Please use this identifier to cite or link to this item: https://hdl.handle.net/11000/37779
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dc.contributor.authorRubio-Portillo, Esther-
dc.contributor.authorOrts, David-
dc.contributor.authorLlorca, Eleuterio-
dc.contributor.authorFernández Aracil, Cleofé-
dc.contributor.authorAnton, Josefa-
dc.contributor.authorFerrer, Consuelo-
dc.contributor.authorGálvez, Beatriz-
dc.contributor.authorEsteban Ronda, Violeta-
dc.contributor.authorRevelles, Elena-
dc.contributor.authorPérez-Martín, Carlos-
dc.contributor.authorGómez Imbernón, Enrique-
dc.contributor.authorAdsuar, Jorge-
dc.contributor.authorPiqueras, Pedro-
dc.contributor.authorAmat, Beatriz-
dc.contributor.authorFranco, José-
dc.contributor.authorColom Valiente, María Francisca-
dc.contributor.otherDepartamentos de la UMH::Producción Vegetal y Microbiologíaes_ES
dc.date.accessioned2025-11-03T11:36:02Z-
dc.date.available2025-11-03T11:36:02Z-
dc.date.created2020-
dc.identifier.citationMicroorganisms. 2020 Nov 2;8(11):1717es_ES
dc.identifier.issn2076-2607-
dc.identifier.urihttps://hdl.handle.net/11000/37779-
dc.description.abstractThis study analyzes the relationship between the mycobiome of the Lower Respiratory Tract (LRT) and the fungi in the domestic environment. Samples studied consisted of Broncho-Alveolar Lavage (BAL) from 45 patients who underwent bronchoscopy for di erent diagnostic purposes, and dust and air from the houses (ENV) of 20 of them (44.4%). Additionally, five bronchoscopes (BS) were also analyzed and negative controls were included for every procedure. All samples were processed for DNA extraction and cultures, which were performed in Sabouraud Dextrose and Potato Dextrose Agar. The fungal Internal Transcribed Spacer (ITS2) was sequenced by the Solexa/Illumina system and sequences were analyzed by QIIME 1.8.0 and compared with the UNITE Database for identification. The similarity between the two fungal communities (BAL and ENV) for a specific patient was assessed via the percentage of coincidence in the detection of specific operational taxonomic units (OTUs), and about 75% of co-occurrence was detected between the mycobiome of the LRT and the houses. Cultures confirmed the presence of the core mycobiome species. However, the low rate of isolation from BAL suggests that most of its mycobiome corresponds to non-culturable cells. This likely depends on the patient’s immune system activity and inflammatory status.es_ES
dc.formatapplication/pdfes_ES
dc.format.extent20es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectfungies_ES
dc.subjectmycobiomees_ES
dc.subjectlower respiratory tractes_ES
dc.subjecthouse dustes_ES
dc.subjectmycobiotaes_ES
dc.subjectbronco-alveolar lavagees_ES
dc.titleThe Domestic Environment and the Lung Mycobiomees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://doi.org/10.3390/microorganisms8111717es_ES
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Artículos - Producción vegetal y microbiología


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