TY - JOUR
T1 - Synthetic peptides derived from ribosomal proteins of leishmania spp. in mucocutaneous leishmaniasis
T2 - Diagnostic usefulness
AU - Flórez, Magda Melissa
AU - De Oliveira, Camila Indiani
AU - Puerta, Concepción
AU - Guzmán, Fanny
AU - Ayala, Martha
AU - Montoya, Gladis
AU - Delgado, Gabriela
N1 - Funding Information:
This work was financed by the Universidad Nacional de Colombia’s Bogotá Research Division (DIB) project 16015, as well as a grant from the Colombian Science, Technology and Innovation Department’s (Colciencias) Young Researchers and Innovators programme "Virginia Gutiérrez de Pineda" (2012) and Colciencias Grant (contract number 03092013, code 57635945-project 6). We Thank to National University of Colombia and its Master program on Microbiology. Thanks to Juqueline Cristal and to FAMETRA group by all their support in the development of the present work.
PY - 2017
Y1 - 2017
N2 - Background: The serological diagnostic methods currently available for mucocutaneous leishmaniasis (MCL) lack specificity when complete parasites are used; however, such specificity increases when protein fractions are used. Ribosomal proteins have been reported to induce antibodies in animal and humans infected with the parasite, making them a worth candidate to assess its diagnosis potential. Objective: This study was thus aimed at evaluating synthetic peptides derived from Leishmania braziliensis ribosomal proteins S25 and S5 as antigen candidates for diagnosing MCL by ELISA Methods: It was used 8 and 13 peptides derived from ribosomal proteins 25 and S5 respectively as antigens in order to detect IgG antibodies by ELISA in people with active MCL, Chagas disease (CH) and autoimmune disease (AID). Results: 4 of these 21 peptides (P4, P6, P19 and P21) had the greatest sensitivity (21.7%, 13.04%, 20% and 20%, respectively) as well as having 95%, 100%, 100% and 82.5% specificity, respectively. Conclusion: The study revealed the limited usefulness of the peptides being studied as a diagnostic tool in the conditions used here, because its low sensitivity, but it is worth highlighting that the use of peptides as antigen in the serodiagnosis of MCL may overcome the cross reaction presented with other antigens, thus avoiding false positives.
AB - Background: The serological diagnostic methods currently available for mucocutaneous leishmaniasis (MCL) lack specificity when complete parasites are used; however, such specificity increases when protein fractions are used. Ribosomal proteins have been reported to induce antibodies in animal and humans infected with the parasite, making them a worth candidate to assess its diagnosis potential. Objective: This study was thus aimed at evaluating synthetic peptides derived from Leishmania braziliensis ribosomal proteins S25 and S5 as antigen candidates for diagnosing MCL by ELISA Methods: It was used 8 and 13 peptides derived from ribosomal proteins 25 and S5 respectively as antigens in order to detect IgG antibodies by ELISA in people with active MCL, Chagas disease (CH) and autoimmune disease (AID). Results: 4 of these 21 peptides (P4, P6, P19 and P21) had the greatest sensitivity (21.7%, 13.04%, 20% and 20%, respectively) as well as having 95%, 100%, 100% and 82.5% specificity, respectively. Conclusion: The study revealed the limited usefulness of the peptides being studied as a diagnostic tool in the conditions used here, because its low sensitivity, but it is worth highlighting that the use of peptides as antigen in the serodiagnosis of MCL may overcome the cross reaction presented with other antigens, thus avoiding false positives.
KW - Diagnosis
KW - Leishmania braziliensis
KW - Mucocutaneous leishmaniasis
KW - Parasite
KW - Ribosomal protein
KW - Synthetic peptide
UR - http://www.scopus.com/inward/record.url?scp=85041688422&partnerID=8YFLogxK
U2 - 10.2174/0929866524666170728143924
DO - 10.2174/0929866524666170728143924
M3 - Article
C2 - 28758598
AN - SCOPUS:85041688422
SN - 0929-8665
VL - 24
SP - 982
EP - 988
JO - Protein and Peptide Letters
JF - Protein and Peptide Letters
IS - 10
ER -