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Molecular Epidemiology of Agents of Human Chromoblastomycosis in Brazil with the Description of Two Novel Species

The human mutilating disease chromoblastomycosis is caused by melanized members of the order Chaetothyriales. To assess population diversity among 123 clinical strains of agents of the disease in Brazil we applied sequencing of the rDNA internal transcribed spacer region, and partial cell division c...

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Autores principales: Gomes, Renata R., Vicente, Vania A., de Azevedo, Conceição M. P. S., Salgado, Claudio G., da Silva, Moises B., Queiroz-Telles, Flávio, Marques, Sirlei G., Santos, Daniel W. C. L., de Andrade, Tania S., Takagi, Elizabeth H., Cruz, Katia S., Fornari, Gheniffer, Hahn, Rosane C., Scroferneker, Maria L., Caligine, Rachel B., Ramirez-Castrillon, Mauricio, de Araújo, Daniella P., Heidrich, Daiane, Colombo, Arnaldo L., de Hoog, G. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5125572/
https://www.ncbi.nlm.nih.gov/pubmed/27893750
http://dx.doi.org/10.1371/journal.pntd.0005102
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author Gomes, Renata R.
Vicente, Vania A.
de Azevedo, Conceição M. P. S.
Salgado, Claudio G.
da Silva, Moises B.
Queiroz-Telles, Flávio
Marques, Sirlei G.
Santos, Daniel W. C. L.
de Andrade, Tania S.
Takagi, Elizabeth H.
Cruz, Katia S.
Fornari, Gheniffer
Hahn, Rosane C.
Scroferneker, Maria L.
Caligine, Rachel B.
Ramirez-Castrillon, Mauricio
de Araújo, Daniella P.
Heidrich, Daiane
Colombo, Arnaldo L.
de Hoog, G. S.
author_facet Gomes, Renata R.
Vicente, Vania A.
de Azevedo, Conceição M. P. S.
Salgado, Claudio G.
da Silva, Moises B.
Queiroz-Telles, Flávio
Marques, Sirlei G.
Santos, Daniel W. C. L.
de Andrade, Tania S.
Takagi, Elizabeth H.
Cruz, Katia S.
Fornari, Gheniffer
Hahn, Rosane C.
Scroferneker, Maria L.
Caligine, Rachel B.
Ramirez-Castrillon, Mauricio
de Araújo, Daniella P.
Heidrich, Daiane
Colombo, Arnaldo L.
de Hoog, G. S.
author_sort Gomes, Renata R.
collection PubMed
description The human mutilating disease chromoblastomycosis is caused by melanized members of the order Chaetothyriales. To assess population diversity among 123 clinical strains of agents of the disease in Brazil we applied sequencing of the rDNA internal transcribed spacer region, and partial cell division cycle and β-tubulin genes. Strains studied were limited to three clusters divided over the single family Herpotrichiellaceae known to comprise agents of the disease. A Fonsecaea cluster contained the most important agents, among which F. pedrosoi was prevalent with 80% of the total set of strains, followed by 13% for F. monophora, 3% for F. nubica, and a single isolate of F. pugnacius. Additional agents, among which two novel species, were located among members of the genus Rhinocladiella and Cyphellophora, with frequencies of 3% and 1%, respectively.
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spelling pubmed-51255722016-12-15 Molecular Epidemiology of Agents of Human Chromoblastomycosis in Brazil with the Description of Two Novel Species Gomes, Renata R. Vicente, Vania A. de Azevedo, Conceição M. P. S. Salgado, Claudio G. da Silva, Moises B. Queiroz-Telles, Flávio Marques, Sirlei G. Santos, Daniel W. C. L. de Andrade, Tania S. Takagi, Elizabeth H. Cruz, Katia S. Fornari, Gheniffer Hahn, Rosane C. Scroferneker, Maria L. Caligine, Rachel B. Ramirez-Castrillon, Mauricio de Araújo, Daniella P. Heidrich, Daiane Colombo, Arnaldo L. de Hoog, G. S. PLoS Negl Trop Dis Research Article The human mutilating disease chromoblastomycosis is caused by melanized members of the order Chaetothyriales. To assess population diversity among 123 clinical strains of agents of the disease in Brazil we applied sequencing of the rDNA internal transcribed spacer region, and partial cell division cycle and β-tubulin genes. Strains studied were limited to three clusters divided over the single family Herpotrichiellaceae known to comprise agents of the disease. A Fonsecaea cluster contained the most important agents, among which F. pedrosoi was prevalent with 80% of the total set of strains, followed by 13% for F. monophora, 3% for F. nubica, and a single isolate of F. pugnacius. Additional agents, among which two novel species, were located among members of the genus Rhinocladiella and Cyphellophora, with frequencies of 3% and 1%, respectively. Public Library of Science 2016-11-28 /pmc/articles/PMC5125572/ /pubmed/27893750 http://dx.doi.org/10.1371/journal.pntd.0005102 Text en © 2016 Gomes et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gomes, Renata R.
Vicente, Vania A.
de Azevedo, Conceição M. P. S.
Salgado, Claudio G.
da Silva, Moises B.
Queiroz-Telles, Flávio
Marques, Sirlei G.
Santos, Daniel W. C. L.
de Andrade, Tania S.
Takagi, Elizabeth H.
Cruz, Katia S.
Fornari, Gheniffer
Hahn, Rosane C.
Scroferneker, Maria L.
Caligine, Rachel B.
Ramirez-Castrillon, Mauricio
de Araújo, Daniella P.
Heidrich, Daiane
Colombo, Arnaldo L.
de Hoog, G. S.
Molecular Epidemiology of Agents of Human Chromoblastomycosis in Brazil with the Description of Two Novel Species
title Molecular Epidemiology of Agents of Human Chromoblastomycosis in Brazil with the Description of Two Novel Species
title_full Molecular Epidemiology of Agents of Human Chromoblastomycosis in Brazil with the Description of Two Novel Species
title_fullStr Molecular Epidemiology of Agents of Human Chromoblastomycosis in Brazil with the Description of Two Novel Species
title_full_unstemmed Molecular Epidemiology of Agents of Human Chromoblastomycosis in Brazil with the Description of Two Novel Species
title_short Molecular Epidemiology of Agents of Human Chromoblastomycosis in Brazil with the Description of Two Novel Species
title_sort molecular epidemiology of agents of human chromoblastomycosis in brazil with the description of two novel species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5125572/
https://www.ncbi.nlm.nih.gov/pubmed/27893750
http://dx.doi.org/10.1371/journal.pntd.0005102
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