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Conceived and designed the experiments: QZ HYH. Performed the experiments: BH QPZ STL SL SHY. Analyzed the data: QZ HD BH. Contributed reagents/materials/analysis tools: SHZ HD. Wrote the paper: QZ HYH.
The genome sequences of Eimeria tenella have been sequenced, but >70% of these genes are currently categorized as having an unknown function or annotated as conserved hypothetical proteins, and few of them have been studied. In the present study, a conserved hypothetical protein gene of E. tenella, designated EtCHP559, was cloned using rapid amplification of cDNA 5'-ends (5'RACE) based on the expressed sequence tag (EST). The 1746-bp full-length cDNA of EtCHP559 contained a 1224-bp open reading frame (ORF) that encoded a 407-amino acid polypeptide with the predicted molecular weight of 46.04 kDa. Real-time quantitative PCR analysis revealed that EtCHP559 was expressed at higher levels in sporozoites than in the other developmental stages (unsporulated oocysts, sporulated oocysts and second generation merozoites). The ORF was inserted into pCold-TF to produce recombinant EtCHP559. Using western blotting, the recombinant protein was successfully recognized by rabbit serum against E. tenella sporozoites. Immunolocalization by using EtCHP559 antibody showed that EtCHP559 was mainly distributed on the parasite surface in free sporozoites and became concentrated in the anterior region after sporozoites were incubated in complete medium. The EtCHP559 became uniformly dispersed in immature and mature schizonts. Inhibition of EtCHP559 function using anti-rEtCHP559 polyclonal antibody reduced the ability of E. tenella sporozoites to invade host cells by >70%. Animal challenge experiments demonstrated that the recombinant EtCHP559 significantly increased the average body weight gain, reduced the oocyst outputs, alleviated cecal lesions of the infected chickens, and resulted in anticoccidial index >160 against E. tenella. These results suggest that EtCHP559 plays an important role in sporozoite invasion and could be an effective candidate for the development of a new vaccine against E. tenella.
Chicken coccidiosis is a protozoal disease caused by infection with several Eimeria species and leads to high annual economical losses in the poultry industry due to high morbidity, reduction of body weight, and treatment costs . At present, the control of Eimeria infection is still based mainly on anticoccidial drugs and live vaccines. However, these measures have been restricted by some reasons, for example, the consumer attention to food safety, the rise of drug resistance, and the high production expenses etc. Therefore, new cost-effective anticoccidial control strategies need to be developed [2,3].
Eimeria are classified in the phylum Apicomplexa, which contains obligate intracellular parasites including medical and veterinary pathogens such as Plasmodium, Toxoplasma, Cryptosporidium, Neospora and Sarcocystis. These protozoan parasites are characterized by a peculiar organelle complex located at the apical end . The life cycle of Eimeria is complex and comprises three distinct phases: sporogony, schizogony and gametogony . These phases involve different life cycle forms which have different morphological characteristics and habitats, including unsporulated oocysts, sporulated oocysts, sporozoites, trophozoites, merozoites and gametocytes. The levels of gene expression among these stages often differ greatly and this increased the difficulty of developing the cost-effective subunit vaccines.
The genomes of all seven Eimeria species that infect chickens have been sequenced and each Eimeria species expresses between 6000 and 9000 proteins throughout its life cycle . However, the annotation of coding sequences is still a major challenge. Among seven Eimeria species, Eimeria tenella is one of the most important species, causing cecal hemorrhage and high mortality. A lot of research on E. tenella has been reported. But more than 70% of the E. tenella genes are currently categorized as unknown function or annotated as conserved hypothetical proteins , so some conserved proteins maybe important for invasion, development and the life cycle of E. tenella. Until now, few genes of the conserved hypothetical proteins have been studied and tested for their function and immunogenicity, although there are nucleotide sequences in GenBank.
In our previous research, some expressed sequence tags (ESTs) that encoded potential interaction proteins with EtAMA1were obtained by screening from the yeast two-hybrid cDNA library of E. tenella sporozoites using EtAMA1 as bait (data unpublished). BLAST searches showed that a protein encoded by ESTs559 (GeneBank accession NO.JZ905777) was annotated as a conserved hypothetical protein. In this study, we used the rapid amplification of cDNA ends (RACE) technique to clone the full-length cDNA sequence based on the EST sequence described above. Then, we identified the molecular characterization, and the immunogenicity of the recombinant protein was checked through chicken challenge experiments.
The protocol was approved and authorized by the Animal Care and Use committee of the Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences.
Newly hatched 1-day-old Chinese Pudong yellow chickens purchased from the hatchery of Min You (Shanghai, China) were raised under coccidian-free conditions. The New Zealand white rabbits were purchased from the Shanghai Experimental Animal Center, Chinese Academy of Sciences. We examined the coccidia from rabbits feces for three days and judged the rabbits as coccidian-free. Then the rabbits were also raised under coccidian-free conditions.
The Shanghai strain of E. tenella was isolated from a sample collected on a chicken farm in Shanghai, China in the 1980s and subsequently maintained in our laboratory . Parasites were propagated by passage through coccidia-free 2-week-old chickens as previously described . Unsporulated oocysts (UO) were obtained after infected chickens with 5× 104 sporulated oocysts per bird and undergone sporulation to become sporulated oocysts (SO). Then unsporulated oocysts and sporulated oocysts were purified using standard procedures [9,10]. Sporozoites (Spz) were purified from cleaned sporulated oocysts by in vitro excystation . Second-generation merozoites(Mrz) were collected from the cecal mucosa of chickens at 115 h post inoculation (p.i.) with 105 sporulated oocysts per bird. Briefly, the ceca contents were discarded. Then the ceca were rinsed with PBS and cut into small pieces. After enzymatic digestion, the merozoites were released from the ceca and purified by filtration, centrifugation, erythrocyte disruption and Percoll density gradient centrifugation .
Total RNA of E. tenella sporozoites was extracted by using TRIzol (Takara, Dalian, China). To avoid DNA contamination, the extracted RNA preparations were additionally treated with RNase-free DNase Ι (Takara) for 30 min at 37°C according to the manufacturer instructions and then inactivated by heating at 75°C for 10 min. RNA was quantified by NanoDrop 2000C (Thermo Scientific, Waltham, MA, USA) and its integrity was verified by 1% agarose denaturing formaldehyde-Dured gel electrophoresis. cDNA was synthesized from the total RNA using an M-MLV Reverse Transcriptase kit (Invitrogen, Beijing, China) with Oligo dT primers. The cDNA was then used as a template for further study.
A yeast two-hybrid cDNA library from sporozoites of E. tenella, constructed in our laboratory previously, was screened with the bait EtAMA1 protein. One of the putative positive clones (Clone No.Et559, GenBank accession No.JZ905777) expected to be the interaction protein with EtAMA1 was chosen for further analysis. The 701 bp EST sequence of the clone had 100% identity with E. tenella hypothetical protein (XM_013376471.1) in NCBI. It contains a poly(A) in the 3' end, so the full-length 5'-ends of the cDNA for the gene were obtained by 5'RACE using GeneRacer kits (Invitrogen). GR5P and GR5N primers supplied with the kit and the GS5P and GS5N gene-specific primers listed in Table 1 were used to amplify the 5' flanking sequence. And gene-specific primers were designed on the basis of the EST sequence. Amplified fragments were gel purified (Qiagen, GmbH, Hilden, Germany) and cloned into the pGEM-T-easy vector (Promega, Madison, WI, USA), and sequenced. After aligning and assembling the resulting sequences with the original EST sequence, the full-length cDNA sequence of the CHP559 gene was obtained and submitted to NCBI GenBank (accession number: KT318394).
The full-length cDNA sequence of the putative EtCHP559 gene was analyzed for similarity using the BLAST programs at NCBI (http://www.ncbi.nlm.nih.gov/BLAST/) and the genome sequence of E. tenella (http://www.genedb.org/Homepage/Etenella). The predicted amino acid sequence was obtained using the ORF Finder at NCBI (http://www.ncbi.nlm.nih.gov/gorf/gorf.html). The molecular mass, and theoretical isoelectric point were acquired using ProtParam tool at the ExPASy server (http://web.expasy.org/protparam/). Signal peptides, transmembrane regions and protein motifs were predicted using SignalP (http://www.cbs.dtu.dk/services/SignalP/), TMHMM (http://www.cbs.dtu.dk/services/TMHMM-2.0/), and Motifscan (http://hits.isb-sib.ch/cgi-bin/motif_scan) computational tools, respectively.
To validate the differential expression of EtCHP559 in the different developmental stages, Total RNA was isolated by the TRIzol reagent (Invitrogen) from the four stages of E. tenella (UO, SO, Spz and Mrz). DNA contamination was removed by DNase I(Invitrogen)treatment. The quality and quantity of total RNA were assessed as describedin above. The cDNA was generated by SuperScriptII reverse transcriptase (Invitrogen) using random primers. Quantitative RT-PCR was performed on a Realplex 4 (Eppendorf, Hamburg, Germany) using the SYBR1 Green Idye method. Four housekeeping genes of E. tenella, 18S rRNA, β-actin, GAPDH and β-tubulin, were used as reference genes for the purposes of normalization. Primers for EtCHP559 (RTS and RTA) and the β-tubulin gene (β-tubulinS and β-tubulinA), were designed manually by the Beacon Designer program (www.premierbiosoft.com). The primers for the 18SrRNA gene (18S and 18A), the β-actin gene (β-actinS and β-actinA) and the GAPDH gene (GAPDHS and GAPDHA) were designed as described previously [12,13]. Each reaction was carried out in triplicate, and the experiment was performed twice. The primer sequences used for the amplification of specific genes by quantitative RT-PCR are shown in Table 1.
The EtCHP559 open reading frame (ORF) was amplified with HD1 and HD2 primers, with BamHI(GCGGATCC) and XhoI (CGCTCGAG) restriction sites at the 5' and 3' ends of the fragment, respectively. The products were digested with BamHI and XhoI, and purified with a gel extraction kit (Tiangen, Beijing, China). The purified fragments were ligated overnight into the expression vector pCold-TF (Takara), digested by the same restriction enzymes at 4°C, and transformed into competent Escherichia coli BL21(DE3) (Tiangen) for protein expression. The recombinant protein was harvested after induction with 1mM isopropylthio-α-D-galactoside (IPTG) (Sigma, St Louis, MO, USA) for 24 h at 16°C. The cell pellet was lysed by sonication and analyzed by 12% SDS-PAGE to confirm the distribution of expressed recombinant protein. rEtCHP559 protein was purified from lysate supernatants using His Bind Resin (Merck, Darmstadt, Germany). The purity of the protein was verified by 12% SDS-PAGE and the concentration of purified protein was determined by the BCA protein assay kit (Beyotime, Haimen, China), using bovine serum albumin (BSA) as a standard. The purified protein was stored in aliquots at −20°Cuntil further use. The TF protein was purified from the lysate supernatants of E. coli BL21 cells transformed with pCold-TF plasmid as same as the methods to rEtCHP559 protein.
The sporozoite protein were prepared using sonication according to the previous description . rEtCHP559 protein or sporozoite protein was used to immunize a 2-month-old male rabbit by intraperitoneal injection of 200 μg protein emulsified in Freund’s complete adjuvant (Sigma) in a 1:1 mixture. The rabbits were boosted three times at 2-week intervals with proteins emulsified in Freund’s incomplete adjuvant (Sigma). Seven days after the final immunization, antiserum against rEtCHP559 and sporozoite protein was collected respectively. Sera collected before protein injection was used as negative sera. All polyclonal antibodies used for sporozoite invasion inhibition experiments were purified from rabbit antiserum using Protein A+G agarose (Beyotime).
Recombinant EtCHP559 proteins were subjected to 12% SDS-PAGE and blotted onto polyvinylidene difluoride transfer membranes (Millipore, Billerica, MA, USA). After blocking with 5% (w/v) skimmed milk powder in TBS-Tween 20 [Tris–HCl 10 mM (pH7.4), NaCl 150 mM, Tween 20 0.5%], membranes were incubated with primary antibodies (sporozoite-immunized rabbit serum at 1:100dilution) or anti-His6 monoclonal antibody (at 1:1000 dilution) or naïve rabbit serum (1:100 dilution) were used as a negative control. Horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG or goat anti-mouse IgG (1:1000 dilution; Sigma) was added as the secondary antibody, and detection used diaminobenzidine (Tiangen).
The chicken embryo fibroblast cell line, DF-1, a derivative of the East Lansing Line (ELL-0) , was used for the infection and immunofluorescence experiments. DF-1 cells (3 × 105 cell per well) were seeded in six-well plates (Corning, NY, USA) with precoated sterile coverslips and cultured in complete medium (Dulbecco’s Modified Eagle’s Medium (DMEM) containing 10% fetal bovine serum, 100 U/mL penicillin/streptomycin, 2 mM L-glutamine) at 37°C and 5% CO2 for 24 h. Freshly purified sporozoites were incubated in phosphate-buffered saline (PBS) or complete medium (CM) for 2 h at 41°C, and air dried on a glass slide before fixation [12,15]. Sporozoites previously incubated in complete medium were used to infect DF-1 cells. At various times post-inoculation, the DF-1 cells were collected, and washed. Sporozoites and cells were fixed in 2% paraformaldehyde in PBS for 15 min, and permeabilized with 1% Triton X-100 in PBS for 15 min, then blocked in PBS containing 2% (w/v) BSA overnight at 4°C. A 1:100 dilution of anti-rEtCHP559 polyclonal antibody was added and incubated for 1 h at 37°C. A 1:400 dilution of a goat anti-rabbit IgG fluorescein-isothiocyanate-conjugated antibody (Sigma) was added, and the slides were incubated for 1 h at 37°C. The nuclei were stained by incubation in 10 μg/mL of 4,6-diamidino-2-phenylindole (Beyotime) for 20 min. After each step described above, the slides were washed three times with PBS containing 0.05% Tween 20. The slides were treated with 60 μL Fluoromount Aqueous Mounting Medium (Sigma) and observed with a florescence microscope (Olympus, Tokyo, Japan). Second-generation merozoites purified from the ceca of chickens were also incubated in PBS or CM for observation.
The invasion inhibition assay was based on previous reports of sporozoites of E. tenella invading DF-1 cells . DF-1 cells (2 × 105 cells per well) were seeded in 24-well plates and cultured in DMEM with 10% fetal bovine serum at 37°C and 5% CO2 for 24 h. Freshly purified sporozoites were counted and labeled with carboxyfluorescein diacetate succinimidyl ester (Beyotime), and incubated at 37°C with 25, 50, 100, 200, 300 or 400 μg/mL purified IgG against rEtCHP559 for 2 h, respectively. The same quantity of IgG from naïve rabbit serum was used as a negative control and the equivalent volume of PBS as a normal control. Sporozoites (105/well) were used to infect 105 DF-1 cells in 24-well plates (Corning) and cultured at 41°C and 5% CO2 for 12 h. Cells were collected, trypsinized, washed, and analyzed by Cytomics FC500 flow cytometry (Beckman Coulter, Indianapolis, IN, USA). Controls were uninfected DF-1 cells. Infected cells, uninfected cells, and free sporozoites were gated using CXP software for counting infected (labeled sporozoites) and uninfected (fluorescence-free) cells. All assays were performed in triplicate. Deduced percentages of infected cells in the presence or absence of inhibitory antibody were used to calculate inhibition rates, as described previously [14,16].
As shown in Table 2, a total of 80 one-week-old chickens were randomly divided into four groups of 20 chickens with equal mean body weights. The experimental group was immunized with 100 μg EtCHP559 recombinant protein emulsified in Montanide ISA 71 adjuvant (Seppic, Puteaux, France) as a 3:7 mixture per chicken, the TF protein control group was given 100 μg of TF protein emulsified in Montanide ISA 71 adjuvant as a 3:7 mixture. The chickens of the challenged control and unchallenged control groups were injected with PBS. A booster immunization was carried out 8days later with the same dose as the primary immunization. Eight days after the second immunization, blood samples were collected to isolate the serum, which was used for the detection of antibody and cytokines. Then, all the chickens except the unchallenged control group, were challenged orally with 1×104 sporulated oocysts of E. tenella. While chickens of unchallenged control were given equal volume PBS orally. The fecal samples from each group were collected separately from 5th day to 8th day post challenge. The 9th day after the challenge, all chickens were weighed and slaughtered. The cecal content for each group was collected separately. Average body weight gain, oocyst decrease ratio, lesion score, and anti-coccidial index (ACI) were calculated as follows.
Protective efficacy was evaluated by the average body weight gain, oocyst output, oocyst decrease ratio, lesion score and ACI. Body weight gain was determined by subtracting the body weight at the time of challenge from the body weight at the end of the experiments. The cecal lesion scores were determined on a graded scale from 0 (normal) to 4 (severe) described by Johnson and Reid . Oocysts per gram of fecal sample and cecal content were counted using McMaster’s technique. Oocyst decrease ratio was calculated as follows: (the number of oocysts from the positive control chickens − immunized chickens)/positive control chickens × 100% [18,19]. ACI is a synthetic criteria for determination of the anticoccidial effect and calculated as follows: (relative rate of weight gain + survival rate) − (lesion value + oocyst value) . According to Merck Sharp & Dohme , ACI ≥180 is considered high performance, ACI 160–179 is considered effective, and ACI <160 is considered ineffective.
The serum IgG antibody responses were measured by ELISA, as described previously . Briefly, the 96-well microtiter plate (Corning) was coated with 100 μL/well (10 μg/mL) rEtCHP559 antigen in 0.05 M carbonate buffer (pH 9.6) and incubated overnight at 4°C. After three washes with PBS containing 0.05% Tween-20 (PBST), the plate was blocked with blocking buffer (PBS containing 0.05% BSA) for 2 h at 37°C, and then the wells were washed with PBST, 100 μL/well serum samples diluted 1:100 in PBST were added, and incubated for 2 h at 37°C. Then, the plate was washed, and 50 μL/well HRP-donkey-anti-chicken IgG antibody (Sigma) diluted 1:1000 in dilution buffer was added and incubated for 2 h at 37°C. After washing, 3,3',5,5'-tetramethylbenzidine (TMB)-ELISA solution was used as a substrate. The OD was measured at 450 nm by a microplate spectrophotometer. All serum samples were included on one plate and tested by ELISA at the same time under the same conditions.
In order to evaluate the protection of immunized chickens, some serum cytokines were measured by ELISA with the Chick Cytokine ELISA Quantitation Kits (catalog numbers: CSB-E13114C, CSB-E14317C, CSB-E08550Ch, CSB-E12835C, and CSB-E04607Ch for sCD4, sCD8, IFN-γ, IL-10, and IL-17 respectively; CUSABIO, Wuhan, China), according to the manual instructions. These cytokines included soluble cluster of differentiation 4 (sCD4), soluble cluster of differentiation 8 (sCD8), interferon-γ (IFN-γ), interleukin-10 (IL-10), and interleukin-17 (IL-17). Every cytokine was tested two times.
Statistical analysis was performed using SPSS for Windows version 22 (SPSS, Chicago, IL, USA). All data, including real-time quantitative PCR (qPCR), invasion inhibition assay results, body weight gain, lesion score, fecal oocyst output and oocyst decrease ratio, were analyzed. Differences among groups were tested by one-way analysis of variance (ANOVA) Duncan test. P<0.05 was considered significant and P<0.01 highly significant.
The 1746 bp full-length cDNA was obtained by overlapping the 5'-RACE fragments with the original 701 bp EST sequence. The full-length cDNA contained a 5'-untranslated region (UTR) of 103 bp, an ORF of 1224 bp and a 3'-UTR of 419 bp (Fig 1). By analysis of the sequence, the ORF was deduced to encode a polypeptide of 407 amino acids (aa) with a calculated molecular mass of 46.04 kDa and a theoretical isoelectric point of 9.12. SignalP program analysis revealed that the Nterminus of EtCHP559 contained a signal peptide of 25 aa, with a hypothetical cleavage site located between alanine and aspartic acid. The EtCHP559 composed a cytoplasmic domain (1–8 aa), a transmembrane domain (9–31 aa) and an ectodomain (32–407 aa), as predicted using TMHMM2.0 (Fig 1). Searches in the Motif Database and Conserved Domain Database revealed the presence of two N-glycosylation sites, five casein kinase II phosphorylation sites, six N-myristoylation sites, six protein kinase C phosphorylation sites, one ankyrin repeat and one tyrosine kinase phosphorylation site, and no conserved domains were found (Fig 1).
A BLAST search of the E. tenella genome database showed that the ORF sequence shared 100% sequence identity with ETH_00024035 on superconting Eth_scaff35: 146391–147790, and that it encoded a conserved hypothetical protein. The amino acid sequence had 100% homology with the E. tenella conserved hypothetical protein (CDJ41175.1) and 92% identity to Eimeria necatrix hypothetical protein (CDJ65043.1) in NCBI. These demonstrated that CHP559 is a conserved protein. So, this gene was designated EtCHP559 (GenBank Accession No. KT318394). It also had 32% identity with Hammondia hammondi dense granule protein 12 (XP008888355.1) and Toxoplasma gondii dense granule protein 12 (ESS30190.1).
Real-time RT-PCR was conducted to analyze UO, SO, Spz and Mrz of E. tenella for the presence of EtCHP559 mRNA. The level of EtCHP559 mRNA in the sporozoites was much higher than that in the other three stages, and the transcripts were almost undetectable in second-generation merozoites (Fig 2).
rEtCHP559 was generated as described above. SDS-PAGE showed that the recombinant protein was found in the lysate supernatants and the inclusion bodies. After purification from the supernatants by chromatography on the Ni2+-nitrilotriacetic acid (Ni-NTA), the protein was seen as a single band with a molecular mass of 98kDa on SDS-PAGE (Fig 3). Because 51.5 kDa of the fusion protein was from the vector and the predicted molecular mass of EtCHP559 protein was about 46kDa. Western blotting showed that the purified protein was recognized by rabbit serum against sporozoites or anti-His6 monoclonal antibody. Naïve rabbit sera failed to detect any protein of the expected size of rEtCHP559 (Fig 3). These results indicated that the rEtCHP559 was recognized specifically by rabbit sera against sporozoite protein and anti-His monoclonal antibody.
Using antibody against rEtCHP559, the localization of EtCHP559 in sporozoites, second-generation merozoites and during first schizogony was investigated in vitro by immunofluorescence. After incubation in PBS, the EtCHP559 protein was mainly distributed on the parasite surface of sporozoites (Fig 4A). When sporozoites were incubated in CM at 41°C for 2 h and incubated with DF-1 cells for 2 h and 24 h, EtCHP559 expression was increased and further distributed throughout the whole cytosol, except in the posterior refractile bodies (Fig 4B–4D). The labeled EtCHP559 eventually became uniformly dispersed in immature and mature schizonts (Fig 4E–4G). When the first-generation merozoites formed, staining became weaker (Fig 4H). Moreover, EtCHP559 was not detected in the parasitophorous vacuole (PV). When second-generation merozoites were collected from the chicken ceca and then incubated in PBS, the staining was very weak, but the staining was increased after incubated in CM at 41°C for 2 h compared to them in PBS (Fig 4I and 4J).
To test whether EtCHP559 protein play a role in E. tenella sporozoite invasion of DF-1 cells, we performed invasion inhibition assays of sporozoites by preincubation with rEtCHP559 antibody before infection. The observed inhibition effect was dose dependent (Fig 5). Pretreatment with antibody significantly affected the capacity of sporozoites to invade the DF-1 cells. Compared with the same dose of naïve rabbit sera IgG (negative control), pretreatment with 25, 50, 100, 200 or 300 μg/mL anti-EtCHP559 IgG highly significantly decreased invasion (P<0.01). Under the experimental conditions, an inhibition plateau of 70.9% was reached at an antibody concentration of 300 μg/mL. However, an inhibition rate of only 17.9% was found with the same dose of the naïve rabbit sera IgG, which did not have a significant effect on invasion.
The immunization efficacies of rEtCHP559 are presented in Table 2. Body weight gains of the challenged control group and TF protein control group were significantly reduced compared with the unchallenged control group (P<0.05). While the body weight gains of chickens immunized with rEtCHP559 protein were significantly increased compared to chickens of the challenged control group and TF protein control group (P<0.05). The oocyst counts and cecal lesions of rEtCHP559-immunized chickens were significantly reduced compared with the challenged control group and TF protein control group (P<0.05). No chicken died from challenge infection in any groups. Chickens immunized with rEtCHP559 protein had an ACI >160.
As depicted in Fig 6, significantly increased levels of rEtCHP559 IgG were present in rEtCHP559- and TF-protein-immunized chickens compared to the control groups (P<0.05). And the levels of sCD8 and IL-17 were significantly increased in chickens immunized with rEtCHP559 protein compared to the control groups (P<0.05). But no significant differences of sCD4, IL-10 and IFN-γ were observed between the immunized and control groups.
In the present work, a new gene of E. tenella was cloned and identified. The entire cDNA of this gene contained 1746 bp, which included a 1224 bp ORF encoding a 407 aa polypeptide with a predicted molecular mass of 46.04 kDa. The bioinformatics analysis predicted that the protein contained two N-glycosylation sites, five casein kinase II phosphorylation sites, six protein kinase C phosphorylation sites, and one tyrosine kinase phosphorylation site. These data suggest that its function might be regulated by post-translational modification. By BLASTP in NCBI, the deduced amino acid sequence had 100% identity with E. tenella conserved hypothetical protein (CDJ41175.1) and 92% identity with Eimeria necatrix conserved hypothetical protein (CDJ65043.1), but no high identity proteins were found in the other Eimeria spp. E. tenella and E. necatrix are the most pathogenic species among the Eimeria spp. and they can all reside in cecal mucosa . Whether this protein is related to the virulence or parasitic site of the parasite needs to be further researched. We found that the sequence had 32% identity with H. hammondi dense granule protein 12 (XP008888355.1) and T. gondii dense granule protein 12 (ESS30190.1). The dense granule proteins are associated with the parasitophorous vacuole (PV) during and after invasion . In the current research, immunofluorescence analysis using antibody against rEtCHP559 showed that EtCHP559 was not found in the PV. Whether this protein was one of the dense granule proteins needs to be further investigated.
The expression of the mRNA transcript was examined in four different development stages of E. tenella. Results from quantitative RT-PCR showed that EtCHP559 mRNA levels were highest in sporozoites, and the lowest was found in second-generation merozoites. This was consistent with the results of immunofluorescence, which showed that staining was weak during the second-generation merozoite stage. Previous studies of E. tenella found that the proteins that are expressed at high levels in sporozoites might participate in invasion. The protein levels of EtCDPK3, EtAMA1 and Etserpin are highest in sporozoites, and indirect immunofluorescence and invasion inhibition assays support their essential role in host invasion [12,14,25]. Both the sporozoites and merozoites of E. tenella are invasive for cells of the chicken cecum epithelium. The previous proteomic comparison of E. tenella found that EtRON2 was found in sporozoites and merozoites but EtRON4 only in merozoites and EtRON5 only in sporozoites. All these proteins are related to invasion, and this suggests that the invasive mechanisms differ between merozoites and sporozoites. It is suggested that EtCHP559 is an essential component in the invasive process of sporozoites.
Using the anti-rEtCHP559 polyclonal antibody, the localization of EtCHP559 in intracellular parasites was investigated. EtCHP559 was found on the parasite surface in free sporozoites incubated in PBS. The bioinformatics analysis predicted that EtCHP559 contained a transmembrane region and six N-myristoylation sites. Myristoylation plays a vital role in signal transduction and membrane targeting in plant responses to environmental stress . These suggested that EtCHP559 was expressed as a membrane protein in this period. However, the EtCHP559 appeared to mainly concentrate in the apical complex of sporozoites after incubation in complete medium or invasion of DF-1 cells. Eimeria is well known for its invasion process via the apical complex present at the apex of invasive forms . When sporozoites come into contact with a host cell surface, a signal is transduced from the surface to the apex, and these processes are involved in the host cell invasion . The vary processes of EtCHP559 localization suggest that EtCHP559 plays a structural role in the signal transduction pathways and this needs to be further studied. Later, the specific staining of EtCHP559 becomes uniformly dispersed in immature and mature schizonts, but decreases in first-generation merozoites, and the staining is weak in the second-generation merozoites. This phenomenon might be that the protein expression of EtCHP559 in merozoites were little. This was consistent with the results of quantitative RT-PCR, which showed that EtCHP559 mRNA levels were the lowest in second-generation merozoites. These results show that EtCHP559 is also possibly related to the development of the schizont stage of E. tenella.
In this study, we found that the distribution of EtCHP559 in sporozoites was different between incubation in PBS and in CM. The previous research showed that EtHsp90 had a homogenous distribution in the cytoplasm of sporozoites incubated in PBS and was concentrated at the apical end of sporozoites incubated in CM on the contrary. The authors also found that the secretion of EtMic2 and EtHsp90 was stimulated by FCS . In our lab previous reports, we found that the different treatments with PBS or CM could affect the distribution of EtSerpin, EtPDIL, and EteIF3s7 [12,31,32]. Moreover, the staining of EtCHP559 in the second-generation merozoites was increased after incubated in CM compared to them in PBS. These suggest that the CM could influence the expression and distribution of some proteins.
Previous studies have shown that apical membrane antigen (AMA)1 of E. tenella is located at the apical end of sporozoites after invasion of DF-1 cells. An invasion inhibition assay has demonstrated that antibody against rEtAMA1 has a remarkable inhibitory effect on parasite invasion . In the present study, invasion inhibition assays revealed that rabbit antiserum against rEtCHP559 also blocked invasion of host cells by >70%. Combined with the results of quantitative RT-PCR and immunofluorescence localization analysis, these data supported a more direct role for EtCHP559 in host invasion. In our previous work, EtCHP559 was obtained by yeast two-hybrid screening and was assumed to be a potentially interacting protein with EtAMA1 (data unpublished). Although the localization of EtCHP559 and EtAMA1 in intracellular parasites overlapped, the Co-Immunoprecipitation and bimolecular fluorescence complementation assays suggested that there was no interaction of EtCHP559 and EtAMA1 (data not shown). The results show that the yeast two-hybrid assay generates false-positive interaction: protein–protein interaction that occurs in yeast cells, but not in the other cells, because the protein modification in yeast cells may not be the same as in other cells .
Animal experiments showed that rEtCHP559 provided protection against an immune challenge by significantly improving the body weight gains, reducing oocyst shedding and alleviating cecal lesions compared to controls. The ACI is commonly used to evaluate the anticoccidial effect . Previous studies of Eimeria spp. proteins have shown that ACI can accurately reflect the protective effect [35–38]. In the present study, rEtCHP559 resulted in an ACI >160 in the animal protective experiment, showing partial protection against E. tenella challenge. Chickens immunized with TF protein did not show any significant protection, indicating that the immune protection against the challenge was produced by rEtCHP559.
The CD4+ and CD8+ lymphocytes can release soluble sCD4 and sCD8 antigens, respectively . The concentrations of sCD4 and sCD8 in serum are consistent with the count of CD4+ and CD8+ lymphocytes . And sCD8 is a sensitive and specific parameter of cytotoxic and suppressor T cell activation . In a previous study, a gradual increase in sCD8 levels was reported in patients with malaria, which was related to malaria-associated immunosuppression . In our study, the concentration of sCD8 increased significantly in chickens that were immunized by rEtCHP559. This suggested that rEtCHP559 could stimulate the recruitment of the T-cell subpopulation. IL-17 is produced by the T helper 17 subset of CD4+ T cells and plays a critical role in host defense against pathogens . A previous study showed that IL-17 was involved in the initiation and migratory response of epithelial cells harboring E.tenella second-generation schizonts during intracellular development and contributed to the maturation of E. tenella schizonts . In the present study, the concentration of IL-17 was significantly increased during immunization with rEtCHP559, and the staining of EtCHP559 became uniformly dispersed in the mature schizonts stages in the immunofluorescence assay. These data suggested that EtCHP559 played a role in schizont maturation. IL-10 has been shown to be crucial for control of Eimeria infections and plays a crucial role in preventing the development of strong IFN-γ-driven responses . However, there was no significantly higher concentrations of IL-10 observed in groups immunized with rEtCHP559. IFN-γ is reported to be associated with protective immune responses to avian coccidiosis . The CD8+ T lymphocytes can secret high levels of IFN-γ in response to the parasite , but IL-17 inhibits the expression of IFN-γ in infection and the immune response . In the present study, there was no significant level of IFN-γ detected and the inconsistency of sCD8 and IL-17 needs to be further researched.
In our study, we determined the serum IgG titers of chickens immunized with rEtCHP559 and TF protein, and the results showed a significantly high level of IgG compared to the other chickens. In the animal experiments, the experimental group was immunized with EtCHP559 recombinant protein which included TF protein and the TF protein control group was immunized with TF protein, respectively. When we measured the serum IgG antibody by ELISA, the antigen used to coat 96-well microtiter plate was purified recombinant EtCHP559 protein which contained the TF. Because TF is a 48-kDa protein whose molecular mass is more than that of EtCHP559 . So the TF immunization could also raise the rEtCHP559 IgG level. Meanwhile western blotting revealed that rEtCHP559 was detected in the sera of rabbits immunized with E. tenella sporozoite protein. This indicates that EtCHP559 can be recognized by the host immune system and enhances the humoral response.
In summary, we successfully obtained the full sequence of a novel gene EtCHP559 using RACE technique. We expressed and characterized this protein. Our results indicate that the protein has an important role in host cell invasion and induces partial protection against an E. tenella challenge. However, the exact roles of EtCHP559 in cell invasion need to be further researched.
This work was supported by grants from National Science Foundation of China (No. 31201699, No. 31572266, No. 31272557) and Central Public Welfare Research Institutions and Basic Scientific Research Business Expenses (No. 2015JB10). The funders had no role in study design, data collection and analysis,decision to publish, or preparation of the manuscript.
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