Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.

Detalhes bibliográficos
Autor(a) principal: Wassano, Natália Sayuri
Data de Publicação: 2020
Outros Autores: Leite, Ariely Barbosa [UNIFESP], Reichert-Lima, Franqueline, Schreiber, Angelica Zaninelli, Moretti, Nilmar S. [UNIFESP], Damasio, André
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://doi.org/10.1007/s42770-020-00253-w
https://hdl.handle.net/11600/62315
Resumo: In recent years, the intensification of the use of immunosuppressive therapies has increased the incidence of invasive infections caused by opportunistic fungi. Considering that, the spread of azole resistance and amphotericin B (AmB) inefficiency against some clinical and environmental isolates has been described. Thus, to avoid a global problem when controlling fungal infections and critical failures in medicine, and food security, new approaches for drug target identification and for the development of new treatments that are more effective against pathogenic fungi are desired. Recent studies indicate that protein acetylation is present in hundreds of proteins of different cellular compartments and is involved in several biological processes, i.e., metabolism, translation, gene expression regulation, and oxidative stress response, from prokaryotes and eukaryotes, including fungi, dem- onstrating that lysine acetylation plays an important role in essential mechanisms. Lysine acetyltransferases (KATs) and lysine deacetylases (KDACs), the two enzyme families responsible for regulating protein acetylation levels, have been explored as drug targets for the treatment of several human diseases and infections. Aspergilli have on average 8 KAT genes and 11 KDAC genes in their genomes. This review aims to summarize the available knowledge about Aspergillus spp. azole resistance mechanisms and the role of lysine acetylation in the control of biological processes in fungi. We also want to discuss the lysine acetylation as a potential target for fungal infection treatment and drug target discovery.
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spelling Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.Drug resistanceLysine acetylationKATsKDACsAspergillus spp.In recent years, the intensification of the use of immunosuppressive therapies has increased the incidence of invasive infections caused by opportunistic fungi. Considering that, the spread of azole resistance and amphotericin B (AmB) inefficiency against some clinical and environmental isolates has been described. Thus, to avoid a global problem when controlling fungal infections and critical failures in medicine, and food security, new approaches for drug target identification and for the development of new treatments that are more effective against pathogenic fungi are desired. Recent studies indicate that protein acetylation is present in hundreds of proteins of different cellular compartments and is involved in several biological processes, i.e., metabolism, translation, gene expression regulation, and oxidative stress response, from prokaryotes and eukaryotes, including fungi, dem- onstrating that lysine acetylation plays an important role in essential mechanisms. Lysine acetyltransferases (KATs) and lysine deacetylases (KDACs), the two enzyme families responsible for regulating protein acetylation levels, have been explored as drug targets for the treatment of several human diseases and infections. Aspergilli have on average 8 KAT genes and 11 KDAC genes in their genomes. This review aims to summarize the available knowledge about Aspergillus spp. azole resistance mechanisms and the role of lysine acetylation in the control of biological processes in fungi. We also want to discuss the lysine acetylation as a potential target for fungal infection treatment and drug target discovery.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)FAPESP: 2018/09948-0CNPq: 424729/2018SBMhttp://lattes.cnpq.br/2131472726202687Wassano, Natália SayuriLeite, Ariely Barbosa [UNIFESP]Reichert-Lima, FranquelineSchreiber, Angelica ZaninelliMoretti, Nilmar S. [UNIFESP]Damasio, André2021-11-26T21:42:52Z2021-11-26T21:42:52Z2020info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://doi.org/10.1007/s42770-020-00253-whttps://hdl.handle.net/11600/62315engBrazilian Journal of Microbiologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-26T11:19:26Zoai:repositorio.unifesp.br/:11600/62315Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-26T11:19:26Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.
title Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.
spellingShingle Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.
Wassano, Natália Sayuri
Drug resistance
Lysine acetylation
KATs
KDACs
Aspergillus spp.
title_short Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.
title_full Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.
title_fullStr Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.
title_full_unstemmed Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.
title_sort Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.
author Wassano, Natália Sayuri
author_facet Wassano, Natália Sayuri
Leite, Ariely Barbosa [UNIFESP]
Reichert-Lima, Franqueline
Schreiber, Angelica Zaninelli
Moretti, Nilmar S. [UNIFESP]
Damasio, André
author_role author
author2 Leite, Ariely Barbosa [UNIFESP]
Reichert-Lima, Franqueline
Schreiber, Angelica Zaninelli
Moretti, Nilmar S. [UNIFESP]
Damasio, André
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv http://lattes.cnpq.br/2131472726202687
dc.contributor.author.fl_str_mv Wassano, Natália Sayuri
Leite, Ariely Barbosa [UNIFESP]
Reichert-Lima, Franqueline
Schreiber, Angelica Zaninelli
Moretti, Nilmar S. [UNIFESP]
Damasio, André
dc.subject.por.fl_str_mv Drug resistance
Lysine acetylation
KATs
KDACs
Aspergillus spp.
topic Drug resistance
Lysine acetylation
KATs
KDACs
Aspergillus spp.
description In recent years, the intensification of the use of immunosuppressive therapies has increased the incidence of invasive infections caused by opportunistic fungi. Considering that, the spread of azole resistance and amphotericin B (AmB) inefficiency against some clinical and environmental isolates has been described. Thus, to avoid a global problem when controlling fungal infections and critical failures in medicine, and food security, new approaches for drug target identification and for the development of new treatments that are more effective against pathogenic fungi are desired. Recent studies indicate that protein acetylation is present in hundreds of proteins of different cellular compartments and is involved in several biological processes, i.e., metabolism, translation, gene expression regulation, and oxidative stress response, from prokaryotes and eukaryotes, including fungi, dem- onstrating that lysine acetylation plays an important role in essential mechanisms. Lysine acetyltransferases (KATs) and lysine deacetylases (KDACs), the two enzyme families responsible for regulating protein acetylation levels, have been explored as drug targets for the treatment of several human diseases and infections. Aspergilli have on average 8 KAT genes and 11 KDAC genes in their genomes. This review aims to summarize the available knowledge about Aspergillus spp. azole resistance mechanisms and the role of lysine acetylation in the control of biological processes in fungi. We also want to discuss the lysine acetylation as a potential target for fungal infection treatment and drug target discovery.
publishDate 2020
dc.date.none.fl_str_mv 2020
2021-11-26T21:42:52Z
2021-11-26T21:42:52Z
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 https://doi.org/10.1007/s42770-020-00253-w
https://hdl.handle.net/11600/62315
url https://doi.org/10.1007/s42770-020-00253-w
https://hdl.handle.net/11600/62315
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Brazilian Journal of Microbiology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv SBM
publisher.none.fl_str_mv SBM
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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