Introduction

Tuberculosis (TB) is an emerging zoonotic disease of captive and free-ranging wildlife species with severe consequences in biodiversity and species conservation. Tuberculosis bacteria has a wide wild life host range which includes Elephants [1,2,3], Sloth Bears [4, 5], Arabian Oryx [6], White tailed Deer [7], Reindeer [8], European Badgers [7, 9, 10], Cervids [8], Rhinoceros [11], Lion [12], Badgers [13] and non-humane primates [2, 14]. So far 60 different wild mammal species were proven to be infected with TB [15, 16]. TB in wild animals is an emerging global concern as some of the wild species were proven to be maintenance and reservoir host for TB [17, 18]. Interspecies transmission of TB at wildlife-livestock-human interface poses public health, conservation and economic threats. Ante-mortern diagnosis of TB in wild life is difficult due to the subclinical nature of the infection and limited choice of diagnostic tests for wild life [19].

Gold standard TB diagnostic test in humans is Mycobacterial culture. However, difficulties in sample collection, long incubation period, cumbersome sample processing and sample transport methods render the test impractical for implementation in wild life. Cell mediated immune (CMI) response based diagnostic methods such as skin testing or interferon-gamma release assays are the commonly employed TB surveillance assays in domestic animals. However, CMI based assays require species specific reagents and skin testing is not practical in wild animals. In this context, sero-diagnosis of TB is an alternative in wild life with a scope for improvement in assay sensitivity and specificity [20]. Rapid pen-side sero-diagnostic kits are preferred for TB diagnosis in wild animals as they are simple, inexpensive, rapid and relatively non-invasive diagnostic methods. Moreover, the sero-diagnostic method does not require bio-containment facility, unlike the Mycobacteria detection by culture methods [21].

Multi-antigen print immunoassay (MAPIA) is being used as an appropriate tool for the identification of sero-dominant antigens of TB organism. The MAPIA methodology was adopted in various animal species such as Cattle [22, 23], Elephants [7], Reindeer [8] and European Badgers [24] for determining antigen recognition patterns of serum samples. Early Secretory Protein-6 (ESAT-6) and culture filtrate protein-10 (CFP-10) are the immuno-dominant antigenic candidates in Elephants [25]. However, the immuno-biology of TB may vary with different species and is poorly understood in wild life. Therefore, sensitivity of the assay can be compromised if only a limited number of antigens are used in the development of sero-diagnostic assays. At the same time wild animals are invariably exposed to environmental nonpathogenic Mycobacterial species [26] and various atypical mycobacterium species outside the Mycobacterium tuberculosis complex. Wild animals can mount an antibody response to environmental Mycobacterium resulting in false positivity in TB diagnosis [27].

The present study was aimed at developing a Rapid TB antibody detection kit using recombinant fusion protein of ESAT-6::CFP-10 along with purified protein derivatives (PPDs) of M. bovis for the improved diagnostic sensitivity and also with PPDs of M. avium for assessing the diagnostic specificity. To the best of our knowledge, this is the first report on the development and evaluation of a point of care kit using the above combination of antigens for the diagnosis of TB.

Materials and Methods

Immunochemicals and Reagents

Purified protein derivatives of Mycobacterium bovis (BoPPD) and Mycobacterium avium sub species avium (AvPPD) were procured from Prionics AG (Wagistrasse, Schlieren-Zurich, Switzerland). Wild animal sera samples were sourced from various zoos, rescue centers and temple elephants around India. Bovine positive and negative reference sera were from Animal and Plant Health Agency (APHA), UK.

Cloning and Expression of Recombinant ESAT-6::CFP-10 Fusion Protein

Coding sequence of ESAT-6 and CFP-10 of M. tuberculosis was synthesized as fusion gene construct (GenScript, USA). The gene construct was cloned into prokaryotic expression vector pET28a (Novagen) and the plasmid clone was used to transform chemically competent E. coli BL21 DE3 cells (Invitrogen). The protein expression was induced in the E. coli clone using 1 mM IPTG for overnight at 25 °C. The HIS6 tagged ESAT-6::CFP10 fusion protein was purified from the soluble fraction of the bacterial lysate using Ni–NTA agarose (immobilized metal affinity chromatography). Briefly, a 5 ml Ni–NTA agarose column was equilibrated with 10 column volumes of tris buffered saline (TBS) and the soluble fraction of the bacterial lysate was passed through the column and the column was washed with 20 column volumes of TBS containing 50 mM imidazole and the recombinant protein was eluted using 500 mM imidazole. The pooled protein fractions were dialyzed against PBS (pH 7.4) and purity of the protein was assessed using SDS-PAGE. The protein was identified in a western blot using anti-His antibody.

LPS Removal from the Purified TB Antigens

LPS from recombinant fusion protein ESAT-6::CFP-10 was removed using Triton X100 as per the procedure [22]. Briefly, Triton X −100 was added to the protein sample to a final concentration of 1% (v/v) and incubated at 4 °C for 1 h with continuous mixing. The sample was centrifuged at 7500 rpm for 10 min at 30 °C and the upper miceller phase was collected without disturbing the LPS rich middle and lower phase. Triton X −100 was added again to the upper phase to a final concentration of 0.5% (v/v) and the remaining steps were repeated as mentioned above. Then, the recombinant protein was analysed in SDS-PAGE and western blot.

Characterization of Recombinant Protein

The ESAT-6::CFP-10 fusion protein was characterized using reference culture positive and culture negative sera samples in immuno-blot. Identity of the protein was further established by LC–MS/MS analysis of the trypsin-treated protein sample.

Lateral Flow Assay (LFA) Design and Manufacture

LFA Design and Principle

Immuno-chromatographic strip test was designed as a two module system using the combination of recombinant fusion protein, BoPPD and AvPPD. BoPPD was used in the test line 1 and the recombinant fusion protein was used in the test line 2of test module 1. Similarly, AvPPD and recombinant fusion protein was used in the test lines 1 and 2, respectively, of module 2. The conjugate pad of the assay kits contained gold conjugated protein G and streptavidin. The protein G could bind to antibodies from wide range of animals. The immune complex migrated along the membrane due to the capillary activity and the TB specific antibodies were trapped by the proteins in the test lines 1 and 2. Streptavidin gold was trapped by the biotin in the control line. Colour development in the test line 1 of the module 1 or test line 2 (either of the modules) indicated the presence of antibodies against pathogenic Mycobacteria whereas the development of colour in test line 1 of the module 2 indicated the presence of antibodies against environmental non-pathogenic Mycobacteria (Fig. 1).

Fig. 1
figure 1

LFA kit modules. In kit module 1, the test line 1 was printed with BoPPD and the test line 2 was printed with recombinant ESAT6::CFP10. Whereas in kit module 2, the test line 1 was printed with AvPPD and the test line 2 was printed with recombinant ESAT6::CFP10

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Gold Conjugation of Protein G Antibodies and Streptavidin

Gold conjugation of the protein G and streptavidin was performed using gold chloride (Sigma Aldrich, USA) as per the method described [28]. Briefly, the proteins were mixed with 50-nm gold solution and pH of the solution was adjusted to 7.2 with 50 mM potassium carbonate (pH 9.6) to achieve a final concentration of 15 μg/ml. The unbound protein G from the gold conjugate solution was removed by washing with 15% bovine serum albumin solution. The gold coupled proteins were resuspended in 2% BSA in 10 mM sodium carbonate (pH 9.6) and stored in a refrigerator until further use. The Protein G-coupled gold particle was diluted in dye dilution buffer containing 1% casein and 100 mM sodium phosphate (pH 7). The diluted gold solution was spread onto conjugation pad presoaked in pretreatment buffer containing 1% NP-40, 20mMEDTA, 0.25% L-7600, 1% polyvinylpyrrolidone, 10 mM sodium phosphate and 0.1% sodium azide (pH 7.0); dried in a lyophilizer; stored in a low-humidity room until further use.

LFA Lamination Assembly and Manufacture

The assay membrane and pads were cut as 4.2 mm wide and 60 mm long composite strips using MDI strip cutter Model- M 70 to fit in a plastic assay device that provides the metrics for even flow of analytes and reagent buffer. The strips were laminated on a 300 mm × 60 mm plastic backing consists of a nitrocellulose detection strip in the middle, flanked at one end by a sample pad followed by conjugation pad and at the other end by an absorption pad. The completely laminated strips were cut into 4.2 mm-wide strips and were housed manually into plastic casing and packed in dehumidified room in an aluminum-plastic pouch with a desiccant to ensure the longevity of the product.

Validation of the Assay Kits

Diagnostic Sensitivity and Specificity of the Assay

17 samples from Sloth Bears with confirmed TB based on the postmortem lesions and acid fast staining which were tuberculosis specific were used for the study. Diagnostic sensitivity of the assay was determined using these known positive sera samples of Sloth Bears (N = 17).

Considering the difficulty in determining the TB infection status in wild animals using other tests such as skin test or IGRA, TB positive and negative bovine sera samples were used to estimate the diagnostic sensitivity and specificity of the assay. For this purpose, 200 cattle sera were obtained from APHA, UK (100 from skin-test positive cattle with culture confirmed M. bovis infection and 100 from TB-free animals). The cattle sera samples were designated negative on the basis of IFN γ release assay (IGRA) and skin test results.

Additional Sera Samples from Sloth Bears and Other Wild Animals

Sloth Bear sera samples (n = 74, including the 17 from animals with confirmed TB, referred to in the previous paragraph) were from Wildlife SOS, India and 48 sera samples from other wild animals such as Elephants (n = 9), Felidae (n = 21), Cervidae (n = 14), Cape Buffaloes(n = 2), Wild dog (n = 1) and Wild Bear (n = 1) were collected from captive animals housed in various zoological parks and temples in India. 17 of those Sloth Bears died later due to TB as described above. The remaining 57Sloth Bear sera samples were from in-contact animals with unknown disease status. The other wild animals were with unknown status for TB infection.

Screening of the Study Sera Samples and Interpretation

Sera samples and the LFA kits were brought to room temperature and a drop of sera sample (approximately 5 µl) was drawn using a disposable dropper. The sample was placed onto the sample pad (middle of sample well ‘S’) by holding the dropper vertically and avoiding air bubbles. Additionally, two drops of sample buffer (PBS) was added to the sample well to enable sample flow, through the membrane. The results were read in the results window after 10 min.

Sera samples with positive line in either of the test lines (T1 and T2) of test kit 1 or both the test lines in test kit 1 was considered as seropositive against tuberculosis. Positive line for the recombinant fusion protein was the indication of sero-positivity against pathogenic Mycobacteria. Development of positive line only for the AvPPD (Kit 2—T1) was interpreted as sero-reactivity against non-tuberculous mycobacteria. However, for the routine testing positive line only for T1 of kit 1 (BoPPD) warrants the use of kit 2.

Batch Quality Control for Assembled LFA

Every batch of the kit was checked for its performance using known positive and negative sera.

Batch Signal Strength

The signal strength of the device was considered sufficient when apparently visible lines developed with 5 µl of known positive sera.

Batch Reactivity

Aliquots of positive and negative reference sera samples of Sloth Bear (n = 4), Elephant sera samples (n = 4) and bovine sera samples (n = 4) were stored in −20° C and each batch of the LFA kits were tested with these reference sera samples.

Batch Specificity

Cross reactivity of every batch of LFA kits were tested with reference sera samples of other animal diseases such as Infectious Bovine Rhinotrachitis, Foot and Mouth Disease, Leptospirosis and PPR.

Ethics Statement

The study did not involve any experimental animal usage. The study was conducted using the sera samples available in the repository of Wildlife SOS, India. Testing of bovine sera samples were performed at APHA, UK using the samples available in their repository.

Results

Cloning and Expression of Recombinant Protein

The genetically fused coding sequences of ESAT6 and CFP 10 were cloned into prokaryotic expression vector and the ESAT6::CFP10 fusion protein was expressed as double His6 tagged protein and the positive clones were selected based on the identification of 28 kDa protein band in the immuno-blot using anti-His antibody. The recombinant protein was purified using Ni–NTA agarose column and the purified protein was verified by SDS-PAGE followed by staining with Coomassie brilliant blue. Protein estimation was done using BCA kit and the protein was aliquoted and stored at −80 °C. The protein yield was approximately 20 mg/lt of shake flask culture.

Characterization of Recombinant Protein

Each batch of the ESAT6::CFP10 recombinant protein was verified in SDS-PAGE for purity and the protein was also subjected to immune-blot using anti-His antibody, TB positive cattle sera and TB negative cattle sera. The immuno-blots using anti-His antibody and TB positive reference sera produced a protein band of ~ 28 kDa as shown in Supplementary Fig. I  and II whereas the TB negative reference sera did not react with the recombinant protein. In the MALDI TOF analysis, the fusion protein had 100% amino acid identity with the available ESAT-6 and CFP-10 amino acid sequences of M. tuberculosis and M. bovis.

Kit assembly and Batch Release Criteria

Line drawing and LFA kit assembly was carried out as mentioned in the methods section. Batch quality of the kits was assessed using reference positive and negative sera samples. The following parameters were assessed for batch clearance: 1. Reference positive sera developed lines with the recombinant fusion protein and BoPPD (Fig. 2 Panel A); 2. Reference culture negative sera developed only the control lines (Fig. 2 Panel B); 3. Rabbit hyper-immune sera against PPD of M. avium developed specific line with AvPPD (Fig. 2 Panel C). Additionally a visible control line should appear in all the tests. All the batches of the LFA kits were cleared based on the above mentioned batch release criteria.

Fig. 2
figure 2

Panel A: a1: Reference positive sera in Kit1 developed positive lines for Fusion protein and BoPPD. a2: Reference positive sera in Kit2 developed positive line only in Fusion protein. b1 and b2: Reference negative sera developed only control lines. c1 and c2: Avian PPD immunized sera developed only control lines in Kit1 and developed line for Avian PPD in Kit2

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Interpretation of Result Using the LFA Kits

Reactivity of the kit was verified against sera samples from various wild life species as mentioned in the materials and methods sections. Antibody responses against the recombinant fusion protein, BoPPD and AvPPD were assessed using the kit. Reactivity of the sera samples against the recombinant fusion protein or BoPPD or both was considered positive test result in the LFA. Reactivity against AvPPD alone in the absence of any positive lines against ESAT6::CFP10 and BoPPD was classified as antibody response against non-pathogenic Mycobacteria.

Application of the Kit for Cattle Samples

To benchmark test performance, particularly in respect to specificity, which is very challenging to determine in wildlife species without samples from confirmed uninfected animals, we tested well characterized samples from GB cattle (100 skin test positive cattle with culture-confirmed bovine TB and 100 from TB-free cattle). The results of these experiments are presented in Tables 1 and 2. Applying the interpretation criteria as stipulated above, we estimated test sensitivity and specificity to be 81% (71.93–88.16% at 95% CI) and 90% (82.38–95.10% at 95% CI), respectively in cattle (Tables 1 and 2).

Table 1 Interpretation of results and result summary of known positive cattle sera using the LFA kit
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Table 2 Interpretation of results and result summary of known negative cattle sera using the LFA kit
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Diagnostic Sensitivity in Wildlife Species

Given the constraints of working with wild life and the low number of samples typically available for any study, the present kit was evaluated using a total of 74 Sloth Bear sera samples and 48 sera samples from other wild life species. 17 out of the 74 Sloth Bears were confirmed for tuberculosis based on post mortem granuloma lesions and acid fast bacillias shown in Fig. 3. The post mortem granuloma samples were also confirmed in PCR for Mycobacteria. These 17 Sloth Bear sera were considered as known positive samples to estimate diagnostic sensitivity of the rapid wild TB kit. 16/17 of these sera samples gave positive responses using the LFA kit which indicated 94% diagnostic sensitivity (71.31–99.85% at 95% CI; Fig. 4 - I).

Fig. 3
figure 3

Postmortem confirmation of TB specific granuloma lesions in Sloth Bear lungs. Arrows indicate the pustular lesions

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Fig. 4
figure 4

Venn diagram depicting the reactivity of Sloth Bear sera samples against BoPPD, ESAT-6::CFP-10 and AvPPD using the LFA kit. I: Sera from TB positive sloth bear (n = 17). The LFA kit had 94% diagnostic sensitivity (71.31–99.85% at 95% CI); II: sera from in-contact Sloth Bear (n = 57)

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We next assessed the complete set of 122 wildlife samples including the 17 samples described in the previous paragraph. The Reactivity of these wild animal sera samples (n = 122) against recombinant fusion protein, BoPPD and AvPPD is provided in Fig. 5. Twenty seven out of the 57 live-in-contact Sloth Bear sera samples were positive using the LFA kit indicating 47.4% (Fig. 4 - II) positivity for TB. This experiment was conducted in a Bear rescue center where TB is prevalent. None of these in-contact sloth bears showed any obvious symptoms of TB. However 27 of these animals were diagnosed positive by the kit. These animals were followed subsequently and seven of these positive animals (7 out of 27) died so far. All these seven animals showed typical TB granulomas (subsequently confirmed in the lab test also) during post mortem examination indicating that the kit detected these asymptomatic TB positive animals.

Fig. 5
figure 5

Venn diagram depicting the reactivity towards BoPPD, ESAT-6::CFP-10, AvPPD using the LFA kit for all the wild animals sera samples (n = 122) of the present study

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Sera samples from Elephants (n = 9), Felidae (n = 21), Cervidae (n = 14), Cape Buffaloes (n = 2), Wild Bear (n = 1) and Wild Dog (n = 1) were also tested and the seropositivity in these animals was 25%. Reactivity of individual antigens in the LFA kit for the sera samples from Sloth Bears (n = 74), Elephants (n = 9), Felidae (n = 21), Cervidae (n = 14), Cape Buffaloes (n = 2), Wild Bear (n = 1) and Wild Dog (n = 1) were presented in Table 3.

  1. 1.

    19.67% of all samples tested (n = 122) produced positive lines for the recombinant ESAT6::CFP10 fusion protein as well as BoPPD.

  2. 2.

    18.85% were reactive against one of these two proteins in the LFA.

  3. 3.

    4.91% of samples were reactive against all the three proteins in the test (ESAT6::CFP10, BoPPD and AvPPD).

  4. 4.

    One of the negative wild animal samples (negative by the kit of the present study) produced visible line for AvPPD alone (one out of 66 negative samples).

Table 3 Interpretation of results and result summary of sera samples from wild animals (n = 122) using the LFA kit
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Therefore, these animals were seropositive against pathogenic mycobacteria (Sr. No. 1 and 2 of the above combination), environmental mycobacteria (Sr. No. 4) and a combination of pathogenic and non-pathogenic mycobacteria (Sr. No. 3).

Apart from the above mentioned combination of results, other interesting combinations of sero-reactivity were also observed. Two of the positive samples were reactive against the BoPPD and AvPPD with no visible line for the fusion protein. Similarly, one of the positive samples produced visible lines for the fusion protein and AvPPD.

Based on the above results, it was decided that the Kit 1 (with BoPPD and recombinant protein) was to be used routinely for the sero-diagnosis of TB. The Kit 2 would be used whenever the kit 1 produced visible line against BoPPD alone which was 12.29% of our study samples.

Advantage of Using Combination of TB Specific Proteins Over Single Proteins

Using both the fusion protein and BoPPD, sensitivity of the kit had increased considerably. 41.07% of the positive sera (or 18.85% of the total wild animal sera samples tested) produced line for only one of the two antigens.

  1. 1.

    26.78% of the positive sera had produced line for PPD of M. bovis alone

  2. 2.

    14.28% of the positive sera had produced line for recombinant ESAT6::CFP10 fusion protein alone.

Specificity of the diagnostic method was assessed using AvPPD. Only two out of 124 wild animal sera generated positive lines both in BoPPD and AvPPD without any line development for the fusion protein. Cross reactivity with the environmental Mycobacteria is not ruled out in these animals. In such cases, the test may be repeated after some time using fresh sera and the diagnostic decision can be arrived based on the reactivity against ESAT6::CFP10. Additionally, the diagnostic decision can be based on the disease prevalence and local rules of the country wherein the requirement of ‘ruling out’ or ‘ruling in’ of TB in wild animals can determine the diagnostic decision.

Discussion

India is endemic for tuberculosis and the disease is prevalent in humans, domestic and wild animals. The populations of TB susceptible wild animals such as elephants, bears and boar are high in Asian and African countries. However, the data on TB epidemiology is limited in these countries with a severe effect on the management and control of TB [18, 29]. In developing countries both zoonosis and reverse zoonosis of TB are common; Mycobacterium species isolates from animals include M. tuberculosis and M. bovis in India and other developing countries [30,31,32]. M. tuberculosis also infects animals with similar virulence like M. bovis. The antigen complements of both organisms are almost completely identical. Thus a test detecting M. bovis will also detect M. tuberculosis, i.e. bovine PPD responses will also detect M. tuberculosis and human PPD will detect M. bovis infection. Indeed in early bovine TB control programs for cattle, human PPD was used successfully. As both M. tuberculosis and M. bovis can infect animals including wild life and cause severe pathogenesis a differential diagnosis between M. bovis and M. tuberculosis is not required nor is possible given the degree of antigen identity between these two pathogens. Wild-animals infected with either of the species are culled or segregated depending on the country’s law.

Aim of the current kit is to identify animals which are sero-positive for pathogenic TB (which includes M. tuberculosis and M. bovis) and help in the zoo or wild-life authorities to make appropriate decision or to study the TB sero-prevalence of tuberculosis in wild life.

Additionally, differentiating the pathogenic Mycobateria from environmental Mycobateria (such as M. avium sub sp. avium) is more important in the context of animal infections. Genome wide sequence search of M. avium subsp. paratuberculosis and M. avium subsp. avium revealed absence of any sequences with similarity to ESAT 6 and CFP 10 and the proteins were useful for the specific diagnosis of tuberculous Mycobacteria [33]. These proteins or their peptides had been used in IGRAs for the specific diagnosis of Tuberculosis [23]. The degree of specificity in general of these two antigens is high and they are also the mainstay of TB diagnosis both in cattle and humans [34,35,36]. Thus, many of the FDA and OIE approved kits such as QuantiFERON® and BOVIGAM® 2G uses ESAT6 and CFP10 peptides due to their proven ability to differentiate pathogenic TB (M. tuberculosis and M. bovis) from environmental Mycobacteria and BCG [37]. Mycobacterial species like M. marinum or M. klansasii express almost identical homologues of ESAT6 and CFP 10 [38, 39]. However, infection with these Mycobacteria is rare (both in humans and animals) and therefore, not considered to be major confounders. These two bacilli can also cause pathology and have zoonotic potential and removal of animals infected with these species will be advantageous. However, and most importantly, the homology (and therefore cross-reactivity) of M. bovis/M. tuberculosis ESAT6 and CFP10 compared to other more prevalent environmental Mycobacteria like M. avium sub sp. avium or M. avium sub sp. paratuberculosis is low.

Tuberculin skin testing and IGRA are the common TB diagnostic methods in domestic animals and humans. However, point of care serology assays are more practical for TB diagnosis in wild animals. To improve the sensitivity of detecting intracellular bacteria such as TB using sero-diagnostic kits, cocktails of antigens are required [40, 41]. At the same time, cross reactivity in antibody response due to the exposure to environmental Mycobacteria should also be taken care of while selecting the antigens for serology [42].

In the present study, BoPPD was used for increasing the sensitivity of the assay and AvPPD was used to mitigate against the cross reactivity from environmental bacteria. Tuberculosis antigen recognition pattern varies from species to species in serological assays. ESAT 6 or ESAT 6::CFP 10 fusion proteins were the earliest and most frequently recognized antigens in elephants infected with tuberculosis. The antibody response against the proteins was much earlier than the diagnosis by detecting the organism in trunk washes [2]. Though, MPB 83 and MPB 70 were the sero-dominant proteins in cattle and deer, ESAT 6 and CFP10 were also detected in majority of the tuberculosis infected animals [23, 34]. Moreover, the cross reacting antibodies from other Mycobacteria can also detect MPB 83 and MPB 70 resulting in a reduction in specificity of the assay. Therefore, a ESAT6::CFP10 fusion protein was used in the current diagnostic kit to enhance the specificity of the assay.

Performance of the point of care immuno-chromatographic strip test was assessed using Sloth Bear sera samples. 16 out of the 17 known positive sera samples turned positive in the LFA kit also. All the 16 samples were detected by the recombinant fusion protein and 27 of the in-contact Sloth Bear samples were detected by the protein. 6 out of 44 positive Sloth Bear sera samples reacted with AvPPD and all those six samples were positive for the fusion protein indicating the infection with pathogenic Mycobacteria. Therefore, the use of fusion protein aids in making the diagnostic decisions. To benchmark test performance against a larger number of animals with confirmed TB, the sensitivity and specificity of the kit was estimated using reference cattle sera (n = 100), which was lower (81%) than the estimate in sloth bears although the small sample size of our Sloth Bear assessment resulted in large confidence intervals overlapping those estimated with the cattle sera. The sero-dominant TB proteins in cattle are MPB 83 and MPB 70, and current kit did not contain these proteins as an individually expressed protein. These proteins were not included in the current kit to avoid detecting the cross reacting antibodies from environmental Mycobacteria.

A commonly encountered limitation of testing wildlife samples is the lack of samples from animals that are confirmed TB-free. Specificity estimates are therefore difficult to ascertain. To partially overcome this limitation, we have used cattle sera from TB-free animals. Thus, the specificity of the assay was determined using known negative cattle sera from TB-free herds in TB-non-endemic areas of GB. Further, freedom of infection of individual cattle was confirmed by negative tuberculin skin and interferon-gamma test results. Using these TB-free cattle sera (n = 100) the LFA kit showed 90% specificity. This is comparable to the data by Da Silva et al. [43] reported a sensitivity and specificity of 82 and 91% for their indirect ELISA using BCG as coating antigen. Similar kind of tuberculosis antibody detection kits were tested in wild animals earlier. DPP vet TB kit was tested in white tailed deer (sensitivity 65.1 and specificity 97.8%) [44] and South American Camelids (sensitivity 74 and specificity 98%) [45]. Elephant TB STAT-PAK Kit was tested in Asian and African elephants and the reported sensitivity and specificity was 100% and 95–100%, respectively [3]. Similarly, Prima TB STAT-PAK kit was tested in Non-Human primates and the reported sensitivity and specificity was 90 and 99% respectively [46].

The major difference between the other LFA kits and the current kit is the combination of proteins present in the kit. The other kits uses MPB83 protein and ESAT6/CFP10 fusion protein. The kit which is described in the current manuscript uses ESAT6::CFP10 fusion protein and native Mycobacterial proteins (BoPPD and AvPPD). Inclusion of BoPPD in the kit had increased the sensitivity by 41% in cattle (Table 1). However, BoPPD can compromise the specificity of the kit and therefore, AvPPD was included in the kit to detect the cross reactivity (if any) from the environmental Mycobacteria. One out of 100 negative cattle (Table 2; Sr No. 6) showed BoPPD positive line which may be due to the cross reactivity of environmental mycobacteria. Considerable percentage of positive samples (41.07%) were reactive against either BoPPD or fusion protein alone. Sero-reactivity against tuberculosis varies between the species and use of multiple proteins as in MAPIA increased the sensitivity of detection. Instead, BoPPD which is a mix of Mycobacterial proteins was used in the present kit for enhancing the sensitivity. 26.78% of positive samples were reactive against BoPPD alone. Use of kit II which contained AvPPD was recommended in those circumstances to rule out any cross reactivity with antibodies against environmental Mycobacteria. Two of the total 122 samples were reactive against BoPPD and AvPPD. These animals may be tested again to confirm the TB sero-positivity.

The kit was used in wide range of wild animals including Elephants (n = 9), Felidae (n = 21), Cervidae (n = 14), Cape Buffalo (n = 2), Wild Bear (n = 1) and Wild Dogs (n = 1). Use of protein A and Protein G conjugate (instead of anti-species antibody) enabled the kit to be used universally for any of the wild species.

The results indicated that 47.4% of in-contact Sloth Bear samples which were tested using the kit turned sero-positive for tuberculosis. 25% of samples from other wild species were also positive by the test. This indicates the high prevalence of TB in Indian wild animals. The situation is further complicated by the extensive wild animal and human (animal handlers of captive wild animals and tribes in the periphery of the forest areas) as well as wild and domestic animal interactions. In India the disease is highly prevalent in domestic animals and humans. These results emphases the need for systematic TB surveillance and control programs in India for wild animals.

Sero-diagnosis of tuberculosis in wild animals was permitted in countries like USA and UK (OIE 2014), since the conventional TB diagnosis by culture/IGRA/skin testing have serious practical difficulties in implementing them in wild animals [47, 48]. For an efficient surveillance and management of Wild TB, rapid, accurate, affordable and reliable TB diagnostic kits are needed. The available commercial sero-diagnostic kit was licensed for use in few countries and the kit is for fewer species. Moreover, the cost of the kit is too high for developing countries like India. The current kit addresses some of these problems.

In the present study, a rapid TB sero-diagnostic kit which can detect antibodies due to pathogenic as well as environmental Mycobacteria infection in wild animals was developed and validated using the sera samples of wild animals. Using this kit, sero-diagnosis of TB in wild animals is enabled.