Profiling the resting venom gland of the scorpion Tityus stigmurus through a transcriptomic survey
© Almeida et al.; licensee BioMed Central Ltd. 2012
Received: 15 October 2011
Accepted: 27 June 2012
Published: 1 August 2012
The scorpion Tityus stigmurus is widely distributed in Northeastern Brazil and known to cause severe human envenoming, inducing pain, hyposthesia, edema, erythema, paresthesia, headaches and vomiting. The present study uses a transcriptomic approach to characterize the gene expression profile from the non-stimulated venom gland of Tityus stigmurus scorpion.
A cDNA library was constructed and 540 clones were sequenced and grouped into 153 clusters, with one or more ESTs (expressed sequence tags). Forty-one percent of ESTs belong to recognized toxin-coding sequences, with transcripts encoding antimicrobial toxins (AMP-like) being the most abundant, followed by alfa KTx- like, beta KTx-like, beta NaTx-like and alfa NaTx-like. Our analysis indicated that 34% of the transcripts encode “other possible venom molecules”, which correspond to anionic peptides, hypothetical secreted peptides, metalloproteinases, cystein-rich peptides and lectins. Fifteen percent of ESTs are similar to cellular transcripts. Sequences without good matches corresponded to 11%.
This investigation provides the first global view of gene expression of the venom gland from Tityus stigmurus under resting conditions. This approach enables characterization of a large number of venom gland component molecules, which belong either to known or non yet described types of venom peptides and proteins from the Buthidae family.
Scorpion morphology has changed little over the last four hundred million years. In the other hand, they naturally developed venom glands as a special weapon used in prey and defense. Tityus stigmurus belongs to the Buthidae family, widely distributed around the world and comprising all the species considered of medical interest . In Brazil, scorpions from the genus Tityus are responsible for most reported envenomation accidents, primarily Tityus serrulatus, Tityus stigmurus and Tityus bahiensis. T. stigmurus is the main causal agent of scorpionism in the Northeast; its envenomation is often characterized by local symptoms, such as: pain (94.4%), hyposthesia (30%), edema (17.8%), erythema (17.8%) and paresthesia (15.6%) . Nishikawa  reported that T. stigmurus venom is the most toxic (DL50 = 0.773mg/kg) when compared to T. serrulatus and T. bahiensis. Nevertheless, T. serrulatus is the only species that has been significantly studied.
In addition to their clinical relevance, scorpion venoms are known to contain a very complex mixture of biologically active compounds . Of these, neurotoxins are the most studied and play a key role in the pathogenesis of scorpionism. These toxins are small peptides that interact with several types of ion channels, modifying the electrical activity of excitable cells . The most widely known ion channels recognized by these molecules are Na+ channels , K+ channels , ryanodine sensitive Ca2+ channels , T-type Ca2+ channels [10, 11] and Cl- channels . Their properties make these peptides useful as molecular and pharmacological tools for studying ion channels. Another noteworthy class of molecules present in the venom gland are antimicrobial peptides, which may be involved in ancient innate immunity . There are an estimated 150,000 distinct polypeptides found in the approximately 1500 known scorpion species worldwide , representing a broad scope for drug research and development.
The venoms of T. stigmurus T. serrulatus and T. bahiensis have similar toxic components and display a high degree of cross reactivity between specific antiserums [15–18]. Earlier studies reported the sequence of some T. stigmurus toxins, homologous to the previously known gama, III-8 and IV-5 toxins from T. serrulatus. These were named Tst-1, Tst-2 and Tst-3, respectively,  and are toxic to mice, recognizing Na-channels through different modes of action [19, 20]. Holaday et al.  purified butantoxin, a K-channel blocker from the three medically important Tityus species mentioned above. Potassium channel toxins were also predicted in Tityus stigmurus venom using a proteomic approach .
Although the scorpion venom repertoire has been extensively investigated by PCR-based methods conducted with cDNA libraries [23–25], this strategy, in addition to cloning, isolation and characterization procedures, is limited by the specificity of the PCR primers used. In recent years, the number of proteomic and transcriptomic analyses performed has increased [26–35], since they are better able to assess venom diversity. Thus, in addition to known venom peptides and proteins, non yet described molecules can also be obtained. Moreover, transcriptomics has the advantage of providing insight into biological processes occurring in venom gland cells.
Previous investigations have used milked scorpion glands to achieve an enriched toxin library [26, 27, 29, 30]; however, only one used a so called “replete” venom gland not actively engaged in regenerating venom . Few scorpion nucleotide sequences are currently deposited in public databases, particularly for the Tityus genus, despite its clinical importance. The present study describes the transcriptomic expression of T. stigmurus scorpion from non-stimulated venom glands, using specimens collected in the urban area of Natal, Brazil.
Results and discussion
Overview of ESTs from the venom gland of T. stigmurus
Sequence clusters were denominated TSTI0001C to TSTI0037C, for clusters with more than one EST, or TSTI0038S to TSTI0153S for those containing only one EST. When compared to data from GenBank and dbEST, we found that of the 153 clusters (540 clones) identified, 113 exhibited significant similarities to known cDNA and protein sequences. This corresponds to 486 clones (90%); the remaining 54 (10%) were not identified and defined as “no hit”. Six clusters exclusively matching mitochondrial DNAs, mRNAs and ribosomal RNAs were also found and excluded from quantitative analyses.
Identification of high-abundance transcripts present in T. stigmurus venom glands
Number of clusters
Number of clones
% of total
hypothetical secreted peptide*
Potassium channel toxins (α-KTX, β-KTX)
TSTI0003C may be a new member of this orthologous genes family, displaying greater similarity to β-KTX genes from T. costatus (gb|Q0GY45) and T. trivitattus (gb|Q0GY42) when compared to the other family members (Figure5B).
Sodium channel toxins (α-NaTX, β-NaTX)
Another similar case was that of Hottentota judaicus scorpion “resting” venom glands, where sodium channel toxins were underrepresented and the αNaTx:βNaTx ratio inversed . Sequences matching Tst-1 (TSTI0051S), Tst-2 (TSTI0033C) and Tst-3 (TSTI0151S) were also found in this group.
AMPs (antimicrobial peptides)
Other possible venom molecules
Some transcripts found in T. stigmurus venom glands resembled putative molecules with potential toxic activity and were therefore classified as ‘other possible venom molecules’. Five groups fit into this category: Lectins, Metalloproteases, Anionic Peptides, Hypothetical Secreted Peptides and Cystein-Rich peptides.
Lectins have not been reported for scorpions in transcriptomic, proteomic or related approaches. As such, to the best of our knowledge, there are no scorpion lectin sequences currently deposited in public databases, although lectins have been isolated from scorpion venom and hemolymph using chromatographic procedures [47, 48]. Despite the lack of information on lectins in scorpion venoms, they have been studied in other venomous animals, such as fish, snakes and spiders [49–51] and may be involved in innate immunity. Our library contains two clusters (TSTI0068S and TSTI0118S) with arthropod lectin-like sequences.
Alhough scorpion venom research has focused primarily on neurotoxic peptides, proteolytic activity has also been described [53, 54]. Two types of proteases have already been characterized in scorpion venom glands: serineproteases (SPSVs) and metalloproteases [27, 28, 55]. Serine- and metalloproteases were also detected in venom transcriptomic analysis of other animals [51, 56]. Despite the lack of transcripts similar to SPSVs, metalloproteases are significantly represented by 6 clusters (7 clones). Four of these are similar to antareases, a venom protein from T. serrulatus. Antarease is a divalent ion-dependent protease that cleaves vesicle-associated membrane proteins (VAMPs) at specific sites, leading to significant alterations in vesicular transport and secretory mechanisms. This action may be involved in pathogenesis mechanisms, including acute pancreatitis induction . An additional two clusters encode for putative M13 metalloprotease and angiotensin converting enzymes from the Hottentotta Judaicus scorpion.
Hypothetical secreted peptides
Cysteine-rich secretory peptides
Cystein-rich secretory peptides (CRISPs) are widely distributed in the animal, plant and fungal kingdoms, with variable primary sequences [62–64], including different animal venoms [28, 62, 65]. The SCP_CRISP-like domain containing sequence is a cluster with 2 clones (TSTI0017C), similar to other arachnid and insect cysteine-rich peptides. Interestingly, as with helothermine , lizard venom CRISPs block Ca++ transporting ryanodine receptors, while the opposite action is reported for neurotoxins belonging to the calcin family found in scorpions .
The first analysis of a non-Buthidae scorpion resulted in 147 high-quality ESTs, which allowed the authors to examine the molecular repertoire of the venom gland . Similar approaches have been applied with Buthidae and non-Buthidae scorpions species, showing marked differences in diversity and repertoire of toxin-like sequences . The venom components commonly found in transcriptomics are sodium channel toxins, potassium channel toxins, calcines, AMPs, BPPs, phospholipases A2, anionic peptides and glycine-rich peptides. Of these, only calcines, phospholipases A2 and glycine-rich peptides were not found in this study. The main novelty of this investigation is to present some poorly or as yet undescribed transcripts in scorpion venoms such as: lectins, metaloproteases, cystein-rich peptides and hypothetical secreted proteins.
Scorpion venom proteome studies have been previously carried out, although most components have not been sequenced [27, 32, 33, 35]. Thus, a comparative proteomic analysis with other scorpion venoms is difficult to obtain. Nevertheless, the following transcripts match proteins found in Tityus sp. venom itself, using either proteomics or isolation and characterization approaches, as follows: TSTI0022C (hypothetical secreted peptide, similar to Peptide 9797, gb|P0C8X1), TSTI0051S (sodium channel toxin, similar to Tst1, gb|P56612), TSTI0033C (sodium channel toxin, similar to Tst2, gb|P68411), TSTI0151S and TSTI0048S (sodium channel toxin, similar to Tst3, gb|P0C8X5), TSTI0109S (potassium channel toxin, similar to Tst-17, gb|P0C8L2), TSTI0140S (potassium channel toxin, similar to Tst26 gb|P0CB56), TSTI0016C (potassium channel toxin, similar to Ts15 gb|P86270), TSTI0075S (potassium channel toxin, similar to TsPep2, gb|P0C175), TSTI0006C (Hypotensin-II, gb|P84190) and some Antareases-like sequences (gb|P86392).
The majority of transcripts involved in ‘cellular metabolism’ are similar to cytochrome c oxidase (3 clusters/ 12 ESTs), followed by arginine kinase (1 cluster/ 7 ESTs). Clusters TSTI0014C, TSTI0037C and TSTI0065S are similar to cytochrome c oxidase subunits 1 or 2. TSTI0014C resembles cytochrome c oxidase subunit 1 from Centruroides noxius. The terminal oxidase in respiratory chains of eukaryotes and most bacteria, is a multi-chain transmembrane protein located in the inner membrane of mitochondria and the cell membrane of prokaryotes (gb| AY995829.1). In parallel, cluster TSTI0013C (group of 7 ESTs) is similar to arginine kinase (represented in group 8, from Table1) from Litopenaeus vanname shrimp. Members of this enzyme family play a key role in animals as ATP-buffering systems for cells with high and variable rates of ATP turnover (gb| DQ975203.1).
The venom gland is an organ specialized in venom production, with almost 75% of the transcripts ‘known’ or ‘possible’ toxins. We can therefore assume that a substantial metabolic expenditure is required for this task, resulting in a natural demand for energy and transcription/translation functions. The next most abundant transcripts were ‘structural proteins’ (11 clones, 8 clusters) such as actin and myosin. The presence of these transcripts is not surprising, since telson is known to contain compressor muscles, whose function is to press the glands against the cuticle along its exterior lateral and ventral surfaces . Cluster TSTI0018C (group of 3 ESTs) exhibits similarity with myosin light chain 2 from the Avicularia avicularia spider, a Ca2+-binding protein (EF-Hand superfamily) (gb| 3DTP_E).
Other relevant categories were ‘cell regulation’ (6 clusters/ 8 ESTs), ‘processing and sorting’ (3 ESTs) and transcripts with unknown functions (7 clusters/ 8 ESTs). In the last, we found 5 clusters matching ‘hypothetical proteins’ from arachnids (Ixodes scapularis and Tityus discrepans).
Taken together, these results represent important clues for the characterization of cellular and molecular functions in scorpion venom glands. Moreover, the repertoire generated in this approach is relevant in highlighting the transcripts of T. stigmurus venom glands, contributing to the international “Genbank” database and allowing subsequent isolation and application of these molecules.
The present study describes the profile of gene expression present in the venom glands of Tityus stigmurus scorpions using a transcriptomic approach. This profile shows a wide range of structural and functional putative molecules in Tityus stigmurus venom glands. Six known protein types were identified, including ‘potassium channel’ (sub-families α and β) , ‘sodium channel’ (subfamilies α and β), ‘hypotensins’ and ‘antimicrobial peptides’, and five atypical types of venom peptides and proteins, such as ‘lectins’, ‘anionic peptides’, ‘metalloproteases’, ‘hypothetical secreted peptides’ and ‘cystein-rich peptides’. This strategy confirms the highly specialized nature of scorpion venom glands as toxin producers, enabling the description, for the first time, of putative proteins involved in cellular processes relevant to venom gland function of T. stigmurus. In particular, transcripts encoding antimicrobial peptides and anionic peptides were the most representative transcripts in this database. The transcriptome of T. stigmurus did not show high expression of sodium channel toxins as one might expect from a Buthidae scorpion, primarily for subfamily α. This type of toxin is the most studied among scorpions from the genus Tityus and has often been related to the severity of poisoning. Its absence may be associated to environmental conditions, where more antibacterial defenses may be required than neurotoxins for prey, since food is abundant. It may also be a characteristic of scorpion venom-filled glands in a resting stage.
This database of scorpion molecules described here may be an important resource for the investigation and characterization of proteins or peptides potentially applicable in pharmaceutical research and biotechnology.
cDNA library construction
A cDNA library was constructed from total RNA extracted from four telsons. Specimens were collected in the urban region of Natal, Brazil. The 'total RNA isolation system' of Promega (Madison, WI) was used for RNA isolation. With this material, a full-length cDNA library was prepared using the In-Fusion™ SMARTer™ cDNA Library Construction Kit (CLONTECH Lab., Palo Alto, CA). The titre of the non-amplified cDNA library obtained was 2 × 104 cfu/mL with 90% recombinant clones. Reverse transcription used SMARTer II A and 3' SMART CDS Primer II A oligonucleotides. Next, 5' PCR Primer II A was employed for PCR amplification. Resulting cDNAs were bidirectionally cloned in the pSMART2IF plasmid (all components were from the CLONTECH Lab, Palo Alto, CA). Escherichia coli DH10β cells were transformed with cDNA library plasmids and plated on Luria-Bertani agarose plates containing 100 μg/mL ampicilin.
DNA sequencing and bioinformatic analyses
Random clones were grown in antibiotic selective medium for 22 h and plasmid DNA was isolated using alkaline lysis . DNA was sequenced on an ABI 3100 sequencer, using a BigDye2 kit (Applied Biosystems, Foster City, CA) and the standard M13 reverse primer. In order to extract the high quality sequence region, ESTs were subjected to the Phred program, with a cutoff Phred score of 20 in a window length of 75 bases . Sequences were processed by removing vector, adaptors and E. coli DNA sequences using CrossMatch . High-quality ESTs were assembled into contigs, using the CAP3 program  set to combine only those sequences with at least 98% base identity. To assign annotation to the assembled ESTs (clusters), these sequences were searched against nr and nt (E values < 1e-05) for homologous comparison using BLASTX and BLASTN , supported by the Blast2GO . Metadata and bibliographic information, when available, were manually inspected to assign putative functional classification of the cluster. Additionally, proteins coded by the clusters were grouped according to possible participation in the venom. Three categories were established: 'known toxins', 'other possible venom molecules' or 'cellular proteins' for proteins with best hits to well-known scorpion venom toxins, proteins with hits to non-scorpion toxin sequences exhibiting activities compatible with toxic venom action, and other products related to cellular functions without evidence of being toxins, respectively. The presence of conserved domains, using the nr protein database or SMART  and Pfam , was also used to guide functional attribution. The occurrence of signal peptide was predicted with the SignalP 3.0 program , using both neural networks (NN) and hidden Markov models (HMM). A secretory protein was considered when both methods showed a signal peptide according to their default parameters (mean S > 0.048 and mean D score 0.43 > in NN and signal peptide probability > 0.5 in HMM).
Alignment and dendogram
This research was supported by grants from CNPq. MdFF–P, IdLMJ–d–A, KCS, LFA-L and SRBM are researchers from CNPq.
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