ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

Antigenic characterization of 52-55 kDa protein isolated from Trypanosoma evansi and its application in detection of equine trypanosomosis

Yadav, SC and Kumar, Ritesh and Kumar, Jaideep and Singh, Meetali and Bera, BC and Kumar, Rajender and Tatu, U and Tehri, Kanika (2017) Antigenic characterization of 52-55 kDa protein isolated from Trypanosoma evansi and its application in detection of equine trypanosomosis. In: RESEARCH IN VETERINARY SCIENCE, 114 . pp. 455-460.

[img] PDF
Res_Vet_Sci_114_445_2017.pdf - Published Version
Restricted to Registered users only

Download (642kB) | Request a copy
Official URL: http://doi.org/10.1016/j.rvsc.2017.07.034

Abstract

Trypanosome evansi is a haemo-protozoan parasite responsible for the disease surra, an economically important disease of wide range of domestic and wild animals. The present diagnostic methods using soluble antigens have inherent problems like lack of standardized and reproducible antigens, as well as ethical issues. This entails further efforts for search of defined antigenic molecules with satisfying sensitivity and specificity for sero-epidemiology of trypanosomosis. In present investigation, we have identified and purified 52-55 kDa immunodominant protein cluster in molecular mass ranges by preparatory SDS-PAGE methods from T. evansi proteome. The purified protein was further characterized by hyper immune serum raised in rabbits and also further evaluated for its immunodiagnostic potential using experimentally infected horse serum samples by different immunological tests. The immunoblot, ELISA and dot blot assay using purified cluster in infected pooled serum samples showed detection of infection early as 10th days post infection till termination of experiment. The observations revealed that purified cluster is expressed not only at early stage but also persisted and detected throughout course of infection. Further, whole cell lysate antigen separated out and detected 141 spots by 2-D gel electrophoresis. The isoelectric focussing (PI) of 52-55 kDa was determined in pH range between 6.9 and 7.5 along with two other cluster of proteins recognised by immune sera of ponies infected with T. evansi. MS/MS analysis of the purified protein cluster identified five proteins i.e. pyruvate kinase 1, beta tubulin, paraflagellar rod protein, alanine aminotransferase and variable surface glycoprotein showing homology to protein present in Trypanosome database. These identified proteins may be useful for development of vaccines and diagnostic targets against animal trypanosomosis.

Item Type: Journal Article
Publication: RESEARCH IN VETERINARY SCIENCE
Additional Information: Copy right for this article belongs to the ELSEVIER SCI LTD, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND
Department/Centre: Division of Biological Sciences > Biochemistry
Date Deposited: 07 Dec 2017 09:40
Last Modified: 07 Dec 2017 09:40
URI: http://eprints.iisc.ac.in/id/eprint/58400

Actions (login required)

View Item View Item