Hsp90 regulates Paracoccidioides brasiliensis proliferation and ROS levels under thermal stress and cooperates with calcineurin to control yeast to mycelium dimorphism
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.3109/13693786.2012.725481 http://repositorio.unifesp.br/handle/11600/36264 |
Resumo: | Paracoccidioidomycosis is a systemic human mycosis in Latin America caused by Paracoccidioides brasiliensis, a dimorphic pathogenic fungus that lives as a mold in the environment and as yeast during infections of human lungs. in this work, we provide evidence that the inhibition of Hsp90 by geldanamycin (GDA) impairs the proliferation of the yeast, but has no effect on mycelial development. Treatment with cyclosporin A (CsA), an inhibitor of the Hsp90 client protein calcineurin, did not increase the effect of GDA. in contrast, GDA prevented mycelial to yeast differentiation through a mechanism partially dependent on calcineurin, whereas differentiation from yeast to mycelia occurred independent of GDA or CsA. A significant increase in reactive oxygen species (ROS) levels was detected in GDA-treated yeast at 42 degrees C. However, the levels of ROS remained unchanged in GDA-treated yeast or mycelia incubated at 37 degrees C, suggesting that Hsp90 plays different roles under normal and thermal stress conditions. We propose that Hsp90 strengthens the stress response of P. brasiliensis at 37 degrees C through a mechanism that does not involve ROS. Moreover, we suggest that Hsp90 has calcineurin-dependent functions in this organism |
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Hsp90 regulates Paracoccidioides brasiliensis proliferation and ROS levels under thermal stress and cooperates with calcineurin to control yeast to mycelium dimorphismParacoccidioides brasiliensisHsp90calcineurinthermal stressdimorphismParacoccidioidomycosis is a systemic human mycosis in Latin America caused by Paracoccidioides brasiliensis, a dimorphic pathogenic fungus that lives as a mold in the environment and as yeast during infections of human lungs. in this work, we provide evidence that the inhibition of Hsp90 by geldanamycin (GDA) impairs the proliferation of the yeast, but has no effect on mycelial development. Treatment with cyclosporin A (CsA), an inhibitor of the Hsp90 client protein calcineurin, did not increase the effect of GDA. in contrast, GDA prevented mycelial to yeast differentiation through a mechanism partially dependent on calcineurin, whereas differentiation from yeast to mycelia occurred independent of GDA or CsA. A significant increase in reactive oxygen species (ROS) levels was detected in GDA-treated yeast at 42 degrees C. However, the levels of ROS remained unchanged in GDA-treated yeast or mycelia incubated at 37 degrees C, suggesting that Hsp90 plays different roles under normal and thermal stress conditions. We propose that Hsp90 strengthens the stress response of P. brasiliensis at 37 degrees C through a mechanism that does not involve ROS. Moreover, we suggest that Hsp90 has calcineurin-dependent functions in this organismUniv Vale Parailba UNIVAP, Inst Pesquisa & Desenvolvimento, São Paulo, BrazilUniversidade Federal de São Paulo UNIFESP, Inst Ciencia & Tecnol, São Paulo, BrazilUniversidade Federal de São Paulo UNIFESP, Inst Ciencia & Tecnol, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)FAPESP: 10/50078-8Informa HealthcareUniv Vale Parailba UNIVAPUniversidade Federal de São Paulo (UNIFESP)Matos, Tatiana G. F.Morais, Flavia V.Campos, Claudia Barbosa Ladeira de [UNIFESP]2016-01-24T14:31:39Z2016-01-24T14:31:39Z2013-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion413-421http://dx.doi.org/10.3109/13693786.2012.725481Medical Mycology. London: Informa Healthcare, v. 51, n. 4, p. 413-421, 2013.10.3109/13693786.2012.7254811369-3786http://repositorio.unifesp.br/handle/11600/36264WOS:000317592600010engMedical Mycologyinfo:eu-repo/semantics/openAccesshttp://informahealthcare.com/userimages/ContentEditor/1255620309227/Copyright_And_Permissions.pdfreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T12:31:39Zoai:repositorio.unifesp.br/:11600/36264Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-01-24T12:31:39Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Hsp90 regulates Paracoccidioides brasiliensis proliferation and ROS levels under thermal stress and cooperates with calcineurin to control yeast to mycelium dimorphism |
title |
Hsp90 regulates Paracoccidioides brasiliensis proliferation and ROS levels under thermal stress and cooperates with calcineurin to control yeast to mycelium dimorphism |
spellingShingle |
Hsp90 regulates Paracoccidioides brasiliensis proliferation and ROS levels under thermal stress and cooperates with calcineurin to control yeast to mycelium dimorphism Matos, Tatiana G. F. Paracoccidioides brasiliensis Hsp90 calcineurin thermal stress dimorphism |
title_short |
Hsp90 regulates Paracoccidioides brasiliensis proliferation and ROS levels under thermal stress and cooperates with calcineurin to control yeast to mycelium dimorphism |
title_full |
Hsp90 regulates Paracoccidioides brasiliensis proliferation and ROS levels under thermal stress and cooperates with calcineurin to control yeast to mycelium dimorphism |
title_fullStr |
Hsp90 regulates Paracoccidioides brasiliensis proliferation and ROS levels under thermal stress and cooperates with calcineurin to control yeast to mycelium dimorphism |
title_full_unstemmed |
Hsp90 regulates Paracoccidioides brasiliensis proliferation and ROS levels under thermal stress and cooperates with calcineurin to control yeast to mycelium dimorphism |
title_sort |
Hsp90 regulates Paracoccidioides brasiliensis proliferation and ROS levels under thermal stress and cooperates with calcineurin to control yeast to mycelium dimorphism |
author |
Matos, Tatiana G. F. |
author_facet |
Matos, Tatiana G. F. Morais, Flavia V. Campos, Claudia Barbosa Ladeira de [UNIFESP] |
author_role |
author |
author2 |
Morais, Flavia V. Campos, Claudia Barbosa Ladeira de [UNIFESP] |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Univ Vale Parailba UNIVAP Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Matos, Tatiana G. F. Morais, Flavia V. Campos, Claudia Barbosa Ladeira de [UNIFESP] |
dc.subject.por.fl_str_mv |
Paracoccidioides brasiliensis Hsp90 calcineurin thermal stress dimorphism |
topic |
Paracoccidioides brasiliensis Hsp90 calcineurin thermal stress dimorphism |
description |
Paracoccidioidomycosis is a systemic human mycosis in Latin America caused by Paracoccidioides brasiliensis, a dimorphic pathogenic fungus that lives as a mold in the environment and as yeast during infections of human lungs. in this work, we provide evidence that the inhibition of Hsp90 by geldanamycin (GDA) impairs the proliferation of the yeast, but has no effect on mycelial development. Treatment with cyclosporin A (CsA), an inhibitor of the Hsp90 client protein calcineurin, did not increase the effect of GDA. in contrast, GDA prevented mycelial to yeast differentiation through a mechanism partially dependent on calcineurin, whereas differentiation from yeast to mycelia occurred independent of GDA or CsA. A significant increase in reactive oxygen species (ROS) levels was detected in GDA-treated yeast at 42 degrees C. However, the levels of ROS remained unchanged in GDA-treated yeast or mycelia incubated at 37 degrees C, suggesting that Hsp90 plays different roles under normal and thermal stress conditions. We propose that Hsp90 strengthens the stress response of P. brasiliensis at 37 degrees C through a mechanism that does not involve ROS. Moreover, we suggest that Hsp90 has calcineurin-dependent functions in this organism |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-05-01 2016-01-24T14:31:39Z 2016-01-24T14:31:39Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3109/13693786.2012.725481 Medical Mycology. London: Informa Healthcare, v. 51, n. 4, p. 413-421, 2013. 10.3109/13693786.2012.725481 1369-3786 http://repositorio.unifesp.br/handle/11600/36264 WOS:000317592600010 |
url |
http://dx.doi.org/10.3109/13693786.2012.725481 http://repositorio.unifesp.br/handle/11600/36264 |
identifier_str_mv |
Medical Mycology. London: Informa Healthcare, v. 51, n. 4, p. 413-421, 2013. 10.3109/13693786.2012.725481 1369-3786 WOS:000317592600010 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Medical Mycology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://informahealthcare.com/userimages/ContentEditor/1255620309227/Copyright_And_Permissions.pdf |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://informahealthcare.com/userimages/ContentEditor/1255620309227/Copyright_And_Permissions.pdf |
dc.format.none.fl_str_mv |
413-421 |
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 |
biblioteca.csp@unifesp.br |
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1814268389273632768 |