z-logo
open-access-imgOpen Access
Identification of Proteins in Promastigote and Amastigote-like Leishmania Using an Immunoproteomic Approach
Author(s) -
Vinicio T. S. Coelho,
Jamil S. Oliveira,
Diogo G. Valadares,
Miguel Á. ChávezFumagalli,
Mariana C. Duarte,
Paula S. Lage,
Manuel Soto,
Marcelo M. Santoro,
Carlos A. P. Tavares,
Ana Paula Fernandes,
Eduardo Antônio Ferraz Coelho
Publication year - 2012
Publication title -
plos neglected tropical diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.99
H-Index - 135
eISSN - 1935-2735
pISSN - 1935-2727
DOI - 10.1371/journal.pntd.0001430
Subject(s) - amastigote , leishmania infantum , leishmania , antigen , proteome , biology , visceral leishmaniasis , leishmaniasis , virulence , virology , proteomics , microbiology and biotechnology , immunology , biochemistry , parasite hosting , world wide web , computer science , gene
Background The present study aims to identify antigens in protein extracts of promastigote and amastigote-like Leishmania (Leishmania) chagasi syn. L. (L.) infantum recognized by antibodies present in the sera of dogs with asymptomatic and symptomatic visceral leishmaniasis (VL). Methodology/Principal Findings Proteins recognized by sera samples were separated by two-dimensional electrophoresis (2DE) and identified by mass spectrometry. A total of 550 spots were observed in the 2DE gels, and approximately 104 proteins were identified. Several stage-specific proteins could be identified by either or both classes of sera, including, as expected, previously known proteins identified as diagnosis, virulence factors, drug targets, or vaccine candidates. Three, seven, and five hypothetical proteins could be identified in promastigote antigenic extracts; while two, eleven, and three hypothetical proteins could be identified in amastigote-like antigenic extracts by asymptomatic and symptomatic sera, as well as a combination of both, respectively. Conclusions/Significance The present study represents a significant contribution not only in identifying stage-specific L. infantum molecules, but also in revealing the expression of a large number of hypothetical proteins. Moreover, when combined, the identified proteins constitute a significant source of information for the improvement of diagnostic tools and/or vaccine development to VL.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom