Back to Search Start Over

High immunological response against a Trypanosoma equiperdum protein that exhibits homology with the regulatory subunits of mammalian cAMP-dependent protein kinases.

Authors :
Mendoza, Emiliana
Bubis, José
Pérez-Rojas, Yenis
Montilla, Alejandro J.
Spencer, Lilian M.
Bustamante, Floritza
Martínez, Juan C.
Source :
Journal of Immunoassay & Immunochemistry. 2018, Vol. 39 Issue 4, p451-469. 19p.
Publication Year :
2018

Abstract

Previously, we have identified a protein in Trypanosoma equiperdum that possesses homology with the regulatory (R) subunits of the mammalian cAMP-dependent protein kinase (PKA). The recombinant T. equiperdum PKA R-like protein was expressed in bacteria and purified to homogeneity. Mice polyclonal antibodies were raised against the recombinant R-like protein to serologically evaluate its humoral immune response. High titers of specific sera antibodies were obtained against the parasite R-like protein by indirect enzyme-linked immunosorbent assay (ELISA), and immunoblots revealed that this protein was specifically recognized by the hyperimmune mice sera. Cellular proliferation assays using splenic B cells from the immunized mice showed higher values when the recombinant T. equiperdum R-like protein was employed than when concanavalin A was utilized as an unspecific mitogen. Two healthy horses that were experimentally infected using either T. equiperdum or Trypanosoma evansi showed a curve response characterized by the appearance of anti-T. equiperdum PKA R-like protein antibody production in sera using indirect ELISA. The recombinant parasite PKA R-like protein was also recognized by sera from naturally trypanosome-infected horses using western blotting. These findings demonstrated that the T. equiperdum PKA R-like protein is an antigen that exhibits cross-reaction with T. equiperdum and T. evansi. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15321819
Volume :
39
Issue :
4
Database :
Academic Search Index
Journal :
Journal of Immunoassay & Immunochemistry
Publication Type :
Academic Journal
Accession number :
132044133
Full Text :
https://doi.org/10.1080/15321819.2018.1506930