Molecular Characterisation and Functions of Fis1 and PDCD6 Genes from Echinococcus granulosus

Cystic echinococcosis, a parasitic zoonosis that causes significant economic losses and poses a threat to public health, is caused by larvae of the tapeworm Echinococcus granulosus. Infection causes infertile cysts in intermediate hosts that cannot produce protoscoleces (PSCs) or complete the life cycle. Herein, we cloned, expressed, and characterised mitochondrial fission protein 1 (Eg-Fis1) and programmed cell death protein 6 (Eg-PDCD6) from E. granulosus, and explored their functions related to infertile cysts. Eg-Fis1 and Eg-PDCD6 encode putative 157 and 174 residue proteins, respectively, and Western blotting indicated good reactogenicity for both. Eg-Fis1 and Eg-PDCD6 were ubiquitously distributed in all stages of E. granulosus. Furthermore, mRNAs of Eg-Fis1 and Eg-PDCD6 were upregulated following H2O2 treatment which induced apoptosis in PSCs. To investigate the regulation of apoptosis in response to oxidative stress, RNA interference (RNAi) and terminal deoxynucleotidyl transferase dUTP nick-end labelling (TUNEL) assays were performed. The apoptotic rate of the Eg-Fis1 RNAi group was significantly lower than non-interference group, but there was no such difference for Eg-PDCD6. In conclusion, Eg-Fis1 promotes apoptosis induced by oxidative stress, whereas Eg-PDCD6 does not appear to be a key regulator of apoptosis.


Introduction
The larval stage of Echinococcus granulosus (Platyhelminthes, Cestoda) causes cystic echinococcosis (CE), which is a significant global public health concern in many rural, grazing areas of South America, North and East Africa, and Australia [1,2]. This parasitic disease is listed as one of the neglected tropical diseases in the World Health Organisation (WHO) "Accelerating work to overcome the global impact of neglected tropical diseases-a roadmap for implementation" document [3]. A wide range of domestic and wild mammals, as well as humans, can serve as intermediate hosts in the life cycle of this parasite [1]. Hydatid cysts develop in the intermediate host, mainly in internal organs, such as liver and lungs, and cause compression, mechanical damage, or even death [3,4]. Two types of hydatid cysts occur; fertile cysts, in which protoscoleces (PSCs) are found both joined to the germinal layer and free in the hydatid fluid filling the cyst cavity, and infertile cysts, which do not produce PSCs and are, therefore, unable to complete the life cycle of the parasite [5][6][7].
Mitochondrial fission protein 1 (Fis1) is known to mediate mitochondrial fission, which plays a key role in the process of mitochondrial membrane disruption [8][9][10]. Mitochondrial fusion and fission processes are vital for maintenance of organellar morphology and distribution, but also for cell proliferation and cell differentiation [10]. A previous study showed that increasing mitochondrial fission can promote apoptosis. Programmed cell death protein 6 (PDCD6), also known as apoptosis-linked gene-2 (ALG-2), is a calcium-binding modulator protein involved in cell proliferation and death [11,12]. It was identified in a cell death trap assay as a pro-apoptotic protein in a functional screen of T-cell hybridoma cells, and it was linked to calcium-dependent apoptosis [13][14][15][16]. Fis1 and PDCD6 have been reported to play an important role in promoting apoptosis in organisms [17,18]. However, their functions in E. granulosus are not yet clear.
In the present study, genes encoding Fis1 and PDCD6 from E. granulosus were cloned, expressed, and characterised. Their locations during different life cycle stages were investigated by immunolocalisation, gene expression following H 2 O 2 treatment was evaluated, and their functions in PSCs, in vitro, were explored using RNA interference (RNAi).

Bioinformatic Analysis of Eg-Fis1 and Eg-PDCD6
The full-length Eg-Fis1 cDNA comprises a 474 bp gene encoding a protein of 157 amino acids (aa) with no signal peptide, but with a single transmembrane region (aa 129−157). The predicted molecular weight (MW) of Eg-Fis1 is 16.93 kDa. The cDNA sequence of Eg-PDCD6 contains an open reading frame (ORF) of 525 bp encoding a polypeptide of 174 aa without a signal peptide or a transmembrane region, and the deduced protein has a MW of 20.34 kDa. InterPro analysis showed that Eg-Fis1 has two functional domains comprising a tetratricopeptide-like helical domain (aa 26−146) and a C-terminal tetratricopeptide repeat domain (aa 78−120), while Eg-PDCD6 has an EF-hand domain (aa 7−169).
Amino acid sequences of Fis1 and PDCD6 from various species were retrieved from GenBank and GeneDB database, and multiple sequence alignment revealed that Fis1 genes are highly variable. Eg-Fis1 shares highest sequence identity with Echinococcus multilocularis Fis1 (90.51%), followed by 63.03% with Hymenolepis microstoma Fis1, and 38.32% and 34.13% with Clonorchis sinensis and Schistosoma mansoni, respectively ( Figure 1). By contrast, PDCD6 genes among species are highly conserved. Eg-PDCD6 is most similar to E. multilocularis PDCD6 (98.85%), and shares 89.08% and 71.43% sequence identity with PDCD6 from Taenia solium and H. microstoma, respectively, but shares lower identity with sequences from other nematodes, such as Globodera pallida and Ascaris suum ( Figure 1).

Expression of Recombinant rEg-Fis1 and rEg-PDCD
The Eg-Fis1 and Eg-PDCD genes were amplified from PSCs, and recombinant rEg-Fis1 and rEg-PDCD proteins were successfully expressed in Escherichia coli. After purification, the His-tagged rEg-Fis1 protein yielded a single band close to the predicted size of 35 kDa following separation by 15%

Expression of Recombinant rEg-Fis1 and rEg-PDCD
The Eg-Fis1 and Eg-PDCD genes were amplified from PSCs, and recombinant rEg-Fis1 and rEg-PDCD proteins were successfully expressed in Escherichia coli. After purification, the His-tagged rEg-Fis1 protein yielded a single band close to the predicted size of 35 kDa following separation by 15% sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE), while the rEg-PDCD6 band was close to the expected size of 37 kDa (Figure 3).
In Western blotting assays, both rEg-Fis1 and rEg-PDCD reacted with cystic echinococcosis (CE)-positive sheep sera, and with anti-Eg-Fis1 and anti-Eg-PDCD6 rabbit sera, respectively ( Figure 3). Moreover, anti-Eg-Fis1 and anti-Eg-PDCD6 rabbit sera IgGs recognised their respective native proteins in PSC extracts. As expected, specific bands were not observed following incubation with sera from non-infected sheep or pre-immunised rabbit. sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE), while the rEg-PDCD6 band was close to the expected size of 37 kDa ( Figure 3). In Western blotting assays, both rEg-Fis1 and rEg-PDCD reacted with cystic echinococcosis (CE)positive sheep sera, and with anti-Eg-Fis1 and anti-Eg-PDCD6 rabbit sera, respectively ( Figure 3). Moreover, anti-Eg-Fis1 and anti-Eg-PDCD6 rabbit sera IgGs recognised their respective native proteins in PSC extracts. As expected, specific bands were not observed following incubation with sera from non-infected sheep or pre-immunised rabbit.

Localisation of Eg-Fis1 and Eg-PDCD6 during Different E. granulosus Life Cycle Stages
In immunofluorescence analysis, anti-Eg-Fis1 and anti-Eg-PDCD6 rabbit IgGs were applied for detection of their respective native proteins in adult worms, cyst walls (from fertile and infertile cysts), and PSCs in E. granulosus. The results indicated that both Eg-Fis1 and Eg-PDCD6 were distributed in all tissues of E., including the inner body and tegument of adult worms, the germinal layer (GL) of the cyst wall, and the parenchymal region and tegument of PSCs, but both were absent from the laminated layer (LL) of the cyst wall ( Figure 4).

Localisation of Eg-Fis1 and Eg-PDCD6 during Different E. granulosus Life Cycle Stages
In immunofluorescence analysis, anti-Eg-Fis1 and anti-Eg-PDCD6 rabbit IgGs were applied for detection of their respective native proteins in adult worms, cyst walls (from fertile and infertile cysts), and PSCs in E. granulosus. The results indicated that both Eg-Fis1 and Eg-PDCD6 were distributed in all tissues of E., including the inner body and tegument of adult worms, the germinal layer (GL) of the cyst wall, and the parenchymal region and tegument of PSCs, but both were absent from the laminated layer (LL) of the cyst wall ( Figure 4). sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE), while the rEg-PDCD6 band was close to the expected size of 37 kDa ( Figure 3). In Western blotting assays, both rEg-Fis1 and rEg-PDCD reacted with cystic echinococcosis (CE)positive sheep sera, and with anti-Eg-Fis1 and anti-Eg-PDCD6 rabbit sera, respectively ( Figure 3). Moreover, anti-Eg-Fis1 and anti-Eg-PDCD6 rabbit sera IgGs recognised their respective native proteins in PSC extracts. As expected, specific bands were not observed following incubation with sera from non-infected sheep or pre-immunised rabbit.

Localisation of Eg-Fis1 and Eg-PDCD6 during Different E. granulosus Life Cycle Stages
In immunofluorescence analysis, anti-Eg-Fis1 and anti-Eg-PDCD6 rabbit IgGs were applied for detection of their respective native proteins in adult worms, cyst walls (from fertile and infertile cysts), and PSCs in E. granulosus. The results indicated that both Eg-Fis1 and Eg-PDCD6 were distributed in all tissues of E., including the inner body and tegument of adult worms, the germinal layer (GL) of the cyst wall, and the parenchymal region and tegument of PSCs, but both were absent from the laminated layer (LL) of the cyst wall ( Figure 4).

Expression of Eg-Fis1 and Eg-PDCD6 in Response to Oxidative Stress
According to previous studies, clear indications of apoptosis were apparent in PSCs following treatment with H 2 O 2 , and the degree of apoptosis increased gradually with increasing treatment time [19]. In our present study, PSCs were treated with 10 mM H 2 O 2 for 8 h to induce apoptosis, and collected every 2 h. Quantitative PCR (qPCR) was then performed to assess Eg-Fis1 and Eg-PDCD6 mRNA expression levels in PSCs using β-actin (actb) as a reference gene.
The results showed that Eg-Fis1 mRNA expression was upregulated at the beginning of H 2 O 2 treatment, and levels continued to increase by up to 4-fold after an 8 h incubation. The mRNA levels were also gradually upregulated with increasing treatment time, but not significantly so ( Figure 5).

Expression of Eg-Fis1 and Eg-PDCD6 in Response to Oxidative Stress
According to previous studies, clear indications of apoptosis were apparent in PSCs following treatment with H2O2, and the degree of apoptosis increased gradually with increasing treatment time [19]. In our present study, PSCs were treated with 10 mM H2O2 for 8 h to induce apoptosis, and collected every 2 h. Quantitative PCR (qPCR) was then performed to assess Eg-Fis1 and Eg-PDCD6 mRNA expression levels in PSCs using β-actin (actb) as a reference gene.
The results showed that Eg-Fis1 mRNA expression was upregulated at the beginning of H2O2 treatment, and levels continued to increase by up to 4-fold after an 8 h incubation. The mRNA levels were also gradually upregulated with increasing treatment time, but not significantly so ( Figure 5). Figure 5. Expression profile analysis of Eg-Fis1 and Eg-PDCD6 in response to H2O2 treatment. Data are presented as the mean ± SD of triplicate experiments. Statistically significant differences between the 0 h group (control) and the other groups were determined using Student's t-tests (* p < 0.05).

Small Interfering RNA (siRNA)-Mediated Knockdown of Eg-Fis1 and Eg-PDCD6
Specific siRNAs were applied by soak transfection to silence target gene transcription, and the transfection efficiency was estimated to be ~60%, as determined by the control siRNA (siRNA-CON) and the 6-carboxyfluorescein (FAM) fluorescence label.

Measurement of Apoptotic Rate in PSCs Following RNAi Treatment
To investigate whether Eg-Fis1 and/or Eg-PDCD6 are responsible for regulating the apoptosis response to oxidative stress, terminal deoxynucleotidyl transferase dUTP nick-end labelling (TUNEL) assays were performed (Table 1 and Figure 6). In the negative control group, the fluorescence signal from apoptotic cells in PSCs was minimal (13.95%, 42/301), but a significant increase in apoptotic rate was observed in all H2O2 treatment groups (p < 0.05). In the Eg-Fis1 RNAi group (Fis1-IG), the fluorescence signal from apoptotic cells was decreased after H2O2 treatment relative to the non-interference group (NIG); the apoptotic rate for the Fis1-IG group was 53.85% (182/338), compared with 63.87% (76/119) for the NIG. By contrast, the difference in fluorescence signal between the Eg-PDCD6 RNAi group (PDCD6-IG) and the NIG was not significant (p > 0.05); the apoptotic rate in the PDCD6-IG was 65.07% (285/438).

Small Interfering RNA (siRNA)-Mediated Knockdown of Eg-Fis1 and Eg-PDCD6
Specific siRNAs were applied by soak transfection to silence target gene transcription, and the transfection efficiency was estimated to be~60%, as determined by the control siRNA (siRNA-CON) and the 6-carboxyfluorescein (FAM) fluorescence label.

Measurement of Apoptotic Rate in PSCs Following RNAi Treatment
To investigate whether Eg-Fis1 and/or Eg-PDCD6 are responsible for regulating the apoptosis response to oxidative stress, terminal deoxynucleotidyl transferase dUTP nick-end labelling (TUNEL) assays were performed (Table 1 and Figure 6). In the negative control group, the fluorescence signal from apoptotic cells in PSCs was minimal (13.95%, 42/301), but a significant increase in apoptotic rate was observed in all H 2 O 2 treatment groups (p < 0.05). In the Eg-Fis1 RNAi group (Fis1-IG), the fluorescence signal from apoptotic cells was decreased after H 2 O 2 treatment relative to the non-interference group (NIG); the apoptotic rate for the Fis1-IG group was 53.85% (182/338), compared with 63.87% (76/119) for the NIG. By contrast, the difference in fluorescence signal between the Eg-PDCD6 RNAi group (PDCD6-IG) and the NIG was not significant (p > 0.05); the apoptotic rate in the PDCD6-IG was 65.07% (285/438).

Discussion
Previous studies on the Fis1 gene have mainly concentrated on mammals, and reports on parasites are scarce [20]. PDCD6 is named after its role in the apoptosis of T cells, but the mechanism underpinning its role in the regulation of apoptosis is still unclear. Herein, we cloned, expressed, and characterised the Fis1 gene (Eg-Fis1) and PDCD6 gene (Eg-PDCD6) from E. granulosus, and explored their functions.
Our results showed that Eg-Fis1 encodes a protein of 157 aa with a predicted MW of 16.93 kDa. Its N-terminal region was predicted to be exposed to the cytosol, and it likely adopts a novel tetratricopeptide repeat (TPR)-like helical bundle. This structure is known to stimulate mitochondrial fission and combine with other proteins [21]. In Fis1 mutant strains, mitochondrial fission was significantly suppressed, which demonstrates that Fis1 is required for the proper assembly,

Discussion
Previous studies on the Fis1 gene have mainly concentrated on mammals, and reports on parasites are scarce [20]. PDCD6 is named after its role in the apoptosis of T cells, but the mechanism underpinning its role in the regulation of apoptosis is still unclear. Herein, we cloned, expressed, and characterised the Fis1 gene (Eg-Fis1) and PDCD6 gene (Eg-PDCD6) from E. granulosus, and explored their functions.
Our results showed that Eg-Fis1 encodes a protein of 157 aa with a predicted MW of 16.93 kDa. Its N-terminal region was predicted to be exposed to the cytosol, and it likely adopts a novel tetratricopeptide repeat (TPR)-like helical bundle. This structure is known to stimulate mitochondrial fission and combine with other proteins [21]. In Fis1 mutant strains, mitochondrial fission was significantly suppressed, which demonstrates that Fis1 is required for the proper assembly, membrane distribution, and function of Dnm1-containing complexes during fission [22]. The transmembrane region of Fis1 is known to be very important for its function, since cytoplasmic localisation results in loss of the ability to promote mitochondrial fission when the transmembrane region is missing [8][9][10]. Multiple sequence alignment revealed that Fis1 genes were highly variable, and evolutionary analysis showed that Fis1 from E. granulosus shares higher homology with Fis1 from congeneric cestodes than with other species.
Eg-PDCD6 encodes a polypeptide of 174 aa with a predicted MW of 20.34 kDa. Protein functional domain prediction revealed an EF-hand domain that likely facilitates binding to Ca 2+ [23]. Indeed, PDCD6 (ALG-2) possesses two high-affinity Ca 2+ -binding sites, and binding alters the structure of the PDCD6 protein, exposing its hydrophobic region to allow it to interact with other proteins, facilitating a wider range of biological functions [24]. Moreover, PDCD6 genes are highly conserved among species [13,25]. PDCD6 from humans is almost 100% identical to the mouse gene, and homologs are present in mammals and plants.
In our present study, localisation of Eg-Fis1 and Eg-PDCD6 in adult and larval stages of E. granulosus was confirmed by immunofluorescence, and both proteins were widely distributed in all tissues of E. granulosus. These findings suggest that Eg-Fis1 and Eg-PDCD6 might be involved in many important physiological functions in this organism.
In many cells, mitochondria are highly dynamic and regularly undergo fusion and fission [26], hence mitochondrial DNA and mitochondrial proteins can be continuously exchanged and distributed throughout the whole mitochondrial population [27][28][29]. Fis1 is the main mitochondrial fission factor in mammalian cells [10]. The wide distribution of Eg-Fis1 in E. granulosus is likely required to support normal life activities and metabolic needs.
Research has revealed novel functions of PDCD6 in addition to pro-apoptotic activity. Changes in protein conformation allow PDCD6 to interact with other proteins, and thereby induce various biological effects. Therefore, the widespread distribution of Eg-PDCD6 suggests that this protein might be involved in metabolic processes in E. granulosus.
In multicellular organisms, harmful stimuli can lead to excessive production of highly reactive molecules, such as reactive oxygen species (ROS) that cause oxidative damage [30], which can affect the structure and function of cells, causing tissue damage and pathological changes. Apoptosis is a fundamental biological phenomenon in multicellular organisms, and parasite load in hosts can be regulated by apoptosis to enhance host survival [31]. Previous studies demonstrated that oxidative DNA damage can exceed DNA repair mechanisms, triggering death of PSCs and apoptosis in the germinal layer, leading to infertility of hydatid cysts [19,32,33]. Thus, H 2 O 2 was used as an apoptosis inducer to treat PSCs in our study, and expression profiles of Eg-Fis1 and Eg-PDCD6 following H 2 O 2 exposure were analysed to further confirm whether these two proteins respond to oxidative stress. Expression of Eg-Fis1 was significantly upregulated with increasing duration of H 2 O 2 treatment, and levels continued to increase up to 4-fold during an 8 h incubation. These results are similar to those of previous studies; Zhang and colleagues treated human lung cancer cells with UV irradiation to induce apoptosis, and Fis1 levels were slightly, but significantly, elevated after UV treatment [34]. This demonstrates that Fis1 is upregulated to mediate mitochondrial fission during UV irradiation-induced apoptosis. Furthermore, the mRNA expression level of Eg-PDCD6 was also upregulated, but the increase was not significant, suggesting that Eg-PDCD6 does not play a key role in the response to oxidative stress, although the functions of both genes requires further study.
To further confirm the functions of Eg-Fis1 and Eg-PDCD6 in PSCs during oxidative stress-induced apoptosis, RNAi experiments were performed, and the apoptotic rate in PSCs was determined. In the Eg-Fis1 RNAi group, the fluorescence signal from apoptotic cells was lower than the non-interference group (NIG), which indicates that lack of Eg-Fis1 could reduce apoptosis in E. granulosus. Fluorescence resonance energy transfer and coimmunoprecipitation analysis has already proven that Fis1 can interact with Drp1, and overexpression of human Fis1 causes mitochondrial fragmentation [8,9], while silencing of Fis1 leads to the extension and interconnection of mitochondria [10]. Since apoptosis induced by oxidative stress is one of the mechanisms causing infertility of hydatid cysts [19,32,33], further studies will be carried out to evaluate whether Eg-Fis1 is involved in regulating the production of infertile cysts.
By contrast, the difference in fluorescence signal between the Eg-PDCD6 RNAi group and NIG was not significant. To study the function of PDCD6 (ALG-2) under physiological conditions, Jang et al. generated PDCD6-deficient mice using a gene-targeting approach, and the results indicated that the general development and survival of mutant mice, as well as their immune system development and differentiation, was normal, consistent with our current results. Of interest, TCR-, Fas-, and dexamethasone-induced apoptosis of T-cells was not significantly impaired in the absence of PDCD6 [15]. We therefore speculate that Eg-PDCD6 is unlikely to be a key regulator of apoptosis.

Animals and Parasites
E. granulosus (G1 genotype) cysts were collected from the livers of infected sheep at a local abattoir in Sichuan Province, China. Cysts containing PSCs in hydatid fluid were confirmed as fertile, while the rest were identified as infertile [35]. Cyst walls (including the GL and LL) from fertile and infertile cysts and PSCs were separated and treated as previously described [36]. Fresh PSCs at a concentration of 2000 mL −1 were cultured in complete RPMI 1640 medium (Hyclone, Logan, UT, USA), containing 100 µg·mL −1 streptomycin, 100 U·mL −1 penicillin G (Sigma, St. Louis, MO, USA), and 10% fetal calf serum (Hyclone), in an atmosphere containing 5% CO 2 at 37 • C. A four-month-old dog was artificially infected with 30,000 PSCs, and adult worms were obtained from the small intestine after 35 days.

Cloning and Expression of Recombinant rEg-Fis1 and rEg-PDCD6
Total parasite RNA was isolated from PSCs using TRIzol reagent (Tiangen, Beijing, China) following the manufacturer's instructions, and cDNAs were synthesised using a Reverse Transcription System (Thermo Fisher, Waltham, MA, USA). The sequence encoding Eg-Fis1 was amplified by PCR with sense primer 5 -CGCGGATCCATGGAATTACTGGATTTGAATG-3 and antisense primer 5 -CCGCTCGAGTTATTGTCCTTTGCCCTTCT-3 containing BamHI and XhoI restriction enzyme sites, respectively. Eg-PDCD6 was amplified from cDNAs using sense primer 5 -CGCGGATCCATGAGCCAACCCTTTTCG-3 containing a BamHI site, and antisense primer 5 -CCGCTCGAGTTATGTGAACACGGTAAAGACAC-3 containing an XhoI site. PCR cycling involved an initial denaturation for 5 min at 94 • C followed by 35 cycles at 95 • C for 45 s, 60 • C for 30 s, and 72 • C for 45 s. Recombinant Eg-Fis1 and Eg-PDCD6 were cloned into pET-32a, expressed, and purified as described in our previous study [38]. Purified rEg-Fis1 and rEg-PDCD6 were separated by 15% SDS-PAGE, and the final protein concentration was determined using a BCA protein assay kit (Beyotime, Shanghai, China).

Preparation of Polyclonal Antibodies
Polyclonal antibodies against rEg-Fis1 and rEg-PDCD6 were produced from four 3-month-old female New Zealand white rabbits using an immunisation strategy described previously [38]. Rabbit sera were collected before and after immunisation and the antibody titre was determined. Afterwards, IgGs were isolated from sera using a protein G Sepharose column (Bio-Rad, Richmond, VA, USA), following the manufacturer's instructions.
Fertile and infertile cyst walls, PSCs, and adult worms were fixed for 36 h with 4% paraformaldehyde, embedded in paraffin, and sliced into sections. Pre-treatment of sections was implemented as described previously [38] followed by incubation with anti-Fis1/anti-rEg-PDCD6 rabbit IgG or native rabbit IgG (1:500 v/v dilutions in PBS) at 4 • C overnight. Sections were then incubated with fluorescein isothiocyanate (FITC)-conjugated sheep anti-rabbit IgG (1:200 v/v dilution in 0.1% Evan's Blue) in the dark at 37 • C for 1 h, glycerine was added after washing four times with PBS, and images were collected using a fluorescence microscope (Nikon 55i, Tokyo, Japan).

Eg-Fis1 and Eg-PDCD6 Expression in PSCs Following H 2 O 2 Treatment
In 6-well microplates, PSCs were cultured for 2 days then treated with 10 mM H 2 O 2 for 8 h to induce apoptosis. PSCs were collected every 2 h and placed immediately in liquid nitrogen until further study.

RNA Interference Assay
To further investigate the role of Eg-Fis1 and Eg-PDCD6 in PSCs in E. granulosus, expression levels were knocked down by RNAi. To target the cDNA sequences of Eg-Fis1 and Eg-PDCD6, three specific small interfering RNAs (siRNAs) were respectively designed and synthesised by GenePharma Co., Ltd. (Shanghai, China). We also synthesised a random siRNA with the FAM fluorescence label to determine the transfection efficiency (Table 2).  PSCs for which the survival rate was >95% were divided into seven groups. In each group, 4000 PSCs were cultured in 3 mL of RPMI 1640 medium, and treated with 10 µL of transfection reagent (Engreen Biosystem, Beijing, China) plus the specific or random siRNA at a final concentration of 200 µM at days 0 and 2. Medium was replaced every day.
Eg-Fis1 and Eg-PDCD6 mRNA levels were determined by qPCR as described above. PSCs were collected for RNA isolation and cDNA synthesis at 24 h after the final addition of RNAi.
Afterwards, PSCs treated with the most efficient siRNA were selected and incubated with 10 mM H 2 O 2 for 8 h in an atmosphere containing 5% CO 2 at 37 • C (interference group, IG). PSCs treated with siRNA-CON were also incubated with H 2 O 2 under the same conditions (non-interference group, NIG). After treatment, PSCs were collected and stored in liquid nitrogen for further study. A negative control group (NCG) cultured without any siRNA and H 2 O 2 was also included.

Terminal Deoxynucleotidyl Transferase dUTP Nick End Labelling (TUNEL) Assay
After 8 h of exposure, PSCs were collected and prepared for TUNEL assays as described previously [39] and assays were performed using an In Situ Cell Death Detection Kit (Roche, Basel, Switzerland) following the manufacturer's instructions. Samples were eventually stained with 1 µg·mL −1 of 4 ,6-diamidino-2-phenylindole (DAPI) reagent (Sigma-Aldrich, St. Louis, MO, USA) at room temperature for 10 min, and cells marked with green fluorescence were confirmed as positive cells. The apoptotic rate of cells in PSCs was calculated as the percentage of positive cells (the number of positive cells/total cell number × 100) using Image-Pro Plus 6.0 (Media Cybernetics, Inc., Rockville, MD, USA).

Statistical Analysis
All data are presented as mean ± standard deviation (SD). For comparison between groups, Student's unpaired t-tests and one-way analysis of variance (ANOVA) were performed using SPSS 13.0, and p-values < 0.05 were considered statistically significant.

Conclusions
In this study, Eg-Fis1 and Eg-PDCD6 were cloned, expressed, and characterised. Both Eg-Fis1 and Eg-Fis1 were ubiquitously distributed in adult worms, PSCs, and the GL of the cyst wall. Expression of both Eg-Fis1 and Eg-PDCD6 was upregulated after triggering of apoptosis following H 2 O 2 treatment, but the increase in Eg-PDCD6 expression was not significant. In addition, the apoptotic rate was significantly decreased after RNAi knockdown of Eg-Fis1, but there was no difference between the Eg-PDCD6 RNAi group and the non-interference group. In conclusion, Eg-Fis1 promotes apoptosis induced by oxidative stress in E. granulosus, and thereby stimulates the production of infertile cysts, whereas Eg-PDCD6 does not appear to be a key regulator of apoptosis.