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dc.contributor.authorHernando Ortiz, Ainara ORCID
dc.contributor.authorEraso Barrio, María Elena ORCID
dc.contributor.authorQuindós Andrés, Guillermo
dc.contributor.authorMateo Alesanco, Estibaliz ORCID
dc.date.accessioned2021-12-29T07:52:59Z
dc.date.available2021-12-29T07:52:59Z
dc.date.issued2021-11-23
dc.identifier.citationJournal of Fungi 7(12) : (2021) // Article ID 998es_ES
dc.identifier.issn2309-608X
dc.identifier.urihttp://hdl.handle.net/10810/54772
dc.description.abstractCandida albicans is the major etiological agent of invasive candidiasis but the increasing prevalence of emerging species of Candida, such as Candida glabrata and phylogenetically closely related species, Candida nivariensis and Candida bracarensis, requires special attention. Differences in virulence among these species and their therapeutic responses using in vivo non-mammalian models are scarcely analysed. The aim of this study was analyse the survival of G. mellonella and host-pathogen interactions during infection by C. glabrata, C. nivariensis and C. bracarensis. Moreover, therapeutic responses to echinocandins were also assessed in the G. mellonella model of candidiasis. These three species produced lethal infection in G. mellonella; C. glabrata was the most virulent species and C. bracarensis the less. Haemocytes of G. mellonella phagocytised C. bracarensis cells more effectively than those of the other two species. Treatment with caspofungin and micafungin was most effective to protect larvae during C. glabrata and C. nivariensis infections while anidulafungin was during C. bracarensis infection. The model of candidiasis in G. mellonella is simple and appropriate to assess the virulence and therapeutic response of these emerging Candida species. Moreover, it successfully allows for detecting differences in the immune system of the host depending on the virulence of pathogens.es_ES
dc.description.sponsorshipThis research was supported by grants from the Spanish Ministry of Economy and Competitiveness (MINECO) [SAF2017-86188-P and PID2020-117983RB-I00] and from the Consejería de Educación, Universidades e Investigación of Gobierno Vasco-Eusko Jaurlaritza [GIC15/78 IT-990-16]. Ainara Hernando-Ortiz was funded by Ph.D. grants from the University of the Basque Country (PIF 16/39).es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/SAF2017-86188-Pes_ES
dc.relationinfo:eu-repo/grantAgreement/MCI/PID2020-117983RB-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectemerging pathogenes_ES
dc.subjectpathogenesises_ES
dc.subjectantifungal susceptibilityes_ES
dc.subjectinvertebrate modelses_ES
dc.titleCandidiasis by Candida glabrata, Candida nivariensis and Candida bracarensis in Galleria mellonella: Virulence and Therapeutic Responses to Echinocandinses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2021-12-23T15:06:45Z
dc.rights.holder© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/2309-608X/7/12/998es_ES
dc.identifier.doi10.3390/jof7120998
dc.departamentoesInmunología, microbiología y parasitología
dc.departamentoeuImmunologia, mikrobiologia eta parasitologia


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© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).