Antifungal Efficacy during Candida krusei Infection in Non-Conventional Models Correlates with the Yeast In Vitro Susceptibility Profile
ABSTRACT: The incidence of opportunistic fungal infections has increased in recent decades due to the growing proportion of immunocompromised patients in our society. Candida krusei has been described as a causative agent of disseminated fungal infections in susceptible patients. Although its preval...
- Autores:
-
Mesa Arango, Ana Cecilia
de Lucas, María Pilar
Scorzoni, Liliana
Fusco Almeida, Ana Marisa
Lozano, Encarnación
Cuenca Estrella, Manuel
Mendes Giannini, María José
Zaragoza, Oscar
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2013
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/39059
- Acceso en línea:
- https://hdl.handle.net/10495/39059
- Palabra clave:
- Anfotericina B - uso terapéutico
Amphotericin B - therapeutic use
Antifúngicos - uso terapéutico
Antifungal Agents - therapeutic use
Caenorhabditis elegans
Candida
Candidiasis
Fluconazol
Fluconazole
Lepidópteros
Lepidoptera
Pirimidinas
Pyrimidines
Triazoles
Voriconazol
Voriconazole
https://id.nlm.nih.gov/mesh/D000666
https://id.nlm.nih.gov/mesh/D000935
https://id.nlm.nih.gov/mesh/D017173
https://id.nlm.nih.gov/mesh/D002175
https://id.nlm.nih.gov/mesh/D002177
https://id.nlm.nih.gov/mesh/D015725
https://id.nlm.nih.gov/mesh/D007915
https://id.nlm.nih.gov/mesh/D011743
https://id.nlm.nih.gov/mesh/D014230
https://id.nlm.nih.gov/mesh/D065819
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by/4.0/
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|
| dc.title.spa.fl_str_mv |
Antifungal Efficacy during Candida krusei Infection in Non-Conventional Models Correlates with the Yeast In Vitro Susceptibility Profile |
| title |
Antifungal Efficacy during Candida krusei Infection in Non-Conventional Models Correlates with the Yeast In Vitro Susceptibility Profile |
| spellingShingle |
Antifungal Efficacy during Candida krusei Infection in Non-Conventional Models Correlates with the Yeast In Vitro Susceptibility Profile Anfotericina B - uso terapéutico Amphotericin B - therapeutic use Antifúngicos - uso terapéutico Antifungal Agents - therapeutic use Caenorhabditis elegans Candida Candidiasis Fluconazol Fluconazole Lepidópteros Lepidoptera Pirimidinas Pyrimidines Triazoles Voriconazol Voriconazole https://id.nlm.nih.gov/mesh/D000666 https://id.nlm.nih.gov/mesh/D000935 https://id.nlm.nih.gov/mesh/D017173 https://id.nlm.nih.gov/mesh/D002175 https://id.nlm.nih.gov/mesh/D002177 https://id.nlm.nih.gov/mesh/D015725 https://id.nlm.nih.gov/mesh/D007915 https://id.nlm.nih.gov/mesh/D011743 https://id.nlm.nih.gov/mesh/D014230 https://id.nlm.nih.gov/mesh/D065819 |
| title_short |
Antifungal Efficacy during Candida krusei Infection in Non-Conventional Models Correlates with the Yeast In Vitro Susceptibility Profile |
| title_full |
Antifungal Efficacy during Candida krusei Infection in Non-Conventional Models Correlates with the Yeast In Vitro Susceptibility Profile |
| title_fullStr |
Antifungal Efficacy during Candida krusei Infection in Non-Conventional Models Correlates with the Yeast In Vitro Susceptibility Profile |
| title_full_unstemmed |
Antifungal Efficacy during Candida krusei Infection in Non-Conventional Models Correlates with the Yeast In Vitro Susceptibility Profile |
| title_sort |
Antifungal Efficacy during Candida krusei Infection in Non-Conventional Models Correlates with the Yeast In Vitro Susceptibility Profile |
| dc.creator.fl_str_mv |
Mesa Arango, Ana Cecilia de Lucas, María Pilar Scorzoni, Liliana Fusco Almeida, Ana Marisa Lozano, Encarnación Cuenca Estrella, Manuel Mendes Giannini, María José Zaragoza, Oscar |
| dc.contributor.author.none.fl_str_mv |
Mesa Arango, Ana Cecilia de Lucas, María Pilar Scorzoni, Liliana Fusco Almeida, Ana Marisa Lozano, Encarnación Cuenca Estrella, Manuel Mendes Giannini, María José Zaragoza, Oscar |
| dc.contributor.researchgroup.spa.fl_str_mv |
GRID - Grupo de Investigación Dermatológica |
| dc.subject.decs.none.fl_str_mv |
Anfotericina B - uso terapéutico Amphotericin B - therapeutic use Antifúngicos - uso terapéutico Antifungal Agents - therapeutic use Caenorhabditis elegans Candida Candidiasis Fluconazol Fluconazole Lepidópteros Lepidoptera Pirimidinas Pyrimidines Triazoles Voriconazol Voriconazole |
| topic |
Anfotericina B - uso terapéutico Amphotericin B - therapeutic use Antifúngicos - uso terapéutico Antifungal Agents - therapeutic use Caenorhabditis elegans Candida Candidiasis Fluconazol Fluconazole Lepidópteros Lepidoptera Pirimidinas Pyrimidines Triazoles Voriconazol Voriconazole https://id.nlm.nih.gov/mesh/D000666 https://id.nlm.nih.gov/mesh/D000935 https://id.nlm.nih.gov/mesh/D017173 https://id.nlm.nih.gov/mesh/D002175 https://id.nlm.nih.gov/mesh/D002177 https://id.nlm.nih.gov/mesh/D015725 https://id.nlm.nih.gov/mesh/D007915 https://id.nlm.nih.gov/mesh/D011743 https://id.nlm.nih.gov/mesh/D014230 https://id.nlm.nih.gov/mesh/D065819 |
| dc.subject.meshuri.none.fl_str_mv |
https://id.nlm.nih.gov/mesh/D000666 https://id.nlm.nih.gov/mesh/D000935 https://id.nlm.nih.gov/mesh/D017173 https://id.nlm.nih.gov/mesh/D002175 https://id.nlm.nih.gov/mesh/D002177 https://id.nlm.nih.gov/mesh/D015725 https://id.nlm.nih.gov/mesh/D007915 https://id.nlm.nih.gov/mesh/D011743 https://id.nlm.nih.gov/mesh/D014230 https://id.nlm.nih.gov/mesh/D065819 |
| description |
ABSTRACT: The incidence of opportunistic fungal infections has increased in recent decades due to the growing proportion of immunocompromised patients in our society. Candida krusei has been described as a causative agent of disseminated fungal infections in susceptible patients. Although its prevalence remains low among yeast infections (2–5%), its intrinsic resistance to fluconazole makes this yeast important from epidemiologic aspects. Non mammalian organisms are feasible models to study fungal virulence and drug efficacy. In this work we have used the lepidopteran Galleria mellonella and the nematode Caenorhabditis elegans as models to assess antifungal efficacy during infection by C. krusei. This yeast killed G. mellonella at 25, 30 and 37uC and reduced haemocytic density. Infected larvae melanized in a dose-dependent manner. Fluconazole did not protect against C. krusei infection, in contrast to amphotericin B, voriconazole or caspofungin. However, the doses of these antifungals required to obtain larvae protection were always higher during C. krusei infection than during C. albicans infection. Similar results were found in the model host C. elegans. Our work demonstrates that non mammalian models are useful tools to investigate in vivo antifungal efficacy and virulence of C. krusei. |
| publishDate |
2013 |
| dc.date.issued.none.fl_str_mv |
2013 |
| dc.date.accessioned.none.fl_str_mv |
2024-04-17T23:16:57Z |
| dc.date.available.none.fl_str_mv |
2024-04-17T23:16:57Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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Scorzoni L, de Lucas MP, Mesa-Arango AC, Fusco-Almeida AM, Lozano E, Cuenca-Estrella M, Mendes-Giannini MJ, Zaragoza O. Antifungal efficacy during Candida krusei infection in non-conventional models correlates with the yeast in vitro susceptibility profile. PLoS One. 2013;8(3):e60047. doi: 10.1371/journal.pone.0060047. Epub 2013 Mar 28. PMID: 23555877; PMCID: PMC3610750. |
| dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/10495/39059 |
| dc.identifier.doi.none.fl_str_mv |
10.1371/journal.pone.0060047 |
| dc.identifier.eissn.none.fl_str_mv |
1932-6203 |
| identifier_str_mv |
Scorzoni L, de Lucas MP, Mesa-Arango AC, Fusco-Almeida AM, Lozano E, Cuenca-Estrella M, Mendes-Giannini MJ, Zaragoza O. Antifungal efficacy during Candida krusei infection in non-conventional models correlates with the yeast in vitro susceptibility profile. PLoS One. 2013;8(3):e60047. doi: 10.1371/journal.pone.0060047. Epub 2013 Mar 28. PMID: 23555877; PMCID: PMC3610750. 10.1371/journal.pone.0060047 1932-6203 |
| url |
https://hdl.handle.net/10495/39059 |
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eng |
| language |
eng |
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PLoS ONE. |
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13 |
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1 |
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8 |
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PLoS ONE |
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13 páginas |
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Mesa Arango, Ana Ceciliade Lucas, María PilarScorzoni, LilianaFusco Almeida, Ana MarisaLozano, EncarnaciónCuenca Estrella, ManuelMendes Giannini, María JoséZaragoza, OscarGRID - Grupo de Investigación Dermatológica2024-04-17T23:16:57Z2024-04-17T23:16:57Z2013Scorzoni L, de Lucas MP, Mesa-Arango AC, Fusco-Almeida AM, Lozano E, Cuenca-Estrella M, Mendes-Giannini MJ, Zaragoza O. Antifungal efficacy during Candida krusei infection in non-conventional models correlates with the yeast in vitro susceptibility profile. PLoS One. 2013;8(3):e60047. doi: 10.1371/journal.pone.0060047. Epub 2013 Mar 28. PMID: 23555877; PMCID: PMC3610750.https://hdl.handle.net/10495/3905910.1371/journal.pone.00600471932-6203ABSTRACT: The incidence of opportunistic fungal infections has increased in recent decades due to the growing proportion of immunocompromised patients in our society. Candida krusei has been described as a causative agent of disseminated fungal infections in susceptible patients. Although its prevalence remains low among yeast infections (2–5%), its intrinsic resistance to fluconazole makes this yeast important from epidemiologic aspects. Non mammalian organisms are feasible models to study fungal virulence and drug efficacy. In this work we have used the lepidopteran Galleria mellonella and the nematode Caenorhabditis elegans as models to assess antifungal efficacy during infection by C. krusei. This yeast killed G. mellonella at 25, 30 and 37uC and reduced haemocytic density. Infected larvae melanized in a dose-dependent manner. Fluconazole did not protect against C. krusei infection, in contrast to amphotericin B, voriconazole or caspofungin. However, the doses of these antifungals required to obtain larvae protection were always higher during C. krusei infection than during C. albicans infection. Similar results were found in the model host C. elegans. Our work demonstrates that non mammalian models are useful tools to investigate in vivo antifungal efficacy and virulence of C. krusei.COL005083913 páginasapplication/pdfengPublic Library of ScienceSan Francisco, Estados Unidoshttps://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Antifungal Efficacy during Candida krusei Infection in Non-Conventional Models Correlates with the Yeast In Vitro Susceptibility ProfileArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAnfotericina B - uso terapéuticoAmphotericin B - therapeutic useAntifúngicos - uso terapéuticoAntifungal Agents - therapeutic useCaenorhabditis elegansCandidaCandidiasisFluconazolFluconazoleLepidópterosLepidopteraPirimidinasPyrimidinesTriazolesVoriconazolVoriconazolehttps://id.nlm.nih.gov/mesh/D000666https://id.nlm.nih.gov/mesh/D000935https://id.nlm.nih.gov/mesh/D017173https://id.nlm.nih.gov/mesh/D002175https://id.nlm.nih.gov/mesh/D002177https://id.nlm.nih.gov/mesh/D015725https://id.nlm.nih.gov/mesh/D007915https://id.nlm.nih.gov/mesh/D011743https://id.nlm.nih.gov/mesh/D014230https://id.nlm.nih.gov/mesh/D065819PLoS ONE.13318PLoS ONEPublicationORIGINALArangoCecilia_2013_AntifungalEfficacyInfectionCorrelatesInVitro.pdfArangoCecilia_2013_AntifungalEfficacyInfectionCorrelatesInVitro.pdfArtículo de investigaciónapplication/pdf5825619https://bibliotecadigital.udea.edu.co/bitstreams/8a00297e-59d2-4fe9-b36d-152d962f42f4/download68753bbc2e4368a300525e0f9ddcf6b1MD51trueAnonymousREADCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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