Dual localization of Mdj1 in pathogenic fungi varies with growth temperature

Detalhes bibliográficos
Autor(a) principal: Dourado, Itala Bruna Z. [UNIFESP]
Data de Publicação: 2014
Outros Autores: Batista, Wagner L. [UNIFESP], Longo, Larissa V. G. [UNIFESP], Mortara, Renato A. [UNIFESP], Puccia, Rosana [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/37341
http://dx.doi.org/10.1093/mmy/myt002
Resumo: Paracoccidioides brasiliensis and P. lutzii are temperature-dependent dimorphic fungi that cause paracoccidioidomycosis (PCM). Previously, we characterized the PbMDJ1 gene. This gene encodes P. brasiliensis chaperone Mdj1, which in yeast is a mitochondrial member of the J-domain family, whose main function is to regulate cognate Hsp70 activities. We produced rabbit polyclonal antibody antirecombinant PbMdj1 (rPbMdj1), which labeled the protein not only in mitochondria but also at the cell wall of P. brasiliensis yeasts of isolate Pb18. Here we used anti-rPbMdj1 in confocal microscopy to localize Mdj1 in Pb18 and other fungal isolates grown at different temperatures. Dual intracellular and cell surface pattern were initially seen in yeast-phase P. brasiliensis Pb3, Pb18 (control), P. lutzii Pb01, and Histoplasma capsulatum. Pb18 and Aspergillus fumigatus hyphae as well as Pb3 pseudo hyphae formed at 36 degrees C were labeled predominantly along the cell surface. Preferential surface localization was observed by 72 h of yeast-mycelium thermotransition. It was interesting to observe that anti-rPbMdj1 concentrated at the surface tip and branching points of A. fumigatus hyphae grown at 36 degrees C, suggesting a role in growth, whereas at 23 degrees C, anti-rPbMdj1 was distributed along the hyphal surface. in Pb3, Pb18, and Pb01 mitochondrial extracts, the antibodies revealed a specific 55-kDa band, which corresponds to the processed Mdj1 size. the presence of Mdj1 on the fungal cell wall suggests that this protein could also play a role in the interaction with the host.
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spelling Dourado, Itala Bruna Z. [UNIFESP]Batista, Wagner L. [UNIFESP]Longo, Larissa V. G. [UNIFESP]Mortara, Renato A. [UNIFESP]Puccia, Rosana [UNIFESP]Universidade Federal de São Paulo (UNIFESP)2016-01-24T14:35:11Z2016-01-24T14:35:11Z2014-02-01Medical Mycology. London: Informa Healthcare, v. 52, n. 2, p. 187-195, 2014.1369-3786http://repositorio.unifesp.br/handle/11600/37341http://dx.doi.org/10.1093/mmy/myt00210.1093/mmy/myt002WOS:000339911800009Paracoccidioides brasiliensis and P. lutzii are temperature-dependent dimorphic fungi that cause paracoccidioidomycosis (PCM). Previously, we characterized the PbMDJ1 gene. This gene encodes P. brasiliensis chaperone Mdj1, which in yeast is a mitochondrial member of the J-domain family, whose main function is to regulate cognate Hsp70 activities. We produced rabbit polyclonal antibody antirecombinant PbMdj1 (rPbMdj1), which labeled the protein not only in mitochondria but also at the cell wall of P. brasiliensis yeasts of isolate Pb18. Here we used anti-rPbMdj1 in confocal microscopy to localize Mdj1 in Pb18 and other fungal isolates grown at different temperatures. Dual intracellular and cell surface pattern were initially seen in yeast-phase P. brasiliensis Pb3, Pb18 (control), P. lutzii Pb01, and Histoplasma capsulatum. Pb18 and Aspergillus fumigatus hyphae as well as Pb3 pseudo hyphae formed at 36 degrees C were labeled predominantly along the cell surface. Preferential surface localization was observed by 72 h of yeast-mycelium thermotransition. It was interesting to observe that anti-rPbMdj1 concentrated at the surface tip and branching points of A. fumigatus hyphae grown at 36 degrees C, suggesting a role in growth, whereas at 23 degrees C, anti-rPbMdj1 was distributed along the hyphal surface. in Pb3, Pb18, and Pb01 mitochondrial extracts, the antibodies revealed a specific 55-kDa band, which corresponds to the processed Mdj1 size. the presence of Mdj1 on the fungal cell wall suggests that this protein could also play a role in the interaction with the host.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Universidade Federal de São Paulo, EPM UNIFESP, Dept Microbiol Imunol & Parasitol, Escola Paulista Med, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Ciencias Biol, São Paulo, BrazilUniversidade Federal de São Paulo, EPM UNIFESP, Dept Microbiol Imunol & Parasitol, Escola Paulista Med, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Ciencias Biol, São Paulo, BrazilWeb of Science187-195engInforma HealthcareMedical Mycologyhttp://informahealthcare.com/userimages/ContentEditor/1255620309227/Copyright_And_Permissions.pdfinfo:eu-repo/semantics/openAccessMdj1cell wallmitochondriapathogenic fungitemperatureDual localization of Mdj1 in pathogenic fungi varies with growth temperatureinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlereponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/373412022-02-08 11:52:12.716metadata only accessoai:repositorio.unifesp.br:11600/37341Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652022-02-08T14:52:12Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Dual localization of Mdj1 in pathogenic fungi varies with growth temperature
title Dual localization of Mdj1 in pathogenic fungi varies with growth temperature
spellingShingle Dual localization of Mdj1 in pathogenic fungi varies with growth temperature
Dourado, Itala Bruna Z. [UNIFESP]
Mdj1
cell wall
mitochondria
pathogenic fungi
temperature
title_short Dual localization of Mdj1 in pathogenic fungi varies with growth temperature
title_full Dual localization of Mdj1 in pathogenic fungi varies with growth temperature
title_fullStr Dual localization of Mdj1 in pathogenic fungi varies with growth temperature
title_full_unstemmed Dual localization of Mdj1 in pathogenic fungi varies with growth temperature
title_sort Dual localization of Mdj1 in pathogenic fungi varies with growth temperature
author Dourado, Itala Bruna Z. [UNIFESP]
author_facet Dourado, Itala Bruna Z. [UNIFESP]
Batista, Wagner L. [UNIFESP]
Longo, Larissa V. G. [UNIFESP]
Mortara, Renato A. [UNIFESP]
Puccia, Rosana [UNIFESP]
author_role author
author2 Batista, Wagner L. [UNIFESP]
Longo, Larissa V. G. [UNIFESP]
Mortara, Renato A. [UNIFESP]
Puccia, Rosana [UNIFESP]
author2_role author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Dourado, Itala Bruna Z. [UNIFESP]
Batista, Wagner L. [UNIFESP]
Longo, Larissa V. G. [UNIFESP]
Mortara, Renato A. [UNIFESP]
Puccia, Rosana [UNIFESP]
dc.subject.eng.fl_str_mv Mdj1
cell wall
mitochondria
pathogenic fungi
temperature
topic Mdj1
cell wall
mitochondria
pathogenic fungi
temperature
description Paracoccidioides brasiliensis and P. lutzii are temperature-dependent dimorphic fungi that cause paracoccidioidomycosis (PCM). Previously, we characterized the PbMDJ1 gene. This gene encodes P. brasiliensis chaperone Mdj1, which in yeast is a mitochondrial member of the J-domain family, whose main function is to regulate cognate Hsp70 activities. We produced rabbit polyclonal antibody antirecombinant PbMdj1 (rPbMdj1), which labeled the protein not only in mitochondria but also at the cell wall of P. brasiliensis yeasts of isolate Pb18. Here we used anti-rPbMdj1 in confocal microscopy to localize Mdj1 in Pb18 and other fungal isolates grown at different temperatures. Dual intracellular and cell surface pattern were initially seen in yeast-phase P. brasiliensis Pb3, Pb18 (control), P. lutzii Pb01, and Histoplasma capsulatum. Pb18 and Aspergillus fumigatus hyphae as well as Pb3 pseudo hyphae formed at 36 degrees C were labeled predominantly along the cell surface. Preferential surface localization was observed by 72 h of yeast-mycelium thermotransition. It was interesting to observe that anti-rPbMdj1 concentrated at the surface tip and branching points of A. fumigatus hyphae grown at 36 degrees C, suggesting a role in growth, whereas at 23 degrees C, anti-rPbMdj1 was distributed along the hyphal surface. in Pb3, Pb18, and Pb01 mitochondrial extracts, the antibodies revealed a specific 55-kDa band, which corresponds to the processed Mdj1 size. the presence of Mdj1 on the fungal cell wall suggests that this protein could also play a role in the interaction with the host.
publishDate 2014
dc.date.issued.fl_str_mv 2014-02-01
dc.date.accessioned.fl_str_mv 2016-01-24T14:35:11Z
dc.date.available.fl_str_mv 2016-01-24T14:35:11Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Medical Mycology. London: Informa Healthcare, v. 52, n. 2, p. 187-195, 2014.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/37341
http://dx.doi.org/10.1093/mmy/myt002
dc.identifier.issn.none.fl_str_mv 1369-3786
dc.identifier.doi.none.fl_str_mv 10.1093/mmy/myt002
dc.identifier.wos.none.fl_str_mv WOS:000339911800009
identifier_str_mv Medical Mycology. London: Informa Healthcare, v. 52, n. 2, p. 187-195, 2014.
1369-3786
10.1093/mmy/myt002
WOS:000339911800009
url http://repositorio.unifesp.br/handle/11600/37341
http://dx.doi.org/10.1093/mmy/myt002
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Medical Mycology
dc.rights.driver.fl_str_mv http://informahealthcare.com/userimages/ContentEditor/1255620309227/Copyright_And_Permissions.pdf
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://informahealthcare.com/userimages/ContentEditor/1255620309227/Copyright_And_Permissions.pdf
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 187-195
dc.publisher.none.fl_str_mv Informa Healthcare
publisher.none.fl_str_mv Informa Healthcare
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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