes are a newly evolved and derived type of PRC rather than a primitive one. Since pigmented eyes in Clitellata are only present in two distinct and clearly separated terminal branches, convergent evolution of eyes is the most probable explanation. This scenario is congruent with the different modes of life style observed in Clitellata, which began with a change to an almost entirely endobenthic mode of life in the stem lineage of Clitellata [35, 39, 40, 52]. During these changes most of the photoreceptive features typically present in polychaetes got lost except for a residual function of light detection in a specific cell type, the phaosomal PRC, taken from the rhabdomeric PRC present in the pigmented polychaete eyes. In two clitellate lineages, namely naidids and leeches, a second evolutionary trait led to colonization of epibenthic habitats and these lineages are characterized by possessing pigmented eyes which most likely evolved de novo in convergent evolutionary lines.
Material and methods
The study was conducted on two laboratory strains of Helobdella robusta (Shankland et al., 1991); one from Austin, Texas, one from Sacramento, California. Both strains, abbreviated as H. robusta TX and H. robusta CA, were obtained from Prof. Weisblat, University of California, Berkley, USA (identifiers in ): TXAU-3 for the strain from Texas and CASA-4 for the strain from California). From the latter the genome has been sequenced  and for the former an in situ protocol was available. Animals were kept at room temperature in 1% artificial sea water and fed with freshwater snails. For experiments the anterior ends of juveniles which already had pigmented eye spots were used.
For transmission electron microscopy juveniles at an age of more than eight days were chosen. Animals were relaxed in carbonated water prior to fixation. They were fixed in 2.5% glutaraldehyde in a 0.1 M phosphate buffer (pH 7.2) for 2.5 h at 4°C. After initial fixation, the anterior part was cut off and further processed. After rinsing in the same phosphate buffer (2.5 h, 7 changes, 4°C) specimens were post-fixed in a buffered 1% solution of OsO4 (1 h, 4°C). After a short wash with buffer (5 min) specimens were dehydrated in a graded ethanol series (starting with 30% and ending with 100% ethanol). Ethanol was successively replaced by the intermedium propylene oxide followed by a 1:3 mixture of the embedding medium with the intermedium. Propylene oxide was allowed to evaporate overnight and then final embedding took place in an Epon-Araldite mixture (polymerization at 60°C for 2 d). Ultrathin sections of the eye region from two specimens and the brain region of one specimen were obtained with a diamond knife (Diatome 45°) on Leica Ultracut E or Leica UCT ultramicrotomes. Ribbons of sections were collected on single slot grids coated with pioloform support films in order to obtain almost complete series of ultrathin sections. They were stained with 2% aqueous uranyl acetate for 40 minutes at 20°C and lead citrate (2.66 g Pb(NO3)2 + 3.52 g Na3C6H5O7 × 2 H2O in 100 ml H2O) for 6 minutes at 20°C in a Nanofilm Phoenix Ultrostainer. Finally the sections were examined using a Zeiss EM 902A electron microscope. Images were recorded digitally on a CCD camera.
Juvenile animals, which already had pigmented eye spots, were removed from the adults and starved for at least three days to avoid contamination with nucleic acids of the snails the leeches fed on. When there was no visible gut outline anymore the juveniles were transferred as dry as possible to 1.5 ml tubes which were immediately placed into liquid nitrogen for 5 to 10 minutes.
To homogenize the tissue a stone mortar and pestle, which were sterilized by 10 minutes incubation in 0.5 M sodium hydroxide, rinsed with ddH2O and autoclaved, were placed on dry ice. After the tools were chilled the frozen tissue was quickly ground to fine particles which were finally mixed with 1 ml peqGOLD Tri-Fast™ reagent (Peqlab Biotechnologie GmbH, Erlangen, Germany).
After successful homogenization of the tissue RNA was extracted according to the TRIzol® reagent protocol (Life Technologies, Inc., Gaitersburg, USA) with an addition of a high-salt precipitation solution (0.8 M sodium citrate, 1.2 M sodium chloride) during the RNA precipitation step to avoid contaminations with proteoglycan and polysaccharides. The quality of the extracted RNA was assessed using a NanoDrop ND-1000 spectrophotometer (Peqlab).
For the generation of all complementary DNAs (cDNAs) the SMART™ RACE cDNA amplification kit (Clontech Laboratories, Inc., Mountain View, USA) was used. The recommended reverse transcriptase was substituted by SuperScript™ II RNase H- Reverse Transcriptase (Invitrogen Corporation, Carlsbad, USA). Sequence predictions for four opsins were found and Dr. Florian Raible, Max F. Perutz Laboratories, Vienna, provided predictions for two g-q-alpha proteins based upon the published genome of Helobdella robusta (CASA-4) [http://genome.jgi-psf.org/Helro1/Helro1.home.html]. The specific primers based on these predictions were always used to amplify the DNA fragments in both H. robusta strains. The following primer combinations were used: H. robusta CA-RopsA: CCCCATTGGTGGAAGTACCATGAC (forward), ATTAATTGTGCTTGTCAGCGCAATGG (reverse); H. robusta TX-RopsA: GATAGCGTCACGTGGTACAAAGAC (forward), ATTAATTGTGCTTGTCAGCGCAATGG (reverse); H. robusta CA-RopsB: GGTGGCTTCATGATAATCCTGGG (forward), TGTTGGGACCTCCTGAG (reverse);
H. robusta TX-R opsB: GGTGGCTTCATGATAATCCTGGG (forward), GATCCCTCCGTCTTCCACTGC (reverse); H. robusta CA-RopsC: CCAGGACTCCAATACTGCGAACCC (forward), CACCAACATCACTCCTCCTACTCC (reverse); H. robusta TX-RopsC: CCAGGACTCCAATACTGCGAACCC (forward), CACCAACATCACTCCTCCTACTCC (reverse); H. robusta CA-gq: TGGCGTGTTGTCTAAGTGAGGAG (forward), CGTCAAATAAAACATCCGTGTTC (reverse); H. robusta TX-t23d: CACGACGAACACCTCTTCATAGTTACTC (forward), TTACACAGCGCTTAATTCTGCAGTCAG (reverse); H. robusta TX-sepr: AATTGGTAGATGTTATTTCACCAC (forward), CATAGAAGAACGTTCTGTTTGATAACCG (reverse). The amplified PCR fragments were cloned into the plasmid pCRII®-TOPO® (Invitrogen) according to the protocol for One Shot® Chemical Transformation provided in the manual.
In situ hybridization
Whole mount in situ hybridization (WMISH). The linearization and transcription of the RNA probes was done for all samples according to the Platynereis standard protocol . Following linearization of plasmids by restriction digestion using QIAquick® Nucleotide Removal Kit (Qiagen) the transcription was purified with the QIAGEN RNeasy® Mini Kit QIAGEN according to the RNA cleanup protocol. WMISH was carried out according to the protocol from Weisblat and Kuo . As the specimens used were older juveniles and not embryos, the penetration of the probes was enhanced by using only the amputated anterior ends and an incubation for 30 min in 10 μg/ml ProteinaseK (from Tritirachium album; Merck) without shaking at room temperature. In addition a few similar WMISH experiments with adults were carried out as well.
Anti-acetylated α-Tubulin (Sigma, T7451, produced in mouse) was diluted 1:200, and the anti-DIG-Fab (Roche Deutschland Holding GmbH, Grenzach-Wyhlen, Germany) 1:4000 with blocking solution. The animals were incubated over night at 4°C followed by 1 hour at RT. The antibody solution was washed off with two rinses, 3 × 15 min, 3 × 1 hr in PTW. After the NBT/BCIP staining reaction the animals were blocked for 1hour at RT and then incubated over night at 4°C in Anti-Mouse FITC (diluted 1:125) and DAPI (1 μg/ml).
In situ Hybridization on sections. Paraffin embedding, sectioning and ISH on paraffin sections were carried out according to Cardona et al. . Individuals of adult H. robusta (TX & AU) were fixed in 2%PFA/ 0.1% glutaraldehyde/ 1xPBS. Probe concentration was 2 ng/μl according to the standard leech protocol. The embedded animals were sectioned into 10 μm slices.
Phylogenetic analyses of opsin sequences
Sequence analyses. The sequenced cDNA fragments were translated into Protein sequences and aligned with sequences obtained from NCBI using the in BioEdit incorporated ClustelW algorithm. The phylogenetic tree was calculated with RaXml using the protein model ‘LG’ obtained through ProtTest . The substitution model was complemented with invariable substitutions and CAT based.
Accession numbers for opsin sequences. H. robusta CA RopsA [jgi|Helro1|85596 |e_gw18.104.22.168], H. robusta TX RopsA [KF613602], H. robusta CA RopsB [jgi|Helro1|132379|gw22.214.171.124], H. robusta TX RopsB [KF613603], H. robusta CA RopsC [jgi|Helro1|84106|e_gw126.96.36.199], H. robusta TX RopsC [KF613604], H. robusta CA RopsD [jgi|Helro1|129809|gw188.8.131.52], Capitella teleta Rops [jgi|Capca1|202516|fgenesh1_pg.C_scaffold_376000014], Platynereis dumerillii Rops1 [CAC86665.1], Schistosoma mansoni Rho [AAF73286.1], Schistosoma mansoni Opn2 [XP_002581174.1], Schistosoma japonicum Opn4 [CAX73070.1], Dugesia japonica [CAD13146.1], Schmidtea mediterranea Rops [AAD28720.1], Todarodes pacificus Rho [P31356.2], Loligo forbesi Rho [P24603.1], Sepia officinalis Rho [O16005.1], Octopus dofleini Rho [P09241.1], Limulus polyphemus ocellar opsin [P35361.1], Limulus polyphemus lateral opsin [P35360.1], Drosophila melanogaster Rho4 [AAA28856.1], Manduca sexta opsin [O02464.2], Mizuhopecten yessoensis Gq-coupled Rho [BAA22217], Danio rerio [AAL83431.1], Homo sapiens opsin3 [AAH36773.1], Platynereis dumerillii ciliary opsin [AAV63834.1], Anopheles gambiae GPCR receptor1 [AGAP002443-PA], Anopheles gambiae GPCR receptor2 [AGAP002444-PA], Bos taurus Rho [NP_001014890.1], Homo sapiens RGR [NP_001012740.1], Mus musculus RGR [NP_067315.1], Drosophila melanogaster 5HT-dro2B receptor [CAA77571.1], Drosophila melanogaster Tyramine/octopamine receptor [P22270.2], Mus musculus Histamine H1 receptor [NP_001239572.1], Mus musculus Melanocortin 5 receptor [AAI00721.1 GI: 71682941].
Accession numbers for other sequences. H. robusta CA tryptophan 2,3 dioxygenase [scaffold_18|1087627|1088299 (673 bp)], H. robusta TX t23d [KF613600], H. robusta CA sepiapterin reductase [scaffold_77|451749|452651 (903 bp)], H. robusta TX sptr [KF613601], H. robusta CA Gq [jgi|Helro1|184821|estExt_fgenesh4_kg.C_10016].
Images were recorded digitally and further processed using Adobe Photoshop® and Adobe Illustrator®. 3D reconstructions (Figure 4E’, E”) were carried out by Raju Tomer, EMBL Heidelberg, with Imaris 5.7.1 (Bitplane AG, Zurich, Switzerland).
Pigmented supportive cell
Kozmik Z, Ruzickova J, Jonasova K, Matsumoto Y, Vopalensky P, Kozmikova I, Strnad H, Kawamura S, Piatigorsky J, Paces V, Vlcek C: Assembly of the cnidarian camera-type eye from vertebrate-like components. Proc Natl Acad Sci USA. 2008, 105: 8989-8993. 10.1073/pnas.0800388105.
Arendt D, Hausen H, Purschke G: The “division of labor” model of eye evolution. Phil Trans R Soc B. 2009, 364: 2809-2817. 10.1098/rstb.2009.0104.
Richter S, Loesel R, Purschke G, Schmidt-Rhaesa A, Scholtz G, Stach T, Vogt L, Wanninger A, Brenneis G, Döring C, Faller S, Fritsch M, Grobe P, Heuer CM, Kaul S, Møller OS, Müller CHG, Rieger V, Rothe BH, Stegner MEJ, Harzsch S: Invertebrate neurophylogeny - suggestions of terms and definitions for a neuroanatomical glossary. Front Zool. 2010, 7 (29): 1-49.
Eakin RM: Continuity and diversity in photoreceptors. Visual cells in evolution. Edited by: Westfall JA. 1982, New York: Raven, 91-106.
Arendt D: Evolution of eyes and photoreceptor cell types. Int J Dev Biol. 2003, 47: 563-571.
Gehring W, Seimiya M: Eye evolution and the origin of Darwin’s eye prototype. Ital J Zool. 2010, 77: 124-136. 10.1080/11250001003795350.
Arendt D: The evolution of cell types in animals: emerging principles from molecular studies. Nat Rev. 2008, 9: 868-882. 10.1038/nrg2416.
Arendt D, Tessmar-Raible K, Snyman H, Dorresteijn AW, Wittbrodt J: Ciliary photoreceptors with a vertebrate-type opsin in an invertebrate brain. Science. 2004, 306: 869-871. 10.1126/science.1099955.
Isoldi MC, Rollag MD, Castrucci AM, Provencio I: Rhabdomeric phototransduction initiated by the vertebrate photopigment melanopsin. Proc Natl Acad Sci USA. 2005, 102: 1217-1221. 10.1073/pnas.0409252102.
Koyanaigi M, Kubokaea K, Tsukamoto H, Shichida Y, Terakita A: Cephalochordate melanopsin: evolutionary linkage between invertebrate visual cells and vertebrate photosensitive retinal ganglion cells. Curr Biol. 2005, 15: 1065-1069. 10.1016/j.cub.2005.04.063.
Plachetzki DC, Degnan BM, Oakley TH: The origins of novel protein interactions during animal opsin evolution. PLoS One. 2007, 2: e1054-10.1371/journal.pone.0001054.
Suga H, Schmid V, Gehring JW: Evolution and functional diversity of jellyfish opsins. Curr Biol. 2008, 18: 51-55. 10.1016/j.cub.2007.11.059.
Purschke G, Arendt D, Hausen H, Müller MCM: Photoreceptor cells and eyes in Annelida. Arthr Struct Dev. 2006, 35: 211-230. 10.1016/j.asd.2006.07.005.
Eakin RM, Hermans CO: Eyes. The ultrastructure of Polychaeta. Edited by: Westheide W, Hermans CO. 1988, Microfauna Marina, 4: 135-156.
Jamieson BGM: Oligochaeta. Microscopic Anatomy of Invertebrates. Vol 7. Annelida. Edited by: Harrison FW, Gardiner SL. 1992, New York: Wiley Liss, 217-322.
Purschke G: Ultrastructure of the phaosomous photoreceptors in Stylaria lacustris (Naididae, Oligochaeta, Clitellata) and their importance for the position of the Clitellata in the phylogenetic system of the Annelida. J zool Syst Evol Res. 2003, 41: 100-108. 10.1046/j.1439-0469.2003.00203.x.
Clark AW: The fine structure of the eye of the leech Helobdella stagnalis. J Cell Sci. 1967, 2: 342-348.
Hirata K, Ohsako N, Mabuchi K: Fine structure of the photoreceptor cell of the earthworm, Eisenia foetida. Rep Facult Sci Kagoshima Univ (earth Sci, Biol). 1969, 2: 127-142.
Myhrberg HE: Fine structural analysis of the basal epidermal receptor cells in the earthworm (Lumbricus terrestris). Cell Tiss Res. 1979, 203: 1873-1884.
Röhlich P, Aros B, Vrágh S: Fine structure of photoreceptor cells in the earthworm, Lumbricus terrestris. Z Zellforsch. 1970, 104: 345-357. 10.1007/BF00335687.
Drewes CD, Fourtner CR: Hindsight and rapid escape in a freshwater oligochaete. Biol Bull. 1989, 177: 363-371. 10.2307/1541596.
Fernández J, Téllez V, Olea N: Microscopic Anatomy of Invertebrates. Volume 7. Annelida. Edited by: Harrison FW, Gardiner SL. 1992, New York: Wiley Liss, 323-394.
Hesse R: Untersuchungen über die Organe der Lichtempfindung bei Thieren. III. Die Sehorgane der Hirudineen. Z wiss Zool. 1897, 62: 671-707.
Sawyer RT: Leech Biology and Behaviour. Vol. 1. Anatomy, Physiology, and Behaviour. 1986, Oxford: Clarendon Press
Ukhanov K, Walz B: The phosphoinositide signalling cascade is involved in photoreception in the leech Hirudo medicinalis. J Comp Physiol A. 2001, 186: 1171-1183. 10.1007/s003590000169.
Raible F, Tessmar-Raible K, Arboleda E, Kaller T, Bork P, Arendt D, Arnone MI: Opsins and clusters of sensory G-protein-coupled receptors in the sea urchin genome. Devel Biol. 2006, 300: 461-475. 10.1016/j.ydbio.2006.08.070.
Guy K: Development and molecular characterization of adult and larval eyes in Platynereis dumerilii (Polychaeta, Annelida, Lophotrochozoa). 2008, Heidelberg: PhD Thesis
Weisblat DA, Huang FZ: An overview of glossiphoniid leech development. Can J Zool. 2001, 79: 218-232. 10.1139/z00-199.
Jamieson BGM: Oligochaete ultrastructure. The ultrastructure of Polychaeta. Edited by: Westheide W, Hermans CO. 1988, Microfauna Mar, 4: 397-428.
Purschke G: Sense organs in polychaetes (Annelida). Hydrobiologia. 2005, 535/536: 53-78. 10.1007/s10750-004-4358-5.
Röhlich P, Török LJ: Elektronenmikroskopische Beobachtungen an den Sehzellen des Blutegels, Hirudo medicinialis L. Z Zellforsch. 1964, 63: 618-635. 10.1007/BF00339910.
Jékely G, Colombelli J, Hausen H, Guy K, Stelzer E, Nedelec F, Arendt D: Mechanism of phototaxis in marine zooplankton. Nature. 2008, 456: 395-399. 10.1038/nature07590.
Suschenko D, Purschke G: Ultrastructure of pigmented adult eyes in errant polychaetes (Annelida): implications for annelid evolution. Zoomorphology. 2009, 128: 75-96. 10.1007/s00435-008-0075-3.
Struck TH, Paul C, Hill N, Hartmann S, Hösel C, Kube M, Lieb B, Meyer A, Tiedemann R, Purschke G, Bleidorn C: Phylogenomic analyses unravel annelid evolution. Nature. 2011, 471: 95-98. 10.1038/nature09864.
Rhode B: Larval and adult eyes in Capitella spec. I (Annelida, Polychaeta). J Morphol. 1993, 217: 327-335. 10.1002/jmor.1052170307.
Struck TH: Direction of evolution within Annelida and the definition of Pleistoannelida. J zool Syst Evol Res. 2011, 49: 340-345. 10.1111/j.1439-0469.2011.00640.x.
Kaller T: Molekulare und ultrastrukturelle Charakterisierung von Photorezeptorzellen und Augen bei Annelida. 2011, Berlin: PhD Thesis
Westheide W: The direction of evolution within the Polychaeta. J Nat Hist. 1997, 31: 1-15. 10.1080/00222939700770011.
Purschke G: On the ground pattern of Annelida. Org Divers Evol. 2002, 2: 181-196. 10.1078/1439-6092-00042.
Bartolomaeus T, Purschke G, Hausen H: Polychaete phylogeny based on morphological data – a comparison of current attempts. Hydrobiologia. 2005, 535/536: 341-356. 10.1007/s10750-004-1847-5.
Barnes RD Harrison FW: Introduction. Microscopic Anatomy of Invertebrates. Vol 7. Annelida. Edited by: Harrison FW, Gardiner SL. 1992, New York: Wiley Liss, 1-9.
Viscontini M, Hummel W, Fischer A: Pigmente von Nereiden (Annelida, Polychaeta). Isolierung von Pterindimeren aus den Augen von Platynereis dumerilii (Audouin & Milne-Edwards) 1833. Helv Chim Acta. 1970, 53: 1207-1209. 10.1002/hlca.19700530538.
Erséus C: Phylogeny of oligochaetous Clitellata. Hydrobiologia. 2005, 535/536: 357-372. 10.1007/s10750-004-4426-x.
Sjöllin E, Erséus C, Källersjö M: Phylogeny of Tubificidae (Annelida, Clitellata) based on mitochondrial and nuclear sequence data. Mol Phyl Evol. 2005, 35: 431-441. 10.1016/j.ympev.2004.12.018.
Jamieson BGM, Ferraguti M: Non-leech Clitellata. Reproductive biology and phylogeny of Annelida. Edited by: Rouse GW, Pleijel F. 2006, Enfield: Science Publishers, 235-393.
Sidall ME, Bely AE, Borda E: Hirudinea. Reproductive biology and phylogeny of Annelida. Edited by: Rouse GW, Pleijel F. 2006, Enfield: Science Publishers, 393-429.
Scriban IA, Autrum H: 2. Ordnung der Clitellata: Hirudinea = Egel. Handbuch der Zoologie. Vol 2.8 Vermes Polymera. Edited by: Kükenthal W, Krumbach T. 1932–1934, Berlin: De Gruyter, 119-352.
Walz B: Ca2+-sequestring smooth endoplasmic reticulum in an invertebrate photoreceptor. I. Intracellular topography as revealed by OsFeCN staining and in situ Ca accumulation. J Cell Biol. 1982, 93: 839-848. 10.1083/jcb.93.3.839.
Golding DW, Whittle AC: Secretory end feet, extracerebral cells, and cerebral sense organs in certain limnicole oligochaete annelids. Tiss Cell. 1975, 7: 469-484. 10.1016/0040-8166(75)90019-1.
Rota E, de Eguilor M, Grimaldi A: Ultrastructure of the head organ: a putative compound georeceptor in Grania (Annelida, Cliteallata, Enchytraeidae). Ital J Zool. 1999, 66: 11-21. 10.1080/11250009909356231.
Locke JM: Ultrastructure of the statocyst of the marine enchytraeid Grania americana (Annelida: Clitellata). Inv Biol. 2000, 119: 83-93.
Purschke G: Is Hrabeiella periglandulata (Annelida, “Polychaeta”) the sister group of Clitellata? Evidence from an ultrastrutural analysis of the dorsal pharynx in H. periglandulata and Enchytraeus minutus (Annelida, Clitellata). Zoomorphology. 2003, 122: 55-66.
Bely AE, Weisblat DA: Lessons from leeches: a call for DNA barcoding in the lab. Evol Devel. 2006, 8: 491-501. 10.1111/j.1525-142X.2006.00122.x.
Tessmar-Raible K, Steinmetz PRH, Snyman H, Hassel M, Arendt D: Fluorescent two-color whole mount in situ hybridization in Platynereis dumerilii (Polychaeta, Annelida), an emerging marine molecular model for evolution and development. Biotechniques. 2005, 39: 460-464. 10.2144/000112023.
Weisblat DA, Kuo DH: In situ hybridization of Helobdella (leech) embryos. Cold Spring Harb Protoc. 2009, doi:10.1101/pdb.prot5194, 4
Cardona A, Fernández J, Solana J, Romero R: An in situ hybridization protocol for planarian embryos: monitoring myosin heavy chain gene expression. Dev Genes Evol. 2005, 215: 482-488. 10.1007/s00427-005-0003-1.
Abascal F, Zardoya R, Posada D: ProtTest: selection of best-fit models of protein evolution. Bioinformatics. 2005, 21: 2104-2105. 10.1093/bioinformatics/bti263.
We thank Professor David Weisblat and Dr Stephanie Gline, Berkeley, USA for providing a culture stock of H. robusta and a WMISH protocol. Dr. Mette Handberg-Thorsager kindly gave advice to carry out in situs on paraffin sections. Help in gene predictions by Drs. Tobias Kaller and Florian Raible, Berlin and Heidelberg, are gratefully acknowledged. Dr. Torsten Struck, Bonn, helped in phylogenetic analyses of opsin sequences. We thank Dr. Raju Tomer, EMBL Heidelberg for doing the 3D reconstruction. Heidi Snyman, EMBL, Heidelberg, Werner Mangerich and Kerstin Etzold, both Osnabrück, gave various technical supports. The study was supported by a grant from the DFG (Pu 84/3-1, Pu 84/6-2) in the priority program 1174 “deep phylogeny”.
The authors declare that they have no competing interests.
GP, DA and HH conceived the study. CD conducted most of the experimental work except for TEM and took the lead of data collection. JG carried out the TEM observations. KTR aided substantially in performing the molecular studies. HH and CD carried out the gene predictions. GP took the lead on writing the manuscript; GP and CD were the main contributors to the writing. HH, DA and KTR contributed substantially to the writing of the manuscript. All authors read and approved the final manuscript.
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Döring, C., Gosda, J., Tessmar-Raible, K. et al. Evolution of clitellate phaosomes from rhabdomeric photoreceptor cells of polychaetes – a study in the leech Helobdella robusta (Annelida, Sedentaria, Clitellata). Front Zool 10, 52 (2013) doi:10.1186/1742-9994-10-52
- Cell type
- Photoreceptor cell