Novel recombinant Mce-truncated protein based ELISA for the diagnosis of Mycobacterium avium subsp. paratuberculosis infection in domestic livestock

Johne’s disease (JD) is an infectious wasting condition of ruminants caused by Mycobacterium avium subsp. paratuberculosis (MAP) in domestic livestock of every country that has been investigated. Controlling JD is problematic due to the lack of sensitive, specific, efficient, and cost-effective diagnostic tests. A major challenge in the development of diagnostics like ELISA is the selection of an ideal antigen/(s) that is pathogen-specific and allows sensitive recognition. Therefore, the purpose of this study was to identify and use Mce-truncated protein-based ELISA assay for the diagnosis of MAP infection with high sensitivity and specificity. In silico epitope prediction by epitope mapping throughout the whole length of MAP2191 protein revealed that C-terminal portion of this protein presented potential T- and B-cell epitopes. Therefore, a novel Mce-truncated protein encoded by the selected region of MAP2191 gene was expressed, purified with Ni-NTA gel matrix and confirmed by SDS PAGE and western blot. A profiling ELISA assay was developed to evaluate sera from MAP infected and non-infected ruminant species for antibodies against Mce-truncated protein to infer the immunogenicity of this protein in the host. Using this Mce protein-based ELISA, 251 goats, 53 sheep, 117 buffaloes, and 33 cattle serum samples were screened and 49.4, 51.0, 69.2, and 54.6% animals, respectively, were found positive. Comparing with i-ELISA, the new Mce-based ELISA kit showed a relatively higher specificity but suffered from slightly reduced sensitivity. Mce-based ELISA excluded apparently false positive results of i-ELISA. Mce protein was found to be antigenic and Mce-ELISA test could be employed as a diagnostic test for JD in domestic livestock in view of the a relatively higher specificity and accuracy. The antigenic potential of Mce antigen can also be exploited for the development of a new vaccine for the control of MAP infection.

were included in this study. Animals were in variable age mainly from females and they have mixed physical conditions and 30-35% of the animals were suffering from clinical to advance clinical JD. All these animals were ear-tagged for identification.For the collection of blood samples goats and sheep by restraining manually by side of chest and gently holding the the head towards one side. Cattle and buffaloes were properly restrained in cattle crush and blood (2-3 ml) was collected in vacutainers, after properly sterilizing the jugular vein with 70.0% ethyl alcohol. Institute Animal Ethics committee (IAEC) of the CIRG, Mathura, UP, India has approved the technical program of the project. Samples were stored at -20˚C until screened. Status of the animals with respect to MAP infection was determined using 'Gold Standard'fecal culture, fecal microscopy and fecal IS900-PCR before screening through i-ELISA and Mce-ELISA.

Morphological and molecular characterization
Reference strain of MAP 'S 5' Indian Bison Type was provided by CIRG, Mathura, UP, India. Strain used in this study was recovered from an advance case of JD (terminally sick, extremely weak and recumbent) in a Jamunapari breed of goat [29], which later succumbed to disease [30]. The MAP strain was sub-cultured and colonies identified morphologically on Herrold's egg yolk (HEY) agar medium, mycobactin dependency and acid fast (Ziehl-Neelsen) staining of smears. Method for fecal culture and decontamination methods explained in the text. Briefly, ingredients of HEYM weighed (Mineral salt solution-MSS) and pH was made 7.8 after adding glycerol. Agar powder added and MSS (870 mil) was autoclaved. Egg yolk (120 ml from 8 eggs) harvested after sterilizing in isopropanol. Antibiotic free eggs from local poultry farmers used. Harvested yolk and 5 ml of 2.0% malachite green were added to MSS at 560C and HEYM was stirred for 2 hr at 500C. Mycobactin J was added to HEYM and dispensed. Fecal smears were made from middle layer after triturating feces (2 gm) in 10 ml sterilized water and centrifuged at 5000 rpm for 60 min. Molecular characterization of the strain was done using IS900, IS1311 PCR and IS1311 PCR-REA [29].

Identification of antigenicity mce gene by in-silico analysis
In Silico analysis of the MAP2191 protein was carried out using CLC Genomics Workbench 7.5.1 program (CLC bio, QIAGEN, Germany) and Major histocompatibility complex (MHC) binding peptide prediction algorithms through Immune Epitope Database and Analysis Resource (IEDB-AR) site (http://www.iedb.org/). MAP2191 protein full-length coding sequence was subjected to a basic local alignment search (BLASTp) analysis at the National Center for Biotechnology Information (NCBI) GenBank. After that T cell MHC class I and II epitopes prediction were performed using the IEDB-AR analysis consensus tool, which combines predictions from the Artificial neural network (ANN), Stabilized matrix method (SMM) and combLib [13,[31][32][33][34]. T cell epitopes prediction were calculated on the basis of their binding affinity to MHC alleles of the mouse, using the half-maximal inhibitory concentration (IC50) values as follows: IC50s <50 nm (high-affinity binding); IC50s <500 nm (intermediate-affinity binding), and IC50s <5,000 nm (low-affinity binding). A lower IC50 for MAP2191 protein indicates a higher affinity of binding to host MHC alleles. Mouse MHC alleles H-2Db, H-2Dd, H-2Kb, H-2Kd, H-2Kk, and H-2Ld were used for peptide binding affinity to MHC-I epitopes and H-2IAb, H-2IAd, and H-2IEd were used for peptide binding affinity to MHC-II epitopes [31][32][33]. For the prediction of linear and conformational B cell epitopes, the MAP2191 protein sequence was subjected to an ElliPro suite [35]. We obtained a score for each predicted epitope defined by PI average over each amino acid residue present in the MAP2191 protein. Predicted B cell epitopes of MAP2191 protein had scores of between 0.5 and 0.9; the minimum prediction cutoff score was set at 0.80.

Amplification and cloning of mce-truncated gene in TA-cloning vector
Mce-truncated gene (Accession number: MG754208) was successfully amplified with the help of primers designed to have BamHI and HindIII restriction enzyme sites (Table 1). Thermocycling was done in Veriti 96 well thermal cycler (Applied Biosystem), with initial hot start denaturation step for 5 min at 94˚C, followed by 37 cycles of 94˚C for 1 min, 58˚C for 30 sec, and 72˚C for 1 min. Subsequently, a final extension at 72˚C for 10 min was carried out. Purified mce-truncated was confirmed by nucleic acid sequencing and cloned with pTZ57R/T cloning vector. Ligation products were successfully transformed into E. coli DH5α/E. coli XL10-Gold ultra-competent cells followed by plating on Luria Bertani (LB) agar (Merck, Germany) containing X-gal, IPTG, Ampicillin, Tetracycline, and Chloramphenicol. Final confirmation of purified clones was done using restriction digestion followed by sequencing.

Cloning and confirmation of mce-truncated gene in expression vector
Expression plasmid was generated by cloning mce-truncated gene of MAP using pET28a (+) expression vector as per   [36] with some modifications. Prior to ligation reaction, pET28a vector was restricted with HindIII and BamHI endonuclease, de-phosphorylated by a fast alkaline phosphatase enzyme (Fermentas, USA) with 10X FastAP buffer, and gel purified. For ligation reaction, mce-truncated gene fragment was digested from a pTZ57R/T vector with HindIII and BamHI, gel purified, and ligated with de-phosphorylated and digested using pET28a plasmid. Ligation product was transformed into E. coli DH5α/XL-10 competent cells followed by plating on LB-agar containing 50 μg ml -1 Kanamycin. Six to ten colonies were picked for mce-truncated colony PCR for the confirmation of the insert. Plasmid DNA of

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concern clones was isolated and digested with HindIII and BamHI enzymes. In order to further confirm the insert, one of the confirmed pET28a-mce-truncated cloning vectors was sequenced using T7 universal primers.

Expression and purification of Mce-recombinant protein
To express Mce-truncated protein, cloned vector was further transformed into E. coli Rosetta and E. coli BL-21 (DE3) competent cells; a single colony was picked up and propagated in 10 ml fresh Luria Bertani broth supplemented with Kanamycin (50 μg ml -1 ) at 37˚C with shaking (180 rpm) overnight. For expression, 500 ml LB-broth containing Kanamycin were inoculated with 1% overnight grown culture and propagated until the absorbance reached approximately 0.5 at 600 nm. In the next step, cells were induced with different concentrations of IPTG and cultures were grown at different temperatures for different time intervals. One ml of uninduced cells (as negative control) were collected just before the addition of IPTG and from the induced cells at different time intervals, i.e. 2, 4, 6, 8, 10, 20 and 24 hrs. post induction. Collected culture was centrifuged and the pellet was harvested.
Purification of His-tagged Mce-truncated protein was carried out by affinity chromatography on a nickel-nitrilo triacetic acid (Ni-NTA) gel matrix (Qiagen, USA) using batch method. In brief, Rosetta and BL21 cells, harboring mce-truncated pellets, were suspended by gentle stirring in 15 ml equilibration buffer (50 mm Tris. HCl, 200 mm NaCl, 5mm DTT, 1mm PMSF, pH 8.0). The 14 ml cell suspension was lysed on ice using sonication at 30% amplitude for 20 cycles (20 sec pulse on, 20 sec pulse off). Then, a 50 ml conical tube containing 12 ml crude lysate was equilibrated with 1ml of pre-washed Ni-NTA resin in a horizontal position for 8 hours at 4˚C while mixing. After incubation, the equilibrated suspension was centrifuged (2000 rpm, 10 min, 4˚C) and the pellet was washed three times with wash buffer. Captured Mce-truncated proteins were eluted by increasing the imidazole concentration to 250 mM in the elution buffer.

SDS-PAGE and western blotting
Expression of Mce-truncated protein was analyzed by 12% Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE) to investigate the desired size of expressing proteins. For western blotting, Mce-truncated protein band was transferred to nitrocellulose membrane (GE water and process technologies) with a Transblot Turbo1 (Biorad, USA) apparatus operated at 60 volts for 2 hrs. The unbound membrane sites were first blocked by incubation for 30 min in blocking buffer (3% skimmed milk powder) at room temperature (RT). Blocking buffer was removed, followed by three rounds of washing with phosphate buffer saline with tween 20 (PBST buffer). The membrane was dipped with anti His Tag monoclonal antibody (Sigma-Aldrich, Germany; 1:10000 dilutions) for 1 hr. at RT. After 3 final washing with PBS-Tween-20, the membrane was immersed in 0.02% substrate solution (diaminobenzidine (DAB) / Roche Applied Science) suspended in PBS containing 0.03 Hydrogen Peroxide. Color was developed by incubation in the dark at RT for 5-10 min until a deep brown band appeared. Concentration of the purified Mce-truncated protein was estimated by Bradford protein estimation assay. In Addition, another Western blotting was also performed on SDS-PAGE gel with sera from tuberculosis infected animals, to determine the cross reactivity of Mce-truncated protein. Serum samples used to check cross reactivity of protein, were obtained from six tuberculin positive cattle.

Recombinant Mce-truncated protein (antigen)
Recombinant protein Mce (MAP2191) was identified on the basis of it's moleculara weight by SDS-PAGE and it's immunoreactivity in western blot assay.

Mce-ELISA
Mce-ELISA was performed to quantify titer of the antibody in serum samples of naturally infected, suspected, and non-infected (Healthy) animals. Concentrations of serum (1:50), antigen and conjugate (1:8000 for goats and sheep; 1:6000 for cattle and buffaloes) were optimized by checker board analysis. Flat bottom 96-well Microtiter plates (Cat. No. 655061, Greiner bio-one, made in Germany) were coated with 100 μl of recombinant Mce-truncated protein containing 0.02 μg of antigen in coating buffer. Coated plates were incubated over-night at 4˚C. After incubation, antigen-coated plates were washed one time with washing buffer (1X PBS containing 0.05% [v/v] Tween-20). Uncoated surfaces were blocked (100 μl/well) with blocking buffer (3.0% skimmed milk) for one hour at 37˚C. Following three washes with washing buffer, 100 μl of diluted serum (1:50) in serum dilution buffer (1.0% BSA) were added in duplicate to each well. Plates were incubated at 37˚C for one hour, emptied, and washed three times with washing buffer. Secondary antibodies used in this assay were peroxidase-labelled anti-species whole IgG antibody produced in rabbits (Cat. numbers A8919 for goats/sheep and A5295 for cattle/buffaloes, Sigma-Aldrich, Inc.), at 1:8000 dilution for goats and sheep and 1:6000 for cattle and buffaloes in 1xPBS. 100 μl of secondary anti-species antibody was added to each well and incubated for 50 minutes at 37˚C. After washing four times, 100 μl of chromogenic substrate solution of O-Phenylenediamine dihydrochloride (OPD) (Cat. number P3804, Sigma-Aldrich, Inc.) was prepared as per manufacturer's recommendation and added to each well. Plates were incubated for 10-15 minutes in the dark at 37˚C. Extent of the color development (optical density) was measured at the absorbance of 450 nm using Bio-RAD i-mark ELISA plate reader. Positive and negative controls were selected from the animals that were fully characterized on cultural/ morphological characteristics (Ziehl-Neelsen staining), molecular characteristics (IS900 PCR, IS1311PCR and Real time PCR), serological screening (ELISA and Dot-ELISA) and other tests (LAT and FAT).

Indigenous ELISA kit (i-ELISA)
A robust and extensive validated indigenous ELISA kit based on semi-purified Protoplasmic antigen (sPPA) prepared from the characterized strain (S 5) 'Indian Bison Type' bio-type of MAP of goat origin (provided by CIRG) was used for the comparative studies. PPA used in this kit was harvested as whole cell sonicate. Lysate was centrifuged and supernatant was used as antigen after protein estimation. Initially, i-ELISA was developed for the screening of goats and sheep [30,37,38] and has since been standardized for screening cattle and buffaloes [39]. Serum samples were used in 1:50 dilution and anti-species horseradish peroxidase conjugates (Sigma Aldrich, USA) at the dilution of 1:5000 for goats and sheep and 1:4000 for cattle and buffaloes in 1xPBS. Serum samples from culture positive and negative animals were used as positive and negative controls, respectively. S/P ratio for Mce: Optical densities (OD) were expressed as sample-to-positive (S/P) ratios as per Collins (2002) by the following formula (Table 2).

Statistical analyses
Statistical differences between the results of Mce-ELISA and i-ELISA were analyzed by McNemar's and kappa agreement was applied to measure the statistical significance between the results of the two tests (GraphPad software, USA).

Morphological and molecular characteristics of MAP
Colonies of the MAP reference strain (S 5) appeared on the slants of HEY medium. Colonies were small, straw color, translucent, hemispherical, raised with nipple, smooth, and glistening ( Fig 1A). Staining of smears from MAP colonies by ZN-stain exhibited short pink staining cocco-bacillary nature (Fig 1B). Yield of specific PCR products in IS900 PCR, confirmed the presence of MAP (Fig 1C and 1D).

Bioinformatics analysis
Alignment and comparison of MAP K-10 and MAP (S 5) strain sequences illustrated highly conserved sequences, likely to be cross-reactive, as most epitopes were shared. Moreover, MAP2189-MAP2194 cluster organization was also conserved in both the strains. Based on Bioinformatics analysis, MAP2191 gene from MAP was of 1065bp and encodes for a typical linear Mce protein that has 354 amino acids with an estimated molecular weight of 37.510 kDa. Possible secondary structure of the MAP2191 protein was predicted using SOPMA website and analyzed results revealed that this protein consisted of 41.53% α-Helix, 16.95% extended strand, 11.58% β-turn and 29.94% random coils. C-terminal portion of MAP2191 protein was successfully expressed and purified in this study. Partial Mce-truncated protein sequence (amino acids 154 to 354) was chosen based on the predicted sequence to contain most dominant B-and T-cell epitopes. CLC software analysis also revealed that selected region of MAP2191 protein had high antigenic index and was more hydrophilic.

Amplification, cloning, and sub-cloning of mce-truncated gene
Whole DNA was isolated from MAP (S 5) strain, and target region of MAP2191 gene was successfully amplified by PCR. Agarose gel electrophoresis of PCR products showed a single band of 621bp amplicon (603bp mce gene and extra 18bp were used to restrict sites and bring the coding sequence in-frame) as positive for the truncated gene (Fig 2A). Mce-truncated amplicon was sequenced and the sequence results were aligned using BLASTp analysis; no mismatch was reported in sequence data. The amplified mce-truncated fragment was purified and ligated into pTZ57R/T TA cloning vector and transformed into E. coli competent cells. Transformants were confirmed for the presence of mce-truncated insert by specific colony PCR and restriction analysis (Fig 2B). Gene sequencing results confirmed the presence of mce-truncated gene segment in pTZ57R/T vector. Purified mce-truncated gene from TA-cloning vector was sub-

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cloned into pET28a (+) expression vector between the restriction sites BamHI and HindIII and transformed into XL10-Gold ultra-competent cells for the high percentage of recombinant plasmid yields. Presence of the insert was approved by colony PCR and double digestion using

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restriction enzymes (Fig 2C). Gene sequencing results confirmed the presence of mce-truncated gene in the pET28a vector.

Expression and purification of Mce-recombinant protein
The pET28a-mce-truncated plasmid was transformed into Rosetta/BL-21 cells. Transformed cells were induced for expression with optimized concentration of 1.5 mM IPTG (Fig 3A). Samples were collected at different time intervals and were analyzed using 12.0% SDS-PAGE, along with the protein ladder (Precision plus make). The~28-30 kDa Mce-truncated protein was expressed from 2 hrs post induction, while zero hour sample and mock controls showed no observable expression; distinct bands of intensity increased with time between 2 and 24 hrs as shown in Fig 3B. Optimized time interval for the best expression of Mce-truncated protein after induction with IPTG was 20 hrs. Expressed proteins were purified by nickel-nitrilotriacetic acid (Ni-NTA) gel matrix (Qiagen, USA) using batch method; purified Mce-truncated protein run on SDS-PAGE showed single band with an approximate expected molecular mass of

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~28-30 kDa (Fig 4A). Mce-truncated proteins were confirmed using anti-His tagged mouse monoclonal antibody (Sigma Aldrich, Inc.) (Fig 4B). Final yield of pure Mce-truncated protein per liter for E. coli culture was approximately 0.8 gr/L using Bradford method. Cross reactions analysis by western blot also showed that the expressed Mce-truncated protein reacted with sera of MAP infected animals, but did not react with tuberculosis-infected ones (Fig 5). The result suggested that the recombinant Mce-truncated protein had no cross reactions with non-MAP mycobacterial infections, such as tuberculosis.

Antibody response with Mce-ELISA
Newly developed Mce-truncated protein based-ELISA was compared with i-ELISA (an in house ELISA using a semi-purified protoplasmic extract of the S5 'Indian Bison' MAP biotype) ( Table 3). Sample OD values (at 450 nm) were converted to sample-to-positive (S/P) ratios as per Collins (2002) [40]. Serum samples in the positive and strong positive categories were considered positive for MAP infection (Table 3) (Table 4). Though i-ELISA appeared to be more sensitive of the two tests applied, but Mce-ELISA was more specific than i-ELISA (Table 5).
Sheep. Of the 53 serum screened by Mce-ELISA and i-ELISA, 27 (51.0%) and 31 (58.5%) were positive and 26 (49.0%) and 22 (41.5%) were negative, respectively (Table 3). I-ELISA showed higher number of serum samples positive and lower number as negatives than Mce-ELISA. Only 4 (7.5%) positive samples in i-ELISA were missed by Mce-ELISA (Table 4). Here too, i-ELISA was more sensitive, though specificity was lower than Mce-ELISA (Table 5).   (Table 3). Results were comparable; only 3 (2.5%) positive serum in i-ELISA were missed by Mce-ELISA (Table 4). These results showed higher specificity and lowered sensitivity in case of Mce-ELISA as compared to i-ELISA in buffaloes (Table 5).

Statistical analysis
Mc-Nemar test and kappa agreement were used for statistical analysis. P value and kappa agreement were calculated. P values were 0.0071, 0.1336, 0.5050 and 0.2482, and Kappa agreements were 0.785, 0.849, 0.815 and 0.814 in goats, sheep, cattle, and buffaloes, respectively. The strength of agreement was substantial in goats and perfect in another three livestock species (sheep, buffaloes, cattle), respectively (Table 6).

Discussion
MAP, the cause of JD in domestic livestock [41], has also been associated with CD and other auto-immune disorders in human beings [2,4,5,8]. Developing effective strategies for the diagnosis and control of MAP infection remains a major challenge for optimizing the animal health [42]. ELISA test being sensitive, quick and cost effective is preferred as 'screening test' in chronic infections like MAP [37]. Present study described genetic expression of a new Mce protein that could be possibly used as potential antigenic candidate for the development of a new ELISA test for the diagnosis of MAP infection.
Proteins of Mce-family of pathogenic mycobacteria have been associated with virulence by enhancing invasive power and survival in macrophages and various mammalian cell lines [15,[43][44][45][46]. Mce encoded products were found to conferring invasive attribute to otherwise a nonpathogenic strain of E. coli, invading non-phagocytic HeLa cells [16,24,47]. Kumar et al. [48] analyzed and compared the expression profiles of the mce operons of Mycobacterium tuberculosis, Mycobacterium bovis, and Mycobacterium smegmatis under different growth conditions and found the expression of mce1, mce3, and mce4 operons present in tissues collected from infected guinea pigs and rabbits. Hou et al. [49] found that genes similar to MTB mce genes were expressed by Mycobacterium avium during growth in macrophages. Another previous study also revealed presence of mce and PE/ PPE family genes in MAP as virulence factors [50]. In a study conducted by Wu et al. [51], showed that there were islands in both M. avium subsp. avium (MAC) and MAP which encode for different mce genes that were analogous in all the mycobacteria, indicating their functional importance. MAP2191 gene is one of the mce5 operons (MAP2189 to MAP2194) of the MAP; mce5 cluster which has previously been identified as important for invasion and survival of bacilli within macrophages and also virulence of MAP [25,26]. Eight putative Mce-encoding genes have been identified in the MAP strain K-10 genome. Some studies have been carried out to find the unique MAP-specific protein targets, which may elicit strong immune responses in the host [13,52]. Targeting of the MAP2191 gene was based on the identification of putative Band T-cell epitopes in MAP proteins encoded by the mce5 gene cluster and asses their antigenicity during infection. Using Bioinformatics analyses, we identified B-and T-cell epitopes in the C-terminal region of the MAP2191 putative Mce protein. The selected region of MAP2191 protein had a high antigenic index and was more hydrophilic as crevealed by the CLC software analysis. In this study, we generated and cloned a truncated MAP2121 DNA sequence, and subsequently generated the His-tagged recombinant protein in an E. coli host. Our purification method with Ni-NTA agarose resin was very effective and we obtained a large amount of soluble and purified Mce-truncated peptide.
Currently, antigen-based ELISA tests for detecting MAP with a mixture of proteins are available including avian or johnin, a MAP-PPD, whole-cell sonicated extract, protoplasmic antigens etc., [53]. Because analysis and sequencing of the entire MAP genome has been recorded [54], immune reactivity of several specific proteins of the MAP genome have been investigated [55]. In the present study also, serological ELISA assays were conducted and results have been reported for the new ELISA test developed using truncated MAP Mce protein and the traditional i-ELISA kit.
This in house i-ELISA kit has been validated with other commercial ELISA kits (ID-VET, Allied Monitor Inc., USA, antigen based indirect ELISA, Ethanol Vortex ELISA (EV-ELISA), recombinant secretory proteins based cocktail ELISA (c_ELISA) and natural secretory proteins-based ELISA test [10,35,37,56,57] and compared its efficacy in different livestock species (goats, sheep, cattle and buffaloes) [12,58,59]. In this series, Mce-ELISA is the most recently developed ELISA and used for the diagnosis of MAP infection. I-ELISA has been the most validated and robust test was used for evaluating newly developed Mce-ELISA in terms of specificity and sensitivity.
Our earlier studies reported enhanced sensitivity and specificity of the i-ELISA as compared to the other commercially available ELISA kits for the diagnosis of Johne's disease in domestic livestock [38,39]. For example, in a study, i-ELISA kit showed greater diagnostic efficiency than other commercial ELISA kits [38] and improved the detection rate of MAP in test samples [60]. We used S/P-ratios-based categorization of OD values as per Collin (2002), wherein serum samples in the positive and strong positives categories, were considered as positive for MAP infection. This type of categorization exhibited good correlation with fecal culture in some of our other studies [39,61]. Chaubey et al. (2015) compared i-ELISA (Indigenous g-ELISA) with commercial antigen-based b-ELISA and commercial sr-ELISA and found 100% sensitivity. In another report, 91.4% sensitivity of i-ELISA was observed when compared with EV-ELISA kit [57]. These and other findings from other studies confirmed the enhanced sensitivity and specificity of i-ELISA in the detecting of MAP infection in domestic livestock in the country [35,38].
In our study, Mce-truncated protein yielded higher absorbance values against the confirmed positive pooled serum samples, and low-level (but above background) antibody reactivity was also observed with confirmed negative pooled serum samples. The ELISA test using Mce-truncated protein was able to discriminate between the most positive and negative serum samples used in this study. However, the Mce-based ELISA showed a relatively higher specificity than i-ELISA but suffered from slight reduction in sensitivity. These results highlighted the potential capability of Mce-truncated ELISA in preventing false-positive reactions that occur when a milieu of antigens is used in i-ELISA tests. Mce-ELISA has shown perfect agreement with i-ELISA and there is no cross-reactivity with anti-M.bovis antibodies. Therefore, this test could be a better choice for screening of paratuberculosis especially in the region where bovine-TB is endemic. Overall the Mce-based ELISA was comparable to the the highly sensitive and robust 'i-ELISA test', indigenously developed for the screening of livestock population.
In conclusion, this is the first report of a Mce surface protein-based ELISA as new modified ELISA test, as diagnostic test against MAP infection. Affinity of purified Mce-truncated protein was detected by serum antibodies from animals infected with JD and supported the hypothesis that MAP Mce protein was immunogenic and highly expressed protein during MAP infection. True achievement of this study was the isolation and expreseeion of the Mce protein, 'a new antigen' with the huge potential to be further exploited not only as a diagnostic tool but also a new target antigen for the development of a highly effective vaccine for the control and eradication of the incurable Johne's disease in domestic livestock.