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Synthetic Peptides Mimic gp75 from Paracoccidioides brasiliensis in the Diagnosis of Paracoccidioidomycosis

Paracoccidioidomycosis (PCM) is a systemic granulomatous disease, endemic in Latin America, caused by the thermal dimorphic fungus Paracoccidioides brasiliensis. Although some fungal antigens have already been characterized and used for serological diagnosis, cross-reactions have been frequently obs...

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Autores principales: Caldini, Camila Pistelli, Xander, Patricia, Kioshima, Érika Seki, Bachi, André Luis Lacerda, de Camargo, Zoilo Pires, Mariano, Mário, Lopes, José Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368115/
https://www.ncbi.nlm.nih.gov/pubmed/22249604
http://dx.doi.org/10.1007/s11046-011-9518-3
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author Caldini, Camila Pistelli
Xander, Patricia
Kioshima, Érika Seki
Bachi, André Luis Lacerda
de Camargo, Zoilo Pires
Mariano, Mário
Lopes, José Daniel
author_facet Caldini, Camila Pistelli
Xander, Patricia
Kioshima, Érika Seki
Bachi, André Luis Lacerda
de Camargo, Zoilo Pires
Mariano, Mário
Lopes, José Daniel
author_sort Caldini, Camila Pistelli
collection PubMed
description Paracoccidioidomycosis (PCM) is a systemic granulomatous disease, endemic in Latin America, caused by the thermal dimorphic fungus Paracoccidioides brasiliensis. Although some fungal antigens have already been characterized and used for serological diagnosis, cross-reactions have been frequently observed. Thus, the examination of fungal forms in clinical specimens or isolation of P. brasiliensis by culture is still the most frequent method for the diagnosis of this mycosis. In this study, a random peptide phage display library was used to select mimotopes of P. brasiliensis, which were employed as antigens in an indirect enzyme-linked immunosorbent assay. The protective monoclonal antibody against experimental PCM (anti-gp75) was used as molecular target to screen a phage display library. That approach led to a synthetic peptide named P2, which was synthesized and tested against PCM patients’ sera to check whether it was recognized. There was significant recognition of P2 by sera of untreated PCM patients when compared with normal human sera. Sera from treated PCM group, patients with other mycosis or co-infected with HIV had much lower recognition of P2 than untreated patient group. The test showed a sensitivity of 100 and 94.59% of specificity in relation to human sera control. These data indicate a potential use of P2 as diagnostic tool in PCM. Its application for serological diagnosis of PCM may contribute to the development and standardization of simpler, faster and highly reproducible immunodiagnostic tests at low cost.
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spelling pubmed-33681152012-06-14 Synthetic Peptides Mimic gp75 from Paracoccidioides brasiliensis in the Diagnosis of Paracoccidioidomycosis Caldini, Camila Pistelli Xander, Patricia Kioshima, Érika Seki Bachi, André Luis Lacerda de Camargo, Zoilo Pires Mariano, Mário Lopes, José Daniel Mycopathologia Article Paracoccidioidomycosis (PCM) is a systemic granulomatous disease, endemic in Latin America, caused by the thermal dimorphic fungus Paracoccidioides brasiliensis. Although some fungal antigens have already been characterized and used for serological diagnosis, cross-reactions have been frequently observed. Thus, the examination of fungal forms in clinical specimens or isolation of P. brasiliensis by culture is still the most frequent method for the diagnosis of this mycosis. In this study, a random peptide phage display library was used to select mimotopes of P. brasiliensis, which were employed as antigens in an indirect enzyme-linked immunosorbent assay. The protective monoclonal antibody against experimental PCM (anti-gp75) was used as molecular target to screen a phage display library. That approach led to a synthetic peptide named P2, which was synthesized and tested against PCM patients’ sera to check whether it was recognized. There was significant recognition of P2 by sera of untreated PCM patients when compared with normal human sera. Sera from treated PCM group, patients with other mycosis or co-infected with HIV had much lower recognition of P2 than untreated patient group. The test showed a sensitivity of 100 and 94.59% of specificity in relation to human sera control. These data indicate a potential use of P2 as diagnostic tool in PCM. Its application for serological diagnosis of PCM may contribute to the development and standardization of simpler, faster and highly reproducible immunodiagnostic tests at low cost. Springer Netherlands 2012-01-17 2012 /pmc/articles/PMC3368115/ /pubmed/22249604 http://dx.doi.org/10.1007/s11046-011-9518-3 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
Caldini, Camila Pistelli
Xander, Patricia
Kioshima, Érika Seki
Bachi, André Luis Lacerda
de Camargo, Zoilo Pires
Mariano, Mário
Lopes, José Daniel
Synthetic Peptides Mimic gp75 from Paracoccidioides brasiliensis in the Diagnosis of Paracoccidioidomycosis
title Synthetic Peptides Mimic gp75 from Paracoccidioides brasiliensis in the Diagnosis of Paracoccidioidomycosis
title_full Synthetic Peptides Mimic gp75 from Paracoccidioides brasiliensis in the Diagnosis of Paracoccidioidomycosis
title_fullStr Synthetic Peptides Mimic gp75 from Paracoccidioides brasiliensis in the Diagnosis of Paracoccidioidomycosis
title_full_unstemmed Synthetic Peptides Mimic gp75 from Paracoccidioides brasiliensis in the Diagnosis of Paracoccidioidomycosis
title_short Synthetic Peptides Mimic gp75 from Paracoccidioides brasiliensis in the Diagnosis of Paracoccidioidomycosis
title_sort synthetic peptides mimic gp75 from paracoccidioides brasiliensis in the diagnosis of paracoccidioidomycosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368115/
https://www.ncbi.nlm.nih.gov/pubmed/22249604
http://dx.doi.org/10.1007/s11046-011-9518-3
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