Most organisms modulate their motility in response to environmental variables such as nutrients, abiotic and biotic stress [1,2]. A recent study shows that, organisms probably randomized their motility in such an environment [3]. These movements range from sliding to gliding over a substrate, rotation, swimming or streaming in a suitable medium with the help of organelles such as flagella or cilia that support such motions. The once vestigial organelle, the flagellum, and its evolution is of enormous interest to biologists because the three known varieties (eukaryotic, bacterial, and archaeal flagella) represent an advanced protein-based structure that requires the interaction of its components within itself and with many systems; their molecular mechanism of motility and sensory transduction remaining elusive. An approach to the evolutionary origin of any cellular component(s) is to devise in silico homology searches among the protein or nucleotide sequences of the two components that one is trying to find evolutionary relatedness. This very approach has suggested that a subset of the bacterial flagellar components is similar to the Type III secretory and transport system; the latter defensive systems provide the function of injecting a toxin into eukaryotic cells. On the other hand, the recently elucidated archaeal flagellum has been analogous, not homologous, to the bacterial one. While there is no sequence similarity among the genes of the two systems and that the archaeal flagellum appears to grow from the base and not the tip; sequence comparison shows that the archaeal flagellum is homologous to Type IV pili [4].

The evolutionary origin of the eukaryotic flagellum offers two competing models; the Margulis’ model disputes that the eukaryotic flagellum evolved from a symbiotic spirochete that attached to a primitive unicellular eukaryote or archaebacteria. Endogenous, autogenous and direct filiation model states that the cilium developed from pre-existing components of the eukaryotic cytoskeleton (which has tubulin and dynein) as an extension of the mitotic spindle apparatus. The first line of evidence is seen in the various early branching singlecelled eukaryotes that have a microtubule basal body, where microtubules on one end form a spindle-like cone around the nucleus, and those on the other end point away from the cell to form the cilium. A second connection is that the centrioles, homologous to the cilium, and have often been the basal body from which the cilium grows. Regarding the origin of the individual protein components, and in particular on the evolution of dyneins, the complex protein family of ciliary dynein has an apparent ancestor in a simpler cytoplasmic dynein (which itself has evolved from the AAA protein family that occurs widely in all archea, bacteria and eukaryotes). Long-standing suspicions that tubulin was homologous to FtsZ (based on very weak sequence similarity and some behavioral similarities) were confirmed by the independent resolution of the 3-D structures of the two proteins [5]. While the flagella lineage is traced back to the secretory systems of bacteria, the pili themselves is a piece of evolutionary enigma.

Notwithstanding, the flagella and not the pili are therefore, the organelles used as one of the parameters in taxonomy. Among motile rod-shaped bacteria, the number of flagella per cell, the shape of flagella and their points of origin of the cell (polar versus peritrichous), are a primary taxonomic criterion [6] with immense clinical significance [7]. Flagellar arrangement may be a feature with enough stability and uniqueness to classify flagellated bacteria into several groups [8]. Conventionally, four arrangements are popular, the monotrichous, amphitrichous, lophotrichous and polytrichous. However, variations on the classical flagellum does exist, possession of both lateral and polar flagella on the same cell, and the periplasmic flagella of spirochetes [9,10]. The number and position of flagellum filaments on the surface of bacterial cells are highly conserved traits, with the polar and peritrichous arrangements being frequent. Though the type of cell flagellation used as an extra taxonomic key to distinguish motile bacteria, little is known about the mechanisms regulating its the number and position [11]. The same criterion need not be used for eukaryotic species’ classification. This kind of robustness, therefore, calls for the uniqueness of the flagella system across evolution. If the origin of flagella is considered, the need is to analyze the common as well as differing features in these structures throughout evolution.

An unbiased peek into the cellular position of flagella at the morphological level was attempted in the present study; with the flagella characteristics of the phyla across all the kingdoms being scored. The overall results show that the flagellar arrangement on both uniand multicellular organisms may have evolved with a function; the position on the cell where the flagella are arranged would not have been a random selection. Whatever the purpose, our observations show a gradual shift in the arrangement of flagella from polar, peritrichous, sub-apical, apical to lateral throughout evolution; such an arrangement shifting functionally from the polar, chemo-tactically motile to the lateral, non-motile cilia types. We propose a model for multicellularity based on the arrangement of flagella; a phenomenon that is robust and reproducible from one generation to the other among all species. And, if natural selection favored motility, at least for the sake of costbenefits, arrangement of the flagella seemed critical.

The present study is divided into two modules namely Module A and Module B.

The first primitive cell, assumed as a non-motile coccus

Table 1. OTU of prokaryotes.

Table 2. OTU of eukaryotes.

was probably carried by currents present in the primordial milieu. From here on, two forms of movements were notably seen; cells with gas vesicles and those that harbored flagella. Gas vesicles are found rampantly among the unicellular organisms; but, flagella are found equally among both the unicellular and multicellular organisms. The latter might have originated from groups of single cells that need to show high interaction and co-operation between one another and be nearly free of variance [13]. The evolution of flagella has always been a curiosity to biologists, particularly in the context of non-similarities in the ultrastructure, development and motion dynamics of the three known varieties (viz. Eukaryotic, bacterial, and the archaeal types) [14-17]. Some overlaps in the gene/protein sequence similarities have led many to believe that the eubacterial flagella originated from the T3SS, while the archebacterial flagella originated from the T4SS [14-17]. With two competing views on the evolutionary origin of the eukaryotic flagellum, the one that seems largely favored in terms of gene/protein sequence similarity is the endogenous or direct filiation model. The pre-existing components of the eukaryotic cytoskeleton such as tubulin and dynein are extensions of the mitotic spindle apparatus. Dynein evolution shows that the complex protein family of ciliary dynein has evolved from a simpler cytoplasmic dynein that evolved from the AAA protein family that occurs widely in all archaea, bacteria and eukaryotes [15]. These support, mainly vertical inheritance for the components of this unique motility system, and probably an ancient horizontal gene transfer event of a whole flagellum-coding gene cluster among Euryarchaeota and Crenarchaeota [18]. In the context of all these sequence similarities and an associated functional significance of cilia in motility, sensory transduction and development, we set out to know whether there an order or randomness in the rather simple attribute, namely, flagellar arrangement of cells across all the six kingdoms? And, could this arrangement serve as a paradigm to draw a similarity tree, akin to a phylogenetic tree so as to reveal the relatedness between species, if any?

The study, initiated by surveying the flagella literature (290 primary references, and references therein amounting to ~6000) for flagella presence with respect to the arrangement; irrespective of their internal ultrastructure (flagellin-based or tubulin-based), number, length and functionality (motile, non-motile or sensory) of the organelle on the cell. The comparison and purpose behind the work are entirely based on the common features in their physical properties and functions across species; this being, property of locomotion, sensory perception, made up of protein polymers, have ATPase or proton-motive forces, anchored to a basal body, sizes are about 2 mm - 40 mm, complex and made up of several proteins. In order to avoid the data being skewed, flagella information from 357 species (Eubacteria—115, Archaebacteria—129, Protista—37, Fungi—19, Plantae—19 and Animalia—38) are provided in this study. Such a survey led to a database for the presence or absence of the organelle, and its arrangement vis-à-vis the species classified using the classical method of taxonomical classification. As detailed in the methods, the database was queried and the percentage of species that have flagella within each phylum calculated. The percentages were calculated by the number of phyla having flagella verses total phyla in that particular kingdom. As depicted in Figure 1, the percentages of organisms (multicellular and/or unicellular) harboring or not harboring flagella varied with the phyla among all the kingdoms. For example, 80% of the phyla among Eubacteria have flagella, while only 20% of phyla in Archaebacteria showed flagella. In Protista, 77% phyla have flagella while in Fungi 10% phyla have flagella. In Plantae, 70% phyla have flagella. All the phyla (100%) in the Animalia kingdom have flagella or cilia. A noteworthy comment is that the flagella in the Fungi and Plantae kingdoms belong to the cells of the reproductive system (zoöspores).

Having depicted the gross variability in the presence and/or absence of flagella among different kingdoms, the flagellar arrangement of the cells was then categorized. Detailed observation of images of cells bearing flagella helped in making twenty-four categories of flagellar arrangements (Figure 2(a)). While, twenty-four arrangements of flagella were totally observed; any other arrangement considered “cryptic”; the latter type being the most prevalent (~23%; Figure 2(b)). Among the known categories, the predominating flagellar arrangements were of the polar type (~15%) followed by peritrichous (~11%) and lateral (~10%; Figure 2(b)). However, the other types of arrangements (multilateral, monopolar polytrichous, multitrichous, monotrichous, polar multiple

flagella, non motile monopolar, non motile monotrichous, polar monotrichous, polar polytrichous, longitudinal and transverse, subpolar, polar bundle, anterior, polytrichous, tufts, polar tufts, non motile flagella lateral, bipolar, apical, monopolar, polar and peritrichous, periplasmic, non motile, non motile cilia lateral, sub apical and non motile cilia, motile cilia, lateral) varied from 0.4% - 10% and were mere variations of the polar and peritrichous types (Figure 2(b)). Since flagella and/or cilia have an associated function of motility and therefore, a correlation between flagellar arrangements vis-à-vis motility sought (Figure 2(c)). Among all the motile flagella/cilia, the lateral (30%) arrangement was the most prevailing followed by polar (16%), peritrichous (14%) and secondary cilia (13%; Figure 2(c)). Flagellar arrangement diversity among motile organisms was vast; although the total number of organisms harboring such a variety ranged between 0.5% - 5% only. On the other hand, among the non-motile flagella/cilia, the primary cilia (seen in the Animalia kingdom) are the most widespread, followed by the peritrichous, monoand polytrichous categories (Figure 2(d)). Therefore, the first observation remains that the flagella which offer motility are predominately polar and peritrichous in nature and are prevalent among the Eubacteria (Figure 2(c)); the lateral flagella being found in fungi, plants and animals. Meanwhile, the flagella on non-motile cells are mainly found in Archaebacteria and Animalia kingdoms, predominate being monoor polytrichous group (Archaebacteria) (Figure 2(d)).

To gain an evolutionary perspective, the organisms harboring flagella from various kingdoms were separately scored for their flagellar arrangements (Figures 3(a)-(f)). These results show that flagellar arrangement diversity between the prokaryotes is higher (~13 in numbers) than that of eukaryotes (between 3 - 5). Nonetheless, the main flagellar arrangement remains of the polar and peritrichous types in prokaryotes and lateral among all the eukaryotes. In the Eubacteria kingdom, the polar flagella (34%) group predominates, followed by the peritrichous (28%) arrangement (Figure 3(a)). As observed, the peritrichous flagella are mainly seen in the pathogenic species of Eubacteria kingdom [19]. This further supports the idea put forth by Jensen in 1909 that the most primitive form of life would have been cells with polar flagella and in accordance, ancestors of prokaryotes [20,21]. Also, flagella conversion from one form to another is reported only among prokaryotes [8-10,22]. Incidentally, certain bacteria when grown at a higher temperature shed their flagella [23]. We observed that most of the organisms in Archaebacteria are without flagella (Figure 1). And among these 20% which harbor flagella, fifteen arrangements with the polar and peritrichous as widespread (Figure 3(b)). Those which have flagella are further classified based on cell motility. The flagella of non-motile cells have predominately peritrichous flagella. This flagella type is thinner than the peritrichous flagella seen in motile cells [24,25]. The flagella of motile cells are mainly polar type. As observed in Archaebacteria, similarly, most species in Protista kingdom are without flagella (Figure 1). In contrast, those that have flagella are of lateral, apical, sub-apical, anterior or longitudinal transverse types; the sub-apical (39%) is of the major type, followed by lateral (33%; Figure 3(c)). It is also observed that liverworts have unequal length flagella. In these unequal flagella, the shorter one is tensile and the longer one has the whiplash kind of movement [26]. From among the fungal species, the flagella are mainly found on the zoöspores and these are the lateral, apical and sub-apical types (Figure 3(d)). Except for some unicellular algal cells, the dominant type of flagella is lateral in the Plantae kingdom, (Figure 3(e)), and these are present on zoöspores. It is noteworthy that the apical and sub-apical type of flagellar arrangement is particularly found among lower marine plants such as seaweed and sea lettuce [27]. Along with the flagella, cilia are also observed throughout the Animalia kingdom; these are both motile and non-motile. The flagella are mainly on sperms, and the position is predominantly lateral (Figure 3(f)). In summary, if one considers only two major types of arrangements of flagella across kingdoms, and then looks closely at these types and their variations, one observes that variations of polar and peritrichous types are mostly among the bacterial species and not among the eukaryotes (Table 3). A clear transition from the polar, peritrichous to the only peritrichous types across evolution is markedly clear.

With the flagellar arrangement into consideration, a Dendogram (Figure 4) was constructed based on “flagella types” whose values were represented as “P” and “A” indicating presence or absence of flagella type respectively. During this process, differences between the Prokaryotic and Eukaryotic flagella types were observed to be stark and hence were segregated as two different classes. To get an in-depth insight of eukaroytic flagellar evolution, the protista and algal kingdoms were separated. The resultant Dendogram (Figure 4) gave an insight of organismal evolution based on the flagella types. Contrary to expectations, the tree depicts similarity between the Eubacteria and Archaebacteria with a similarity distance of 14 forming the first neighborhood. Protista, Algae, Fungi, Plantae, Animalia form a second neighborhood. Protista and Algae are more similar to one another and are joined at a similarity distance of 1. The composite taxon (1) Protista and algae is similar to Fungi at a similarity distance of 1.5 and hence forms the next composite taxon (2). The taxon (2) is similar to Plantae at a similarity distance of 1 forming taxon (3), while taxon (3) is similar to Animalia at a similarity distance of 6.75. The distinct arrival of two neighborhoods may be interpreted as the two distinct types of flagellar ultrastructures and proteomes in the prokaryotes and eukaryotes, respectively.

In conclusion, our hypothesis restricts to the understanding of flagellar position on prokaryotes in contrast to eukaryotes; this, because work on the molecular understanding about the flagella position on prokaryotes is well understood contrary to that in eukaryotes. Our working model (Figure 5) states that the primitive cell may have been non-motile coccus, with the propensity to form the Mycoplasmas or a rod-shaped bacterium. Suitable conditions, unknown until now, may have converted this bacterium into the motile, polar cell. Flagellum

Table 3. Flagellar and cellular parameters across evolution. Summary of various flagellar parameters used to compare across evolution. Note the increase in flagellation, motility, laterality and multicellularity with evolution.

position on such a bacterium would be decided by energy costs, the geometry of the cell versus placement of the flagellum and simultaneous origin of the genes responsible for deciding flagellum position on the cell; a wrong geometry would be a misfit and eventually be discarded. The gene responsible for the position and number of flagella per cell is guanosine 5c-triphosphate (GTP) -binding protein (FlhF); it correctly localizes the flagella in several bacterial species [11,28-31]. Furthermore, an interaction between the FlhF and another protein FlhG regulates the number of polar flagella in V. alginolyticus cells. FlhF, localized at the pole probably promotes the flagella assembly at the initiation point, namely, the MS ring. FlhG, a cytoplasmic protein that harbors a ras-like GTPase interacts with FlhF and inhibits its localization at the pole, thus repressing excessive flagellation [29-31]. On the other hand, a cell over-expressing FlhG protein, has no FlhF molecules to localize at the pole, thus failing to produce a polar flagellum. With no FlhG, most of the FlhF localizes at the pole, such cells producing multiple flagella or tufts at the pole. We conclude therefore, that a critical ratio of FlhF and FlhG protein expression eventually leads to variations in the flagella; and mutations within these genes leading to higher or lower ratios are essentially speciation events throughout evolution. Although homologs of FlhF and FlhG are found in eukaryotes, their role in flagella position and the number is something to our knowledge not been investigated. Hence, although energy costs of locomotion are small for bacteria, fluid mechanical forces in its environment (namely, the primordial soup) may have played a significant role during the evolution of the flagellum [32]. On the lines of changing the arrangements on the cell, it seems that stress plays a vital role. In contemporary bacteria, motility being associated with chemotaxis; the response to signals from the environment modulates the motion within the cell harboring the flagella. Such changes within the environment, associated with stress have shown that bacteria can change its flagellar arrangement from one form to the other [9,10,22], causing biofilms to form that again requires flagella help. However, a recent finding indicates that motility may have evolved before chemotaxis or favored without chemotaxis [3]; flagellar arrangement for the sole function of motility is over scored among bacteria in which they are predominantly polar to peritrichous. A curiously strange phenomenon seen in the organism, Candidatus Magnetoglobus multicellularis, a multicellular, magnetotactic prokaryote from a hypersaline environment is that, it forms structures with peritrichous flagella-a signature that reflects multicellularity in terms of our working hypothesis [33]. We, therefore, attribute a changing environment (stressful niches) that may regulate the levels of FlhF and/or FlhG genes, an added function of signal transduction and multicellularity as the chief factors responsible for the evolving arrangements in the flagella of cells from polar, peritrichous, sub-apical, apical to lateral throughout evolution. Analogously, eukaryotes with the classical “9 + 2” flagella/cilia arrangement also show changes from anterior flagella (Chlamydomonas reinhardtii) to the peritrichous form (Volvox carteri); this being a testable hypothesis [34].

Financial support to JSD was provided by the UM-DAE CBS, India.