Journal of Immunology and Immunopathology
  • Year: 2013
  • Volume: 15
  • Issue: 2

PCR-based Identification of Trypanosoma evansi targeting Internaltranscribed Spacer 1 of rDNA in experimentally infected Mice

  • Author:
  • Shashi Kant Kankar1, Sachin Kumar Goyal2, Parvati Sharma2, Deepak Kumar Gaur3, Souti Prasad Sarkhel4, Rajender Kumar5,
  • Total Page Count: 5
  • Page Number: 210 to 214

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

Abstract

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.

Keywords

Trypanosma evansi, Surra, ITS-1, PCR, rDNA, Equine