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A Model for Trans-Kingdom Pathogenicity in Fonsecaea Agents of Human Chromoblastomycosis

The fungal genus Fonsecaea comprises etiological agents of human chromoblastomycosis, a chronic implantation skin disease. The current hypothesis is that patients acquire the infection through an injury from plant material. The present study aimed to evaluate a model of infection in plant and animal...

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Autores principales: Fornari, Gheniffer, Gomes, Renata Rodrigues, Degenhardt-Goldbach, Juliana, dos Santos, Suelen Silvana, de Almeida, Sandro Rogério, dos Santos, Germana Davila, Muro, Marisol Dominguez, Bona, Cleusa, Scola, Rosana Herminia, Trindade, Edvaldo S., Bini, Israel Henrique, Ferreira-Maba, Lisandra Santos, Kestring, Daiane Rigoni, do Nascimento, Mariana Machado Fidelis, Lima, Bruna Jacomel Favoreto de Souza, Voidaleski, Morgana F., Steinmacher, Douglas André, Soley, Bruna da Silva, Deng, Shuwen, Bocca, Anamelia Lorenzetti, da Silva, Moises B., Salgado, Claudio G., de Azevedo, Conceição Maria Pedroso e Silva, Vicente, Vania Aparecida, de Hoog, Sybren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189323/
https://www.ncbi.nlm.nih.gov/pubmed/30356683
http://dx.doi.org/10.3389/fmicb.2018.02211
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author Fornari, Gheniffer
Gomes, Renata Rodrigues
Degenhardt-Goldbach, Juliana
dos Santos, Suelen Silvana
de Almeida, Sandro Rogério
dos Santos, Germana Davila
Muro, Marisol Dominguez
Bona, Cleusa
Scola, Rosana Herminia
Trindade, Edvaldo S.
Bini, Israel Henrique
Ferreira-Maba, Lisandra Santos
Kestring, Daiane Rigoni
do Nascimento, Mariana Machado Fidelis
Lima, Bruna Jacomel Favoreto de Souza
Voidaleski, Morgana F.
Steinmacher, Douglas André
Soley, Bruna da Silva
Deng, Shuwen
Bocca, Anamelia Lorenzetti
da Silva, Moises B.
Salgado, Claudio G.
de Azevedo, Conceição Maria Pedroso e Silva
Vicente, Vania Aparecida
de Hoog, Sybren
author_facet Fornari, Gheniffer
Gomes, Renata Rodrigues
Degenhardt-Goldbach, Juliana
dos Santos, Suelen Silvana
de Almeida, Sandro Rogério
dos Santos, Germana Davila
Muro, Marisol Dominguez
Bona, Cleusa
Scola, Rosana Herminia
Trindade, Edvaldo S.
Bini, Israel Henrique
Ferreira-Maba, Lisandra Santos
Kestring, Daiane Rigoni
do Nascimento, Mariana Machado Fidelis
Lima, Bruna Jacomel Favoreto de Souza
Voidaleski, Morgana F.
Steinmacher, Douglas André
Soley, Bruna da Silva
Deng, Shuwen
Bocca, Anamelia Lorenzetti
da Silva, Moises B.
Salgado, Claudio G.
de Azevedo, Conceição Maria Pedroso e Silva
Vicente, Vania Aparecida
de Hoog, Sybren
author_sort Fornari, Gheniffer
collection PubMed
description The fungal genus Fonsecaea comprises etiological agents of human chromoblastomycosis, a chronic implantation skin disease. The current hypothesis is that patients acquire the infection through an injury from plant material. The present study aimed to evaluate a model of infection in plant and animal hosts to understand the parameters of trans-kingdom pathogenicity. Clinical strains of causative agents of chromoblastomycosis (Fonsecaea pedrosoi and Fonsecaea monophora) were compared with a strain of Fonsecaea erecta isolated from a living plant. The clinical strains of F. monophora and F. pedrosoi remained concentrated near the epidermis, whereas F. erecta colonized deeper plant tissues, resembling an endophytic behavior. In an invertebrate infection model with larvae of a beetle, Tenebrio molitor, F. erecta exhibited the lowest survival rates. However, F. pedrosoi produced dark, spherical to ovoidal cells that resembled muriform cells, the invasive form of human chromoblastomycosis confirming the role of muriform cells as a pathogenic adaptation in animal tissues. An immunologic assay in BALB/c mice demonstrated the high virulence of saprobic species in animal models was subsequently controlled via host higher immune response.
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spelling pubmed-61893232018-10-23 A Model for Trans-Kingdom Pathogenicity in Fonsecaea Agents of Human Chromoblastomycosis Fornari, Gheniffer Gomes, Renata Rodrigues Degenhardt-Goldbach, Juliana dos Santos, Suelen Silvana de Almeida, Sandro Rogério dos Santos, Germana Davila Muro, Marisol Dominguez Bona, Cleusa Scola, Rosana Herminia Trindade, Edvaldo S. Bini, Israel Henrique Ferreira-Maba, Lisandra Santos Kestring, Daiane Rigoni do Nascimento, Mariana Machado Fidelis Lima, Bruna Jacomel Favoreto de Souza Voidaleski, Morgana F. Steinmacher, Douglas André Soley, Bruna da Silva Deng, Shuwen Bocca, Anamelia Lorenzetti da Silva, Moises B. Salgado, Claudio G. de Azevedo, Conceição Maria Pedroso e Silva Vicente, Vania Aparecida de Hoog, Sybren Front Microbiol Microbiology The fungal genus Fonsecaea comprises etiological agents of human chromoblastomycosis, a chronic implantation skin disease. The current hypothesis is that patients acquire the infection through an injury from plant material. The present study aimed to evaluate a model of infection in plant and animal hosts to understand the parameters of trans-kingdom pathogenicity. Clinical strains of causative agents of chromoblastomycosis (Fonsecaea pedrosoi and Fonsecaea monophora) were compared with a strain of Fonsecaea erecta isolated from a living plant. The clinical strains of F. monophora and F. pedrosoi remained concentrated near the epidermis, whereas F. erecta colonized deeper plant tissues, resembling an endophytic behavior. In an invertebrate infection model with larvae of a beetle, Tenebrio molitor, F. erecta exhibited the lowest survival rates. However, F. pedrosoi produced dark, spherical to ovoidal cells that resembled muriform cells, the invasive form of human chromoblastomycosis confirming the role of muriform cells as a pathogenic adaptation in animal tissues. An immunologic assay in BALB/c mice demonstrated the high virulence of saprobic species in animal models was subsequently controlled via host higher immune response. Frontiers Media S.A. 2018-10-09 /pmc/articles/PMC6189323/ /pubmed/30356683 http://dx.doi.org/10.3389/fmicb.2018.02211 Text en Copyright © 2018 Fornari, Gomes, Degenhardt-Goldbach, Santos, Almeida, Santos, Muro, Bona, Trindade, Bini, Ferreira-Maba, Soley, Kestring, Nascimento, Lima, Voidaleski, Steinmacher, Scola, Deng, Bocca, da Silva, Salgado, de Azevedo, Vicente and de Hoog. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Fornari, Gheniffer
Gomes, Renata Rodrigues
Degenhardt-Goldbach, Juliana
dos Santos, Suelen Silvana
de Almeida, Sandro Rogério
dos Santos, Germana Davila
Muro, Marisol Dominguez
Bona, Cleusa
Scola, Rosana Herminia
Trindade, Edvaldo S.
Bini, Israel Henrique
Ferreira-Maba, Lisandra Santos
Kestring, Daiane Rigoni
do Nascimento, Mariana Machado Fidelis
Lima, Bruna Jacomel Favoreto de Souza
Voidaleski, Morgana F.
Steinmacher, Douglas André
Soley, Bruna da Silva
Deng, Shuwen
Bocca, Anamelia Lorenzetti
da Silva, Moises B.
Salgado, Claudio G.
de Azevedo, Conceição Maria Pedroso e Silva
Vicente, Vania Aparecida
de Hoog, Sybren
A Model for Trans-Kingdom Pathogenicity in Fonsecaea Agents of Human Chromoblastomycosis
title A Model for Trans-Kingdom Pathogenicity in Fonsecaea Agents of Human Chromoblastomycosis
title_full A Model for Trans-Kingdom Pathogenicity in Fonsecaea Agents of Human Chromoblastomycosis
title_fullStr A Model for Trans-Kingdom Pathogenicity in Fonsecaea Agents of Human Chromoblastomycosis
title_full_unstemmed A Model for Trans-Kingdom Pathogenicity in Fonsecaea Agents of Human Chromoblastomycosis
title_short A Model for Trans-Kingdom Pathogenicity in Fonsecaea Agents of Human Chromoblastomycosis
title_sort model for trans-kingdom pathogenicity in fonsecaea agents of human chromoblastomycosis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189323/
https://www.ncbi.nlm.nih.gov/pubmed/30356683
http://dx.doi.org/10.3389/fmicb.2018.02211
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