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...

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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/
Description
Summary: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.