Cutaneous granulomas in dolphins caused by novel uncultivated Paracoccidioides brasiliensis

Detalhes bibliográficos
Autor(a) principal: Raquel Virgínia Rocha Vilela
Data de Publicação: 2016
Outros Autores: Gregory Dana Bossart, Judy A. St. Leger, Leslie M. Dalton, John S. Reif, Adam M. Schaefer, Peter J. McCarthy, Patricia A. Fair, Leonel Mendoza
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFMG
Texto Completo: http://dx.doi.org/10.3201/eid2212.160860
http://hdl.handle.net/1843/40188
Resumo: Cutaneous granulomas in dolphins were believed to be caused by Lacazia loboi, which also causes a similar disease in humans. This hypothesis was recently challenged by reports that fungal DNA sequences from dolphins grouped this pathogen with Paracoccidioides brasiliensis. We conducted phylogenetic analysis of fungi from 6 bottlenose dolphins (Tursiops truncatus) with cutaneous granulomas and chains of yeast cells in infected tissues. Kex gene sequences of P. brasiliensis from dolphins showed 100% homology with sequences from cultivated P. brasiliensis, 73% with those of L. loboi, and 93% with those of P. lutzii. Parsimony analysis placed DNA sequences from dolphins within a cluster with human P. brasiliensis strains. This cluster was the sister taxon to P. lutzii and L. loboi. Our molecular data support previous findings and suggest that a novel uncultivated strain of P. brasiliensis restricted to cutaneous lesions in dolphins is probably the cause of lacaziosis/lobomycosis, herein referred to as paracoccidioidomycosis ceti.
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spelling 2022-03-17T15:53:42Z2022-03-17T15:53:42Z2016221220632069http://dx.doi.org/10.3201/eid2212.1608601080-6059http://hdl.handle.net/1843/40188Cutaneous granulomas in dolphins were believed to be caused by Lacazia loboi, which also causes a similar disease in humans. This hypothesis was recently challenged by reports that fungal DNA sequences from dolphins grouped this pathogen with Paracoccidioides brasiliensis. We conducted phylogenetic analysis of fungi from 6 bottlenose dolphins (Tursiops truncatus) with cutaneous granulomas and chains of yeast cells in infected tissues. Kex gene sequences of P. brasiliensis from dolphins showed 100% homology with sequences from cultivated P. brasiliensis, 73% with those of L. loboi, and 93% with those of P. lutzii. Parsimony analysis placed DNA sequences from dolphins within a cluster with human P. brasiliensis strains. This cluster was the sister taxon to P. lutzii and L. loboi. Our molecular data support previous findings and suggest that a novel uncultivated strain of P. brasiliensis restricted to cutaneous lesions in dolphins is probably the cause of lacaziosis/lobomycosis, herein referred to as paracoccidioidomycosis ceti.engUniversidade Federal de Minas GeraisUFMGBrasilFAR - DEPARTAMENTO DE ANÁLISES CLÍNICAS E TOXICOLÓGICASEmerging Infectious DiseasesParacoccidioidesParacoccidioidomicoseGranulomaFungosGolfinhosCutaneous granulomas in dolphins caused by novel uncultivated Paracoccidioides brasiliensisinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://wwwnc.cdc.gov/eid/articles/issue/22/12/table-of-contentsRaquel Virgínia Rocha VilelaGregory Dana BossartJudy A. St. LegerLeslie M. DaltonJohn S. ReifAdam M. SchaeferPeter J. McCarthyPatricia A. 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dc.title.pt_BR.fl_str_mv Cutaneous granulomas in dolphins caused by novel uncultivated Paracoccidioides brasiliensis
title Cutaneous granulomas in dolphins caused by novel uncultivated Paracoccidioides brasiliensis
spellingShingle Cutaneous granulomas in dolphins caused by novel uncultivated Paracoccidioides brasiliensis
Raquel Virgínia Rocha Vilela
Paracoccidioides
Paracoccidioidomicose
Granuloma
Fungos
Golfinhos
title_short Cutaneous granulomas in dolphins caused by novel uncultivated Paracoccidioides brasiliensis
title_full Cutaneous granulomas in dolphins caused by novel uncultivated Paracoccidioides brasiliensis
title_fullStr Cutaneous granulomas in dolphins caused by novel uncultivated Paracoccidioides brasiliensis
title_full_unstemmed Cutaneous granulomas in dolphins caused by novel uncultivated Paracoccidioides brasiliensis
title_sort Cutaneous granulomas in dolphins caused by novel uncultivated Paracoccidioides brasiliensis
author Raquel Virgínia Rocha Vilela
author_facet Raquel Virgínia Rocha Vilela
Gregory Dana Bossart
Judy A. St. Leger
Leslie M. Dalton
John S. Reif
Adam M. Schaefer
Peter J. McCarthy
Patricia A. Fair
Leonel Mendoza
author_role author
author2 Gregory Dana Bossart
Judy A. St. Leger
Leslie M. Dalton
John S. Reif
Adam M. Schaefer
Peter J. McCarthy
Patricia A. Fair
Leonel Mendoza
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Raquel Virgínia Rocha Vilela
Gregory Dana Bossart
Judy A. St. Leger
Leslie M. Dalton
John S. Reif
Adam M. Schaefer
Peter J. McCarthy
Patricia A. Fair
Leonel Mendoza
dc.subject.other.pt_BR.fl_str_mv Paracoccidioides
Paracoccidioidomicose
Granuloma
Fungos
Golfinhos
topic Paracoccidioides
Paracoccidioidomicose
Granuloma
Fungos
Golfinhos
description Cutaneous granulomas in dolphins were believed to be caused by Lacazia loboi, which also causes a similar disease in humans. This hypothesis was recently challenged by reports that fungal DNA sequences from dolphins grouped this pathogen with Paracoccidioides brasiliensis. We conducted phylogenetic analysis of fungi from 6 bottlenose dolphins (Tursiops truncatus) with cutaneous granulomas and chains of yeast cells in infected tissues. Kex gene sequences of P. brasiliensis from dolphins showed 100% homology with sequences from cultivated P. brasiliensis, 73% with those of L. loboi, and 93% with those of P. lutzii. Parsimony analysis placed DNA sequences from dolphins within a cluster with human P. brasiliensis strains. This cluster was the sister taxon to P. lutzii and L. loboi. Our molecular data support previous findings and suggest that a novel uncultivated strain of P. brasiliensis restricted to cutaneous lesions in dolphins is probably the cause of lacaziosis/lobomycosis, herein referred to as paracoccidioidomycosis ceti.
publishDate 2016
dc.date.issued.fl_str_mv 2016
dc.date.accessioned.fl_str_mv 2022-03-17T15:53:42Z
dc.date.available.fl_str_mv 2022-03-17T15:53:42Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/1843/40188
dc.identifier.doi.pt_BR.fl_str_mv http://dx.doi.org/10.3201/eid2212.160860
dc.identifier.issn.pt_BR.fl_str_mv 1080-6059
url http://dx.doi.org/10.3201/eid2212.160860
http://hdl.handle.net/1843/40188
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dc.relation.ispartof.pt_BR.fl_str_mv Emerging Infectious Diseases
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dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv FAR - DEPARTAMENTO DE ANÁLISES CLÍNICAS E TOXICOLÓGICAS
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
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