Septins of Platyhelminths: Identification, Phylogeny, Expression and Localization among Developmental Stages of Schistosoma mansoni

Septins are a family of eukaryotic GTP binding proteins conserved from yeasts to humans. Originally identified in mutants of budding yeast, septins participate in diverse cellular functions including cytokinesis, organization of actin networks, cell polarity, vesicle trafficking and many others. Septins assemble into heteroligomers to form filaments and rings. Here, four septins of Schistosoma mansoni are described, which appear to be conserved within the phylum Platyhelminthes. These orthologues were related to the SEPT5, SEPT10 and SEPT7 septins of humans, and hence we have termed the schistosome septins SmSEPT5, SmSEPT10, SmSEPT7.1 and SmSEPT7.2. Septin transcripts were detected throughout the developmental cycle of the schistosome and a similar expression profile was observed for septins in the stages examined, consistent with concerted production of these proteins to form heterocomplexes. Immunolocalization analyses undertaken with antibodies specific for SmSEPT5 and SmSEPT10 revealed a broad tissue distribution of septins in the schistosomulum and colocalization of septin and actin in the longitudinal and circular muscles of the sporocyst. Ciliated epidermal plates of the miracidium were rich in septins. Expression levels for these septins were elevated in germ cells in the miracidium and sporocyst. Intriguingly, septins colocalize with the protonephridial system of the cercaria, which extends laterally along the length of this larval stage. Together, the findings revealed that schistosomes expressed several septins which likely form filaments within the cells, as in other eukaryotes. Identification and localization demonstrating a broad distribution of septins across organs and tissues of schistosome contributes towards the understanding of septins in schistosomes and other flatworms.

The diversity and the number of septin-encoding genes diverge among species, ranging from one in algae [2] to 13 in humans [19]. Based on phylogenetic analysis, the metazoan septins can be classified into four groups, termed SEPT6, SEPT7, SEPT2 and SEPT3 [20]. Septins form filaments, which are composed of hetero-oligomeric complexes of septins from different groups. It has been postulated that each position of the hetero-oligomeric complex is specifically occupied by a septin group member and those cannot be replaced by member of another group [4]. Diversity among human members within most of the groups allows a multiplicity of potential complexes of human septins, with the permutation of different members of a same group in each of the hetero-oligomeric positions of the complex. However, an exception is the SEPT7 group which displays a single representative in the human genome and therefore its single member may not be replaced [4].
Schistosomiasis is considered the most important of the human helminth diseases in terms of morbidity and mortality (see [21]). Unusual among flatworms, schistosomes are dioecious, with sexual dimorphism and division of labor between sexes in the adult developmental stage [22]. Draft genome sequences for the three major species of schistosomes parasitizing humans are available [23][24][25]. Among these genomes, we identified putative septinencoding sequences of Schistosoma mansoni and reported here four schistosome septins termed SmSEPT5, SmSEPT10, SmSEPT7.1, and SmSEPT7.2, based on sequence identity with numbered human orthologues. Phylogenetic analyses in tandem with expression profiles of transcripts among developmental stages point to structural roles for these septin-like proteins in this pathogen. Confocal imaging revealed tissue-specific and/or ubiquitous localization of septins, suggesting specialized functions in schistosomes, and in flatworms at large, in addition to cytokinesis. To our knowledge, this is the first report of septins in any member of the phylum Platyhelminthes, or indeed in any Lophotrochozoan -a major evolutionary branch of the Bilateria [26].

Ethics statement
Mice infected with S. mansoni were obtained from the Biomedical Research Institute (BRI), Rockville, MD and housed at the Animal Research Facility of the George Washington University Medical School, which is accredited by the American Association for Accreditation of Laboratory Animal Care (AAALAC no. 000347) and has an Animal Welfare Assurance on file with the National Institutes of Health, Office of Laboratory Animal Welfare, OLAW assurance number A3205-01. All procedures employed were consistent with the Guide for the Care and Use of Laboratory Animals. Maintenance of the mice and recovery of schistosomes were approved by the Institutional Animal Care and Use Committee of the George Washington University. Procedures used for the production of antibodies were performed in accordance with the National Research Council's guide for care and use of laboratory animals [27].

Developmental stages of Schistosoma mansoni
Biomphalaria glabrata snails and Swiss-Webster mice infected with the NMRI (Puerto Rican) strain of S. mansoni were supplied by Drs.
Fred Lewis and Matt Tucker, Biomedical Research Institute, Rockville, MD under NIH-NIAID contract HHSN272201000 005I. Developmental stages of schistosomes were obtained as described [28][29][30]. In brief, adult developmental stages of the worms were recovered from infected mice by portal perfusion. Eggs were isolated from livers of schistosome-infected mice and newly hatched miracidia obtained by hatching these eggs. Primary sporocysts were obtained by transferring miracidia into sporocyst medium, as described [28] and cultured for two days [28]. Cercariae released from infected snails were snap frozen at 280uC or transformed mechanically into schistosomula which were cultured in Basch's medium [31] at 37uC under 5% CO 2 in air.

Bioinformatics and sequence analysis
Coding regions deduced in the genome of Schistosoma mansoni [23,32] were used as a database to identify septin genes through the tBLASTn program, using all human septins as queries. Four putative orthologues of septin were identified: Smp_041060, Smp_060070, Smp_003620 and Smp_029890. The multiple sequence alignment of the GTPase domain from these four S. mansoni septins with septins from Homo sapiens, Caenorhabditis elegans, Drosophila melanogaster, Strongylocentrotus purpuratus and Ciona intestinalis was accomplished using ClustalX2 [33]. Additional alignment was performed with GTPases domains from several platyhelminths using the same approach. Phylogenetic analyses were performed using a Bayesian inference method implemented in MrBayes (v3.1.2) [34]. All analyses were run using default parameters, except by the use of the command ''prset aamodelpr = mixed'', which allows the use of a mixture of amino acid models with fixed rate to estimate the appropriate model for the analysis. Analyses were stopped after 1,000,000 generations, with samplings every one hundredth generation. Tree information was summarized utilizing the ''sumt burnin = 2500'', which discards the first 250,000 generations. In all cases, the measured potential scale reduction factor (PSRF), obtained using the ''sump burnin = 2500'' command, was equal to 1, indicating a convergence of the analysis. Amino acids models chosen by the program for each tree were: Tree 1 (Figs. 1, 2), WAG (posterior probability = 1.0); Tree 2 ( Figure S1), WAG (posterior probability = 0.877) and Jones (posterior probability = 0.123). The resulting tree together containing the posterior probability for each branch was visualized using TreeView [35].

Recombinant expression of schistosome septins; antiseptin antisera
Full length transcripts encoding the septins SmSEPT5 and SmSEPT10 of S. mansoni were amplified by PCR using the following primers: SmSept5 forward primer, 59-GCTAGCATG GCA AA T ATT CCG CGT TTT GG-39; SmSept5 reverse primer 59-GGA TCCTCAAGACGCTTGTTGACCAGTTAC-39; SmSept10 forward primer 59-GCTAGCATGACTGCAGATGTTCTAAAAG CATTG-39; SmSept10 reverse primer ACTAGCTGTACTCT CGTCAGGATCCTTATTTCC-39 (restriction enzyme sites underlined). Reverse transcription from total mRNAs from mixed sex adult schistosomes (BH, a Brazilian strain) was accomplished and cDNA served as template for PCRs using the primers above. Amplicons of expected sizes were ligated into pTZ57R/T (Thermo Scientific), integrity of the inserts confirmed by nucleotide sequencing (3130 Genetic Analyzer, Applied Biosystems), and the septin-encoding sequences sub-cloned into the expression vector pET28a(+) (Novagen), which introduces a His-Tag at the N-terminus of the polypeptide. Recombinant septins were expressed in E. coli Rosetta (DE3) strain cells transformed

Author Summary
Schistosoma mansoni is one of the causative agents of schistosomiasis, a neglected tropical disease affecting over 230 million people in the developing world. Research on new therapies for this parasitic disease has been facilitated by the recent publication of a curated draft sequence of the schistosome genome. Here, we describe proteins from the septin family found in the genome of S. mansoni. The septins are increasingly recognized as central components of the cytoskeleton of eukaryotic cells. They are linked to numerous cellular functions, although the precise role(s) of these proteins is not fully understood. Schistosome septins were seen in the miracidium and sporocyst larval stages, on superficial structures, within epidermal plates and in muscles. Notably, septins were prominently expressed in the germ cells of larval stages of the blood fluke. In addition, septins were ubiquitously immuno-localized throughout the organs and tissues of the schistosomulum stage of the parasite. This is the first report on septins in schistosomes; these proteins are broadly distributed among organs and tissues of the parasite where they likely perform diverse functions. Identification and localization demonstrating a broad distribution of septins across organs and tissues of schistosome contributes towards the understanding of septins in schistosomes and other flatworms.
with pET28 constructs, with expression induced by IPTG at 0.4 mM in LB medium for 16 h at 18uC with shaking. Rosetta cells were lysed by sonication in 50 mM Tris-HCl pH 8.0, 800 mM NaCl, 10% glycerol, 10 mM b-mercaptoethanol (buffer A), after which lysates were clarified by centrifugation at 20,000 g for 30 min. Supernatants were fractionated by affinity chromatography on Ni-NTA resin (Qiagen) equilibrated in buffer A. Immobilized proteins were eluted in 50 mM Tris-HCl pH 8.0, 300 mM NaCl, 500 mM imidazole, 10% glycerol, 10 mM, bmercaptoethanol (buffer B). Subsequently, eluates were separated through a column of Superdex 200 10/300 GL resin (GE Healthcare Life Sciences) fitted to a liquid chromatography system (AKTA purifier, GE Healthcare Life Sciences). Purity of eluates was assessed by Coomassie stained SDS-PAGE.
Polyclonal antibodies against recombinant SmSEPT5 and SmSEPT10 were raised in mice. Anti-septin immunoglobulins were isolated from mouse sera by affinity chromatography using immobilized recombinant schistosome septins conjugated to HiTrap NHS resin (GE Healthcare Life Sciences). Western blot analysis was employed to examine the specificity of antibodies to recombinant SmSEPT5, SmSEPT10 (each at 0.5 mM) and proteins extracted from mixed sex, adult worms (50 mg). After resolution by SDS-PAGE, proteins were transferred to nitrocellulose using the Trans-blot Semi-dry Transfer cell (Bio-Rad), 30 min at 10 V.
Membranes were washed three times (15 min each) with TBS-T (10 mM Tris, 150 mM NaCl, 0.1% Tween-20) and incubated with blocking buffer (5% nonfat milk powder in TBS-T) for 2 h at 4uC. Incubation with the primary antibody, anti-SmSEPT5 or anti-SmSEPT10 diluted 1:1,000 in TBS-T was performed for 2 h at 4uC, followed by washes as above. Thereafter, membranes were probed with goat anti-mouse IgG (whole molecule)-alkaline phosphatase (Sigma-Aldrich), diluted 1:5,000 in TBS-T, for 2 h at 4uC, and washed as above. Signals were developed using Bio-Rad's Alkaline Phosphatase Conjugate Substrate Kit after which membranes were photographed.

Expression profiles of schistosome septins
Total RNA was recovered from developmental stages of schistosomes using the RNAqueous-4PCR system (Ambion). Any residual DNA in the RNA was removed by digestion with DNase (TurboDNase, Ambion). RNA concentration, purity and integrity were determined by Nanodrop 1000 spectrophotometer and Agilent 2100 Bioanalyzer; cDNA was synthesized from 150 ng RNA using the iScript cDNA Synthesis Kit (Bio-Rad). Quantitative polymerase chain reaction (qPCR) employing iQ SYBR Green Supermix (Bio-Rad), each primer at 0.3 mM in 20 ml reaction volume, was performed in a thermocycler (iCycler, Bio-Rad) fitted with real time detector (Bio-Rad iQ5). Septins-specific Efficiency of the PCR for each pair of septin specific primers was estimated by titration analysis to be 100%65 [36] (not shown).The qPCRs were performed in triplicate followed an initial denaturation at 95uC for 3 min and 40 cycles of 30 sec at 95uC and 30 sec of 55uC. The specificity of the PCR product was verified by a melting curve: 1 min at 95uC, 1 min at 55uC and a ramp from 55 to 95uC with an increasing rate of 1uC/min. Absolute quantification was undertaken using copy number standards, i.e. 10-fold serial dilutions of each septin clone. Copy number of each clone dilution was calculated through the relationship between the molecular mass of the clone and the Avogadro constant. Absolute copy number of septin transcripts was estimated by interpolation of the sample PCR signals from a standard curve [36]. Biological replicates were performed. In addition, relative quantification was undertaken in order to evaluate the expression of the four septin genes within developmental stages of S. mansoni. S. mansoni glyceraldehyde 3-phosphate dehydrogenase (SmGAPDH; GenBank M92359), forward primer, 59-TGTGAAAGAGATCCAGCAAAC-39; reverse primer, 59-GA TATTACCTGAGCTTTATCAATGG-39 was employed as a reference gene, with these PCRs carried out as above. The E 2DCt method, a variation of the Livak method that incorporates the amplification efficiency values (E) for each pair of primers, was employed to determine the expression of septins relative to SmGAPDH, within each sample, i.e. each developmental stage analyzed [37]. Bioinformatics analyses were performed using RNA-seq reads from libraries of adult worms and of cercariae [32]. A tally of the RNA-seq reads aligning to the transcripts encoding the four septins was compiled based on outcomes of a blastn search, to assess relative abundance of each septin.

Confocal imaging
Developmental stages (miracidium, sporocyst, cercaria and schistosomulum) of S. mansoni were dispensed in tissue culture medium into cell culture inserts incorporating polyethylene terephthalate track-etched membranes with a pore size of 8 mm (BD Falcon, BD Biosciences, Durham NC), mounted in wells of plastic 24-well tissue culture plates. Schistosomes were fixed in 4% paraformaldehyde (PFA) by diluting 16% PFA (EMS, Electron Microscopy Sciences) in 16 phosphate-buffered saline (PBS) for 1 h at 4uC. Subsequent steps were performed on a laboratory shaker. Worms were permeabilized with Triton X-100 in PBS (0.2%) for 60 min at 25uC, followed by three washes in PBS with 0.05% of Tween-20 (PBS-T). The blocking step was carried out overnight at 4uC in PBS containing 5% normal goat serum (NGS), followed by incubation with the primary antibody (1:50 dilution) for 2 d at 4uC. Samples were washed three times with PBS-T and incubated in 5% NGS for 20 min at 25uC as a second blocking step. Anti-mouse IgG conjugated to Alexa Fluor 633 Goat (Invitrogen) was added to the blocking solution to a final dilution of 1:300, after which samples were incubated in the dark for 90 min at 37uC. The samples were subsequently stained for 30 min at 25uC with 49,6-diamidino-2-phenylindole (DAPI) at 300 nM and Alexa Fluor 568 phalloidin (Invitrogen) at 165 nM in PBS containing 1% bovine serum albumin (BSA) for 30 min at 25uC. After samples were air dried, they were mounted in Fluoromount-G (EMS) on glass slides.
Confocal images were obtained using a Carl Zeiss LSM 710 system, which includes a Zeiss Axio Examiner Z1 microscope and a Quasar 32-channel spectral detector. Samples were scanned sequentially using a Plan-Apochromat 636/1.40 Oil DIC objective. For acquisition of signals from the DAPI channel, targets were excited with a 405 diode laser line and emission was filtered in a band between 410 and 585 nm. Immunolabeling (Alexa Fluor 633) was revealed by excitation with a diode 633 laser line, with emission recorded between 638-747 nm. Phalloidin labeling of actin filaments was excited with a 561 diode laser and emission recorded from 572 to 630 nm. Optical confocal sections were generated by adjusting the pinhole to one Airy unit using the most red-shifted channel, producing an optical section of ,0.7 mm in all channels. Confocal images were captured in sequential acquisition mode to avoid excitation bleed-through, particularly apparent with DAPI. Image frames measured 102461024 pixels with a pixel dimension of 0.132 mm. Images manipulation was undertaken with the assistance of Zen 2009 software (Carl Zeiss). Manipulations were limited to adjustment of brightness, cropping, insertion of scale bars and the like; image enhancement algorithms were applied in linear fashion across the image and not to selected aspects. Control images were adjusted similarly.

Schistosomes displays four discrete septins
Four genes, Smp_041060, Smp_060070, Smp_003620 and Smp_029890, encoding putative septins were identified in the S. mansoni genome by interrogating the database in a tBLASTn search with all described human septin protein sequences as queries. Eventual discrepancies between gene predictions and actual transcript data were assessed. Utilizing the database of S. mansoni ESTs for a BLASTn search with each of four newly predicted S. mansoni septins, we observed that Smp_041060 included 59 residues that did not correspond entirely with any EST and ESTs AM042809 and AM043866 exhibited a different 59 terminus. These sequences were aligned to assemble a putative sequence for this transcript. Confirmation of the existence of this transcript was investigated by reverse transcription PCR utilizing primers flanking the full-length coding sequence (CDS) of the putative gene, followed by nucleotide sequencing. Sequences of the other three predicted transcripts were similarly confirmed. The sequences of the full-length CDS of SmSEPT5, SmSEPT7.1, SmSEPT7.2 and SmSEPT10 have been assigned GenBank accessions KC916723, KC916724, KC916725 and KC916726, respectively.
Sequence alignment of the four polypeptides predicted to be encoded by these transcripts using BLASTp with the 13 human septins as a database indicated that two of the S. mansoni septins, Smp_003620 and Smp_060070, displayed higher identity with the human septin SEPT7 (47% and 55% identity, respectively). Hence we termed the putative proteins SmSEPT7.1 and SmSEPT7.2. The other S. mansoni septins, Smp_029890 and Smp_041060, displayed higher identities with human septin 10 (65% identity) and septin 5 (57% identity); there have been named SmSEPT10 and SmSEPT5, respectively. The four schistosome septins have predicted molecular masses of 48-58 kDa and display hallmarks of the septin family: a highly conserved GTPase domain containing the G1 (GXXXXGKS/T), G3 (DXXG) and G4 (XKXD) motifs [38], a septin unique region [39], a variable N-terminus, and a C-terminal region predicted to form a coiled coil structure (COILS program [40]) (Figure 1).
A phylogenetic tree established using Bayesian inference of a multiple alignment of the conserved GTPase domains of the four S. mansoni septins with septins from selected deuterostomes and protostomes revealed that the orthologous S. mansoni septins SmSEPT 5, SmSEPT10, and SmSEPT 7.1 with SmSEPT 7.2 clustered in the groups SEPT2, SEPT6 and SEPT7, respectively, with strong statistical support (Figure 2). Proteins from these groups comprise a known human hetero-oligomeric septin complex [18]. Examination of the phylogenetic tree presented in Figure 2 indicated, with high posterior probability, that all the septin groups are monophyletic and their branches have an origin in the center of the tree, predicting that divergence of all septin groups preceded the protostome-deuterostome split.
It is noteworthy that schistosomes, like the other protostomes sampled, lacked septins of the SEPT3 group, suggesting that this gene was lost early in this branch of evolution. The phylogram also indicated with strong statistical support that deuterostome genes encoding groups SEPT7 and SEPT6 form a monophyletic branch. This suggested that only a single copy from each of these families was present in the last common ancestor of deuterostomes and protostomes. Gene duplications that resulted in several copies of septins from group SEPT6 in humans likely occurred after the divergence of the two lineages. A peculiar scenario was evident in the SEPT2 group, in which septins of protostomes and deuterostomes did not segregate in the branch structure. This suggests that at least one event of gene duplication in this family preceded the divergence between species analyzed here. The only gene duplication observed among the four new schistosome septins was in the SEPT7 group. Curiously, a similar duplication did not occur in the orthologous human group, where only one form of SEPT7 is known [4].
Access to genome sequences of several other species of the phylum Platyhelminthes [41] facilitated analysis of putative septin sequences among flatworms at large. Phylogenetic analyses of the tapeworms Echinococcus multilocularis, E. granulosus, Taenia solium and Hymenolepis microstoma revealed the presence of four septin genes that cluster into the same groups of schistosome septins ( Figure  S1), indicative of a conservation of septin structures among trematodes and cestodes. The expression profile of septins in developmental stages of the S. mansoni was investigated by quantitative PCR. At the outset, absolute quantification was employed to normalize septin expression among different developmental stages [42][43][44][45]. (Gene expression analysis based on normalization to a reference gene, by contrast, may be challenging in the absence of accurate information on the reference gene expression throughout the developmental stages analyzed in the present study.) The expression profile of the four septin genes exhibited similar trends among the developmental stages ( Figure 3). This outcome was confirmed in a biological replicate ( Figure S2).Given the propensity of septins to form hetero-filaments [18], this coordinated expression of all septin groups suggested that functional filaments of septins in schistosomes may be composed of multiple septin proteins. In order to further investigate the coordinated expression of the four septin genes, relative quantification was undertaken using SmGAPDH as a reference gene. The relative expression levels of the four septins were detected within each individual stage. In concordance to the findings with absolute quantification PCR (Figure 3), the relative abundance of the four septin transcripts was similar among the stages studied ( Figure S3). Additionally, the relative contribution of each septin gene in the adults and cercarial stages of S. mansoni, was assessed by interrogation of publicly available RNA-seq data for these two stages [32]; a similar pattern of transcript abundance was apparent ( Figure S4). Together, analyses by absolute and relative qPCR and of RNA-seq libraries [32] indicated that schistosome septins exhibit coordinated expression during the development cycle of the parasite.

Ubiquitous expression in the schistosomulum
Immunolocalization analyses were undertaken using affinity purified antibodies raised against two of the four S. mansoni septins, SmSEPT5 and SmSEPT10. At the outset, western blots were performed with two recombinant schistosome septins and lysates of adult schistosomes to ascertain the specificity of the antibodies. Minimal cross-reactivity was apparent even to excessive quantities of septins. Anti-SmSEPT5 immunoglobulin recognized SmSEPT5 strongly and SmSEPT10 weakly. In similar fashion, anti- SmSEPT10 immunoglobulin recognized SmSEPT10 strongly but only weakly recognized SmSEPT5 ( Figure S5, panels A, C). Moreover, only single bands reacted in soluble lysates of adult schistosomes, incubated with anti-SmSEPT5 or anti-SmSEPT10 ( Figure S5, panels B, D), indicating negligible cross-reactivity at physiological concentrations of the targets. The same trend of expression was revealed by the imaging analysis regardless of the antibody used -anti-SmSEPT5 or anti-SmSEPT10, consistent with the proposition that schistosome septins form hetero-oligomeric complexes. Representative images labeled with anti-SmSEPT5 and anti-SmSEPT10 in two developmental stages are presented in the Figures S6 and S7 to illustrate the similarity of the localization profiles. Images from samples incubated in the secondary antibody only showed minimal, though marginally detectable, signals in the septin channel ( Figure S8).
In parallel to the immunolocalization with anti-septin antibodies, filaments of schistosome actin were labeled with phalloidin, a ligand of fungal origin that binds actin polymers. Two-and 14day-old schistosomula exhibited similar immunofluorescence profiles (Movies S1, S2). Septin fibers could be identified at the worm surface, along with actin fibers (Figure 4). Septins were also evident in deeper layers, usually at the periphery of the cells ( Figure 5). Three-dimensional renderings of confocal images including signals from the DAPI, phalloidin and septin probes revealed ubiquitous expression of septins ( Figure 6). By contrast, actin was more prominent in muscle layers and the gut ( Figure 6B).

Septins localize in superficial structures and germ cells of the miracidium and sporocyst
Miracidia and sporocysts cultured for two days were permeabilized and probed with anti-septin immunoglobulins, followed by incubation with an Alexa Fluor 633-conjugated secondary antibody. Confocal imaging allowed the sampling of increasingly deeper (internal) layers of these stages of the blood fluke which, in turn, precisely localized septins in organs and tissues (Movie S3; Figures S9, S10). The superficial layers of the miracidium expressed septins on the epidermal plates (Figure 7), which contain the cilia of the motile larva. Images of superficial layers of the sporocyst revealed colocalization of actin and septin in the longitudinal and circular muscle layers ( Figure 7D). Moreover, septins were prominent in optical sections of germs cell in miracidia ( Figure 8A) and two-day-old sporocysts ( Figure 8B). Colocalization of septin and actin was observed in the superficial optical sections of these larval stages, though not in deeper sites.

Protonephridial ducts of the cercaria are septin rich structures
Robust staining of septin was seen in the cercaria along the protonephridial ducts that extend laterally down both sides of the larva; characteristic flame cells are located at the termini of the canals (Figure 9, arrows; Movie S4). The protonephridium consists of a network of osmoregulatory tubules comprising the excretory system of the larva and extends nearly the entire length of the body [46,47]. Septins appear to occur at the collecting tubules of this osmoregulatory system (Figure 9); the role of septins in these structures remains to be elucidated.

Discussion
Septins are cytoskeleton components formed from heterooligomeric complexes which assemble into higher-order structures such as filaments and rings. Whereas septins are evolutionarily conserved and widely distributed among eukaryotes, until now septins have not been reported in schistosomes or indeed in any flatworm. Four schistosome septins are reported here; they are members of three discrete septin groups, with a duplication verified in SEPT7 group. A similar gene organization was apparent in the genomes of four cyclophyllidean tapeworms including E. multilocularis. The conserved gene organization between trematodes and cestodes indicates an essential role of these proteins across the phylum.
The flukes and tapeworms investigated displayed members of the same three septin groups described previously in some other invertebrates, including Drosophila melanogaster and Caenorhabditis elegans. The SEPT3 group appears to be absent from these taxa [20,48], suggesting that a deletion occurred in a common ancestor. Despite the absence of one of the groups, the functional assembly of septins into heter-oligomeric structures is maintained [49,50]. Phylogenetic analysis involving nine metazoans [20], including the sea urchin Strongylocentrotus purpuratus and the sea squirt Ciona intestinalis which, as representatives of the echinoderms and nonvertebrate chordates, respectively, occupy informative phylogenetic positions with respect to the evolution of mammals, revealed that they share orthologues of all human septin groups. This suggests that these four septins groups evolved before the appearance of the vertebrates and supports the hypothesis of a deletion event in some lineages of the invertebrates. Moreover, schistosomes exhibited only one isoform for groups SEPT2 and SEPT6 in contrast to the situation in humans where several isoforms of the groups occur. Septin configuration in schistosomes may resemble an ancestral arrangement, whereas successive duplications and mutations have endowed the human isoforms with a more specialized role(s).
Real-time PCR analyses indicated that transcription of genes encoding the four schistosome septin was maintained at approx-imately the same ratio throughout the developmental cycle. This suggested that a septin heterocomplex might exhibit a similar composition in the diverse morphological stages of the schistosome, although deeper investigation will be required to precisely define the proportion of the different group members of the septin heterocomplex in S. mansoni. Confocal imaging revealed that muscle layers were rich in actin and septin, suggesting cell specific co-expression of these cytoskeleton elements. Their co-localization was more evident in the sporocyst, which undergoes shedding of ciliated epidermal plates and the emergence of a new tegument during infection of the snail [51]. Co-localization of actin and septin is well-known in mammals [52,53]. Rapid-freeze, deep-etch immuno-replica electron micrographs reveal associations of septins with actin-based membrane skeletons of kidney cells [54]. Septins can be recruited to an actin bundle through the interaction with the adaptor protein anillin of Xenopus laevis [53]. BLASTp searches using X. laevis anillin allowed the identification of a homologue from S. mansoni (XP_002576415.1; 43% similar over 177 positions). Analysis using the CDD tool at NCBI (not shown) revealed an anillin pleckstrin homology (PH) domain (cd01263) in the schistosome orthologue, suggesting that it performs a similar role.
Confocal immunolocalization micrographs revealed septins in the ciliated epidermal plates of the miracidium. Septins are required for ciliogenesis and constitute a diffusion barrier at the base of the ciliary membrane in mammalian cells and Xenopus embryos [49,55]. The cilium of the miracidium exhibits microtubules with a 9+2 pattern [56], typical of eukaryotic motile cilia [57]. Since the cilium is a highly conserved organelle in eukaryotes [57], septins in the epidermal plates of the miracidium likely display a similar organization to the septins found in cilia of mammalian cells, and may perform a similar role. The prominent expression of septins in germ cells of both the miracidium and the  mother sporocyst and absence of phalloidin staining in this tissue together indicated that actin and septins of schistosomes do not always act in concert. In like fashion, earlier reports indicate that actin was not detectable in germ cells when miracidia and sporocysts were probed with phalloidin [47,58,59]. A pattern of staining for b-tubulin in the germ cells has been reported [48] that is similar to the localization of septins in germ cells described here, which together suggests a cellular co-expression of these filaments as well. Associations of septins and microtubules are well known [60][61][62][63]. In D. melanogaster, Peanut, SEPT1 and SEPT2 have been identified in male germ cells [64]. Likewise, septins are known from the mammalian germ cells. Sept4 null male mice are sterile due to immotile spermatozoa with defective annulus [65,66], and diminished expression of SEPT12 transcripts is evident in the testicles of infertile men [65]. Moreover, septin 12 plays a key role in terminal differentiation of germ cells in both humans and mice [67]. Septins are best known for their role in cytokinesis [9][10][11][12][13][14] and we speculate that the role of septins in miracidial and sporocyst germ cells might be related to the mitotic activity of these cells.
Schistosomula cultured for two or 14 days showed ubiquitous localization of septin in contrast to a more restricted distribution in the other stages. Ubiquitous septin localization has also been reported for some human septins [68]; it is feasible that septins are involved in some similar functions in human and schistosome cells and tissues. To conclude, this is the first description of septins of a schistosome or any platyhelminth. Four septins were identified and they were differentially expressed among developmental stages of the blood fluke. Confocal imaging indicated that schistosome septins undertake specialized roles in this pathogen. Detailed evaluation of schistosome septins can be expected to clarify the relationship of this category of proteins with cellular and physiological functions and to deliver deeper understanding of schistosome physiology and anatomy and its roles in the hostparasite relationship.