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The peptidergic signaling system is an ancient cell–cell communication mechanism that is involved in numerous behavioral and physiological events in multicellular organisms. We identified two novel neuropeptides in the neuronal projections innervating the salivary glands of the blacklegged tick, Ixodes scapularis (Say, 1821). Myoinhibitory peptide (MIP) and SIFamide immunoreactivities were colocalized in the protocerebral cells and their projections terminating on specific cells of salivary gland acini (types II and III). Immunoreactive substances were identified by matrix-assisted laser desorption/ionization-time of flight (MALDITOF) analysis: a 1,321.6-Da peptide with the sequence typical for MIP (ASDWNRLSGMWamide) and a 1,395.7-Da SIFamide (AYRKPPFNGSIFamide), which are highly conserved among arthropods. Genes encoding these peptides were identified in the available Ixodes genome and expressed sequence tag (EST) database. In addition, the cDNA encoding the MIP prepropeptide was isolated by rapid amplification of cDNA ends (RACE). In this report, we describe the anatomical structure of specific central neurons innervating salivary gland acini and identify different neuropeptides and their precursors expressed by these neurons. Our data provide evidence for neural control of salivary gland by MIP and SIFamide from the synganglion, thus leading a basis for functional studies of these two distinct classes of neuropeptides.
Ticks are obligatory external parasites that feed on the blood of mammals, birds, and reptiles and often transmit pathogenic viruses, Rickettsiae, bacteria, and protozoa. Tick-borne diseases cause substantial economic loss in the animal industry and present risks for human health. The black-legged tick, Ixodes scapularis, transmits the most important tick-borne pathogen, Borrelia burgdorferi, which causes Lyme disease. More than 20,000 new cases are reported per year in the United States, in 46 states. This species also transmits other diseases, including human babesiosis Babesia microti and human granulocytic ehrlichiosis.
Salivary secretions of ticks are essential during feeding for manipulation and suppression of host defense responses and might represent key components in the transmission of pathogens. The salivary glands of the tick consist of numerous spherical acini (also named alveoli) that form grape-like clusters on the branches of excretory ducts. There are three different types of acini in female ticks: I, II, and III. Nongranular (type I) acini, attached to the main salivary duct, do not change size during feeding, whereas other acini increase in size. Granular acini (types II and III) differ in the number and structure of granule-secreting cells; acini III are more peripherally located (Binnington, 1978; Coons and Roshdy, 1973; Krolak et al., 1982). Each type of acinus contains multiple cell types, including different types of secretory and epithelial cells (Balashov et al., 1983; Sauer et al., 1995; Sonenshine, 1993). Studies with transmission electron microscopy have discovered that axon terminals reach the basal region of the acini, indicating that there is neuronal control of the salivary glands (Balashov et al., 1983; Coons and Alberti, 1999). Recently, we have described the neuroanatomy of peptidergic cells in the nervous system, including the neurons and axonal projections that innervate tick salivary glands (Šimo et al., 2009).
Previous immunohistochemical studies have indicated that the tick nervous system is a rich source of diverse neuropeptides related to those that have been identified in insects, crustaceans, and vertebrates (Davis et al., 1994;Šimo et al., 2009; Zhu and Oliver, 1991; Zhu et al., 1995). Periviscerokinin was the first conserved neuropeptide identified in ticks by using matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) analysis of single neurons (Neupert et al., 2005). Molecular cloning and functional analysis of the G-protein-coupled receptor for a kinin-like peptide in the southern cattle tick, Boophilus microplus, further suggested that ticks produce multiple neuropeptides and receptors similar to those identified in other arthropods (Holmes et al., 2000, 2003; Taneja-Bageshwar et al., 2006). We recently described the complex neuroendocrine network present in the central and peripheral nervous systems of the hard tick, Rhipicephalus appendiculatus, by using 15 different antibodies that recognize various neuropeptides (Šimo et al., 2009). Four of these antibodies identified peptidergic neurons innervating the main salivary ducts (RFamide and tachykinin) or salivary gland acini [myoinhibitory peptide (MIP) and pigment-dispersing factor (PDF)]. In the present study, we further explored the peptidergic system in the salivary glands of I. scapularis by using MALDI and identified MIP and SIFamide. The genes encoding these peptides were cloned. By using immunohistochemistry and in situ hybridization, we detected coexpression of these neuropeptides in a pair of giant central neurons that projected axons along salivary ducts and terminated on specific acini type II and III.
Unfed I. scapularis female ticks were obtained from the tick-rearing facility at Oklahoma State University. A colony of I. scapularis was kept in polypropylene vials (9 × 2.5 cm) with the openings covered by cotton plugs. Each vial contained approximately 30 females and a small sheet (4 × 1 cm) of filter paper. These vials were kept in a dark and humid chamber at 4°C. All experiments described in this study were performed with 1–2-month-old unfed females.
Search in NCBI trace archives, the EST database and VectorBase (www.vectorbase.org) yielded fragments of DNA sequences encoding putative MIP and SIFamide, respectively. Multiple EST clones encoding SIFamide were found in addition to the gene fragment identified in the genome sequence. To obtain the entire cDNA sequence encoding MIP, we designed primers on the basis of the predicted coding sequences and performed reverse transcript polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends (RACE). The PCR product was cloned into the pGEM-T-easy vector (Promega, Madison, WI) and sequenced. The forward primers used for amplification of the mip gene for 3′RACE were 5′-GACTGGAACGCGCTGTCAGGC-3′ and nested 5′-AGCGACTGGAATCGCCTCT-3′, corresponding to positions 203–223 and 242–260, respectively (Fig. 1B). The reverse primers used for 5′RACE were 5′-TGTGTCGAAGCCGCGCGCTTCC-3′ and nested 5′-GATCGTTCCAGTGGTTCTCCCG-3′, corresponding to positions 430–451 and 386–407, respectively (Fig. 1B). We used the Signal P 3.0 server for annotations of signal peptides (Emanuelsson et al., 2007).
Single-stranded DNA containing digoxygenin dNTP was prepared by using asymmetric PCR. A 248-nucleotide probe for mip (203–451 in Fig. 1B) was generated by using the primers 5′-GACTGGAACGCGCTGTCAGGC-3′ (forward) and 5′-TGTGTCGAAGCCGCGCGCTTCC-3′ (reverse). For sifamide, a 190-nucleotide probe (119–308 in Fig. 2B) was made by using the primers 5′-TGGTGATGGCGGTCATGATGAA-3′ (forward) and 5′-TGTCGCTACTGCGCGCCATCCT-3′ (reverse). Freshly dissected synganglia were fixed in 4% paraformaldehyde for 2 hour at room temperature (RT) and washed in PBST (PBS + 0.2% Triton). The tissues were treated with 10 μg/ml proteinase K for ~12 minutes at RT. The reaction was terminated by adding PBST-glycine (2 mg/ml glycine) for 5 minutes. Samples were refixed in 4% paraformaldehyde at RT and washed in PBST three times for 5 minutes each. Prehybridization (10–20 minutes) was followed by hybridization with the respective probes in hybridization solution (HS; 50% formamide, 5× SSC, 50 μg/ml heparin, 0,1% Tween 20, and 100 μg/ml salmon sperm DNA) containing the digoxigenin-labeled probe (Roche Molecular Bio-chemicals) for ~27 hours at 48°C in a humidified chamber. After hybridization, tissues were washed sequentially in HS (48°C), HS-PBST (1:1), and PBST twice at RT. After blocking in 100 μl 1% BSA in PBST for 20–30 minutes in RT, the tissues were immediately incubated with sheep antidigoxigenin-AP (alkaline phosphatase; Roche Diagnostick, Germany) at 1:1,000 in PBST overnight at 4°C. Tissues were washed three times with alkaline phosphatase (AP) buffer (100 mM Tris, pH 9.5, 50 mM MgCl2, 100 mM NaCl, and 0.1% Tween 20). Color was developed by incubation with NBT-BCIP (nitroblue tetra-zolium chloride and 5-bromo-4-chloro-3-indol phosphate; Roche) solution diluted in AP buffer at 1:50. The synganglia were mounted in glycerol and examined under a microscope (Nikon Eclipe E800) with Nomarski differential interference optics. Digital image were captured with a CoolSnap ES2 and enhanced in Adobe Photoshop 7.0.
Extracts of synganglia and salivary glands were analyzed by a MALDI-TOF mass spectrometer. Ten synganglia and ten pairs of salivary glands were dissected simultaneously in 20 μl ice-cold PBS containing 1% trifluoroacetic acid (TFA; Fisher Scientific, Fair Lawn, NJ), pH 4. Each tissue was sonicated for 10 seconds in a glass tube and centrifuged at 12,000g for 5 minutes at RT. The resulting supernatant was loaded onto an equilibrated ZipTip C18 column (Millipore, Bedford, MA) and eluted with 4 μl of a solution containing 0.1% TFA and 70% acetonitrile (ACN; Fisher Scientific). Matrix α-cyano-4-hydroxycinnamic-acid (CHCA; saturated solution in ACN/0.1% TFA acid 1:2) was freshly prepared. A 4-μl volume of CHCA was mixed with 1 μl of eluted sample, and 1 μl of the admixture (matrix/sample 4:1) was spotted and dried on a MALDI sample plate at RT.
We used an Ultraflex II TOF/TOF mass spectrometer (Bruker Daltonics, Bremen, Germany). Mass spectra were acquired in reflector positive ion mode. All acquisitions were made in manual mode in Flex Control 3.0 software. Tandem mass spectrometry of the two peaks [M + H]+ 1,322 and 1,396 provided partial sequences under laser-induced dissociation (LID) conditions upon analysis with the Flex Analysis 3.0 software package. The obtained partial sequences were compared with the genomic sequence data. For final confirmation of the sequences, we compared the MALDI-TOF results with synthetic MIP (ASDWNRLSGMWamide) and SIFamide (AYRKPPFNGSIFamide). Both synthetic peptides had ~80% or higher purity on MALDI and HPLC analyses (Bio Basic Inc., Canada).
For whole-mount immunohistochemical staining of tick synganglia and salivary glands, we followed a procedure that had previously been successfully used for staining insect endocrine cells (Žitňanová et al., 2001). Ticks were dissected in ice-cold phosphate-buffered saline (PBS: 137 mM NaCl, 1.45 mM NaH2PO4, 20.5 mM Na2HPO4, pH 7.2). Isolated synganglia and salivary glands were cleaned from remaining blood and fixed in Bouin’s solution (37% formaldehyde and saturated solution of picric acid 1:3) at RT for 2 hours, followed by a wash in PBS containing 1% Triton X-100 (PBST). The tissues were then preabsorbed with 5% normal goat serum (Sigma, St. Louis, MO) in PBST for 10 minutes and subsequently incubated with the either a monoclonal antibody originally raised against Manduca MIP1 (Kim et al., 2006) or polyclonal antiserum for Drosophila SIFamide (Terhzaz et al., 2007) at dilutions of 1:1,000 for 2 days. After three washes with PBST, the tissues were incubated overnight in a mixture of goat anti-mouse IgG conjugated with Alexa 488 and goat anti-rabbit IgG conjugated with Alexa 594 (Molecular Probes, Carlsbad, CA). Stained tissues were washed in PBST and mounted in glycerol containing 300 nM 4′,6′-diamino-2-phenylindole (DAPI; 2 μg ml−1; Sigma). Images were observed and acquired with a confocal microscope (Zeiss 510 Meta). Schematic drawings were made in Adobe Photoshop 7.0 or Canvas 8.0.
The immunogen for MIP peptide was ManseMIP1 containing conserved W(6x)Wamide motif (Table 1, Fig. 1A) and for SIFamide peptide was DromeSIFamide having identical sequence to the SIFamide of I. scapularis (Table 1, Fig. 2A). Both antibodies recognized only neuronal cell bodies and projections in I. scapularis synganglion. The immunohistochemistry was validated by similar staining patterns in the in situ hybridizations, particularly for the PcSG neurons. Negative controls included preadsorption with each diluted antibody and 1 μM of the corresponding antigen for 24 hours. Preadsorbed antibodies were used for immunohistochemistry as described above. This treatment invariably abolished all immunohistochemical staining.
For naming peptidergic neurons, we followed a nomenclature previously used for the hard tick, R. appendiculatus, by Šimo et al. (2009). The first two letters refer to the position of each neuron in a specific lobe of the synganglion [cheliceral (Ch), palpal (Pa), stomodeal (St), prothocerebral (Pc), pedal 1–4 (Pd1–4), opisthosomal (Os), preoesophageal (Pe) or postoesophageal (Po)], and the letters that follow refer to the anatomical location of the neuron: dorsal (D), ventral (V), anterior (A), posterior (P), medial (M) or lateral (L). Neurons projecting axons onto the surface of the putative neurohemal periganglionic sheath or lateral segmental organs were considered neurosecretory cells (NC), whereas interneurons (IN) arborized within the synganglion. Neurons innervating acini of salivary glands were labeled SG.
The staining pattern of MIP in the synganglion of I. scapularis was similar to that previously described for R. appendiculatus (Šimo et al., 2009). On the dorsal side, the antibody detected neurons in the protocerebrum (PcAM, PcIN, PcSG), palpal lobe (PaD1,2), cheliceral lobe (ChD1–3), pedal lobes 2 and 3 (Pd2DL, Pd3DM1,2), and postoesophageal areas (PoDM) of the synganglion (Figs. 3A,C, ,4A).4A). One additional pair of small dorsal neurons was found in the pedal lobe 4 (Pd4DM1,2) of I. scapularis (Fig. 4A) that was not observed in R. appendiculatus. On the ventral side, staining was found in the protocerebrum (PcVM), pedal lobes 2–4 (Pd2–4VM), and opistosomal lobe (OsVM, OsIN1–5), which is similar to the staining patterns observed in R. appendiculatus. Some small ventral neurons were uniquely stained in I. scapularis, particularly in the stomodeal lobe (StVM1–3), pedal lobe 1 (Pd1VL1,2), and lateral segmental neurons in pedal lobes 1–4 (Pd1–4VL; Figs. 3D, ,4C);4C); these were not found in R. appendiculatus.
Antisera against SIFamide peptide showed immunoreactivity in various neurons on the dorsal and ventral sides of the synganglion. Two pairs of small interneurons were found in the central region of the dorsal protocerebrum (PcIN1,2; Figs. 3B, ,4B).4B). A single pair of giant neurons (PcSG) showing coexpression of SIFamide and MIP was located in the posterior part of the protocerebrum (Figs. 3A–C, 4A,B). We also detected four SIFamide-immunoreactive medial neurons on the ventral side of the protocerebrum (PcVM1–4). Those neurons projected a loop of paired axons posteriorly that arborized in the pedal lobe regions within the synganglion (Figs. 3E,F, ,4D).4D). The cheliceral lobes included a pair of SIFamide-immunoreactive neurons on the dorsal side (ChD). The dorsal pedal region contained a pair of small lateral neurons (Pd1DL1,2, Pd2DL1,2) and medial neuronal cells (Pd3DM1,2), which showed coexpression with SIFamide and MIP (Figs. 3A–C, 4A,B). Two small medial neurons (PoDM) and two small interneurons (OsIN) were detected in the posterior synganglion (Fig. 4B), whereas a pair of small medial neurons was found in each pedal lobe 3 (Pd3VM; Fig. 4D).
In situ hybridization confirmed the immunohistochemistry in a subset of neuronal cell bodies. In the in situ hybridization of mip, strong reactions were detected in protocerebrum cells PcIN and PcSG (Fig. 5A,B). We also recognized weak reactions in small neurons in cheliceral lobes and pedal lobes 2–4 (ChD1–3, Pd2DL, Pd2–4VM; Fig. 5A,B). In situ hybridization of sifamid revealed the reactivity in cheliceral neurons (ChD), protocerebrum (PcIN1,2, PcSG), and pedal lobes 2–3 (Pd1DL1, Pd2DL1,2, Pd3DM1,2; Fig. 5C,D).
By using MIP and SIFamide antibodies, we identified a pair of neurons in the synganglion that innervated the salivary glands of I. scapularis. Double staining with both antibodies revealed coexpression of MIP and SIFamide in a pair of giant neurons (PcSG) in the protocerebral lobe, each projecting a single thick axonal process without varicosities in a loop, which is often not visible (Figs. 3A–C, 4A,B). The axonal projection exited the synganglion through the palpal nerve and salivary nerve I (Fig. 4A,B), ran along salivary duct surface, and produced multiple branches and terminated in salivary acini types II and III, but not in type I (Figs. 6A–L, 7A–C). Each axonal branch entered individual acini through the neck region and arborized into four or five and three or four axon terminals containing varicosities on types II and III acini, respectively. These axon terminals were likely in contact with the luminal surface of the acini (Figs. 6A–L, 7B,C).
The coding sequence of MIP is 496 bp and is transcribed from a gene composed of four exons interrupted by three large introns. The open reading frame (ORF) encodes 132 amino acid residues of the MIP prepropeptide and contains three putative MIP-like sequences (Fig. 1B). Three putative MIP-related peptides were identified: MIP1 (-DWNALSGMWamide), which had an unknown N-terminus; MIP2 (ASDWNRLSGMWamide) and MIP3 (-WNDLSGYW), with unknown N-terminus and containing canonical Gly (G) for possible amidation but lacking cleavage amino acid(s) at the C-terminus (Fig. 1B). So far, only the presence of MIP2 has been confirmed in the CNS and salivary gland extracts by MALDI-TOF analysis.
A search for the SIFamide motif in the I. scapularis sequence database identified six EST sequences (GenBank Accession Nos. EW859993, EW859992, EL516526, EW878394, EL516675, and EL515586) and revealed a 515-bp transcript containing an ORF for 74 amino acid residues of the SIFamide prepropeptide. By comparison with the genome sequence, we identified four exons interrupted by three introns (677, 8,104, and 3,134 bp; Fig. 2B). The mature peptide AYRKPPFNGSIFamide, which was identified in the MALDI-TOF analysis, was located immediately after the predicted signal peptide and was followed by canonical amidation and cleavage signals (GKR). Notably, there were polymorphisms observed upon comparison among multiple EST clones and genome sequences; however, the sequence that we present is based on the genome sequence (Fig. 2B).
We predicted that neuropeptides produced by central neurons and delivered via axonal projections to salivary ducts and acini could be detected in MALDI peaks that were present in both the extracts of the synganglia and the salivary glands. Indeed, two MALDI peaks were present in both extracts: [M + H]+ 1,322 and 1,396 Da (Fig. 8A–D). Tandem mass spectrometry of these peaks provided partial sequences and amino acid compositions, but accurate determination of the whole sequence was not possible. Combining this information with data from the I. scapularis sequence database yielded sequences corresponding to MIP2 (ASDWNRLSGMWamide [M + H]+: 1,321.6106 Da) and SIFamide (AYRKPPFNGSIFamide [M + H]+: 1,395.7532 Da) as the best matches. Ultimately, MIP2 and SIFamide were chemically synthesized and run on MALDI. We found that the tandem mass spectrometry profiles of these synthetic peptides were nearly identical to patterns found for the 1,322- and the 1,396-Da peaks of the synganglia extract (Fig. 9A–D). Both the extracts of the synganglia and the salivary glands contained another peak (1,394 Da), which almost overlapped with SIFamide (1,396 Da), but its identity is still unknown (Fig. 8B,D).
Various components of tick salivary secretions have been extensively studied. These secretions contain multiple cement proteins important for attachment and feeding of ticks as well as anticoagulants and immunosuppressive polypeptides that modulate the host’s immune responses (Bishop et al., 2002; Trimnell et al., 2005). Feeding ticks may efficiently transfer various pathogens, causing serious diseases to their host. Therefore, disruption of tick salivary function has been attempted to prevent infections with the tick-borne pathogens by vaccination of mammalian hosts with selected salivary proteins (Wikel, 1996). However, the mechanism underlying neural and hormonal control of salivary secretion is poorly understood. Several studies have focused on identification of aminergic regulatory pathways controlling the secretory activity of tick salivary glands (Kaufman, 1978; Sauer et al., 1995, 2000). Dopamine has been found to activate salivary secretion through the D1-type (excitatory) receptor, which is likely a G-protein-coupled receptor (GPCR; Sauer et al., 1994; Schmidt et al., 1981). The downstream signaling pathway involves the G-protein alpha subunit S, cyclic AMP, and protein kinases for the excretion of water. A separate calcium-dependent pathway is activated for the production of prostaglandin E2 (PGE2; Maritz-Olivier et al., 2005). Additional biogenic amines, such as adrenaline, pilocarpine (muscarinic acetylcholine agonist), and high concentrations of octopamine, also activate salivary secretion (Kaufman, 1978; Kaufman and Wong, 1983). Additionally, a single report suggests that an unidentified peptide or protein from brain extracts elicits formation of inositol phosphates in salivary glands (McSwain et al., 1989).
Our recent studies indicate that complex mechanisms control the functions of the salivary glands, including peptidergic regulatory pathways. We have previously described MIP-like immunoreactivity in coupled giant neurons and their projections to salivary glands in the tick R. appendiculatus (Šimo et al., 2009). In this report, we identified two neuropeptides (MIP and SIFamide) and corresponding genes expressed in these neurons in the black-legged tick, I. scapularis. Close association of MIP- and SIFamide-immunoreactive axon termini with specific cells in salivary acini indicates the importance of peptidergic regulation of salivary gland activity.
MIPs (also called allatostatins B) have been identified in a number of insect species. These short neuropeptides are generally characterized by two conserved tryptophan residues contained within a W(6x)Wamide motif (Fig. 1A). In D. melanogaster and Tribolium castaneum, the mip gene encodes five or six homologous peptides, whereas multiple copies of seven closely related MIPs are expressed in Bombyx mori and Manduca sexta (Li et al., 2008). Recently, MIPs have been found in a crustacean by using MALDI analysis (Schmidt et al., 2008), indicating that this conserved class of neuropeptides may exist in most arthropods. The first MIP was originally identified as a potent inhibitor in the locust heartbeat bioassay (Schoofs et al., 1991). Closely related orthologs have since been identified in other species based on their inhibitory effects in various in vitro bioassays, such as the inhibition of juvenile hormone production in crickets (Lorenz et al., 1995a,b), the suppression of ecdysone secretion from prothoracic glands in the silk moth (Hua et al., 1999), and the inhibition of spontaneous peristaltic contractions of the adult M. sexta hindgut (Blackburn et al., 2001). Recently, it was proposed to act as a cotransmitter with other neuropeptides in the regulation of ecdysis behavior in M. sexta and D. melanogaster (Davis et al., 2003; Kim et al., 2006).
SIFamides have been found to be identical neuropeptides in different species of crustaceans and insects, except for the variation of a single amino acid at the N-terminus (Fig. 2A; Hauser et al., 2006; Yasuda et al., 2004). The anatomical structure of SIFamide-immunopositive neurons indicates that this peptide acts as a neuromodulator within the CNS to modulate the olfactory system in the crayfish Procambarus clarkii (Yasuda-Kamatani and Yasuda, 2006; Yasuda et al., 2004). Endocrine cells in the anterior midgut of Cancer sp. are a rich source of SIFamide (Christie et al., 2007). One possible role of this midgut peptide has been examined in the lobster Homarus americanus. Injection of SIFamide elicited myostimulatory action on the pyloric valve, which regulates the flow of food particles from the foregut to the midgut (Christie et al., 2006). SIFamide expression is limited to only four brain interneurons in D. melanogaster and B. mori (Roller et al., 2009; Terhzaz et al., 2007). Targeted ablation of these neurons or RNA interference have shown that SIFamide controls male and female sexual behavior in D. melanogaster (Terhzaz et al., 2007). The gene encoding SIFamide in ticks has been recently described (Christie, 2008; Verleyen et al., 2008), and we provide further details of the gene annotation in this study (Fig. 2B).
MIP and SIFamide immunoreactivities were observed in many regions of the I. scapularis synganglion, but a clear colocalization of these peptides was found only in PcSG and Pd3DM1,2 neurons. It is noteworthy that the MIP-IR in the PcSG cell bodies was stronger than that in axon and axon termini in the acini, whereas SIFamide-IR is weaker in cell bodies and stronger in the axonal projections, although accurate quantification was not possible (data not shown). In situ hybridization for the mip also produced more robust and stronger signals in the PcSG neurons than that for sifamide. PcSG neurons have been identified as a source of innervation of acini II and III in many ixodid ticks, and the innervation patterns of the entire salivary glands in I. scapularis and R. appendiculatus are very similar (Šimo et al., 2009). However, it is noteworthy that axon termini on individual acini of Ixodes spp. (I. scapularis and I. ricinus) are unique compared with those observed in other tick species (D. reticulatus, R. appendiculatus, and A. variegatum; Šimo and Park, unpublished). In Ixodes spp., axon terminals in acini II and III showed the characteristic four or five and three or four branches, respectively, whereas two short branches were commonly observed in other tick species.
Observations of salivary glands using confocal microscopy provided a counterpoint to classical studies that used light microscopy and transmission electron microscopy (Balashov et al., 1983; Coons and Alberti, 1999). Patterns and locations of different nuclei visualized by DAPI were highly reproducible in 3D reconstructions of confocal images (Fig. 6A–L). In acini II, nuclei could be categorized into four groups: small nuclei located on the neck of an acinus, small nuclei located between large nuclei dispersed over the surface of an acinus, the major category of large nuclei in granular cells located basal region of acini, and large nuclei clustered in the apical region of acini. In acini III, at least five types of nuclei were observed: small nuclei located on the neck, large nuclei clustered in the apical region of the acinus, scattered small nuclei in between the large nuclei in the apical region, three or four large nuclei located in the basal part of the acinus, and two large elliptical nuclei neighboring the basal large nuclei. The most probable targets of innervation are four or five basal granular cells in the acini II and three or four basally located cells with large nuclei in acini III. According to the previous anatomical descriptions of tick salivary glands in various species (Binnington, 1978), the basal three or four cells in the acini III might be d-cells, whereas the granular cells in acini II could not be accurately compared with the earlier studies.
The large MALDI peak at [M + H] 1,396 that was characterized as a SIFamide peptide in this study seems to also occur in A. americanum, although we do not know whether this peak represents an identical SIFamide (Šimo and Park, unpublished data). A previous study characterizing periviscerokinin peptides (Neupert et al., 2005) also reported a 1,396-Da peak in the MALDI analysis of single cheliceral neurons in I. ricinus, but successful fragmentation of this peak was not possible. Considering that SIFamide is a highly conserved peptide, the 1,396-Da peaks found in other tick species might represent the SIFamide that we characterized in this study.
Our data provide evidence that projections of PcSG neurons innervating salivary glands contain MIP and SIFamide. However, the functions of these two neuropeptides in the control of the salivary glands have not been elucidated. The generalized functions of these two peptides, MIP and SIFamide, might be antagonistic, with inhibitory function of MIP and stimulatory action of SIFamide. The identification of these neuropeptides and the genes encoding them and the description of their expression patterns in the synganglion and the specific innervation of acini reported in this study will lead to further investigations of salivary gland regulation.
We thank Dr. John Tomich and Dr. Takeo Iwamoto in the Biotechnology/Proteomics Core Lab at Kansas State University for assistance with the MALDI analysis. We are also grateful to Drs. Akira Mizoguchi and Jan Veenstra for providing the MIP and SIFamide antibodies. This is Contribution Number 09-281-J from the Kansas Agricultural Experimental Station. The sequences for mip and sifamide genes were deposited in GenBank with accession numbers GQ214555 and GQ214556, respectively.
Grant sponsor: National Institutes of Health; Grant number: R21 AI081136-01; Grant number: NIH-COBRE-P20-RR017686.
Additional Supporting Information may be found in the online version of this article.