1M.V.Sc. Student, Indian Veterinary Research Institute (IVRI), Izatnagar, Uttar Pradesh, India
2Research Associate, National Research Centre on Equines (NRCE), Hisar, Haryana, India
3Senior Research Fellow, National Research Centre on Equines (NRCE), Hisar, Haryana, India
4Principal Scientist-cum-National Fellow, National Research Centre on Equines (NRCE), Hisar, Haryana, India
5M.V.Sc. student, Lala Lajpat Rai University of Veterinary & Animal Sciences (LUVAS), Hisar, Haryana, India
*Corresponding author email id: rkg@scientist.com
Trypanosoma evansi (T. evansi) is a causative agent of disease called surra, affecting wide range of domestic and wild animals. In this study, a PCR assay was developed using primers targeting ITS-1 region flaking between 5.8 S and 18 S subunits of rRNA. The test was employed using serially diluted DNA extracted from purified trypanosomes ranging from 200 ng/μl to 0.00002 pg/μl and T. evansi infected mice blood ranging from 350 ng/μl to 0.00035 ng/μl. The diagnostic sensitivity of PCR assay was found to be 0.2 pg/μl and 0.035 ng/μl with purified parasite DNA and infected mice blood DNA, respectively.
Trypanosma evansi, Surra, ITS-1, PCR, rDNA, Equine