Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate

Detalhes bibliográficos
Autor(a) principal: Mota, Sandra
Data de Publicação: 2015
Outros Autores: Alves, Rosana, Carneiro, Catarina, Silva, Sónia, Brown, Alistair J., Istel, Fabian, Kuchler, Karl, Sampaio, Paula, Casal, Margarida, Henriques, Mariana, Paiva, Sandra
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.22/7443
Resumo: Candida glabrata is considered a major opportunistic fungal pathogen of humans. The capacity of this yeast species to cause infections is dependent on the ability to grow within the human host environment and to assimilate the carbon sources available. Previous studies have suggested that C. albicans can encounter glucose-poor microenvironments during infection and that the ability to use alternative non-fermentable carbon sources, such as carboxylic acids, contributes to the virulence of this fungus. Transcriptional studies on C. glabrata cells identified a similar response, upon nutrient deprivation. In this work, we aimed at analyzing biofilm formation, antifungal drug resistance, and phagocytosis of C. glabrata cells grown in the presence of acetic acid as an alternative carbon source. C. glabrata planktonic cells grown in media containing acetic acid were more susceptible to fluconazole and were better phagocytosed and killed by macrophages than when compared to media lacking acetic acid. Growth in acetic acid also affected the ability of C. glabrata to form biofilms. The genes ADY2a, ADY2b, FPS1, FPS2, and ATO3, encoding putative carboxylate transporters, were upregulated in C. glabrata planktonic and biofilm cells in the presence of acetic acid. Phagocytosis assays with fps1 and ady2a mutant strains suggested a potential role of FPS1 and ADY2a in the phagocytosis process. These results highlight how acidic pH niches, associated with the presence of acetic acid, can impact in the treatment of C. glabrata infections, in particular in vaginal candidiasis.
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spelling Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetateCandida glabrataAcetateTransportersPhagocytosisAntifungal drug resistanceFluconazoleCandidiasisCandida glabrata is considered a major opportunistic fungal pathogen of humans. The capacity of this yeast species to cause infections is dependent on the ability to grow within the human host environment and to assimilate the carbon sources available. Previous studies have suggested that C. albicans can encounter glucose-poor microenvironments during infection and that the ability to use alternative non-fermentable carbon sources, such as carboxylic acids, contributes to the virulence of this fungus. Transcriptional studies on C. glabrata cells identified a similar response, upon nutrient deprivation. In this work, we aimed at analyzing biofilm formation, antifungal drug resistance, and phagocytosis of C. glabrata cells grown in the presence of acetic acid as an alternative carbon source. C. glabrata planktonic cells grown in media containing acetic acid were more susceptible to fluconazole and were better phagocytosed and killed by macrophages than when compared to media lacking acetic acid. Growth in acetic acid also affected the ability of C. glabrata to form biofilms. The genes ADY2a, ADY2b, FPS1, FPS2, and ATO3, encoding putative carboxylate transporters, were upregulated in C. glabrata planktonic and biofilm cells in the presence of acetic acid. Phagocytosis assays with fps1 and ady2a mutant strains suggested a potential role of FPS1 and ADY2a in the phagocytosis process. These results highlight how acidic pH niches, associated with the presence of acetic acid, can impact in the treatment of C. glabrata infections, in particular in vaginal candidiasis.FrontiersRepositório Científico do Instituto Politécnico do PortoMota, SandraAlves, RosanaCarneiro, CatarinaSilva, SóniaBrown, Alistair J.Istel, FabianKuchler, KarlSampaio, PaulaCasal, MargaridaHenriques, MarianaPaiva, Sandra2016-01-21T12:57:47Z20152015-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.22/7443engMota, S., Alves, R., Carneiro, C., Silva, S., Brown, A. J., Istel, F., Kuchler, K., Sampaio, P., Casal, M., Henriques, M., & Paiva, S. (2015). Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate. Frontiers in Microbiology, 6(article 919), 1–12. https://doi.org/10.3389/fmicb.2015.009191664-302X10.3389/fmicb.2015.00919info: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:RCAAP2023-12-13T01:49:09Zoai:recipp.ipp.pt:10400.22/7443Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:27:55.480831Repositório 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 Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate
title Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate
spellingShingle Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate
Mota, Sandra
Candida glabrata
Acetate
Transporters
Phagocytosis
Antifungal drug resistance
Fluconazole
Candidiasis
title_short Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate
title_full Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate
title_fullStr Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate
title_full_unstemmed Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate
title_sort Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate
author Mota, Sandra
author_facet Mota, Sandra
Alves, Rosana
Carneiro, Catarina
Silva, Sónia
Brown, Alistair J.
Istel, Fabian
Kuchler, Karl
Sampaio, Paula
Casal, Margarida
Henriques, Mariana
Paiva, Sandra
author_role author
author2 Alves, Rosana
Carneiro, Catarina
Silva, Sónia
Brown, Alistair J.
Istel, Fabian
Kuchler, Karl
Sampaio, Paula
Casal, Margarida
Henriques, Mariana
Paiva, Sandra
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Politécnico do Porto
dc.contributor.author.fl_str_mv Mota, Sandra
Alves, Rosana
Carneiro, Catarina
Silva, Sónia
Brown, Alistair J.
Istel, Fabian
Kuchler, Karl
Sampaio, Paula
Casal, Margarida
Henriques, Mariana
Paiva, Sandra
dc.subject.por.fl_str_mv Candida glabrata
Acetate
Transporters
Phagocytosis
Antifungal drug resistance
Fluconazole
Candidiasis
topic Candida glabrata
Acetate
Transporters
Phagocytosis
Antifungal drug resistance
Fluconazole
Candidiasis
description Candida glabrata is considered a major opportunistic fungal pathogen of humans. The capacity of this yeast species to cause infections is dependent on the ability to grow within the human host environment and to assimilate the carbon sources available. Previous studies have suggested that C. albicans can encounter glucose-poor microenvironments during infection and that the ability to use alternative non-fermentable carbon sources, such as carboxylic acids, contributes to the virulence of this fungus. Transcriptional studies on C. glabrata cells identified a similar response, upon nutrient deprivation. In this work, we aimed at analyzing biofilm formation, antifungal drug resistance, and phagocytosis of C. glabrata cells grown in the presence of acetic acid as an alternative carbon source. C. glabrata planktonic cells grown in media containing acetic acid were more susceptible to fluconazole and were better phagocytosed and killed by macrophages than when compared to media lacking acetic acid. Growth in acetic acid also affected the ability of C. glabrata to form biofilms. The genes ADY2a, ADY2b, FPS1, FPS2, and ATO3, encoding putative carboxylate transporters, were upregulated in C. glabrata planktonic and biofilm cells in the presence of acetic acid. Phagocytosis assays with fps1 and ady2a mutant strains suggested a potential role of FPS1 and ADY2a in the phagocytosis process. These results highlight how acidic pH niches, associated with the presence of acetic acid, can impact in the treatment of C. glabrata infections, in particular in vaginal candidiasis.
publishDate 2015
dc.date.none.fl_str_mv 2015
2015-01-01T00:00:00Z
2016-01-21T12:57:47Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.22/7443
url http://hdl.handle.net/10400.22/7443
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Mota, S., Alves, R., Carneiro, C., Silva, S., Brown, A. J., Istel, F., Kuchler, K., Sampaio, P., Casal, M., Henriques, M., & Paiva, S. (2015). Candida glabrata susceptibility to antifungals and phagocytosis is modulated by acetate. Frontiers in Microbiology, 6(article 919), 1–12. https://doi.org/10.3389/fmicb.2015.00919
1664-302X
10.3389/fmicb.2015.00919
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Frontiers
publisher.none.fl_str_mv Frontiers
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