In Vitro and In Vivo Effect of Peptides Derived from 14-3-3 <i>Paracoccidioides </i>spp. Protein

Background: Paracoccidioidomycosis (PCM) is a chronic disease that causes sequelae and requires prolonged treatment; therefore, new therapeutic approaches are necessary. In view of this, three peptides from <i>Paracoccidioides brasiliensis</i> 14-3-3 protein were selected based on its im...

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Main Authors: Liliana Scorzoni, Ana Carolina Alves de Paula e Silva, Haroldo Cesar de Oliveira, Claudia Tavares dos Santos, Junya de Lacorte Singulani, Patricia Akemi Assato, Caroline Maria Marcos, Lariane Teodoro Oliveira, Nathália Ferreira Fregonezi, Diego Conrado Pereira Rossi, Leandro Buffoni Roque da Silva, Carlos Pelleschi Taborda, Ana Marisa Fusco-Almeida, Maria José Soares Mendes-Giannini
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Journal of Fungi
Subjects:
Online Access:https://www.mdpi.com/2309-608X/7/1/52
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spelling doaj-70c2abf83f1244fd9fd2589e4d64b9102021-01-14T00:04:23ZengMDPI AGJournal of Fungi2309-608X2021-01-017525210.3390/jof7010052In Vitro and In Vivo Effect of Peptides Derived from 14-3-3 <i>Paracoccidioides </i>spp. ProteinLiliana Scorzoni0Ana Carolina Alves de Paula e Silva1Haroldo Cesar de Oliveira2Claudia Tavares dos Santos3Junya de Lacorte Singulani4Patricia Akemi Assato5Caroline Maria Marcos6Lariane Teodoro Oliveira7Nathália Ferreira Fregonezi8Diego Conrado Pereira Rossi9Leandro Buffoni Roque da Silva10Carlos Pelleschi Taborda11Ana Marisa Fusco-Almeida12Maria José Soares Mendes-Giannini13School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilDepartment of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, BrazilDepartment of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, BrazilDepartment of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, BrazilSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo 14800-903, BrazilBackground: Paracoccidioidomycosis (PCM) is a chronic disease that causes sequelae and requires prolonged treatment; therefore, new therapeutic approaches are necessary. In view of this, three peptides from <i>Paracoccidioides brasiliensis</i> 14-3-3 protein were selected based on its immunogenicity and therapeutic potential. Methods: The in vitro antifungal activity and cytotoxicity of the 14-3-3 peptides were evaluated. The influence of the peptides in immunological and survival aspects was evaluated in vivo, using <i>Galleria mellonella</i> and the expression of antimicrobial peptide genes in <i>Caenorhabditis elegans</i>. Results: None of the peptides were toxic to HaCaT (skin keratinocyte), MRC-5 (lung fibroblast), and A549 (pneumocyte) cell lines, and only P1 exhibited antifungal activity against <i>Paracoccidioides</i> spp. The peptides could induce an immune response in <i>G. mellonella</i>. Moreover, the peptides caused a delay in the death of <i>Paracoccidioides</i> spp. infected larvae. Regarding <i>C. elegans</i>, the three peptides were able to increase the expression of the antimicrobial peptides. These peptides had essential effects on different aspects of <i>Paracoccidioides</i> spp. infection showing potential for a therapeutic vaccine. Future studies using mammalian methods are necessary to validate our findings.https://www.mdpi.com/2309-608X/7/1/52paracoccidioidomycosis<i>Paracoccidioides</i> spp.14-3-3 protein<i>Galleria mellonella</i><i>Caenorhabditis elegans</i>vaccine
collection DOAJ
language English
format Article
sources DOAJ
author Liliana Scorzoni
Ana Carolina Alves de Paula e Silva
Haroldo Cesar de Oliveira
Claudia Tavares dos Santos
Junya de Lacorte Singulani
Patricia Akemi Assato
Caroline Maria Marcos
Lariane Teodoro Oliveira
Nathália Ferreira Fregonezi
Diego Conrado Pereira Rossi
Leandro Buffoni Roque da Silva
Carlos Pelleschi Taborda
Ana Marisa Fusco-Almeida
Maria José Soares Mendes-Giannini
spellingShingle Liliana Scorzoni
Ana Carolina Alves de Paula e Silva
Haroldo Cesar de Oliveira
Claudia Tavares dos Santos
Junya de Lacorte Singulani
Patricia Akemi Assato
Caroline Maria Marcos
Lariane Teodoro Oliveira
Nathália Ferreira Fregonezi
Diego Conrado Pereira Rossi
Leandro Buffoni Roque da Silva
Carlos Pelleschi Taborda
Ana Marisa Fusco-Almeida
Maria José Soares Mendes-Giannini
In Vitro and In Vivo Effect of Peptides Derived from 14-3-3 <i>Paracoccidioides </i>spp. Protein
Journal of Fungi
paracoccidioidomycosis
<i>Paracoccidioides</i> spp.
14-3-3 protein
<i>Galleria mellonella</i>
<i>Caenorhabditis elegans</i>
vaccine
author_facet Liliana Scorzoni
Ana Carolina Alves de Paula e Silva
Haroldo Cesar de Oliveira
Claudia Tavares dos Santos
Junya de Lacorte Singulani
Patricia Akemi Assato
Caroline Maria Marcos
Lariane Teodoro Oliveira
Nathália Ferreira Fregonezi
Diego Conrado Pereira Rossi
Leandro Buffoni Roque da Silva
Carlos Pelleschi Taborda
Ana Marisa Fusco-Almeida
Maria José Soares Mendes-Giannini
author_sort Liliana Scorzoni
title In Vitro and In Vivo Effect of Peptides Derived from 14-3-3 <i>Paracoccidioides </i>spp. Protein
title_short In Vitro and In Vivo Effect of Peptides Derived from 14-3-3 <i>Paracoccidioides </i>spp. Protein
title_full In Vitro and In Vivo Effect of Peptides Derived from 14-3-3 <i>Paracoccidioides </i>spp. Protein
title_fullStr In Vitro and In Vivo Effect of Peptides Derived from 14-3-3 <i>Paracoccidioides </i>spp. Protein
title_full_unstemmed In Vitro and In Vivo Effect of Peptides Derived from 14-3-3 <i>Paracoccidioides </i>spp. Protein
title_sort in vitro and in vivo effect of peptides derived from 14-3-3 <i>paracoccidioides </i>spp. protein
publisher MDPI AG
series Journal of Fungi
issn 2309-608X
publishDate 2021-01-01
description Background: Paracoccidioidomycosis (PCM) is a chronic disease that causes sequelae and requires prolonged treatment; therefore, new therapeutic approaches are necessary. In view of this, three peptides from <i>Paracoccidioides brasiliensis</i> 14-3-3 protein were selected based on its immunogenicity and therapeutic potential. Methods: The in vitro antifungal activity and cytotoxicity of the 14-3-3 peptides were evaluated. The influence of the peptides in immunological and survival aspects was evaluated in vivo, using <i>Galleria mellonella</i> and the expression of antimicrobial peptide genes in <i>Caenorhabditis elegans</i>. Results: None of the peptides were toxic to HaCaT (skin keratinocyte), MRC-5 (lung fibroblast), and A549 (pneumocyte) cell lines, and only P1 exhibited antifungal activity against <i>Paracoccidioides</i> spp. The peptides could induce an immune response in <i>G. mellonella</i>. Moreover, the peptides caused a delay in the death of <i>Paracoccidioides</i> spp. infected larvae. Regarding <i>C. elegans</i>, the three peptides were able to increase the expression of the antimicrobial peptides. These peptides had essential effects on different aspects of <i>Paracoccidioides</i> spp. infection showing potential for a therapeutic vaccine. Future studies using mammalian methods are necessary to validate our findings.
topic paracoccidioidomycosis
<i>Paracoccidioides</i> spp.
14-3-3 protein
<i>Galleria mellonella</i>
<i>Caenorhabditis elegans</i>
vaccine
url https://www.mdpi.com/2309-608X/7/1/52
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