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Poorly understood but highly diverse microbial communities exist within anoxic and oxygen-depleted marine sediments. These communities often harbour single-celled eukaryotes that form symbiotic associations with different prokaryotes. During low tides in South-western British Columbia, Canada, vast areas of marine sand become exposed, forming tidal pools. Oxygen-depleted sediments within these pools are distinctively black at only 2-3 cm depth; these layers contain a rich variety of microorganisms, many of which are undescribed. We discovered and characterized a novel (uncultivated) lineage of heterotrophic euglenozoan within these environments using light microscopy, scanning and transmission electron microscopy, serial sectioning and ultrastructural reconstruction, and molecular phylogenetic analyses of small subunit rDNA sequences.
Bihospites bacati n. gen. et sp. is a biflagellated microbial eukaryote that lives within low-oxygen intertidal sands and dies within a few hours of exposure to atmospheric oxygen. The cells are enveloped by two different prokaryotic episymbionts: (1) rod-shaped bacteria and (2) longitudinal strings of spherical bacteria, capable of ejecting an internal, tightly wound thread. Ultrastructural data showed that B. bacati possesses all of the euglenozoan synapomorphies. Moreover, phylogenetic analyses of SSU rDNA sequences demonstrated that B. bacati groups strongly with the Symbiontida: a newly established subclade within the Euglenozoa that includes Calkinsia aureus and other unidentified organisms living in low-oxygen sediments. B. bacati also possessed novel features, such as a compact C-shaped rod apparatus encircling the nucleus, a cytostomal funnel and a distinctive cell surface organization reminiscent of the pellicle strips in phagotrophic euglenids.
We characterized the ultrastructure and molecular phylogenetic position of B. bacati n. gen. et sp. Molecular phylogenetic analyses demonstrated that this species belongs to the Euglenozoa and currently branches as the earliest diverging member of the Symbiontida. This is concordant with ultrastructural features of B. bacati that are intermediate between C. aureus and phagotrophic euglenids, indicating that the most recent ancestor of the Symbiontida descended from phagotrophic euglenids. Additionally, the extrusive episymbionts in B. bacati are strikingly similar to so-called "epixenosomes", prokaryotes previously described in a ciliate species and identified as members of the Verrucomicrobia. These parallel symbioses increase the comparative context for understanding the origin(s) of extrusive organelles in eukaryotes and underscores how little we know about the symbiotic communities of marine benthic environments.
The Euglenozoa is a diverse group of single-celled eukaryotes consisting of three main subgroups: euglenids, kinetoplastids and diplonemids. Euglenids are united by the presence of a distinctive pellicle, a superficial system formed by four major components: the plasma membrane, a pattern of repeating proteinaceous strips that run along the length of the cell, subtending microtubules and tubular cisternae of endoplasmic reticulum . The group is widely known for its photosynthetic members (e.g. Euglena and Phacus), but the majority of the species are heterotrophic (osmotrophs or phagotrophs). Photosynthetic euglenids evolved from phagotrophic ancestors with a complex feeding apparatus and a large number of pellicle strips that facilitate a characteristic peristaltic cell movement called "euglenoid movement". This combination of characters allows phagotrophic euglenids to engulf large prey cells, such as eukaryotic algae, which eventually led to the acquisition of chloroplasts via secondary endosymbiosis [2,3]. Euglenids are closely related to kinetoplastids and diplonemids. Kinetoplastids (a group that includes free-living bodonids and parasitic species such as Trypanosoma and Leishmania) are united by the presence of a mitochondrial inclusion of distinctively arranged DNA molecules, called a kinetoplast or kDNA . Kinetoplastids and euglenids share several morphological features, such as flagella with hairs and heteromorphic paraxial rods (e.g. a proteinaceous scaffolding adjacent to the usual 9+2 axoneme) and mitochondria with paddle-shaped (discoidal) cristae [5-7]. Diplonemids, on the other hand, possess a large mitochondrion with flattened cristae and apparently lack flagellar hairs . The monophyly of the Euglenozoa has been established on the basis of both molecular phylogenetic analyses and the following morphological synapomorphies: a tripartite flagellar root system, presence of heteromorphic paraxial rods and tubular extrusomes.
Environmental sequencing of oxygen depleted sediments around the world has shown that these habitats harbour a vast and unknown diversity of microbial lineages [9-14]. Phylogenetic analyses of these data have helped demonstrate the existence of several novel lineages associated with many different eukaryotic supergroups. Although these types of analyses are very effective in revealing the actual diversity of microbes living in a particular environment, these approaches also generate vast amounts of "orphan" data that cannot be linked directly to organisms known from comparative morphology. Nonetheless, some of the environmental sequences recovered from oxygen depleted environments cluster with euglenozoans in phylogenetic analyses but with no clear position within the group [9-11].
Other studies have explored and characterized the microbial diversity in oxygen-depleted environments using microscopical approaches [15-20]. This research has shown that a reoccurring feature of euglenozoans living in low oxygen environments is the presence of episymbiotic bacteria on the cell surface. Here, we report on a highly unusual (uncultivated) euglenozoan isolated from oxygen depleted marine sediments that is covered with two very different morphotypes of episymbionts. We characterized this lineage with light microscopy, SEM, comprehensive TEM, and molecular phylogenetic analyses of SSU rDNA sequences. Our data demonstrate that this organism is the earliest diverging member of the Symbiontida, which is an emerging subclade of euglenozoans composed of anaerobic and microaerophilic flagellates with a superficial layer of mitochondrion-derived organelles that associates closely with a uniform layer of episymbiotic bacteria . Moreover, the comparative ultrastructural data from this novel lineage sheds considerable light onto the phylogenetic position of the Symbiontida, as a whole, within the Euglenozoa.
The cells of Bihospites bacati n. gen. et sp. were elongated with a somewhat rounded posterior end and were 40-120 μm long and 15-30 μm wide (n = 200). The cells contained a brownish (or greenish) body near the posterior end of the cell and a variable number of distinctive black bodies at the anterior half of the cell (Figure 1A, B). The cells of B. bacati had two heterodynamic flagella that were inserted subapically within a depression. The longer anterior (dorsal) flagellum extended forward and continuously probed the substrate during 'gliding' movements (Figure (Figure1B);1B); periodically, the tip of the anterior flagellum would adhere to the substrate and abruptly drag the cell forward. The recurrent (posterior) flagellum was slightly longer than the cell body and trailed freely beneath the cell. The cells of B. bacati were plastic and capable of rhythmic deformations ranging from contracted to relaxed states that were reminiscent of "euglenoid movement" (Figure (Figure1C).1C). The cells divided from anterior to posterior along the longitudinal axis (Figure (Figure1D).1D). Cyst formation or sexual reproduction was not observed. Cells of B. bacati were found all year round, although the abundance of this species decreased significantly during the winter months.
The cell surface of B. bacati was covered with two different morphotypes of episymbiotic bacteria: (1) more abundant rod shaped episymbionts and (2) spherical-shaped episymbionts (Figure (Figure1E,1E, ,2).2). The rod-shaped episymbionts were 3-5 μm long and were arranged in bands, about 7 μm wide, along the longitudinal axis of the host cell (Figure (Figure2A).2A). These bands peeled off when the host cell deteriorated. The longitudinal bands of rod-shaped episymbionts were separated and defined by single or double rows of spherical episymbionts, each about 0.6 μm in diameter (Figure 2A-E). These longitudinal rows usually extended nearly the entire length of the host cell and were helically organized when the host cells were in a contracted state (Figure (Figure1C,1C, ,2A).2A). The rod-shaped episymbionts were connected to the plasma membrane of the host by a glycocalyx-like material (Figure 3A-E). The spherical-shaped episymbionts were attached to the host within a corresponding concavity in the host plasma membrane (Figure (Figure3E).3E). The spherical-shaped episymbionts were highly organized and possessed an extrusive apparatus consisting of an apical "operculum" and a tightly coiled internal thread around a densely stained core (Figure 3D-F). The coiled thread was capable of rapid discharge through an apical pore when disturbed during chemical fixation for electron microscopy (Figure 2A, D-E); the densely stained core was discharged first, and the coiled thread followed (Figure (Figure3F3F).
The ultrastructure of the host cell surface, beneath the episymbionts, consisted of a plasma membrane that was organized into a repeated series of S-shaped folds (i.e., "strips") (Figure (Figure1C,1C, ,3A),3A), a thin layer of glycoprotein, and a corset of microtubules (Figure (Figure3C).3C). The longitudinal rows of spherical-shaped episymbionts were associated with the troughs of the S-shaped folds (Figure (Figure3A).3A). The raised articulation zones between the S-shaped folds were visible in (i) light micrographs of contracted cells (Figure (Figure1C),1C), (ii) scanning electron micrographs near the posterior end of the host cell (Figure (Figure2C),2C), and (iii) transmission electron micrographs (Figure (Figure3A).3A). The corset of microtubules beneath the folds formed a continuous row and was linked together by short "arms" (Figure (Figure3C).3C). Tubular cisternae of endoplasmic reticulum and a layer of double-membrane bound mitochondrion-derived organelles (MtD) were positioned immediately below the superficial corset of microtubules (Figure 3A-C, E-F). The mitochondrion-derived organelles contained a granular matrix and none or very few cristae per TEM profile (Figure (Figure3B).3B). There was no evidence of kinetoplast-like inclusions or any other kind of packed DNA within the matrix of the mitochondrion-derived organelles.
The cytoplasm of the host cell was highly vacuolated and contained clusters of intracellular bacteria within vacuoles (Figure (Figure4A).4A). Batteries of tubular extrusomes, ranging from only a few to several dozen, were also present within the host cytoplasm (Figure (Figure4B).4B). The extrusomes were circular in cross-section and had a densely stained outer region that surrounded a lighter, granular core; a cruciform element was observed in cross-section of some extrusomes (Figure (Figure4C).4C). The extrusomes were approximately 4 μm long, and many of them were positioned immediately beneath the raised articulation zones between the S-shaped surface folds (Figure (Figure3A,3A, ,4D4D).
The nucleus of B. bacati was positioned in the anterior half of the cell and had permanently condensed chromosomes (Figure (Figure1A,1A, ,5A).5A). The nucleus was also closely linked to a robust rod apparatus (Figure (Figure1F).1F). Serial sections through the entire nucleus demonstrated that a C-shaped system of rods formed a nearly complete ring around an indented nucleus (Figure (Figure5A,5A, ,6,6, ,7,7, ,88 and and9).9). The C-shaped system of rods consisted of two main elements: (1) a main rod that was nestled against the indented nucleus (Figure (Figure7,7, ,88 and and9)9) and (2) a folded accessory rod that was pressed tightly against the outer side of the main rod for most of its length. We refer to this two-parted arrangement as the "C-shaped rod apparatus" (Figure (Figure5A,5A, ,6,6, ,7,7, ,88 and and9).9). The main rod was composed of a dense cluster of parallel lamellae that often appeared corrugated, while the accessory rod was composed of striated fibres (SF) (Figure 5A-B, ,6,6, ,77 and and8).8). Granular bodies of approximately 35 nm in diameter were observed in the spaces between the parallel lamellae of the main rod (Figure (Figure5B).5B). The ventral side of the main rod was embedded in an amorphous matrix that became thinner toward the posterior end of the cell, until it disappeared altogether (Figure 6A-D). A single row of longitudinal microtubules lined the external side of the main rod, which delimited the boundary between the main rod and the accessory rod for most of their length (Figure 5A-B).
The anterior ends of both C-shaped rods terminated near the antero-ventral region of the nucleus (Figure (Figure9).9). The posterior end of the main rod was positioned within the posterior region of a feeding pocket (Figure 5C-F, ,9).9). This feeding pocket merged together with the flagellar pocket and formed a common subapical concavity in the cell or a "vestibulum" (Figure (Figure2B,2B, ,5,5, ,9A).9A). A novel "cytostomal funnel" was positioned at the junction, and therefore demarcated the boundary, between the feeding pocket and the flagellar pocket (Figure (Figure5,5, ,6,6, ,9A).9A). The cytostomal funnel was an anterior extension of the posterior end of the accessory rod that eventually opened within the subapical vestibulum (Figure (Figure2B,2B, ,5,5, ,66 and and9A).9A). Some microtubules associated with the posterior end of the accessory rod also extended toward the ventral side of the cell and appeared to become continuous with the (ventral flagellar root) microtubules that reinforced the flagellar pocket (not shown).
The posterior region of the feeding pocket also contained a "congregated globular structure" (CGS) that was associated with the posterior end of the main rod (Figure 6A-B). The posterior end of the folded accessory rod became more robust as the serial sections moved from the posterior end of the feeding pocket toward the posterior end of the cell (Figure (Figure6,6, ,9).9). The posterior end of the folded accessory rod was initially positioned between the feeding apparatus and the flagellar apparatus; the accessory rod then gradually became more robust and more tightly associated with the main rod as both of the rods migrated around the posterior side of the nucleus and toward the dorsal side of the nucleus (Figure 6A-D, ,9).9). Moreover, as the sections continued posteriorly, the feeding pocket and the CGS that surrounded the main rod diminished, and ultimately only the main rod and the accessory rod remained (Figure 6C-D).
Serial sections through the anterior region of the nucleus, moving from anterior to posterior, demonstrated the C-shaped curvature of the rod apparatus (Figure (Figure7,7, ,9).9). These sections also demonstrated how the anterior ends of both the main rod and the accessory rod terminate on the ventral side of the indented nucleus near the vestibulum (Figure (Figure7F).7F). Similarly, serial sections through the posterior region of the nucleus, moving from anterior to posterior, demonstrated the C-shaped curvature of the rod apparatus and its relationship to the indented nucleus (Figure (Figure8,8, ,99).
Two flagella emerged from the base of the flagellar pocket (Figure 2A-B, 10A-F, 11A-E). Each flagellum had a paraxial rod (PR) in addition to the 9+2 arrangement of microtubules forming the axoneme (Figure 10G-H, 11F). The PR in the dorsal flagellum (Df) had a whorled disposition, whereas the PR of the ventral flagellum (Vf) had a lattice-like arrangement of parallel fibres (Figure 11F). No mastigonemes were observed on either flagellum (Figure 2A-B). The dorsal basal body contained a long opaque core (Figure 11B). Both basal bodies were approximately 1.7 μm long and were linked by a connecting fibre (CF) (Figure 10A-B). A cartwheel structure was present at the proximal end of both basal bodies (Figure 10A-B). Two accessory basal bodies (Db' and Vb') were observed on the ventral side of the Db and the dorsal side of the Vb (Figure 10B).
The flagellar root system is described here from the proximal to the distal end of the basal bodies as viewed from the anterior end of the cell. The basal bodies were associated with three asymmetrically arranged flagellar roots. A dorsal root (DR) originated from the dorsal-right side of the Db (Figure 10B, 11B-C) and was formed of approximately six microtubules (Figure 10E). A ventral root (VR) connected to the dorsal-right side of the ventral basal body (Figure 11A, D-E) and was comprised initially of four microtubules (Figure 10D). An intermediate root (IR), originally formed of about eight microtubules (Figure 10F), emerged from the left side of the Vb (Figure 10C-D). The ventral root and the intermediate roots ultimately fused, forming a continuous VR-IR row of microtubules around the flagellar pocket (Figure 10G-H). A band of dorsal microtubules (DMt), not directly associated to the basal bodies, lined the dorsal side of the flagellar pocket (Figure 10C, F; 11A-E). Toward the anterior end of the cell, the number of microtubules increased one by one, until the band reached the dorsal root (DR). The DMt and the DR eventually fused and formed a single band of microtubules around the flagellar pocket (Figure 10G-H).
The DR and VR were associated with two electron dense bodies that elongated to form a dorsal lamina (DL) and a ventral lamina (VL), respectively (Figure 10C-H). Both laminae extended anteriorly and ended up reinforcing the walls of the flagellar pocket (Figure 10G-H). The DR, together with the DL, supported the dorsal-left side of the pocket, and the DMt supported the dorsal-right side. The VR - reinforced by the VL - lined the ventral side of the pocket and was in contact with the IR that lined the ventral-left side of the flagellar pocket. The microtubules of the DMt and the VR became part of the elements forming the cytostomal funnel and accessory rod (i.e., the C-shape rod apparatus in general), and both the DR and the IR became part of the sheet of microtubules underlining the plasma membrane of the entire cell.
In order to infer the phylogenetic position of B. bacati, we PCR-amplified and sequenced the nearly complete SSU rDNA gene (2057 bp) from two independent isolates. The sequences contained expansions typical of euglenozoan SSU rDNA genes. First, we carried out a 40-taxon Maximum likelihood (ML) analysis that included sequences representing all of the major groups of eukaryotes; the resulting phylogeny showed B. bacati grouped strongly within the Euglenozoa (not shown). A second analysis included 37 taxa representing all of the major lineages of euglenozoans. The phylogenetic analyses showed that the euglenozoan sequences clustered in five main subgroups with high statistical support (Figure (Figure12):12): (i) a kinetoplastid clade, (ii) a diplonemid clade, (iii) a bacteriovorous euglenid clade, (iv) a eukaryovorous + phototrophic euglenid clade and (v) the Symbiontida, a newly named clade that includes Calkinsia aureus and several environmental sequences. Bihospites bacati clustered with the Symbiontida with extremely high statistical support (ML bootstrap value = 100% and Bayesian posterior probability > 0.95), as the sister lineage to the rest of this group. Calkinsia aureus branched next within the Symbiontida and formed the sister lineage to several environmental sequences (Figure (Figure12).12). However, the relationship of the Symbiontida to the other main subgroups within the Euglenozoa was unclear.
Bihospites bacati n. gen et sp. possesses all three synapomorphies that unify the Euglenozoa: a tripartite flagellar root system, heteromorphic paraxial rods and tubular extrusomes. Concordantly, our analyses of SSU rDNA sequences clearly places B. bacati within the Euglenozoa, specifically within the Symbiontida. Several studies based on environmental sequences indicated the existence of a novel rDNA clade of euglenozoans [9-11]. However, the Symbiontida was proposed after the ultrastructural description and molecular phylogeny of C. aureus strongly grouped this species with these environmental sequences, as a distinct subgroup within the Euglenozoa . Nonetheless, it was not clear in that study whether the Symbiontida was a new clade of euglenozoans or a subclade within one of the three previously recognized members of the Euglenozoa (i.e., kinetoplastids, diplonemids and euglenids). Our comprehensive characterization of B. bacati sheds considerable light onto this question.
Bihospites bacati possesses a cell surface consisting of S-shaped folds, microtubules and endoplasmic reticulum that is similar to the pellicle of S-shaped strips found in euglenids. In most photosynthetic euglenids, the pellicle strips usually consist of a robust proteinaceous frame that supports and maintains the shape of the cell, even during euglenoid movement [21-23]. However, like in most phagotrophic euglenids, there is no robust proteinaceous frame in B. bacati. Articulation zones between strips in the euglenid pellicle function as 'slipping points' around which the pellicle can change shape rather freely; moreover, the relative number of strips in each euglenid species reflects phylogenetic relationships and the degree of cell plasticity . Due to the extreme flexibility of the cell surface in B. bacati, it was not possible to determine an exact number of S-shaped folds in the cell surface. Nonetheless, the microtubular corset in most euglenids is regularly interrupted, thus forming groups of a few microtubules associated with each pellicle strip, the number of which varies between species [21-23]. By contrast, the microtubules beneath the plasma membrane in B. bacati form a continuous corset over the entire cell, much like that found in several phagotrophic euglenids (e.g., Dinema ) and in symbiontids (C. aureus  and Postgaardi mariagerensis ).
Bihospites bacati possesses a well-developed C-shaped rod apparatus consisting of a main rod and an associated accessory rod. Several heterotrophic euglenids [25-30], and some species of diplonemids [31-36], have been described with feeding apparatuses consisting of two main rods; some species also have corresponding accessory rods (e.g. Peranema trichophorum has two main rods and two folded accessory rods) or have a branched rod that gives the appearance of three main rods (e.g., Entosiphon). Nonetheless, there are several differences between these rods and those described here for B. bacati. Firstly, B. bacati only has one main rod and one folded accessory rod; this configuration has never been described so far. Secondly, the vast majority of this apparatus tightly encircles the nucleus in a C-shaped fashion, the functional significance of which is totally unclear. The straight rods in euglenids support and line a conspicuous feeding pocket, whereas the feeding pocket in B. bacati only associates with the posterior end(s) of the C-shaped rod apparatus. Thirdly, the main C-shaped rod in B. bacati is formed by a highly novel arrangement of tightly packed lamellae, and only a single row of microtubules originating from the VR separates the main C-shaped rod from the folded accessory rod. This row of microtubules demarcates the end of each lamella in the main rod. In all of the previously described euglenozoan species, different rods are formed by different proportions of amorphous material (not parallel lamellae) and microtubules originating from the ventral root of the ventral basal body. Fourthly, the posterior terminus of the accessory rod in B. bacati participates in the formation of a novel cytostomal funnel that extends anteriorly and merges with the subapical vestibulum. The cytostomal funnel presumably closes the connection between the flagellar pocket and the vestibulum during feeding. Although the cytostomal funnel in B. bacati is likely homologous to the "vanes" described in several different phagotrophic euglenids, the unusual ultrastructural features of B. bacati made this inference somewhat tenuous. Nonetheless, the additional "congregated globular structure" (CGS) at the posterior end of the main rod in B. bacati is also present in Calkinsia aureus . However, the feeding apparatus in C. aureus lacks conspicuous rods (or vanes) and consists mainly of a feeding pocket reinforced by microtubules from the VR, similar to the MTR pockets of other euglenozoans (e.g., Petalomonas). Overall, the C-shaped rod apparatus in B. bacati appears to contain some homologous subcomponents with phagotrophic euglenozoans (e.g., a main rod and a folded accessory rod), but, as highlighted above, this apparatus is novel in most respects.
The presence of a highly plastic cell surface, an elaborate feeding apparatus, and brownish bodies, reminiscent of food vacuoles, suggests that B. bacati is capable of engulfing large prey cells such as other eukaryotes [1,3,24,27,29,37]; however, this species was never directly observed preying on (relatively large) microeukaryotic cells present in the environment. Nonetheless, the presence of intracellular bacteria surrounded by vacuoles near the feeding pocket indicates that B. bacati actively feeds on bacteria. It is also possible that B. bacati feeds on the rod shaped episymbiotic bacteria that grow over the host surface and into the subapical vestibulum.
Tubular extrusomes are present in several members of the Euglenozoa [16,19,36] and constitute a synapomorphy for the group. Among the Symbiontida, C. aureus has tubular extrusomes clustered in a single large battery that is longitudinally arranged and anchored to a novel "extrusomal pocket" . Although Bihospites bacati also possesses tubular extrusomes, these organelles are not organized as a single battery. The extrusomes in B. bacati are arranged in several smaller clusters that are distributed in different places throughout the superficial cytoplasm; solitary extrusomes are organized consecutively beneath the articulation zones of the S-shaped pellicular folds or "strips". A similar arrangement of tubular extrusomes has also been observed in P. mariagerensis .
Several distantly related species of euglenozoans have been described with episymbiotic bacteria. These euglenozoans are usually phagotrophs that live in oxygen-depletd to anoxic marine environments, such as that in which B. bacati thrives [15,16,18,19,38,39]. However, two species of euglenids living in well-oxygenated, freshwater environments have also been described as having episymbiotic bacteria: the phototroph Euglena helicoideus , and the phagotroph Dylakosoma pelophilum . The episymbionts so far encountered in euglenozoans are either rod-shaped (in Euglena helicoideus , Postgaardi mariagerensis , Calkinsia aureus [19,38]) or spherical-shaped (D. pelophilum ). Bihospites bacati, however, is the first euglenozoan described with both morphotypes of episymbionts.
Hypotheses about the role of rod-shaped bacteria in symbiotic relationships with eukaryotic hosts usually emphasize commensalism, where the bacteria benefit from metabolic byproducts secreted by the host [15,16,20]. It has also been proposed that the rod-shaped bacteria are chemoautotrophic sulphur or methanogenic-oxydizers and form a mutualistic relationship with the host , whereby the host provides anchorage for the bacteria and the bacteria detoxify the immediate environment for the host [39,42]. The episymbiotic bacteria may also serve as a food-source for the host, as has been observed in one ciliate .
Spherical episymbiotic bacteria have been reported in one other euglenozoan based only on light microscopy: the freshwater euglenid D. pelophilum . However, this species has so far been poorly described and morphological characteristics of the bacteria are very difficult to evaluate; it was reported that the bacteria on the surface of D. pelophilum are 2 μm in diameter, twice the size of those in B. bacati. Spherical episymbiotic bacteria that are nearly identical at the ultrastructural level to those we describe here on B. bacati have been demonstrated on one species of hypotrich ciliate isolated from tidal pools [43-46]. Molecular phylogenetic evidence demonstrates that these episymbionts, called "epixenosomes", are novel lineages of verrucomicrobial bacteria, and experiments indicate that the extrusive nature of the spherical episymbionts function in defense against predators [43,45,46]. Therefore, these episymbionts improve the comparative context for understanding the origin(s) of different types of extrusive organelles in different lineages of eukaryotes (e.g., ejectosomes in cryptophytes and nematocysts in cnidarians and dinoflagellates). A more comprehensive examination and discussion of the biology and origins of the epixenosomes in B. bacati have been incorporated into a companion paper currently in preparation for publication (Breglia, Yubuki and Leander, unpubl. data).
Molecular phylogenetic analyses using SSU sequences place B. bacati as the earliest diverging branch within the Symbiontida. The Symbiontida are anaerobic and microaerophilic euglenozoans covered with rod-shaped bacteria that are in close association with a superficial layer of mitochondrion-derived organelles with reduced or absent cristae; accordingly, it was predicted that rod-shaped episymbionts are present in most (if not all) members of the group . The morphology of B. bacati is concordant with this description, reinforcing the interpretation that the presence of episymbiotic bacteria is a shared derived character of the most recent ancestor of the Symbiontida. This hypothesis is more robustly corroborated when we consider that B. bacati and C. aureus form a paraphyletic assemblage near the origin of the Symbiontida. In other words, episymbiotic bacteria are no longer a character known only in a single lineage within this group. Given this context, current ultrastructural data indicate that P. mariagerensis is also a member of the Symbiontida (e.g., B. bacati, C. aureus and P. mariagerensis all lack flagellar hairs and possess rod-shaped episymbionts, a continuous corset of cortical microtubules, and a superficial layer of mitochondrion-derived organelles) [16,19]. This inference, however, needs to be examined more carefully with an ultrastructural characterization of the flagellar apparatus and feeding apparatus in P. mariagerensis and with molecular phylogenetic data from the host and the episymbionts.
The presence of episymbiotic bacteria and the superficial distribution of mitochondria with reduced cristae in B. bacati, C. aureus and P. mariagerensis indicate a mutualistic relationship that enabled both lineages to diversify within low-oxygen environments. Determining whether the episymbionts on B. bacati, C. aureus and other symbiontids are closely related will more robustly establish the identity and composition of the clade and potentially reveal co-evolutionary patterns between the symbionts and the hosts. The geographic distribution of C. aureus and B. bacati (i.e. seafloor sediments of Santa Barbara Basin, California and coastal sediments of British Columbia, Canada) suggests that the Symbiontida is more widespread and diverse than currently known. This view is supported by the existence of related environmental sequences originating from Venezuela, Denmark and Norway [9,11,13]. Moreover, an organism with striking morphological resemblance to B. bacati has been previously observed in the Wadden Sea, Germany, . More comprehensive sampling of anoxic and low-oxygen sediments around the world will shed considerable light on the abundances and ecological significance of this enigmatic group of euglenozoans.
We described and characterized a novel flagellate from micro-aerobic marine sand: Bihospites bacati n. gen. et sp. Both comparative ultrastructure and molecular phylogenetic analyses strongly support the placement of B. bacati with the Euglenozoa and, more specifically, as a new member of the Symbiontida. An early diverging position of B. bacati within the Symbiontida is consistent with the presence of morphological features that are transitional between those found in C. aureus and phagotrophic euglenids: (1) a cell surface with strip-like S-shaped folds but lacking the proteinaceous frames of the euglenid pellicle, (2) a compact but robust rod-based feeding apparatus, and (3) a dense community of rod-shaped episymbiotic bacteria on the cell surface but without the elaborate extracellular matrix of C. aureus. Therefore, the molecular phylogenetic position and suite of intermediate ultrastructural features in B. bacati suggest that the most recent ancestor of the Symbiontida descended from phagotrophic euglenids. Although the close association of rod-shaped episymbiotic bacteria with the underlying mitochondria is a shared feature of symbiontids, the presence of extrusive verrucomicrobial episymbionts in B. bacati is highly unusual. These rapid-firing episymbionts could provide critical context for understanding the origin(s) of several different types of extrusive organelles in eukaryotes, and their discovery on this novel euglenozoan lineage underscores how little we know about the diverse symbiotic communities present in marine benthic environments.
Sediment samples were collected at low tide from the shoreline of Centennial Beach (Boundary Bay) in South-western British Columbia, Canada (49° 00' 4797''N, 123° 02' 1812''W), during the spring and summer of 2007 and 2008. The samples were taken at a depth of 1-3 cm below the sediment surface, from a conspicuous layer of black sand. The sediment samples were stored in flat containers at room temperature before individually isolated cells were prepared for light microscopy, electron microscopy and DNA extraction. Cells were extracted from the sand samples through a 48-μm mesh using the Uhlig melted seawater-ice method .
Attempts to culture the organism were made using two different media: ATCC 1728 (for growing Isonema) and CCAP 1259/1 (for growing Petalomonas cantuscygni). Both media were diluted in sterile seawater and kept under low oxygen conditions (oxygen content below 1%) using the ANAEROGEN™ COMPACT Kit system for anaerobic incubation; however, the cells did not reproduce and disappeared within 24 hours.
Differential interference contrast (DIC) light micrographs were taken using a Zeiss Axioplan 2 imaging microscope and a Leica DC500 digital chilled CCD camera.
Cells isolated from the British Columbia locality were fixed for scanning electron microscopy (SEM) using the 4% osmium tetroxide vapour protocol described previously . The cells were then transferred onto a 10-μm polycarbonate membrane filter, dehydrated with a graded ethanol series, and critical point dried with CO2 using a Tousimis Critical Point Dryer. The filter was then mounted on an aluminium stub, sputter coated with gold/palladium using a Cressington 208 HR High Resolution Sputter Coater, and observed with a Hitachi S-4700 field emission scanning electron microscope.
Cells isolated from the surrounding sediment were pre-fixed for transmission electron microscopy (TEM) using 4% (v/v) glutaraldehyde in 0.2 M sodium cacodylate buffer (SCB) (pH 7.2) with the addition of 0.3 M sorbitol. The pre-fixed cells were washed in 0.2 M SCB (pH 7.2) three times and embedded in 2% of low melting temperature agarose and post-fixed in 1% (w/v) osmium tetroxide in 0.2 M SCB (pH 7.2) at room temperature for 1 hr, before being dehydrated through a graded series of ethanol and 100% acetone. The dehydrated cells were then infiltrated with acetone-Epon 812 resin mixtures and 100% Epon 812 resin. Ultra-thin serial sections were collected on copper Formvar-coated slot grids, stained with 2% (w/v) uranyl acetate and lead citrate, and observed using a Hitachi H7600 electron microscope.
Genomic DNA was extracted using the MasterPure Complete DNA and RNA purification Kit (Epicentre, WI, USA) from 30 cells that were individually isolated and washed three times in sterile seawater (i.e., "isolate 1"). This procedure was repeated three months later on a different sample of 30 individually isolated cells (i.e., "isolate 2"). Polymerase chain reactions (PCR) were performed using PuRe Taq Ready-To-Go PCR beads kit (GE Healthcare, Buckinghamshire, UK). Nearly the entire eukaryotic SSU rDNA gene was amplified from each isolate using the eukaryotic universal primers 5'- TGATCCTTCTGCAGGTTCACCTAC-3'  and 5'-GCGCTACCTGGTTGATCCTGCCAGT-3' . PCR amplifications consisted of an initial denaturing period (95°C for 3 min), 35 cycles of denaturing (93°C for 45 s), annealing (5 cycles at 45°C and 30 cycles at 55°C, for 45 s), extension (72°C for 2 min), and a final extension period (72°C for 5 min). The amplified DNA fragments were purified from agarose gels using UltraClean 15 DNA Purification Kit (MO Bio, CA, USA), and subsequently cloned into the TOPO TA Cloning Kit (Invitrogen, CA, USA). Two clones of the eukaryotic SSU rRNA gene, from each of the two isolates (i.e., four clones in total), were sequenced with the ABI Big-Dye reaction mix using the vector primers and internal primers oriented in both directions. The new sequences were screened with BLAST, identified by molecular phylogenetic analysis, and deposited into GenBank: HM004353, HM004354.
The SSU rDNA sequences from B. bacati were analyzed within the context of two alignments: (1) a 40-taxon alignment consisting of taxa representing all of the major groups of eukaryotes (988 unambiguously aligned sites) and (2) a 37-taxon alignment consisting of taxa representing all of the major lineages of euglenozoans (760 unambiguously aligned sites). Ambiguously aligned positions and gaps were excluded from both analyses. Phylogenetic relationships were inferred using maximum likelihood (ML) and Bayesian methods with the programs PhyML  and MrBayes , respectively. For ML, the nucleotide datasets were analysed using a general-time-reversible (GTR) model of base substitutions, plus a gamma correction with eight substitution rate categories and the proportion of invariable sites (GTR + I + G). ML bootstrap analysis of 500 replicates was performed with the same parameters described above. For Bayesian analyses, the program MrBayes was set to operate with a gamma correction with eight categories and proportion of invariable sites, and four Monte-Carlo-Markov chains (MCMC) (default temperature = 0.2). A total of 2,000,000 generations was calculated with trees sampled every 50 generations and with a prior burn-in of 100,000 generations (i.e., 2,000 sampled trees were discarded). A majority rule consensus tree was constructed from 18,000 post-burn-in trees with PAUP* 4.0. Posterior probabilities correspond to the frequency at which a given node is found in the post-burn-in trees.
A digital archive of this paper is available from PubMed Central and print copies are available from libraries in the following five museums: Natural History Museum Library (Cromwell Road, London, SW7 5BD, UK), American Museum of Natural History (Department of Library Services, Central Park West at 79th St., New York, NY, 10024, USA), Muséum national d'Histoire naturelle (Direction des bibliothèques et de la documentation, 38 rue Geoffroy Saint-Hilaire, 75005 Paris, France), Russian Academy of Sciences (Library for Natural Sciences of the RAS Znamenka str., 11, Moscow, Russia) and Academia Sinica (Life Science Library, 128 Sec. 2 Academia Rd, Nankang Taipei 115, Taiwan R.O.C.).
Euglenozoa, Cavalier-Smith, 1981 
Symbiontida, Yubuki, Edgcomb, Bernhard & Leander, 2009 
Bihospites n. gen. Breglia, Yubuki, Hoppenrath and Leander 2010
Uninucleate biflagellates; two heterodynamic flagella inserted subapically, with paraxial rods and no mastigonemes; flagella of approximately the cell length; elongated cells with a rounded posterior end; nucleus at anterior end of cell; cell covered with epibiotic bacteria of two different types: rod-shaped and spherical-shaped; cell surface with S-shaped folds; tubular extrusomes with cruciform core; presence of black bodies mainly at the anterior end of cell; rhythmic cell deformations and gliding motility.
Latin Bihospites, with two guests. The generic name reflects the presence of two different episymbiont morphotypes: rod-shaped, and spherical-shaped episymbionts.
Bihospites bacati n. sp. Breglia, Yubuki, Hoppenrath and Leander 2010
Cell elongated with rounded ends; cell size 40-120 μm in length and 15-30 μm in width; two heterodynamic flagella inserted subapically; anterior nucleus; cell covered with epibiotic bacteria of two different types: rod-shaped and spherical-shaped; cell surface with S-shaped folds; mitochondrion-derived organelles with reduced or absent cristae; feeding apparatus with conspicuous C-shaped rod and accessory rod that encircles the indented nucleus; the rod is formed by tightly packed, parallel-arranged lamellae; presence of black bodies, mainly at the anterior end of the cell; rhythmic cell deformations and gliding motility. Small subunit rRNA gene sequences [GenBank: HM004353, HM004354].
Both resin-embedded cells used for TEM and cells on gold sputter-coated SEM stubs have been deposited in the Beaty Biodiversity Research Centre (Marine Invertebrate Collection) at the University of British Columbia, Vancouver, Canada.
Tidal sand-flat at Centennial Beach, Vancouver, British Columbia, Canada (49°00' 4797''N, 123°02'1812''W).
Marine sand, black layer 2-3 cm deep.
Specific epithet, Latin bacati, ornamented with pearls. The etymology for the specific epithet reflects the presence of distinct longitudinal rows of spherical-shaped episymbionts, reminiscent of pearl necklaces.
LSID for article: urn:lsid:zoobank.org:pub:40211D82-B95C-494A-B8D0-7E061E80DD18
LSID for the genus Bihospites: urn:lsid:zoobank.org:act:794D6C7B-BFB1-45C7-8DDA-32D44F3B0E50
LSID for the species B. bacati: urn:lsid:zoobank.org:act:E1549565-5434-4F85-B936-7D0C485596B8
ar: accessory rod; CGS: congregated globule structure; Cyt: cytostome; Db: dorsal basal body; Db': dorsal pro-basal body; Df: dorsal flagellum; DL: dorsal lamina; DMt: dorsal microtubules; DR: dorsal root; E: extrusome; epi: epixenosome; ER: endoplasmic reticulum; FP: flagellar pocket; IR: intermediate root; LM: light microscope; MtD: mitochondrion-derived organelle; N: nucleus; Nu: nucleolus; PR: paraxial rod; r: rod; S: strips; SF: striated fibre; SEM: scanning electron microscope; TEM: transmission electron microscope; tz: transition zone; Vb: ventral basal body; Vb': ventral pro-basal-body; Vf: ventral flagellum; VL: ventral lamina; VR: ventral root; vt: vestibulum.
SAB collected the sediment samples from Boundary Bay; generated the LM, SEM, and SSU rDNA sequence data; and wrote the first draft of the paper. NY generated the TEM data and helped with the phylogenetic analyses and interpretation of the TEM data. MH carried out the sampling, identification and LM work of the German material and helped with the identification of the Canadian material. BSL funded and supervised the collection and interpretation of the ultrastructural and molecular phylogenetic data and contributed to writing the paper. All authors have read, edited and approved the final manuscript.
This research was supported by grants from the Tula Foundation (Centre for Microbial Diversity and Evolution), National Science and Engineering Research Council of Canada (NSERC 283091-09), and the Canadian Institute for Advanced Research, Program in Integrated Microbial Biodiversity.