- Open Access
Cloning and expression of a Trichinella spiralis putative glutathione S-transferase and its elicited protective immunity against challenge infections
Parasites & Vectorsvolume 10, Article number: 448 (2017)
Glutathione-S-transferase (GST) is a widespread multigene family of detoxification enzymes. The vaccination of mice with recombinant GST of 24 kDa from Trichinella spiralis elicited a low immune protection against challenge infection. The objective of this study was to characterize the T. spiralis putative GST gene (TspGST) encoding a 30.8 kDa protein and to evaluate its potential as a candidate antigen for anti-Trichinella vaccine.
The full-length cDNA sequence of TspGST from T. spiralis muscle larvae (ML) was expressed in E. coli. The enzymatic activity and antigenicity of the rTspGST were identified by spectrophotometry, Western blot, and ELISA. The expression of TspGST at T. spiralis various stages was investigated by RT-PCR and indirect immunofluorescent test (IIFT). Serum level of total IgG, IgG1, and IgG2a antibodies against rTspGST were measured by ELISA. The immune protection produced by vaccination with rTspGST against T. spiralis was evaluated.
The sequencing results showed that the cDNA of TspGST was 840 bp, and encoded a protein of 279 amino acids, which had a molecular size of 30.8 kDa and a pI of 5.21. Its amino acid sequence shares 37% similarity with TsGST. The rTspGST protein had enzymatic activity of GST. On Western blot and ELISA analysis, the native TspGST protein with 30.8 kDa in crude antigens derived from adult worms (AW), newborn larvae (NBL), infective intestinal larvae (IIL) and ML was recognized by anti-rTspGST sera, but the ML ES antigens could be not recognized by anti-rTspGST sera. Expression of TspGST was found in all of T. spiralis various stages (AW, NBL, ML, and IIL). An immunolocalization analysis identified TspGST in different stages (mainly in cuticles) of the nematode. The mice vaccinated with the rTspGST elicited Th2-predominant immune responses, showed a 34.38% reduction of adult worms and a 43.70% reduction of muscle larvae.
Immunization with rTspGST produced a partial immune protection, and the rTspGST could be regarded as a potential candidate target for an anti-Trichinella vaccine.
Trichinellosis is a major foodborne parasitic disease resulted from ingesting raw or semi-cooked meat infected with Trichinella infective larvae . Trichinella infection in animals and humans has been recorded in most provinces on the Chinese Mainland, and 15 outbreaks of trichinellosis consisting of 1387 cases and four deaths occurred from 2004 to 2009 [2,3,4]. Pork is the dominating source of infection for trichinellosis outbreaks in China. Swine Trichinella infection is an important hygiene problem for meat product safety and public health . Therefore, an anti-Trichinella vaccine for domestic pigs has become another promising measure to prevent the transmission of trichinellosis from swine to humans [6,7,8,9].
After being ingested, Trichinella spiralis muscle larvae (ML) are released in the stomach with the help of digestive enzymes, migrate to the intestine, and develop into the infective intestinal larvae (IIL) . The IIL penetrate the intestinal epithelium, molt four times, and then develop into adult worms (AW) which copulate and produce newborn larvae (NBL). Since the IIL is the first invasion phase during T. spiralis life-cycle, an anti-Trichinella vaccine against the IIL could potentially prevent the intestinal Trichinella infection, which might block or inhibit the subsequent occurrence of the muscular phase of trichinellosis. Previous studies demonstrated that the T. spiralis glutathione-S-transferase (TsGST) gene (GenBank: XM_003371707.1) encoding a 24 kDa protein was an up-regulated gene in the IIL compared with the ML stage [11, 12], suggesting that the TsGST might be a larval invasion-related protease. However, the vaccination of mice with the rTsGST resulted in a 35.71% reduction of adults in the intestine and a 38.55% reduction of larvae in muscle, indicating that immunization with the rTsGST elicited a low immune protection against T. spiralis infection . In this study, we cloned and expressed a putative T. spiralis GST gene (GenBank: XM_003373603) encoding a 30.8 kDa protein , the characteristics of TspGST was investigated, and the immune protection generated by the rTspGST immunization was evaluated in mice.
Parasites and experimental animals
The T. spiralis isolate (ISS534) used here was from a domestic pig in the Henan Province of China. It was passaged in Kunming mice at 6–8 month intervals in our laboratory. Female BALB/c mice, specific pathogen-free (SPF) and 4–6 weeks of age, were obtained from the Henan Provincial Experimental Animal Center (Zhengzhou, China).
Parasite collection and antigen preparation
The mice were infected orally with 300 T. spiralis ML and euthanized at 42 days post infection (dpi). The carcasses were artificially digested by digestion solution containing 0.33% pepsin (1:31,000; Sigma-Aldrich, St. Louis, MO, USA) and 1% HCl at 43 °C for 2 h, and then the ML were collected [15, 16]. The IIL were recovered from small intestines of experimentally infected mice at 6 h post infection (hpi) , and the AW were respectively collected from the duodenum and jejunum of infected mice at 3 and 6 dpi . The NBL was obtained from female worms incubated in RPMI-1640 medium at 37 °C for 24 h . The soluble proteins (crude antigens) of AW, NBL, ML and IIL, and excretory-secretory (ES) proteins from the ML were prepared [20, 21].
Cloning, expression, and identification of TspGST
The TspGST gene (GenBank accession no. XM_003373603) was amplified by PCR using specific primers with BamHI and Hind III restriction enzyme sites (underlined) (forward: 5′-TAT AGG ATC CAT GAC CAA CAC GTC GAA GAA AGG-3′; reverse, 5′-GCC CAA GCT TTC ATT GAC TTT CAA TAG TCA CTG G-3′). The purified PCR product was cloned into the pMD19-T vector (Takara, Dalian, China), subsequently sub-cloned into the pQE-80 L (Novagen, La Jolla, CA, USA). The recombinant plasmid carrying the TspGST gene was transformed into Escherichia coli BL21 (DE3) (Novagen), and expressed under IPTG induction. The rTspGST was purified using Ni-NTA-Sefinose resin (Sangon Biotech, Shanghai, China). The concentration of the purified rTspGST was assayed as described previously , and identified by SDS-PAGE analysis . The gel was stained with 0.25% Coomassie brilliant blue R-250 (Sigma-Aldrich), and subsequently decolorized.
Assay of rTspGST enzymatic activity
The enzymatic activity of the purified rTspGST was determined spectrophotometrically by observing the production of the thioether (S-2,4-dinitrophenylglutathione) between the reduced form of glutathione and 1-chloro-2,4-dinitrobenzene (CDNB; Sigma-Aldrich). The enzymatic product extinction coefficient ε = 9600 M-1 cm-1 at 25 °C at 340 nm. The reaction was conducted in 1 ml reaction mixture consisting of 1 mM reduced GSH, 7 μg of rTspGST, and 100 mM phosphate buffer. The reaction was started by the addition of 1 mM CDNB as substrates, and the increase in absorbance at 340 nm was recorded for 5 min . The rTsGST samples were repeatedly assayed three times, and the results were shown as mean values ± standard deviation (SD).
Immunization of mice
The mice were randomly divided into three groups (20 animals per group). The vaccination group of mice was subcutaneously inoculated at multiple abdominal sites with 20 μg of rTspGST emulsified with complete Freund’s adjuvant and boosted three times with the rTspGST with incomplete Freund’s adjuvant at an interval of 10 days. Two control groups were inoculated with adjuvant or PBS using the vaccination mentioned above procedure . Tail blood from vaccinated mice was respectively collected at 0, 10, 20, 30 and 40 days after vaccination.
Determination of antibodies to rTspGST
Serum anti-rTspGST IgG of vaccinated mice was assayed by ELISA with crude antigens of ML, IIL, AW and NBL, ML ES antigens, or the rTsGST; the IgG subtypes (IgG1 and IgG2a) were also assayed by ELISA with the rTspGST . The plates (Nunc, Roskilde, Denmark) were coated at 4 °C overnight with 1.5 μg/ml of the rTspGST, and crude antigens of T. spirali various stages. The plates were blocked with 200 μl of PBS-Tween 20 (PBST) containing 5% skimmed milk. Serum samples diluted at 1:100 were added and incubated at 37 °C for 1 h. HRP-conjugated goat anti-mouse IgG, IgG1 or IgG2a (1:5000; Sigma-Aldrich) were used as the secondary antibodies, and o-phenylenediamine dihydrochloride (OPD; Sigma-Aldrich) was used as a substrate. The absorbance at 490 nm was assayed with a microplate reader (Tecan, Schweiz, AG, Switzerland).
Western blot analysis
Proteins included 15 μg/lane of ML crude and ES antigens, and the rTsGST. The proteins were separated by SDS-PAGE at 120 V for 2.5 h, then transferred onto nitrocellulose membranes (Merck Millipore, Billerica, MA, USA) at 20 V for 40 min . The membranes were clipped into strips, blocked by PBST with 5% skimmed milk at 37 °C for 1 h, and incubated at 37 °C for 1 h with 1:100 dilutions of different mouse sera (anti-rTspGST sera, sera from mice infected T. spiralis at 42 dpi and normal mouse sera). After washing, the strips were incubated with HRP-conjugated goat anti-mouse IgG (Sigma-Aldrich). 3, 3′-diaminobenzidine tetrahydrochloride (DAB; Sigma-Aldrich) was used as the substrate .
RT-PCR analysis of TspGST gene transcription
Total RNA was respectively extracted by using Trizol reagent (Invitrogen, Carlsbad, CA, USA) from T. spiralis various stages (AW at 3 and 6 dpi, NBL, ML, and IIL). RT-PCR was conducted as described . A housekeeping gene of T. spiralis (glyceraldehyde-3-phosphate dehydrogenase, GAPDH) was also amplified as a positive control. PBS was used as negative control for all PCRs.
Indirect immunofluorescent test (IIFT)
The IIFT was used to determine the expression and immunolocalization of the native TspGST at T. spiralis diverse stages . The whole intact worms and sections of the parasite tissues were blocked in PBS containing 5% goat sera, reacted with 1:100 dilutions of anti-rTspGST sera, infection sera or normal mouse sera at 37 °C for 1 h. The FITC-labeled goat anti-mouse IgG (Santa Cruz Biotechnology, Dallas, Texas, USA) diluted at 1:100 was used as the secondary antibodies. After washing, the whole worms and tissue sections were observed with a fluorescent microscope (Olympus, Tokyo, Japan).
Ten days after the last vaccination, each mouse of three groups was challenged orally with 300 T. spiralis ML. Ten mice of each group were sacrificed at 5 dpi, and the intestinal AW were recovered and counted [29, 30]. The ML burdens from the other ten mice of each group were investigated at 42 dpi by artificial digestion [13, 31]. The immune protection was evaluated as the reduction rate of recovered AW and larvae per gram (LPG) of muscles of the vaccinated groups versus that of the PBS group .
The statistical analyses of the data were performed via SPSS for Windows, version 17.0. The data of OD values of antibody levels and the AW and ML recovery were shown as the mean value ± standard deviation (SD). One-way ANOVA or Student’s t-test was utilized for the analysis of intra- and intergroup differences, and P < 0.05 was regarded as statistically significant.
Molecular cloning and expression of the cDNA encoding a 30.8 kDa TspGST
The full-length TspGST cDNA was 840 bp and encoded a protein of 279 amino acids, which had a molecular size of 30.8 kDa and a pI of 5.21. SignalP 4.1 Server predicted that the TspGST did not have signal peptides. The TspGST had only the 37% identity with TsGST at the amino acid level, which was aligned by protein BLAST. The pQE-80 L harboring the TspGST gene was successfully transformed into E. coli BL21 (DE3) bacteria. After being induced with 0.5 mM IPTG, recombinant TspGST produced a band of approximately 30.8 kDa protein examined by SDS-PAGE, the molecular weight of the rTspGST protein was compatible with its predicted size. On SDS-PAGE analysis, the rTspGST protein purified by Ni-NTA-Sefinose Column showed a clear single band (Fig. 1).
Enzymatic activity of rTspGST
The enzymatic activity analysis revealed that the enzymatic activity of the rTspGST to conjugate glutathione to CDNB was 115.42 ± 7.71 U/mg protein.
Analysis of rTspGST antigenicity
The rTspGST was identified by anti-rTspGST serum on Western blot analysis. Anti-rTspGST sera also identified the native TspGST protein in ML crude antigens but did not identify the ML ES antigens. Furthermore, the rTspGST was identified by sera of mice vaccinated with ML crude antigens, but not by sera of mice vaccinated with ML ES antigens (Fig. 2). The results were obtained under the current experimental conditions, and it is possible that the TspGST cannot be detected if the expression of TspGST in ML ES antigens is low. Also, the ELISA results showed anti-rTspGST sera was strongly reacted with the rTspGST, and crude antigens of T. spiralis different stages (NBL, AW at 3 and 6 dpi, ML and IIL), but anti-rTspGST sera did not react with the ML ES antigens (Fig. 3). These results suggested that TspGST would be one component of the somatic proteins of T. spiralis different phases, but not from ML ES proteins, which indicates that TspGST would not be secreted, and did not expose to the immune system during the muscular phase of T. spiralis infection.
RT-PCR analysis of TspGST gene transcription at various stages
The TspGST gene (840 bp) was amplified by RT-PCR from T. spiralis various stages (AW at 3 and 6 dpi, NBL, ML and IIL). The housekeeping GAPDH gene was also amplified from all T. spiralis developmental stages as a positive control (570 bp) (Fig. 4).
Expression and immunolocalization of TspGST by IIFT
The IIFT with the intact parasite revealed that green fluorescence staining by anti-rTspGST sera was seen on the surface of AW at 3 and 6 dpi as well as NBL. In contrast, no visible staining was found on the surface of the ML and IIL (Fig. 5). After the worm tissue sections from T. spiralis different phases were probed with anti-rTspGST sera, the positive staining was distributed at the cuticles of the AW, ML and IIL, and the embryos within the female uterus.
Humoral antibody responses elicited by vaccination with rTspGST
Serum specific anti-rTspGST IgG, IgG1, and IgG2a at different time after vaccination were examined by ELISA with the rTspGST. The levels of anti-rTspGST IgG in vaccinated mice were obviously elevated after the first and second vaccination and continued to rise at the end of the experiment (Fig. 6). But all of the mice injected with PBS or adjuvant did not show evidently anti-rTspGST antibody responses. Anti-rTspGST IgG subtype assay demonstrated that after the first and second vaccination, the IgG1 levels were remarkably higher than the IgG2a (t 10d (11) = 16.432, P < 0.0001; t 20d (11) = 13.942, P < 0.0001; t 30d (11) = 27.07, P < 0.0001; t 40d (11) = 27.528, P < 0.0001), indicating that Th2-predominant immune response was induced in the immunized mice. However, it was obvious that the IgG2a was elicited after the second vaccination.
Vaccination with rTspGST protected mice against T. spiralis challenge
Immune protection against T. spiralis challenge infection was evaluated in mice vaccinated with rTspGST. The mice vaccinated with rTspGST exhibited a 34.38% reduction of adult worms in intestines and a 43.70% reduction of larvae in skeletal muscles (Fig. 7) compared with the mice injected with only PBS (F adults (2,25) = 6.45, P = 0.002; F larvae (2,26) = 11.555, P < 0.0001). Moreover, the difference of adult (t (16) = 2.524, P = 0.023) and larval reduction (t (19) = 4.002, P = 0.001) between the vaccination group and adjuvant group was also statistically significant, whereas there was no statistical difference in the adult (P = 0.433) and larval worm (P = 0.558) burden between the alone adjuvant and PBS groups.
Glutathione-S-transferase (GST) is a superfamily of detoxification enzymes catalyzing detoxification reactions. The previous studies demonstrated that the GSTs of Echinococcus granulosus, Fasciola hepatica, Necator americanus, Ancylostoma caninum and Seteria cervi induce the evident immune protection [33,34,35,36,37]. The schistosome GST28 has been identified as an effective protective antigen against Schistosoma infections [38, 39]. The vaccination of mice with the rGST26 from Fasciola gigantica showed a 77 to 84% immune protection of mice against challenge infection . The recombinant GSTs from N. americanus had powerful capacities of binding to and detoxifying the toxic heme, which contributes to the obvious immune protection against challenge infection in hamster vaccine trials . The Na-GST-1 from Necator americanus has been developed as an important hookworm vaccine, the phase 1 clinical trials were carried out in Brazilian and American volunteers, and the prominent antigen-specific IgG responses and protective immunity were produced [41, 42]. The GST seems to be an essential protein for development and survival of the parasite and could be used as a potential target for the vaccine capable of preventing parasite infection. Our previous studies indicated that the vaccination of mice with a 24 kDa rTsGST produced a 35.71% reduction of T. spiralis adults in intestines and a 38.55% reduction of larvae in muscles, the vaccination with rTsGST elicited a low immune protection against challenge infection .
In this study, a T. spiralis putative GST gene encoding a 30.8 kDa protein was expressed in E. coli (BL21). The results revealed that the cDNA of TspGST was 840 bp and encoded a protein of 279 amino acids, and this protein had a molecular size of 30.8 kDa and a pI of 5.21. TspGST has only the 37% identity with TsGST at the amino acid level, suggesting that the TspGST is a significant different protein from the TsGST. The results of ELISA indicated that the immunization with the rTspGST generated the significant specific antibodies against the rTspGST, and induced the higher levels of IgG1 (Th2-predominant humoral immune responses). Anti-rTspGST antibodies recognized the native TspGST distinctly in crude proteins of AW at 3 and 6 dpi, NBL, ML and IIL, but not in the ML ES proteins. Moreover, the rTspGST could be probed by sera from mice immunized with ML crude antigens, but not by sera from mice immunized with the ML ES antigens. Nonetheless, the native TspGST in the ML crude antigens was not probed with mouse infection sera, and the ML ES antigens were not probed with anti-rTspGST sera possible because the TspGST is not an ES protein and might be a cytoplasmic protein. The results suggested that the native TsGST could not be secreted and could not elicit the host to produce an obvious humoral immune response in the process of natural Trichinella infection. Previous other studies also demonstrated the native TsGST was found in soluble somatic proteins of T. spiralis ML by Western blotting and ELISA, but not in the ES proteins of the ML [13, 43]. The results showed that the TsGST could be one component of the somatic proteins of T. spiralis different stages (AW, NBL, ML and IIL), but it was not from the ES protein.
The expression level of the TspGST gene was determined by RT-PCR and IIFT. As shown in Fig. 3, TspGST mRNA is transcribed at T. spiralis various stages (AW, NBL, ML and IIL). The results of IIFT with anti-rTspGST sera demonstrated that the green fluorescent staining was found in all the developmental phases (principally in cuticles, and embryos within the female uterus). The results showed that TspGST was expressed at all the T. spiralis life-cycle stages. It is suggested that TspGST mighty be an obligatory protein for the invasion, growth, and survival in a host of this nematode.
In this experiment, the Th2-predominant immune responses were elicited by vaccination with rTspGST. After being challenged orally with T. spiralis ML, the vaccination with rTspGST resulted in a 34.38% reduction of AW and a 43.70% reduction of ML. The results suggested that the partial immune protection produced by vaccination with rTspGST might be the results of a generation of anti-TspGST antibodies which neutralized the partial enzyme activity of GST [44, 45]. The neutralization of the GST by anti-GST antibodies could decrease the survival of the filarial nematode Wuchereria bancrofti in the host . The GST of Schistosoma spp. is an ES protein, the anti-GST antibodies could sufficiently neutralize the enzyme activity of schistosome GST, which leads to prominent reduction of worm burdens in the vaccinated animals [44, 47]. But the TspGST is not a secretory protein, anti-rTspGST antibodies generated by immunization with rTspGST were not enough to neutralize TsGST enzyme activity in cytoplasm. The vaccination with rTspGST produced a partial immune protection against Trichinella infection. Hence, the oral polyvalent vaccines against the ES proteins of T. spiralis various developmental stages should be exploited in future experiments [8, 32, 48].
The TsGST was expressed in all life-cycle stages of T. spiralis and distributed mainly in the cuticle of the parasitic nematode. The immunization with rTspGST elicited Th2-predominant immune responses and exhibited a partial immune protection against T. spiralis challenge infection. The TsGST could be regarded as a potential candidate target for anti-Trichinella vaccine, but its immune protection ought to be furtherly evaluated in a swine model, and the oral polyvalent vaccines against the ES proteins of T. spiralis various developmental stages should be exploited in future studies.
3, 3′-diaminobenzidine tetrahydrochloride
Indirect immunofluorescent test
Intestinal infective larvae
Larvae per gram
Open reading frame
T. spiralis putative glutathione-S-transferase
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This study was supported by a grant from the National Natural Science Foundation of China (no. 81471981).
Availability of data and materials
The DNA sequence data analyzed during the present study are available in the GenBank database (accession No. XM_003373603 for TspGST).
This study was conducted according to the National Guidelines for Experimental Animal Welfare (MOST of the People’s Republic of China, 2006). All the animal experiments were authorized by the Life Science Ethics Committee, Zhengzhou University (no. 2011–016).
Consent for publication
The authors declare that they have no competing interests.
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