doi:10.5455/vetworld.2013.424-427 Characterization of somatic antigens of adult Toxocara canis

Aim: The objective of this study was characterize the somatic soluble antigens of adult Toxocara canis (Tc-SA) by western blotting. 
 
Materials and Methods: T. canis worms were collected from the naturally infected pups after deworming. The somatic antigen was prepared as per standard procedure with slight modification. These antigens were separated using Sodium dodecyl sulphate-electrophoresis (SDS-PAGE). The specific reactivity of the Tc-SA proteins was checked against the serum of naturally infected dogs as well with the hyperimmune serum raised in the rabbit by western blotting. 
 
Results: On SDS-PAGE recovered proteins ranged in size from 44 to 300 kDa. The immuno-reactivity of the naturally infected dog sera with the Tc-SA antigens showed 12 prominent immunoreactive bands of distinct sizes at 28.61, 32.60, 38.10, 43.04, 49.99, 67.57, 73.22, 105.77, 144.74, 161.11, 177.84 and 196.31 kDa. The immuno-reactivity of the hyper immune serum raised in rabbits against Tc-SA antigens was observed with 10 prominent bands of distinct sizes at 17.11, 24.15, 34.83, 43.46, 52.47, 55.89, 67.57, 70, 74.60 and 105.6 kDa. 
 
Conclusions: Common antigens band were observed at 67 and 105 kDa. These antigens merit further evaluation as candidate for use in diagnosis of toxocarosis in humans and adult dogs.


Introduction
The cross-reactivity with antibodies from other endemic helminth infections is a limitation for the Toxocara canis is a wide spread gastrointestinal development of an accurate serodiagnostic test [Enzyme nematode of dogs and other canids and is the causative Linked Immunosorbent Assay (ELISA)] using the agent of zoonotic disease in humans [1].Larval stages unfractionated excretory-secretory (ES) antigens from of T. canis parasite have an obligatory tissue-migratory the T. canis second-stage larvae (TES Ag) [8].In recent phase, giving rise to a drug resistant reservoir in dogs, years, there have been important methodolo-gical and visceral larva migrans in humans [2,3].
advances in the diagnosis of many infectious diseases, Human infection is present worldwide and is a but there are innumerable difficulties in the laboratory consequence of the habit of keeping dogs and cats for diagnosis of toxocarosis due to the laborious production company, which favours the persistence of the parasite of the antigens or the high costs of commercial diagnostic in the environment and its transmission [4].In India, kits [9].studies on the prevalence of human toxocarosis is very In the absence of parasitological evidence of scarce and reports shows that its prevalence is 32.86% infection, immunological methods are required for its in Kashmir valley and 6.4 % in subjects residing in a diagnosis.The diagnosis of human toxocarosis depends rural area near Chandigarh [5].In the other developing on clinical and serological data because detecting countries, this scenario is probably worse, Children Toxocara larvae by biopsy is difficult [10].Since the playing in areas contaminated with dog faeces, as well development of the ELISA using ES antigens from as people with intimate contact with dogs, are subject TES Ag described by de Savigny et al.
[11] and the to a higher risk of infection [6].In the Developed subsequent western-blot method using the same countries like United States, human toxocarosis is the antigen by Magnaval et al.[12], a general agreement most common human parasitic worm infection and has existed regarding the value of the TES Ag for the affects 13.9% of the population [7] excretory-secretory antigens (rTES-120, rTES-26, response in rabbits experimentally immunized with Tc-rTES-30USM) [13].Presently a Dot-ELISA test for SA antigen as per Wijfells et al. [20].The intensity of toxocarosis is under evaluation which is considered as colour reaction was measured as absorbance in each a reliable one as it presents many advantages as a basic well at 492nm in an ELISA reader.diagnostic test.For example, it is highly stable, it does Western blotting: Western blotting was done to not require specialised tools to analyse the results, it recognize the immunodominant polypeptides of Tc-SA has a lower cost and it can be simultaneously applied to antigen using standard procedure of Burnette [21]with a large number of samples by a basically trained slight modifications.The resolved proteins were technical staff [14,15].subsequently transferred to a Nitrocellulose (NC) There are molecular weight moieties observed in membrane.Blotting was carried out in ATTO semi dry adult worms that may be related to the larval TC-ES blot transfer machine, AE6670 (ATTO Corporation, products [16].The parasite proteins of this antigen Japan) [21].which ellicit an immune response can be identified by immunological techniques.Therefore, this paper Development of blot: The NC paper was recovered includes the identification and characterization of the after electrophoretic transfer and each lane was cut into antigenic components of adult T. canis present in the strips.Successful transfer of the protein to the somatic soluble product using the western blot technique.
membrane was confirmed by staining the membrane with Ponceau's stain.Later, the strips were incubated

Materials and Methods
with naturally infected dog sera diluted in PBS-T and Parasite: Three pups of age group between 1-6 months the hyper immune sera raised against TC-SA antigen in were screened at random.They were examined for the rabbit diluted in PBS-T.Finally, they were incubated natural infection of T. canis by faecal examination.The with goat anti-rabbit IgG-HRP and lately with rabbit adult T. canis worms were then collected from the anti-dog IgG-HRP, followed by development of blot positive pups after deworming with a dose of using diaminobenzidine colour reagent system.piperazine citrate @ 220mg/kg of body weight.The Results expelled worms were identified, washed three times with 0.9 % NaCl and frozen in 70% ethanol at -40°C SDS-PAGE analysis: On SDS-PAGE analysis, Tc-SA until further use.
antigen revealed 14 protein bands ranging in size from 44 to 300 kDa, with a molecular moieties of 300,  1).prepared by homogenization of adult worms in ELISA: Indirect ELISA was performed with two rabbits presence of cocktail of protease inhibitors, thereafter hyperimmunised with Tc-SA antigens and a high titre subjected for sonication at 8-10 micron peak to peak for of IgG immunoglobulin response of 1: 50,000 was 15 cycles with an interval of 30 sec.every time strictly observed (Fig- 2).maintaining the cold chain.toxocarosis in humans and adult dogs.However, kDa antigens was specific and sensitive for the antidetailed studies are required for characterizing the Toxocara antibody, supporting the possibility of using immuno-dominant polypeptides of the adult worm for these two antigens for the immunodiagnosis of human their potential in the diagnosis of toxocarosis in dogs toxocarosis in low-prevalent areas [17].Further there and in humans.are also reports that there is close taxonomic Conclusion relationship between Ascaris sp. and Toxocara sp., and serological diagnosis there may be cross reactions as In the present study, we identified and characthe two ascarids undoubtedly share antigens and terized the somatic soluble antigens of Toxocara canis epitopes [26].adult worm.We observed two common immunodominant bands at 67 and 105kDa.Further tests need to We did a preliminary evaluation on the usefulness be performed to test whether these semi-purified adult of soluble somatic antigens of adult T.canis as potential Toxocara antigens might cross-react with other parasitic immunodiagnostic antigens.Compared to juveniles,

and recombinant Toxocara Characterization of somatic antigens of adult Toxocara canis by western blotting
doi:10.5455/vetworld.2013.424-427 90.43, 69.25, 56.76, 42.50, 40.69, 38, 35.70, 27.91, they are relatively easier to obtain and handle.The 21.98 and 19.29 kDa.Aida, [25] reported the SDSimmunoreactivity of the anti-sera raised against Tc-SA PAGE profile of adult Tc-SA consisting of 7 (125.37, in rabbit was observed at 17.11, 24.15, 34.83, 43.46, 117.73, 90.00, 69.25, 58.36, 47.13 and 46.53 kDa) 52.47, 55.89, 67.57, 70, 74.60 and 105.6 kDa and the protein bands.immunoreactivity with the naturally infected dog sera Peixoto and co-workers [17] identified specific was observed at approximately 28.61, 32.60, 38.10, antigens from the adult stages of T. canis including 42, 43.04, 49.99, 67.57, 73.22, 105.77, 144.74, 161.11, 58, 68 and 97 kDa that may be useful for the 177.84 and 196.31 kDa.We observed common serodiagnosis of human toxocarosis.These antigens immune dominant band at 67 and 105 kDa with both of demonstrated considerable sensitivity and specificity hyperimmune and dog sera.These antigens merit and were considered as promising candidates for further evaluation as candidate for use in diagnosis of immunodiagnosis.The combination of the 58 and 68 SDS-PAGE protein profile of adult T. canis ranging in incomplete adjuvant, 15days apart.Rabbits were bled size from 3.4 to 325 kDa [23].Protein bands of adult T. st nd after 10 days of the 1 and 2 booster and the serum was canis viz.91.04, 67.97 and 44 kDa in the present study 0 collected and stored at -20 C for further use.can be compared to those reported in the study of Sun et al., like 92.8, 69.4 and 48.4 kDa [23].Nawal and Mona Enzyme Linked Immunosorbent Assay (ELISA): Indirect ELISA was performed for detection of antibody [24] reported the electrophoretic analysis of Tc-SA doi:10.5455/vetworld.2013.424-427which revealed 13 polypeptide bands at 250, 125, 117, adult worms may be a better source of antigens because