Evaluation of Diagnostic Potential of Echinococcus granulosus Recombinant EgAgB8/l, EgAgB8/2 and EPC1 Antigens for Cystic Echinococcosis in Goats.
MATERIALS AND METHODS
Three recombinant proteins of E. granulosus including two EgAgB sub-units EgAgB8/1 and EgAgB8/2 and Echinococcus protoscolex calcium binding protein (EPC1) were expressed in the prokaryotic expression vectors. Total RNA was isolated from the protoscolices retrieved from a fertile hydatid cyst from buffalo liver at a local abattoir using Trizol reagent (Invitrogen, USA). Briefly, ~0.2 x104 protoscolices were treated with Trizol reagent (1ml) and manually homogenized with a micropestle in a sterile 2.0 ml microcentrifuge tube. The lysed protoscolices were freeze-thawed at -80[degrees]C for multiple cycles together with manual homogenization to completely lyse the parasites. Total RNA was isolated from the lysed protoscolices following standard RNA isolation protocol (Invitrogen, USA). The RNA was converted to single stranded cDNA using oligodT primer and reverse transcriptase enzyme (MBI Fermentas, USA) following standard protocols of cDNA synthesis. The cDNA coding for each of the above three target proteins was PCR amplified with gene specific primers (Table1). The PCR products of three target cDNAs were cloned in [p.sup.DRIVE] cloning vector (Qiagen, Germany) and sequence confirmed for each cDNA.
Expression of the recombinant EgAgB8 sub-units and EPC1 protein
The cDNAs coding for Eg AgB8/1, EgAgB 8/2 and EPC1 proteins were PCR amplified with primers designed with suitable restriction enzyme sites and expressed in three different prokaryotic expression vectors (Table 1).
Eg AgB8/1 protein was expressed in [p.sup.Rham] vector in frame with solubility enhancing sumofusion protein (Expresso[TM] Rhamnose cloning and expression kit; Lucigen, USA). E. cloni[R] 10G chemically competent cells were transformed with the recombinant pRham vector and a moderate level of the recombinant fusion protein was generated on induction of the culture with 0.2% L-rhamnose for 8 h at 37[degrees]C. The bacterial cells were disrupted with 6 M guanidine hydrochloride in the lysis buffer (pH 8.0) supplemented with 18 mM imidazole and 10 mM a-mercaptoethanol, followed by sonication of the cell lysate with 3 bursts of 30 sec each at 10 micron amplitude. The protein was purified to complete homogeneity using Ni-NTA affinity chromatography. The recombinant protein was bound to Ni-NTA resin (Qiagen, Germany) at room temperature for 2 h with constant shaking. Affinity column was washed with wash buffer (pH 6.0) supplemented with 18 mM imidazole and protein eluted with elution buffer (pH 4.2).
Expression of the Eg AgB8/2 recombinant protein was carried out in [p.sup.ET32a(+)] vector in Escherichia coli BL21 (DE3).The cDNA was PCR amplified and cloned in the expression vector in frame with the vector fusion tag. An optimum level of expression of the EgAgB8/2 recombinant protein was achieved at 6 h post-1mM IPTG induction at 37[degrees]C. The recombinant protein was purified by lysis of the bacterial cells in lysis buffer (pH 8.0) containing 8 M urea and supplemented with 12 mM imidazole and 10 mM a-mercaptoethanol for 2 h at RT. The cell lysate was then sonicated on ice for 5 cycles of 30 sec each at 5 micron amplitude. The recombinant protein was bound to Ni-NTA resin at room temperature for 2 h with constant shaking. The affinity column was washed with wash buffer (pH 6.5) supplemented with 12 mM imidazole and recombinant protein eluted with elution buffer at pH 4.2.
The EPC1 target protein was expressed in [p.sup.PROEXHT-b] vector, with a higher level of expression of the recombinant protein achieved at 8 h post-IPTG induction at 37[degrees]C. E. coli BL21 (DE3) cells induced with 1mM IPTG were disrupted in lysis buffer (pH 8.0) containing 6 M guanidine hydrochloride and supplemented with 16 mM imidazole at room temperature for 2 h and the recombinant protein was purified by Ni-NTA affinity chromatography. The wash buffer (pH 5.9) was supplemented with 16 mM imidazole and recombinant protein was eluted at pH 4.2. The composition of the lysis, wash and elution buffers used in the purification steps of each recombinant protein was 10 mM tris and 100 mM potassium dihydrogen phosphate containing 6M guanidine hydrochloride or 8M urea as protein denaturant.
The purified recombinant fusion proteins EgAgB8/1, EgAgB8/2 and EPC1 resolved at 25, 29 and 10.5 kDa, respectively in the SDS-PAGE.
Collection of goat sera
Goats (n = 116) were screened for hydatid infection at necropsy at the local abattoir. Out of the 116 animals examined at necropsy, 15 were positive for hydatid cysts in the liver or lungs and remaining 101 were negative for hydatid cysts. Sera were retrieved from these animals and screened for anti-hydatid antibodies by IgG-ELISA with the above three recombinant antigens. Sera were also collected from goats infected with other parasites for their cross-reactivity studies. Sera collected from healthy goats, maintained at Indian Veterinary Research Institute, Izatnagar, were used as negative control in the subsequent immunoassays. All experiments on goats were conducted as per the guidelines of the Institute Animal Ethics Committee.
Enzyme Linked Immunosorbent Assay
Checker board titrations were done to optimize the concentration of each antigen. The amount of recombinant EgAgB8/1, EgAgB8/2 and EPC1 antigens coated on each well of the 96-well microtitre plate was optimized to 1.0 [micro]g/ml, 2.0 [micro]g /ml and 2.0 [micro]g/ml of coating buffer, respectively. The optimal dilutions of serum samples and antigoat IgG-HRP conjugate (Sigma Chemicals, USA) used in the assay were 1:100-1:200 and 1:6000-1:12000, respectively for different antigens. Receiver Operating Characteristic (ROC) curve analysis was performed to determine the cut-off value for each recombinant antigen. Levels of sensitivity were plotted against the levels of one minus specificity at each cut-off point on a ROC curve. Cut-off values were selected that gave the highest sum of sensitivity (%) and specificity (%), as described by Amagai et al (11). The area under the ROC curve (AUC) was the parameter used to define the antigen's discriminatory values between ELISA positive and negative animals.
The Eg AgB8/1 antigen showed positive reactivity with 10/15 necropsy positive animals with [OD.sub.492] ranging between 0.22-1.18 above the cut-off value 0.22. However, 5/15 necropsy confirmed positive animals were negative with EgAgB8/1 ELISA leading to the sensitivity of 66.7%. The IgG-ELISA with this antigen showed 29/101 (28.7%) necropsy negative animals for hydatid cyst as seropositive (Fig 1a). With antigen EgAgB8/2, 12/15 necropsy confirmed positive animals were ELISA positive with [OD.sub.492] values above the cut-off (0.29), thereby depicting the sensitivity of 80.0%. The IgG-ELISA with this antigen showed 27/101 (26.7%) necropsy negative animals as ELISA positive (Fig 2a). The EPC1 based ELISA carried out on the same number of sera had a lower sensitivity of 60% with 9/15 necropsy confirmed positive animals showing [A.sub.492] above the cut-off value (0.29) and 6 were sero-negative with A492 below cut-off. A number of necropsy negative animals (26/101) were sero-positive (25.7%) with this antigen with [A.sub.492] above the cut-off (Fig 3 a). The comparative sensitivity, specificity, positive and negative predictive values of the three assays showed that EgAgB 8/2 antigen has higher sensitivity and specificity than the other two antigens (Table 2).
Studies on the cross-reactivity of each recombinant antigen were conducted with goat sera positive for gastrointestinal (GI) strongyle nematodes and Taenia hydatigenia. The EgAgB8/ 1 antigen showed immuno-reactivity with sera of 3/5 GI nematode infected goats and 14/21 T. hydatigena positive goats with OD above cut off (0.22). However, serum of single goat with a mixed infection of T. hydatigena and GI nematodes showed [OD.sub.492] below negative cut-off. All the goats with a mixed infection of hydatid, T. hydatigena and GI nematodes reacted with the antigen Eg AgB8/1(Fig 1b).
The EgAgB8/2 antigen showed reactivity with 4/5 sera positive for GI nematodes and 16/21 T. hydatigena positive sera with [OD.sub.492] above cut off (0.29). The serum of a single goat with mixed infection of T. hydatigena and GI nematodes showed [OD.sub.492] above negative cut-off. Goats with a mixed infection of hydatid, T. hydatigena and GI nematodes also reacted with the antigen Eg AgB8/ 2 (Fig 2b).
The EPC1 antigen showed sero-reactivity with 2/5 GI nematodes, 8/21 T. hydatigena infected goats with [OD.sub.492] above cut-off (0.29). The serum of the goat with a mixed infection of T. hydatigena and GI nematodes reacted with this antigen with [OD.sub.492] above negative cut-off. Goats with a mixed infection of hydatid, T. hydatigena and GI nematodes also reacted with the antigen EPC1 in IgG ELISA (Fig 3b).
Two sub-units of E. granulosus AgB viz. EgAgB8/1 and EgAgB8/2 along with EPC1 were expressed as recombinant proteins and evaluated in the present investigation for the detection of CE in goats. The two antigen B sub-units EgAgB8/1 and EgAgB8/2 showed a sensitivity of 66.7% and 80% and specificity of 71.3% and 73.3%, respectively. However, EPC1 antigen showed a lower sensitivity (60%) but comparable specificity (72.3%). The three recombinant antigens were found to cross-react with the sera of goats infected with gastrointestinal strongyle nematodes and Taenia hydatigenia equally. Likewise, EPC1 that has shown a potential in the immunodiagnosis of human hydatidosis (12-14) also cross-reacted with the above parasites in goat host. The results indicate that these proteins share cross-reacting epitopes between the taeniid cestodes and strongyle nematodes. IgG4 sub-class antibody has been shown to reduce the cross-reactivity of EgAgB8/ 2 in human patients (15, 16) but no such study has been carried out in goats. Therefore, immunoassays using IgG4 isotype of the antibody could be evaluated for better sensitivity and specificity of these antigens in goats. Peptide based ELISA for improving the sensitivity and specificity of these antigens may also be tested.
Immunodiagnosis of CE in different hosts like pig, cattle, goat, buffalo and camel has been investigated but specific and sensitive diagnosis has been compromised due to false positive reactions and weak serological response generated in infected animals (17-19). Serological cross-reactivity of the hydatid cyst antigens with taeniid cestodes including Taenia hydatigena and T. ovis has hindered the accurate serological diagnosis of hydatid infection in sheep (17). Furthermore, natural intermediate host animals produce very poor antibody responses to infection compared with the relatively high levels of specific antibody evident in human infection (17). Different groups have reported different findings on using the same antigenic component in diagnostic assays, with some authors reporting low antibody response in sheep to antigen B (20, 21) while others showing reasonably high and specific antibody reactivity against antigen B in livestock (18, 22-26). Cross-reactivity of antigen B (similar to antigen 5) with other helminth parasites has been a recurrent challenge to the immunodiagnostic potential of these antigens (10).
The cross-reactivity of the three recombinant antigens with other helminths in goats detected in the present study compromises the specificity of the test. However, these antigens can be used in the sero-surveillance of the goat flocks for cystic echinococcosis in the endemic regions of the country. The present results provide first information on the cross-reactivity of the three potent human CE diagnostic molecules EgAgB8/ 1, EgAgB8/2 and EPC1 of E. granulosus with the helminth parasites of goat. This investigation was carried out on a smaller number of goats but screening of larger sample size and determining the cross-reactivity with more species of helminths parasitizing goats is needed for validating the utility of these three antigens in the sero-diagnosis of cystic echinococcosis in goats.
The authors are highly thankful to the Director, Indian Council of Agricultural Research-Indian Veterinary Research Institute, Izatnagar, India for providing necessary facilities for completing the present research work. The first author is also thankful to Department of Science and Technology, Government of India, New Delhi for providing INSPIRE fellowship for her PhD programme.
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Ajayta Rialch, Mary Nisha Tigga, Arun A, S. Samanta and O.K. Raina
Division of Parasitology, Indian Veterinary Research Institute, Izatnagar--243 122, India.
(Received: 18 July 2016; accepted: 03 September 2016)
* To whom all correspondence should be addressed.
Tel.: 919458269041; E-mail: firstname.lastname@example.org
Caption: Fig 1a & b. IgG-ELISA showing immuno-reactivity (a) and cross reactivity (b) of the goat sera with recombinant antigen EgAgB8/1 (Hd--Hydatid positive sera, N--Healthy goat sera (Negative control), GIN--Gastro intestinal nematodes, Tn-Taenia hydatigena positive sera)
Caption: Fig 2a & b. IgG-ELISA showing immuno-reactivity (a) and cross reactivity (b) of the goat sera with recombinant antigen EgAgB8/1 (Hd-Hydatid positive sera, N-Healthy goat sera (Negative control), GIN--Gastro intestinal nematodes, Tn-Taenia hydatigena positive sera)
Caption: Fig 3a & b. IgG-ELISA showing immuno-reactivity (a) and cross reactivity (b) of the goat sera with recombinant antigen EgAgB8/1 (Hd -Hydatid positive sera, N- Healthy goat sera (Negative control), GIN - Gastro intestinal nematodes, Tn-Taenia hydatigena positive sera)
Table 1. Primer sequences designed for PCR amplification (A) and cloning of three cDNAs coding for the recombinant antigens in expression vectors (B). * Sequences with restriction enzyme sites are indicated in bold and sequences for homologous recombination with SUMO /pRham vector sequence are indicated in bold with italics (B). Gene Primer name Primer length A EgAgB8/1 B8/1-FOR B8/1-REV 24 bp 24 bp EgAgB8/2 B8/2-FOR B8/2-REV 21 bp 24 bp EPC1 EPC-FOR EPC-REV 21 bp 22 bp B EgAgB8/1 B8/1-FOR-SUM 39 bp B8/1-REV-SUM 40 bp EgAgB8/2 B8/2-FOR-EX 33 bp B8/2-REV-EX 32 bp EPC1 EPC-FOR-EX 31 bp EPC-REV-EX 32 bp Gene Primer Sequence (51 a 31) Amplicon size A EgAgB8/1 ATG CTT CTC GCT CTG GCT CTC GTC CTA TTC ACC 247 bp TTC AGC AAT CAA CCC EgAgB8/2 AAA GAT GAG CCA AAA GCA CAC TTA CTT TGA ATC 250 bp ATC ATC TTT TTC EPC1 TGC GTT TGT CGT TCC TGC CGT TTA GAA GAG AGC 231 bp CAT TAA CTC A B EgAgB8/1 CGC GAA CAG ATT GGA GGT ATG CTT CTC GCT CTG 281 bp GCT CTC GTG GCG GCC GCT CTA TTA TTC ACC TTC AGC AAT CAA CCC T EgAgB8/2 GGA TCC ATG GGC AAA GAT GAG CCA AAA GCA CAC 270 bp CTC GAA GCT TAC TTT GAA TCA TCA TCT TTT TC EPC1 CCA TGG ATC CTG CGT TTG TCG TTC CTG CCG T 251 bp CGA GTC TAG ATT AGA AGA GAG CCA TTA ACT CA Table 2. Showing sensitivity, specificity and accuracy of IgG-ELISA with three recombinant antigens based on ROC analysis Antigen AUC Cut-off Sensitivity (%) EgAgB8/1 0.690 0.22 66.7 EgAgB8/2 0.740 0.29 80 EPC1 0.558 0.29 60 Antigen Specificity PPV NPV Accuracy (%) (%) (%) (%) EgAgB8/1 71.3 25.6 93.5 70.6 EgAgB8/2 73.3 30.7 96.1 74.1 EPC1 72.3 25.7 92.5 72.4
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|Author:||Rialch, Ajayta; Tigga, Mary Nisha; Arun, A.; Samanta, S.; Raina, O.K.|
|Publication:||Journal of Pure and Applied Microbiology|
|Date:||Mar 1, 2017|
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