Spider Cupiennius Salei Research Articles

Expression patterns of leg genes in the mouthparts of the spider Cupiennius salei (Chelicerata: Arachnida).

The leg genes extradenticle, homothorax, dachshund, and Distal-less define three antagonistic developmental domains in the legs, but not in the antenna, of Drosophila. Here we report the expression patterns of these leg genes in the prosomal appendages of the spider Cupiennius salei. The prosoma of the spider bears six pairs of appendages: a pair of cheliceres, a pair of pedipalps, and four pairs of walking legs. Three types of appendages thus can be distinguished in the spider. We show here that in the pedipalp, the leg-like second prosomal appendage, the patterns are very similar to those in the legs themselves, indicating the presence of three antagonistic developmental domains in both appendage types. In contrast, in the chelicera, the fang-like first prosomal appendage, the patterns are different and there is no evidence for antagonistic domains. Together with data from Drosophila this suggests that leg-shaped morphology of arthropod appendages requires an underlying set of antagonistic developmental domains, whereas other morphologies (e.g. antenna, chelicera) may result from the loss of such antagonistic domains.

Secondary neurons are arrested in an immature state by formation of epithelial vesicles during neurogenesis of the spider Cupiennius salei

BackgroundIn the spider Cupiennius salei about 30 groups of neural precursors are generated per hemi-segment during early neurogenesis. Analysis of the ventral neuromeres after invagination of the primary neural precursor groups revealed that secondary neural precursors arise during late embryogenesis that partially do not differentiate until larval stages.ResultsIn contrast to the primary groups, the secondary invaginating cells do not detach from each other after invagination but maintain their epithelial character and form so-called epithelial vesicles. As revealed by dye labeling, secondary neural precursors within epithelial vesicles do not show any morphological features of differentiation indicating that the formation of epithelial vesicles after invagination leads to a delay in the differentiation of the corresponding neural precursors. About half of the secondary neural precursor groups do not dissociate from each other during embryogenesis indicating that they provide neural precursors for larval and adult stages.ConclusionsSecondary neural precursors are arrested in an immature state by formation of epithelial vesicles. This mechanism facilitates the production of larval neural precursors during embryogenesis. I discuss the evolutionary changes that have occured during neural precursor formation in the arthropod group and present a model for the basal mode of neurogenesis.

Prospero and Snail expression during spider neurogenesis.

Analysis of early neurogenesis in the spider Cupiennius salei (Chelicerata, Aranea, Ctenidae) has shown that the cells of the central nervous system are recruited from clusters of cells that invaginate from the neuroectoderm. This is in contrast to Drosophila, where only single cells delaminate and become neuroblasts, the stem cells of the nervous system. In order to compare the processes further, we have cloned homologues of the pan-neural Drosophila genes prospero and snail from the spider and have analysed their RNA and protein expression pattern. We find that snail expression is transient and only a subset of neural cells expresses Snail protein at any given time, making it difficult to assess whether it is indeed a pan-neural gene in the spider. Prospero protein expression, on the other hand, is seen in all invaginating cells and continues throughout differentiation of the neurons. In contrast to Drosophila, asymmetric localization cannot be detected, even in cells that still divide. Our results provide no evidence for neuroblasts or stem cells in the spider, although there are a limited number of mitoses in the cells that are derived from the invaginating clusters. These aspects of spider neurogenesis are more similar to the neurogenesis process known from vertebrates.

Gene expression in spider appendages reveals reversal of exd/hth spatial specificity, altered leg gap gene dynamics, and suggests divergent distal morphogen signaling

Leg development in Drosophila has been studied in much detail. However, Drosophila limbs form in the larva as imaginal discs and not during embryogenesis as in most other arthropods. Here, we analyze appendage genes in the spider Cupiennius salei and the beetle Tribolium castaneum. Differences in decapentaplegic (dpp) expression suggest a different mode of distal morphogen signaling suitable for the specific geometry of growing limb buds. Also, expression of the proximal genes homothorax (hth) and extradenticle (exd) is significantly altered: in the spider, exd is restricted to the proximal leg and hth expression extends distally, while in insects, exd is expressed in the entire leg and hth is restricted to proximal parts. This reversal of spatial specificity demonstrates an evolutionary shift, which is nevertheless compatible with a conserved role of this gene pair as instructor of proximal fate. Different expression dynamics of dachshund and Distal-less point to modifications in the regulation of the leg gap gene system. We comment on the significance of this finding for attempts to homologize leg segments in different arthropod classes. Comparison of the expression profiles of H15 and optomotor-blind to the Drosophila patterns suggests modifications also in the dorsal—ventral patterning system of the legs. Together, our results suggest alterations in many components of the leg developmental system, namely proximal—distal and dorsal—ventral patterning, and leg segmentation. Thus, the leg developmental system exhibits a propensity to evolutionary change, which probably forms the basis for the impressive diversity of arthropod leg morphologies.

Neurogenesis in the spider: new insights from comparative analysis of morphological processes and gene expression patterns

While there is a detailed understanding of neurogenesis in insects and partially also in crustaceans, little is known about neurogenesis in chelicerates. In the spider Cupiennius salei Keyserling, 1877 (Chelicerata, Arachnida, Araneae) invaginating cell groups arise sequentially and in a stereotyped pattern comparable to the formation of neuroblasts in Drosophila melanogaster Meigen, 1830 (Insecta, Diptera, Cyclorrhapha, Drosophilidae). In addition, functional analysis revealed that in the spider homologues of the D. melanogaster proneural and neurogenic genes control the recruitment and singling out of neural precursors like in D. melanogaster. Although groups of cells, rather than individual cells, are singled out from the spider neuroectoderm which can thus not be homologized with the insect neuroblasts, similar genes seem to confer neural identity to the neural precursor cells of the spider. We show here that the pan-neural genes snail and the neural identity gene Krüppel are expressed in neural precursors in a heterogenous spatio-temporal pattern that is comparable to the pattern in D. melanogaster. Our data suggest that the early genetic network involved in recruitment and specification of neural precursors is conserved among insects and chelicerates.

Involvement of Notch and Delta genes in spider segmentation.

It is currently debated whether segmentation in different animal phyla has a common origin and shares a common genetic mechanism. The apparent use of different genetic networks in arthropods and vertebrates has become a strong argument against a common origin of segmentation. Our knowledge of arthropod segmentation is based mainly on the insect Drosophila, in which a hierarchical cascade of transcription factors controls segmentation. The function of some of these genes seems to be conserved among arthropods, including spiders, but not vertebrates. The Notch pathway has a key role in vertebrate segmentation (somitogenesis) but is not involved in Drosophila body segmentation. Here we show that Notch and Delta genes are involved in segmentation of another arthropod, the spider Cupiennius salei. Expression patterns of Notch and Delta, coupled with RNA interference experiments, identify many similarities between spider segmentation and vertebrate somitogenesis. Our data indicate that formation of the segments in arthropods and vertebrates may have shared a genetic programme in a common ancestor and that parts of this programme have been lost in particular descendant lineages.

From stress and strain to spikes: mechanotransduction in spider slit sensilla.

This review focuses on the structure and function of a single mechanoreceptor organ in the cuticle of spiders. Knowledge emerging from the study of this organ promises to yield general principles that can be applied to mechanosensation in a wide range of animal systems. The lyriform slit sense organ on the antero-lateral leg patella of the spider Cupiennius salei is unusual in possessing large sensory neurons, whose cell bodies are close to the sites of sensory transduction, and accessible to intracellular recording during mechanotransduction. This situation, combined with recent technical developments, has made it possible to observe and experiment with all the major stages of mechanosensation. Important findings include the approximate size, number and ionic selectivity of the ion channels responsible for mechanotransduction, the types of voltage-activated ion channels responsible for action potential encoding, and the mechanisms controlling the dynamic properties of transduction and encoding. Most recently, a complex efferent system for peripheral modulation of mechanosensation has been discovered and partially characterized. Much remains to be learned about mechanosensation, but the lyriform slit sense organ system continues to offer important opportunities to advance our understanding of this crucial sense.

Early neurogenesis in the horseshoe crab Limulus polyphemus and its implication for arthropod relationships.

Early neurogenesis in the horseshoe crab Limulus polyphemus and its implication for arthropod relationships.

Cupiennin 1d*: the cytolytic activity depends on the hydrophobic N-terminus and is modulated by the polar C-terminus

To investigate structural features modulating the biological activity of cupiennin 1 peptides from the spider Cupiennius salei, three truncated cupiennin 1d analogs were synthesized. The fact that their growth inhibiting effect on Gram-negative and Gram-positive bacteria, their lytic activity with human red blood cells and their insecticidal effect on Drosophila melanogaster correlates with structural properties shows that the hydrophobic N-terminal chain segment includes the major determinants of structure and activity. The polar C-terminus seems to modulate peptide accumulation at negatively charged cell surfaces via electrostatic interactions and has no important effect on the peptides’ amphipathic secondary structure.

Parasegmental organization of the spider embryo implies that the parasegment is an evolutionary conserved entity in arthropod embryogenesis

Spiders belong to the chelicerates, which is a basal arthropod group. To shed more light on the evolution of the segmentation process, orthologs of the Drosophila segment polarity genes engrailed, wingless/Wnt and cubitus interruptus have been recovered from the spider Cupiennius salei. The spider has two engrailed genes. The expression of Cs-engrailed-1 is reminiscent of engrailed expression in insects and crustaceans, suggesting that this gene is regulated in a similar way. This is different for the second spider engrailed gene, Cs-engrailed-2, which is expressed at the posterior cap of the embryo from which stripes split off, suggesting a different mode of regulation. Nevertheless, the Cs-engrailed-2 stripes eventually define the same border as the Cs-engrailed-1 stripes. The spider wingless/Wnt genes are expressed in different patterns from their orthologs in insects and crustaceans. The Cs-wingless gene is expressed in iterated stripes just anterior to the engrailed stripes, but is not expressed in the most ventral region of the germ band. However, Cs-Wnt5-1 appears to act in this ventral region. Cs-wingless and Cs-Wnt5-1 together seem to perform the role of insect wingless. Although there are differences, the wingless/Wnt-expressing cells and en-expressing cells seem to define an important boundary that is conserved among arthropods. This boundary may match the parasegmental compartment boundary and is even visible morphologically in the spider embryo. An additional piece of evidence for a parasegmental organization comes from the expression domains of the Hox genes that are confined to the boundaries, as molecularly defined by the engrailed and wingless/Wnt genes. Parasegments, therefore, are presumably important functional units and conserved entities in arthropod development and form an ancestral character of arthropods. The lack of by engrailed and wingless/Wnt-defined boundaries in other segmented phyla does not support a common origin of segmentation.

Neurotoxic Peptides in the Multicomponent Venom of the Spider Cupiennius Salei Part I. Primary Structure of Neurotoxic Peptides in Relation to their Biological Function

Beside other components, spider venom contains neurotoxically acting peptides which predominantly target a variety of different ion channels within the spider's prey. From the multicomponent venom of Cupiennius salei 13 toxic peptides (CSTX-1 – CSTX-13) were purified by a combination of gel filtration, cation-exchange chromatography, and reverse-phase HPLC. The amino acid sequence of two important neurotoxic peptides, CSTX-1 (74 residues, 8352.6 Da) and CSTX-9 (68 residues, 7530.9 Da), as well as CSTX-2a (61 residues, 6865.7 Da), a truncated form of CSTX-1, were determined by Edman degradation. Sequence comparison of CSTX-1 with CSTX-9 revealed an identity of 53% as well as identical positions of all eight cysteine residues. CSTX-1 and CSTX-9 share the same disulphide bridge pattern linking Cys1–Cys4, Cys2–Cys5, Cys3–Cys8 and Cys6–Cys7. This disulphide bridge pattern is also found in other spider toxins such as agatoxins and curtatoxins. CSTX-1 and CSTX-9 belong to the family of the ion channel toxins containing the inhibitor cystine knot structural motif with the consensus sequence: CX3-7CX3-10CX0-7CX1-8CX4-20C. CSTX-2a and CSTX-9, lacking the lysine-rich C-terminal tail of CSTX-1, exhibit a much lower toxicity for Drosophila melanogaster than CSTX-1, providing good evidence for the direct involvement of this lysine-rich C-terminal tail in the toxicity of CSTX-1.

Neurotoxic Peptides in the Multicomponent Venom of the Spider Cupiennius Salei Part II. Elucidation of the Disulphide-Bridge Pattern of the Neurotoxic Peptide CSTX-9 by Tandem Mass Spectrometry

The disulphide-bridge pattern of the CSTX-9 polypeptide present in the multicomponent venom of the spider Cupiennius salei was determined de novo by nano-electrospray tandem mass spectrometry. Cleavage of native CSTX-9 with immobilized trypsin resulted in four disulphide-linked peptides with a mass of 2953.43 Da, which were subjected to low-energy collision-induced dissociation (CID) in a hybrid quadrupole time-of-flight (QqTOF) mass spectrometer. The product ion spectra not only provided sequence information of the peptides, the occurrence of characteristic fragment ions generated by cleavage of the peptide bonds adjacent to the bridged cysteines also allowed the disulphide-bridge pattern to be identified unambiguously. CSTX-9 was found to be a member of the neurotoxic polypeptide family incorporating the inhibitor cystine knot (ICK) structural motif. The results demonstrate the potential of modern analytical instrumentation for elucidation of complex molecular structures.

The venom optimisation hypothesis: a spider injects large venom quantities only into difficult prey types

The spider Cupiennius salei needs 0.01–10 μl venom to kill a prey item. Since its venom glands contain only 10 μl and regeneration requires 8–16 days C. salei should use its venom very economically. By a monoclonal antibody we measured, for the first time, the amounts of venom injected by a spider into different prey types. Crickets and stick insects, as victims without special defence mechanism, received only the minimum amount of venom which is not significantly different from the LD 50. Blowflies and ground beetles received considerably more venom because they are difficult to overwhelm or even endanger the spider by their defence behaviour. These results support our venom optimisation hypothesis which supposes that spiders use their venom as economically as possible.

Conservation and variation in Ubx expression among chelicerates.

Chelicerates are an ancient arthropod group with a distinct body plan composed of an anterior (prosoma) and a posterior portion (opisthosoma). The expression of the Hox gene Ultrabithorax (Ubx) has been examined in a single representative of the chelicerates, the spider Cupiennius salei. In spiders, Ubx expression starts in the second opisthosomal segment (O2). Because the first opisthosomal segment (O1) in spiders is greatly reduced relative to other chelicerates, we hypothesized that the observed Ubx expression pattern might be secondarily modified. Shifts in the anterior boundary of the expression of Ubx have been correlated with functional shifts in morphology within malacostracan crustaceans. Thus, the boundary of Ubx expression between chelicerates with different morphologies in their anterior opisthosoma could also be variable. To test this prediction, we examined the expression patterns of Ubx and abdominal-A (collectively referred to as UbdA) in two basal chelicerate lineages, scorpions and xiphosurans (horseshoe crabs), which exhibit variation in the morphology of their anterior opisthosoma. In the scorpion Paruroctonus mesaensis, the anterior border of early expression of UbdA is in a few cells in the medial, posterior region of the O2 segment, with a predominant expression in O3 and posterior. Expression later spreads to encompass the whole O2 segment and a ventral, posterior portion of the O1 segment. In the xiphosuran Limulus polyphemus, early expression of UbdA has an anterior boundary in the segment. Later in development, the anterior boundary moves forward one segment to the chilarial (O1) segment. Thus, the earliest expression boundary of UbdA lies within the second opisthosomal segment in all the chelicerates examined. These results suggest that rather than being derived, the spider UbdA expression in O2 likely reflects the ancestral expression boundary. Changes in the morphology of the first opisthosomal segment are either not associated with changes in UbdA expression or correlate with late developmental changes in UbdA expression.

Neurogenesis in the spider Cupiennius salei.

To uncover similarities and differences in neurogenesis in arthropod groups, we have studied the ventral neuroectoderm of the spider Cupiennius salei (Chelicerata, Aranea, Ctenidae). We found that invaginating cell groups arose sequentially, at stereotyped positions in each hemisegment and in separate waves, comparable with the generation of neuroblasts in Drosophila. However, we found no evidence for proliferating stem cells that would be comparable with the neuroblasts. Instead, the whole group of invaginating cells was directly recruited to the nervous system. The invagination process is comparable with Drosophila, with the cells attaining a bottle-shaped form with the nuclei moving inwards, while actin-rich cell processes remain initially connected to the surface of the epithelium. This general pattern is also found in another spider, Pholcus phalangioides, and appears thus to be conserved at least among the Araneae. We have identified two basic helix-loop-helix encoding genes -- CsASH1 and CsASH2 -- that share sequence similarities with proneural genes from other species. Functional analysis of the genes by double-stranded RNA interference revealed that CsASH1 was required for the formation of the invagination sites and the process of invagination itself, whereas CsASH2 seemed to be required for the differentiation of the cells into neurones. Our results suggest that the basic processes of neurogenesis, as well as proneural gene function is conserved among arthropods, apart of the lack of neuroblast-like stem cells in spiders.

Arthropod touch reception: stimulus transformation and finite element model of spider tactile hairs.

Striving towards an in depth understanding of stimulus transformation in arthropod tactile hairs, we studied the mechanical events associated with tactile stimulation. A finite element model was developed taking a tarsal tactile hair of the spider Cupiennius salei as an example. Considering hair diameter, wall thickness, and curvature, the hair is subdivided into six regions each with its specific mechanical properties. When the hair is touched from above with a flat surface oriented parallel to the tarsus the point of stimulus contact moves towards the hair base with increasing load and hair deflection. Thereby the effective lever arm is reduced protecting the hair against breaking near its base. At the same time the mechanical working range of the hair increases implying higher mechanical sensitivity for small deflections (about 5x10(-5) N/degrees) than for large deflections (about 1x10(-4) N/degrees). The major stresses within the hair shaft are axial stresses due to bending. The position of stress maxima moves along the shaft with the movement of the stimulus contact point. Remarkably, the amplitude of this maximum (about 1x10(5) N/m2) hardly changes with increasing loading force due to the way the hair shaft is deflected by the stimulus.

ChemInform Abstract: Identification of a New Sex Pheromone from the Silk Dragline of the Tropical Wandering Spider Cupiennius salei.

AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Double-stranded RNA interference in the spider Cupiennius salei : the role of Distal-less is evolutionarily conserved in arthropod appendage formation

Chelicerates represent a basal arthropod group, which makes them an excellent system for the study of evolutionary processes in arthropods. To enable functional studies in chelicerates, we developed a double-stranded RNA-interference (RNAi) protocol for spiders while studying the function of the Distal-less gene. We isolated the Distal-less gene from the spider Cupiennius salei. Cs-Dll gene expression is first seen in cells of the prosomal segments before the outgrowth of the appendages. After the appendages have formed, Cs-Dll is expressed in the distal portion of the prosomal appendages, and in addition, in the labrum, in two pairs of opisthosmal (abdominal) limb buds, in the head region, and at the posterior-most end of the spider embryo. In embryos, in which Dll was silenced by RNAi, the distal part of the prosomal appendages was missing and the labrum was completely absent. Thus, Dll also plays a crucial role in labrum formation. However, the complete lack of labrum in RNAi embryos may point to a different nature of the labrum from the segmental appendages. Our data show that the expression of Dll in the appendages is conserved among arthropods, and furthermore that the role of Dll is evolutionarily conserved in the formation of segmental appendages in arthropods.

Female sex pheromone of a wandering spider (Cupiennius salei): identification and sensory reception.

Females of the wandering spider Cupiennius salei attach a sex pheromone to their dragline. Males encountering the female dragline examine the silk thread with their pedipalps and then typically initiate reciprocal vibratory courtship with the sexual partner. The female pheromone was identified as (S)-1,1'-dimethyl citrate. The male pheromone receptive sensory cells are located in tip pore sensilla and respond to touching the sensillum tip with female silk or pieces of filter paper containing the synthetic pheromone.

Identification of a New Sex Pheromone from the Silk Dragline of the Tropical Wandering Spider Cupiennius salei.

The courtship-inducing pheromone of female Cupiennius salei spiders has been identified as the asymmetric dimethyl citrate 1 by NMR investigations and synthesis. Only the S enantiomer is biologically active. This identification enabled the characterization of a spider pheromone sensillum for the first time.