Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant

Detalhes bibliográficos
Autor(a) principal: Araújo, Daniela
Data de Publicação: 2019
Outros Autores: Azevedo, N., Barbosa, Ana, Almeida, Carina, Rodrigues, M. Elisa, Henriques, Mariana, Silva, Sónia Carina
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/61935
Resumo: Antisense oligomers and their analogues have been successfully utilized to silence gene expression for the treatment of many human diseases; however the control of yeast´s virulence determinants has never been exploited before. In this sense, this work is based on the key hypothesis that if a pathogens genetic sequence is a determinant of virulence, it will be possible to synthesize a nucleic acid mimic based on antisense therapy (AST) that will bind to the mRNA produced, blocking its translation into protein and consequently reducing the pathogen virulent phenotype. EFG1 is an important determinant of virulence that is involved in regulation of Candida albicans switch from yeast to filamentous form. Thus, our main goal was to design and synthesize an antisense oligonucleotide (ASO) targeting the EFG1 mRNA and to validate its in vitro applicability. The results show that the anti-EFG1 2-OMethylRNA (2OMe) oligomer was able to significantly reduce the levels of EFG1 gene expression and of Efg1p protein translation (both approximately 60%), as well as effectively prevent filamentation of C. albicans cells (by 80%). Moreover, it was verified that anti-EFG1 2OMe keep the efficacy in different simulated human body fluids. Undeniably, this work provides potentially valuable information for future research into the management of Candida infections, regarding the development of a credible and alternative method to control C. albicans infections, based on antisense therapy methodology.
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spelling Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinantCandidiasisFilamentationNucleic Acid Mimics2-MethylRNA modification2′-OMethylRNA modificationScience & TechnologyAntisense oligomers and their analogues have been successfully utilized to silence gene expression for the treatment of many human diseases; however the control of yeast´s virulence determinants has never been exploited before. In this sense, this work is based on the key hypothesis that if a pathogens genetic sequence is a determinant of virulence, it will be possible to synthesize a nucleic acid mimic based on antisense therapy (AST) that will bind to the mRNA produced, blocking its translation into protein and consequently reducing the pathogen virulent phenotype. EFG1 is an important determinant of virulence that is involved in regulation of Candida albicans switch from yeast to filamentous form. Thus, our main goal was to design and synthesize an antisense oligonucleotide (ASO) targeting the EFG1 mRNA and to validate its in vitro applicability. The results show that the anti-EFG1 2-OMethylRNA (2OMe) oligomer was able to significantly reduce the levels of EFG1 gene expression and of Efg1p protein translation (both approximately 60%), as well as effectively prevent filamentation of C. albicans cells (by 80%). Moreover, it was verified that anti-EFG1 2OMe keep the efficacy in different simulated human body fluids. Undeniably, this work provides potentially valuable information for future research into the management of Candida infections, regarding the development of a credible and alternative method to control C. albicans infections, based on antisense therapy methodology.This study was supported by the Portuguese Foundation for Science and Technology (FCT), under the scope of the strategic funding of the UID/BIO/04469 unit and COMPETE 2020 (POCI-01-0145-FEDER-006684) and the BioTecNorte operation (NORTE-01-0145-FEDER-000004), funded by the European Regional Development Fund under the scope of a Norte 2020 – Programa Operacional Regional do Norte and Daniela Eira Araújo (SFRH/BD/121417/2016) PhD grant. The authors also acknowledge the project funding by the “02/SAICT/2017 – Projetos de Investigação Científica e Desenvolvimento Tecnológico (IC&DT; POCI-01-0145-FEDER-028893).” The mass spectrometry technique was performed at the Proteomics i3S Scientific Platform with the assistance of Hugo Osório. This work had support from the Portuguese Mass Spectrometry Network, integrated in the National Roadmap of Research Infrastructures of Strategic Relevance (ROTEIRO/0028/2013 and LISBOA-01-0145-FEDER-022125).info:eu-repo/semantics/publishedVersionNature Publishing GroupUniversidade do MinhoAraújo, DanielaAzevedo, N.Barbosa, AnaAlmeida, CarinaRodrigues, M. ElisaHenriques, MarianaSilva, Sónia Carina2019-12-062019-12-06T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/61935engAraújo, Daniela; Azevedo, N.; Barbosa, Ana; Almeida, Carina; Rodrigues, M. Elisa; Henriques, Mariana; Silva, Sónia Carina, Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant. Molecular Therapy-Nucleic Acids, 18, 508-517, 20192162-25312162-253110.1016/j.omtn.2019.09.016https://www.cell.com/molecular-therapy-family/homeinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:53:45Zoai:repositorium.sdum.uminho.pt:1822/61935Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:53:13.410291Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant
title Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant
spellingShingle Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant
Araújo, Daniela
Candidiasis
Filamentation
Nucleic Acid Mimics
2-MethylRNA modification
2′-OMethylRNA modification
Science & Technology
title_short Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant
title_full Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant
title_fullStr Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant
title_full_unstemmed Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant
title_sort Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant
author Araújo, Daniela
author_facet Araújo, Daniela
Azevedo, N.
Barbosa, Ana
Almeida, Carina
Rodrigues, M. Elisa
Henriques, Mariana
Silva, Sónia Carina
author_role author
author2 Azevedo, N.
Barbosa, Ana
Almeida, Carina
Rodrigues, M. Elisa
Henriques, Mariana
Silva, Sónia Carina
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Araújo, Daniela
Azevedo, N.
Barbosa, Ana
Almeida, Carina
Rodrigues, M. Elisa
Henriques, Mariana
Silva, Sónia Carina
dc.subject.por.fl_str_mv Candidiasis
Filamentation
Nucleic Acid Mimics
2-MethylRNA modification
2′-OMethylRNA modification
Science & Technology
topic Candidiasis
Filamentation
Nucleic Acid Mimics
2-MethylRNA modification
2′-OMethylRNA modification
Science & Technology
description Antisense oligomers and their analogues have been successfully utilized to silence gene expression for the treatment of many human diseases; however the control of yeast´s virulence determinants has never been exploited before. In this sense, this work is based on the key hypothesis that if a pathogens genetic sequence is a determinant of virulence, it will be possible to synthesize a nucleic acid mimic based on antisense therapy (AST) that will bind to the mRNA produced, blocking its translation into protein and consequently reducing the pathogen virulent phenotype. EFG1 is an important determinant of virulence that is involved in regulation of Candida albicans switch from yeast to filamentous form. Thus, our main goal was to design and synthesize an antisense oligonucleotide (ASO) targeting the EFG1 mRNA and to validate its in vitro applicability. The results show that the anti-EFG1 2-OMethylRNA (2OMe) oligomer was able to significantly reduce the levels of EFG1 gene expression and of Efg1p protein translation (both approximately 60%), as well as effectively prevent filamentation of C. albicans cells (by 80%). Moreover, it was verified that anti-EFG1 2OMe keep the efficacy in different simulated human body fluids. Undeniably, this work provides potentially valuable information for future research into the management of Candida infections, regarding the development of a credible and alternative method to control C. albicans infections, based on antisense therapy methodology.
publishDate 2019
dc.date.none.fl_str_mv 2019-12-06
2019-12-06T00:00:00Z
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://hdl.handle.net/1822/61935
url http://hdl.handle.net/1822/61935
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Araújo, Daniela; Azevedo, N.; Barbosa, Ana; Almeida, Carina; Rodrigues, M. Elisa; Henriques, Mariana; Silva, Sónia Carina, Application of 2OMethylRNA antisense oligomer to control Candida albicans EFG1 virulence determinant. Molecular Therapy-Nucleic Acids, 18, 508-517, 2019
2162-2531
2162-2531
10.1016/j.omtn.2019.09.016
https://www.cell.com/molecular-therapy-family/home
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 Nature Publishing Group
publisher.none.fl_str_mv Nature Publishing Group
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