Functional characterization of a cystatin from the tick Rhipicephalus haemaphysaloides
© Wang et al.; licensee BioMed Central. 2015
Received: 17 November 2014
Accepted: 9 February 2015
Published: 3 March 2015
Ticks and tick-borne diseases affect animal and human health worldwide and cause significant economic losses in the animal industry. Functional molecular research is important to understand the biological characteristics of ticks at the molecular level. Enzymes and enzyme inhibitory molecules play very important roles in tick physiology, and the cystatins are tight-binding inhibitors of papain-like cysteine proteases. To this end, a novel cystatin, designated RHcyst-1, was isolated from the tick Rhipicephalus haemaphysaloides.
The full-length gene of RHcyst-1 was cloning by RACE. The recombinant protein of RHcyst-1 was expressed in a glutathione S-transferase (GST)-fused soluble form in Escherichia coli, and its inhibitory activity against cathepsin L, B, C, H, and S, as well as papain, was identified by fluorogenic substrate analysis. Expression analysis of RHcyst-1 at different tick stages was performed by quantitative reverse transcription - PCR (qRT-PCR). An RNAi experiment for RHcyst-1 was performed to determine its function for tick physiology.
The full-length cDNA of RHcyst-1 is 471 bp, including an intact open reading frame encoding an expected protein of 98 amino acids, without a signal peptide, having a predicted molecular weight of ~11 kDa and an isoelectric point of 5.66. A sequence analysis showed that it has significant homology with the known type 1 cystatins. The results of proteinase inhibition assays showed that rRHcyst-1 can effectively inhibit the six cysteine proteases’ enzyme activities. An investigation of the RHcyst-1 genes’ expression profile showed that it was more richly transcribed in the embryo (egg) stage. A disruption of the RHcyst-1 gene showed a significant decrease in the rate of tick hatching.
Our results suggested that RHcyst-1 may be involved in the early embryonic development of ticks.
Ticks rank first as arthropod vectors of fungi, protozoa, rickettsiae, bacteria, and viruses, which cause diseases in non-human vertebrates, and rank second only to mosquitoes as vectors of human pathogens . Cystatins are classified, based on characteristic sequence motifs and the number of conserved cystatin domains, into four subfamilies: the type 1 cystatins (also known as stefins), the type 2 cystatins, the type 3 cystatins (kininogens), and the type 4 cystatin-like proteins (fetuins and histidine-rich proteins) . Type 1 cystatins are cytoplasmic proteins that do not have signal peptides; however, the type 2 cystatins are secretion-type proteins containing signal peptides. Cystatins are present in a wide range of organisms, such as vertebrates, invertebrates, and plants, as well as protozoa [3,4]. They are involved in various vertebrate biological processes, such as antigen presentation, immune system development, epidermal homeostasis, neutrophil chemotaxis during inflammation, and apoptosis [5-8]. Over the last decade, several cystatins from different hard and soft ticks were identified and biochemically analyzed to determine their roles in the physiology and blood-feeding lifestyle of ticks .
Rhipicephalus haemaphysaloides is a widespread tick species in China and other south Asian countries, where it transmits animal babesiosis and human Kyasanur Forest disease . In this paper, we report on a novel cystatin molecule, named RHcyst-1, identified from R. haemaphysaloides. This molecule exhibited significant inhibitory activities against cysteine proteinases and may be involved in tick embryonic development.
Ticks and animals
The Hubei strain of R. haemaphysaloides has been maintained by feeding on rabbits for several generations in our laboratory at the Chinese Academy of Agricultural Sciences (Shanghai, China) . The experimental animals were treated following the approved guidelines from the Animal Care and Use Committee of the Shanghai Veterinary Research Institute (SOP-1104-003).
Cloning the full-length gene by RACE and bioinformatic analysis
Rapid amplification of cDNA ends (RACE) was conducted using a SMARTer RACE cDNA amplification kit (Clontech, San Jose, CA, USA) following the manual’s instructions. Cloning was performed using primers from highly conserved regions of cystatin . The gene-specific primers used were 5′-AAGGATGCCGATGACACAGTC-3′ and 5′-CCCTGGAAAGCCTTGTGCGC-3′. The cDNA template primed by an adapter-linked oligodT primer (Clontech) was synthesized from 5 μg of total RNA extracted from ticks that had been partially fed for 4 days. After two rounds of PCR, the PCR fragments were cloned into the pGEM-T plasmid (Promega, Madison, WI, USA) and sequenced. A BLASTx homology search revealed a cDNA encoding a cystatin-like polypeptide. Following contig assembly and singleton identification, gene-specific PCR primers were designed and used to clone the full-length cDNA .
Expression and purification of rRHcyst-1 in Escherichia coli
The open reading frame (ORF) of the cystatin gene in the pGEM-T vector was subcloned into the pGEX-4T-1 E. coli expression vector (Amersham Pharmacia Biotech, Piscataway, NJ, USA). The accuracy of the insertion in the resulting plasmid was confirmed by sequencing. The cystatin gene was expressed as a glutathione S-transferase (GST)-fusion protein in the E. coli BL21 (DE3) strain according to the manufacturer’s instructions (Amersham Pharmacia Biotech). The resulting E. coli cells were washed three times with phosphate-buffered saline (PBS), lysed in PBS containing 1% Triton X-100, sonicated, and then centrifuged at 12,000 × g for 10 min at 4°C. Supernatants containing the soluble GST fusion protein were purified with glutathione-Sepharose 4B beads (Amersham Pharmacia Biotech) according to the manufacturer’s instructions. The purified proteins were dialyzed against PBS for further use. The empty pGEX-4T-1 vector was used to produce the control GST protein, which was expressed and purified using the same procedure as that for the cystatin-GST fusion protein. Recombinant protein expression and purification analyses were carried out by standard SDS–PAGE .
Proteinase inhibition assays
To calculate the inhibitory activity of the recombinant protein, the concentration of rRHcyst-1 at which a 50% inhibition of the proteolytic enzymes’ activities was achieved (IC50) was measured. Recombinant protein was preincubated with each enzyme (0.15 μM) in an assay buffer for 30 min. Then, 0.25 mM of the protease-specific substrates was added to each well and residual enzyme activity monitored . The GST protein was used as control. Enzymes used were as follows: cathepsin L, C, B, S and H, as well as papain. All of these enzymes were purchased from Sigma Company (St. Louis, USA). The assay buffer used consisted of 100 mM sodium acetate, pH 5.5, 100 mM NaCl, 1 mM EDTA, 1 mg/ml cysteine, and 0.005% TritonX-100. The substrates purchased (Sigma company) were as follows: Z-Phe-Arg-AMC·HCl for papain, cathepsin L and cathepsin B; Pro-Arg-4-methoxy-β-naphthylamide acetate salt for cathepsin C; Arg-NMec·HCl for cathepsin H; and Ac-Lys-Gln-Lys-Leu-Arg-AMC for cathepsin S.
Expression analysis of RHcyst-1 in ticks at different developmental stages by qRT-PCR
Relative quantification was carried out using 100 ng of cDNA prepared from the eggs, larvae, nymph, and adult cDNA. To normalize the obtained gene expression, the tick elongation factor 1-alpha gene was selected as a housekeeping gene, as described previously . The specific primers used to quantify the cystatin and elongation factor 1-alpha were 5′-CACAGTCAGGGAGATTTGCG-3′ and 5′-TGCGTGCGATACTTCAGAGG-3′ for RHcyst-1, and 5′-CGTCTACAAGATTGGTGGCATT-3′ and 5′-CTCAGTGGTCAGGTTGGCAG-3′ for elongation factor 1-alpha. The amount of mRNA transcripts of the target genes present in the adult samples were considered equivalent to 1 and were used as references for the expression levels in the other stages. Cycling parameters for all amplifications were 5 min at 95°C followed by 30 cycles of 15 s at 95 C, 30 s annealing at 60°C, and extension at 72°C for 30 s. qPCR was performed using Platinum SYBR Green qPCR SuperMix kit (Invitrogen) using an Applied Biosystems 7500 thermocycler (Applied Biosystems Inc, Foster City, CA, USA). To ensure primer fidelity, dissociation curve analyses and gel electrophoresis of target gene amplicons were performed for each sample following the qPCR step. All qPCR amplifications were performed in triplicate and repeated twice, with the mean values considered for comparison. To check for genomic DNA contamination, controls lacking reverse transcription were performed.
RNA interference of RHcyst-1
cDNA of RHcyst-1 in the pGEM-T vector was amplified by PCR using oligonucleotides, including the T7 promoter sequence at the 5′ end of both primers, as follows: 5′-GGATCCTAATACGACTCACTATAGGGTAGCAGCGCGCGCGATTAG-3′ and 5′-GGATCCTAATACGACTCACTATAGGCGCGTAAAATTTGTTCCTT-3′ for the gene encoding RHcyst-1, and 5′-GGATCCTAATACGACTCACTATAGGGCTTCCATCTTCCAGGGATACG-3′ and 5′-GGATCCTAATACGACTCACTATAGGCGTCCACAAACACAACTCCTCC-3′ for the gene encoding luciferase. The PCR products were gel-purified and used to synthesize RNA by in vitro transcription with T7 RNA polymerase (T7 RiboMAX™ Express RNAi System, Promega, Madison, WI, USA) according to the manufacturer’s protocol. The double-stranded (ds) RNA injection was administered as described previously . In total, 1 μg of the RHcyst-1 dsRNA in 0.5 μl of an injection buffer (10 mM Tris and 1 mM EDTA, pH 7.4) was microinjected into unfed female ticks from the same batch of engorged nymphal ticks (105 ticks in each group). Twelve unfed female ticks that had been removed from the host 5 days after feeding for real-time PCR analysis were not included. In the control group, another 105 unfed ticks were injected with luciferase dsRNA constructed from the vector DNA of pGEM-luc (Promega). The ticks were allowed to rest for 1 day at 25°C and 95% relative humidity, and then each group of ticks (RHcyst-1 and control) was allowed to feed on three rabbits (35 ticks on each rabbit). The attachment rate 24 h after putting the adult ticks onto the host ears, the engorgement rate, the death rate and the larval hatching rate were measured to evaluate the RHcyst-1 functions in tick physiology. To confirm gene-specific silencing, real-time quantitative PCR using SYBR Green technology and gene-specific primers was performed as above described. Statistical analyses for significant differences in the results of the RNAi test were calculated using Student’s t test (P < 0.05).
Cloning and sequence analysis of the full-length cDNA encoding R. haemaphysaloides cystatin
Expression and purification of rRHcyst-1
Proteinase inhibition assays
Protease inhibition assays
RHcyst-1 IC 50 and 95% confidence intervals
89 nM (86 to 92.1 nM)
594.5 nM (305.5 to 1157 nM)
34 nM (9.2 to 125.5 nM)
281.8 nM (244.5 to 324.7 nM)
23.7 nM (22.2 to 25.4 nM)
0.3 nM (~ to 1.4 nM)
Expression analysis of RHcyst-1 in ticks at different developmental stages by qRT-PCR
RNA interference of RHcyst-1
Effect of a novel type 1 cystatin, RHcyst-1, isolated from the tick Rhipicephalus haema physaloides , dsRNA treatment on ticks
Attachment rate after 24 h (%)
63.8 ± 3.3
48.6 ± 2.9
Engorgement rate (%)
42.9 ± 5.7
40 ± 2.9
Death rate (%)
56.2 ± 1.6
59.0 ± 1.6
Hatching rate (%)
80.4 ± 4.1
69.1 ± 2.4
The present study describes the sequence of a novel cystatin, RHcyst-1, from the tick R. haemaphysaloides. The characteristics of the putative RHcyst-1 amino acid sequence indicate that it is a member of the type 1 cystatins.
The capacities of various cystatins to inhibit the activity of cysteine proteases have been characterized. In this study, the GST-fused recombinant cystatin efficiently inhibited the activity of cathepsin L, B, C, H, and S, and papain. rRHcyst-1 effectively inhibited cathepsin S, and it also had quite a high inhibitory efficiency against cathepsin L. However, rRHcyst-1 showed relatively less inhibitory activity against cathepsin B, perhaps due to an occluding loop in the cathepsin B active site that limits the access of both substrates and inhibitors to the active site . The lack of inhibitory activity has been documented previously for other cystatins [12,13,17-19]. In recent studies, cathepsin L and S were considered to be effectively controlled targets of tumor cells, because they play key roles in the invasion and migration of tumor cells [20,21]. The SV-cystatin from snake venom was found to inhibit the invasion and metastasis of mouse melanoma cells and human gastric carcinoma cells . Thus, based on this information, RHcyst-1 may be an important candidate molecule for anti-cancer drug research and development in the future.
All known type 1 tick cystatins, except RHcyst-1, were discovered from five different hard tick species of four genera. Only two type 1 tick cystatins have been biochemically analyzed thoroughly enough to identify their roles in tick physiology . Bmcystatin (GenBank accession number: ABG36931) has a 70% sequence identity with a cytoplasmic salivary protein of Ixodes scapularis (GenBank accession number: AAY66864), which was the first type 1 cystatin identified in the I. scapularis’ sialome [18,23]. Lima et al.  suggested a role for Bmcystatin in the embryogenesis of R. microplus because this cystatin was found to inhibit, in addition to human cathepsin L, a vitellin-degrading cysteine endopeptidase of R. microplus. Hlcyst-1 (GenBank accession number: ABZ89553) was localized in epithelial cells of the tick midgut alongside with HlCPL-A, a cathepsin L-like cysteine protease of H. longicornis . HlCPL-A may play a role in the digestion of host hemoglobin in ticks since it is able to degrade bovine hemoglobin . Hlcyst-1 efficiently inhibited the hemoglobinolytic activity of HlCPL-A, and both gene transcripts were upregulated during the blood feeding of H. longicornis, with their strongest expression levels occurring at 48 h in the midgut cells . Thus, Hlcyst-1 seems to function as a regulator for digesting blood in ticks.
In this study, RHcyst-1 was found to be highly expressed in the embryo (egg) stage, and we hypothesize that it plays a role in early embryonic development. To further confirm the function of RHcyst-1 in tick physiology, an RNAi experiment was performed. The disruption of the RHcyst-1 gene led to a significant decrease in the rate of egg hatching. However, there are several cystatin homologs which may compensate the role of the silenced cystatin, thus affect the result of RHcyst-1 RNAi. And this hypothesis will be tested in our future work. In conclusion, our results suggested that RHcyst-1 may be involved in tick early embryonic development.
This work was supported by grants (No. 31172095 and No. 31311140167) from the National Natural Science Foundation of China (NSFC).
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