The Domestic Environment and the Lung Mycobiome

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Título: The Domestic Environment and the Lung Mycobiome
Autor/es: Rubio-Portillo, Esther | Orts, David | Llorca, Eleuterio | Fernández, Cleofé | Anton, Josefa | Ferrer, Consuelo | Gálvez, Beatriz | Esteban, Violeta | Revelles, Elena | Pérez-Martín, Carlos | Gómez-Imbernón, Enrique | Adsuar, Jorge | Piqueras, Pedro | Amat, Beatriz | Franco, José | Colom, María Francisca
Grupo/s de investigación o GITE: Ecología Microbiana Molecular
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Fisiología, Genética y Microbiología
Palabras clave: Fungi | Mycobiome | Lower respiratory tract | House dust | Mycobiota | Bronco-alveolar lavage
Área/s de conocimiento: Microbiología
Fecha de publicación: 2-nov-2020
Editor: MDPI
Cita bibliográfica: Rubio-Portillo E, Orts D, Llorca E, Fernández C, Antón J, Ferrer C, Gálvez B, Esteban V, Revelles E, Pérez-Martín C, Gómez-Imbernón E, Adsuar J, Piqueras P, Amat B, Franco J, Colom MF. The Domestic Environment and the Lung Mycobiome. Microorganisms. 2020; 8(11):1717. https://doi.org/10.3390/microorganisms8111717
Resumen: This 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 different 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.
Patrocinador/es: This research was funded by the Spanish Association for Respiratory Diseases (SEPAR) through their grant program RESPIRA with number PII026/2016. E. Revelles (2015-16) and J. Adsuar (2018) received a grant from the Spanish Ministry of Education for their contribution in this work. E. Gómez-Imbernon received a grant from the University Miguel Hernandez for his contribution to this work (2017).
URI: http://hdl.handle.net/10045/110255
ISSN: 2076-2607
DOI: 10.3390/microorganisms8111717
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2020 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 (http://creativecommons.org/licenses/by/4.0/).
Revisión científica: si
Versión del editor: https://doi.org/10.3390/microorganisms8111717
Aparece en las colecciones:INV - EMM - Artículos de Revistas

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