Comparative evaluation of agglutination assay with microscopy and polymerase chain reaction for detection of Trypanosoma evansi in bovines of Punjab
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https://doi.org/10.56093/ijans.v85i11.53038
Keywords:
Bovines, CATT, PCR, Punjab, Trypanosoma evansiAbstract
Present investigation was aimed to evaluate the diagnostic efficacy of CATT/T.evansi in comparison to Giemsa stained thin blood smear examination and PCR for detection of bovine trypanosomosis in Punjab. Analysis of 264 blood and sera samples revealed 1.89% (5/264), 34.47% (91/264) and 51.89% (137/264) positivity by GSTBS, CATT/T. evansi and PCR, respectively, for Trypanosoma evansi. Sensitivity of CATT/T. evansi was 100% and 30.65% as compared to GSTBS and PCR, while its specificity was 66.79% and 61.42%, respectively. PCR is more sensitive and specific, and is able to detect the latent infections, however, it is time and cost ineffective technique. CATT/T. evansi is a quick and easy pen-site test suitable for mass screening of T. evansi endemic in developing countries.
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References
Altschul S F, Gish W, Miller W, Myers E W and Lipman D J. 1990. Basic local alignment search tool. Journal of Molecular Biology 215: 403–10. DOI: https://doi.org/10.1016/S0022-2836(05)80360-2
Bajyana S E and Hamers R. 1988. A card agglutination test (CATT) for veterinary use based on early VAT RoTat 1/2 of Trypanosoma evansi. Annales de la Societe belge de medecine tropicale 68 : 233–40.
Coles C A. 1986. Veterinary Clinical Pathology. 4th edn.W.B. Saunders Company. Philadelphia and London.
Desquesnes M and Davila A M R. 2002. Applications of PCRbased tools for detection and identification of animal trypanosomes: a review and perspectives. Veterinary Parasitology 109: 213–31. DOI: https://doi.org/10.1016/S0304-4017(02)00270-4
Gardiner P R and Mahmoud M M. 1999. Salivarian Trypanosomes Causing Disease in Livestock outside Sub-Saharan Africa Parasitic Protozoa. vol. 3, Pp. 1. (Ed.) Baker J R. Academic Press, New York, NY, USA.
Masake R, Njuguna J T, Brown P A O and Majiwa P A O. 2002. The application of PCR –ELISA to the detection of Trypansosoma brucei and Trypanosoma vivax infection in livestock. Veterinary Parasitology 105: 179–89. DOI: https://doi.org/10.1016/S0304-4017(02)00020-1
Nantulya V M. 1990. Trypanosomiasis in domestic animals: the problems of diagnosis. Review Science Technique Office International Epizooties 9: 357–67. DOI: https://doi.org/10.20506/rst.9.2.507
Singla L D, Juyal P D and Kalra I S. 1996. Effects of levamisole on the clinical response of Trypanosoma evansi infection in cow-calves. Indian Veterinary Journal 73: 11– 15.
Sumbria D, Singla L D, Sharma A, Moudgil A D and Bal M S. 2014. Equine trypanosomosis in central and western Punjab: Prevalence, haemato-biochemical response and associated risk factors. Acta Tropica 138: 44–50. DOI: https://doi.org/10.1016/j.actatropica.2014.06.003
Verloo D, Magnus E and Büscher P. 2001. General expression of RoTat 1.2 variable antigen type in Trypanosoma evansi isolates from different origin. Veterinary Parasitology 97: 185– 91. DOI: https://doi.org/10.1016/S0304-4017(01)00412-5
Wuyts N, Chokesajjawatee N and Panyim S. 1994. A simplified and highly sensitive detection of Trypanosoma evansi by DNA amplification. Southeast Asian Journal of Tropical Medicine and Public Health 25: 266–71.
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