Drk1, a dimorphism histidine kinase, contributes to morphology, virulence, and stress adaptation in paracoccidioides brasiliensis

Detalhes bibliográficos
Autor(a) principal: Marcos, Caroline Maria [UNESP]
Data de Publicação: 2021
Outros Autores: de Oliveira, Haroldo Cesar [UNESP], Assato, Patrícia Akemi [UNESP], Castelli, Rafael Fernando, Fusco-Almeida, Ana Marisa [UNESP], Mendes-Giannini, Maria José Soares [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/jof7100852
http://hdl.handle.net/11449/233730
Resumo: P. brasiliensis is a thermally dimorphic fungus belonging to Paracoccidioides complex, causative of a systemic, endemic mycosis limited to Latin American countries. Signal transduc-tion pathways related to important aspects as surviving, proliferation according to the biological niches are linked to the fungal pathogenicity in many species, but its elucidation in P. brasiliensis remains poorly explored. As Drk1, a hybrid histidine kinase, plays regulators functions in other dimorphic fungi species, mainly in dimorphism and virulence, here we investigated its importance in P. brasilensis. We, therefore generated the respective recombinant protein, anti-PbDrk1 polyclonal antibody and a silenced strain. The Drk1 protein shows a random distribution including cell wall location that change its pattern during osmotic stress condition; moreover the P. brasiliensis treatment with anti-PbDrk1 antibody, which does not modify the fungus’s viability, resulted in decreased virulence in G. mellonella model and reduced interaction with pneumocytes. Down-regulating Pb-DRK1 yielded phenotypic alterations such as yeast cells with more elongated morphology, virulence attenuation in G. mellonella infection model, lower amount of chitin content, increased resistance to osmotic and cell wall stresses, and also caspofungin, and finally increased sensitivity to itraconazole. These observations highlight the importance of PbDrk1 to P. brasiliensis virulence, stress adaptation, morphology, and cell wall organization, and therefore it an interesting target that could help develop new antifungals.
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spelling Drk1, a dimorphism histidine kinase, contributes to morphology, virulence, and stress adaptation in paracoccidioides brasiliensisAntisense-RNA silencingCell wallDimorphism regulating-histidine kinaseDrk1Paracoccidioides brasiliensisVirulenceP. brasiliensis is a thermally dimorphic fungus belonging to Paracoccidioides complex, causative of a systemic, endemic mycosis limited to Latin American countries. Signal transduc-tion pathways related to important aspects as surviving, proliferation according to the biological niches are linked to the fungal pathogenicity in many species, but its elucidation in P. brasiliensis remains poorly explored. As Drk1, a hybrid histidine kinase, plays regulators functions in other dimorphic fungi species, mainly in dimorphism and virulence, here we investigated its importance in P. brasilensis. We, therefore generated the respective recombinant protein, anti-PbDrk1 polyclonal antibody and a silenced strain. The Drk1 protein shows a random distribution including cell wall location that change its pattern during osmotic stress condition; moreover the P. brasiliensis treatment with anti-PbDrk1 antibody, which does not modify the fungus’s viability, resulted in decreased virulence in G. mellonella model and reduced interaction with pneumocytes. Down-regulating Pb-DRK1 yielded phenotypic alterations such as yeast cells with more elongated morphology, virulence attenuation in G. mellonella infection model, lower amount of chitin content, increased resistance to osmotic and cell wall stresses, and also caspofungin, and finally increased sensitivity to itraconazole. These observations highlight the importance of PbDrk1 to P. brasiliensis virulence, stress adaptation, morphology, and cell wall organization, and therefore it an interesting target that could help develop new antifungals.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)School of Pharmaceutical Sciences São Paulo State University (UNESP)Instituto Carlos Chagas Fundação Oswaldo Cruz (Fiocruz)Laboratório Central de Multiusuários Faculdade de Ciências Agronômicas Campus Botucatu UNESP—Universidade Estadual PaulistaPrograma de Pós-Graduação em Biologia Parasitária Instituto Oswaldo Cruz Fundação Oswaldo Cruz (Fiocruz)School of Pharmaceutical Sciences São Paulo State University (UNESP)Laboratório Central de Multiusuários Faculdade de Ciências Agronômicas Campus Botucatu UNESP—Universidade Estadual PaulistaCNPq: 164217/2020-7FAPESP: 2015/03700-9FAPESP: 2015/14023-8FAPESP: 2016/17048-4CNPq: 403586/2012-7CAPES: 88881.141306/2017-01Universidade Estadual Paulista (UNESP)Fundação Oswaldo Cruz (Fiocruz)Marcos, Caroline Maria [UNESP]de Oliveira, Haroldo Cesar [UNESP]Assato, Patrícia Akemi [UNESP]Castelli, Rafael FernandoFusco-Almeida, Ana Marisa [UNESP]Mendes-Giannini, Maria José Soares [UNESP]2022-05-01T09:47:27Z2022-05-01T09:47:27Z2021-10-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/jof7100852Journal of Fungi, v. 7, n. 10, 2021.2309-608Xhttp://hdl.handle.net/11449/23373010.3390/jof71008522-s2.0-85117683376Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Fungiinfo:eu-repo/semantics/openAccess2024-06-21T15:19:31Zoai:repositorio.unesp.br:11449/233730Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:36:39.708256Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Drk1, a dimorphism histidine kinase, contributes to morphology, virulence, and stress adaptation in paracoccidioides brasiliensis
title Drk1, a dimorphism histidine kinase, contributes to morphology, virulence, and stress adaptation in paracoccidioides brasiliensis
spellingShingle Drk1, a dimorphism histidine kinase, contributes to morphology, virulence, and stress adaptation in paracoccidioides brasiliensis
Marcos, Caroline Maria [UNESP]
Antisense-RNA silencing
Cell wall
Dimorphism regulating-histidine kinase
Drk1
Paracoccidioides brasiliensis
Virulence
title_short Drk1, a dimorphism histidine kinase, contributes to morphology, virulence, and stress adaptation in paracoccidioides brasiliensis
title_full Drk1, a dimorphism histidine kinase, contributes to morphology, virulence, and stress adaptation in paracoccidioides brasiliensis
title_fullStr Drk1, a dimorphism histidine kinase, contributes to morphology, virulence, and stress adaptation in paracoccidioides brasiliensis
title_full_unstemmed Drk1, a dimorphism histidine kinase, contributes to morphology, virulence, and stress adaptation in paracoccidioides brasiliensis
title_sort Drk1, a dimorphism histidine kinase, contributes to morphology, virulence, and stress adaptation in paracoccidioides brasiliensis
author Marcos, Caroline Maria [UNESP]
author_facet Marcos, Caroline Maria [UNESP]
de Oliveira, Haroldo Cesar [UNESP]
Assato, Patrícia Akemi [UNESP]
Castelli, Rafael Fernando
Fusco-Almeida, Ana Marisa [UNESP]
Mendes-Giannini, Maria José Soares [UNESP]
author_role author
author2 de Oliveira, Haroldo Cesar [UNESP]
Assato, Patrícia Akemi [UNESP]
Castelli, Rafael Fernando
Fusco-Almeida, Ana Marisa [UNESP]
Mendes-Giannini, Maria José Soares [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Fundação Oswaldo Cruz (Fiocruz)
dc.contributor.author.fl_str_mv Marcos, Caroline Maria [UNESP]
de Oliveira, Haroldo Cesar [UNESP]
Assato, Patrícia Akemi [UNESP]
Castelli, Rafael Fernando
Fusco-Almeida, Ana Marisa [UNESP]
Mendes-Giannini, Maria José Soares [UNESP]
dc.subject.por.fl_str_mv Antisense-RNA silencing
Cell wall
Dimorphism regulating-histidine kinase
Drk1
Paracoccidioides brasiliensis
Virulence
topic Antisense-RNA silencing
Cell wall
Dimorphism regulating-histidine kinase
Drk1
Paracoccidioides brasiliensis
Virulence
description P. brasiliensis is a thermally dimorphic fungus belonging to Paracoccidioides complex, causative of a systemic, endemic mycosis limited to Latin American countries. Signal transduc-tion pathways related to important aspects as surviving, proliferation according to the biological niches are linked to the fungal pathogenicity in many species, but its elucidation in P. brasiliensis remains poorly explored. As Drk1, a hybrid histidine kinase, plays regulators functions in other dimorphic fungi species, mainly in dimorphism and virulence, here we investigated its importance in P. brasilensis. We, therefore generated the respective recombinant protein, anti-PbDrk1 polyclonal antibody and a silenced strain. The Drk1 protein shows a random distribution including cell wall location that change its pattern during osmotic stress condition; moreover the P. brasiliensis treatment with anti-PbDrk1 antibody, which does not modify the fungus’s viability, resulted in decreased virulence in G. mellonella model and reduced interaction with pneumocytes. Down-regulating Pb-DRK1 yielded phenotypic alterations such as yeast cells with more elongated morphology, virulence attenuation in G. mellonella infection model, lower amount of chitin content, increased resistance to osmotic and cell wall stresses, and also caspofungin, and finally increased sensitivity to itraconazole. These observations highlight the importance of PbDrk1 to P. brasiliensis virulence, stress adaptation, morphology, and cell wall organization, and therefore it an interesting target that could help develop new antifungals.
publishDate 2021
dc.date.none.fl_str_mv 2021-10-01
2022-05-01T09:47:27Z
2022-05-01T09:47:27Z
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.uri.fl_str_mv http://dx.doi.org/10.3390/jof7100852
Journal of Fungi, v. 7, n. 10, 2021.
2309-608X
http://hdl.handle.net/11449/233730
10.3390/jof7100852
2-s2.0-85117683376
url http://dx.doi.org/10.3390/jof7100852
http://hdl.handle.net/11449/233730
identifier_str_mv Journal of Fungi, v. 7, n. 10, 2021.
2309-608X
10.3390/jof7100852
2-s2.0-85117683376
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Fungi
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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