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The Domestic Environment and the Lung Mycobiome
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 t...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693370/ https://www.ncbi.nlm.nih.gov/pubmed/33147738 http://dx.doi.org/10.3390/microorganisms8111717 |
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author | Rubio-Portillo, Esther Orts, David Llorca, Eleuterio Fernández, Cleofé Antón, 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 |
author_facet | Rubio-Portillo, Esther Orts, David Llorca, Eleuterio Fernández, Cleofé Antón, 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 |
author_sort | Rubio-Portillo, Esther |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7693370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76933702020-11-28 The Domestic Environment and the Lung Mycobiome Rubio-Portillo, Esther Orts, David Llorca, Eleuterio Fernández, Cleofé Antón, 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 Microorganisms Article 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. MDPI 2020-11-02 /pmc/articles/PMC7693370/ /pubmed/33147738 http://dx.doi.org/10.3390/microorganisms8111717 Text en © 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/). |
spellingShingle | Article Rubio-Portillo, Esther Orts, David Llorca, Eleuterio Fernández, Cleofé Antón, 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 The Domestic Environment and the Lung Mycobiome |
title | The Domestic Environment and the Lung Mycobiome |
title_full | The Domestic Environment and the Lung Mycobiome |
title_fullStr | The Domestic Environment and the Lung Mycobiome |
title_full_unstemmed | The Domestic Environment and the Lung Mycobiome |
title_short | The Domestic Environment and the Lung Mycobiome |
title_sort | domestic environment and the lung mycobiome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693370/ https://www.ncbi.nlm.nih.gov/pubmed/33147738 http://dx.doi.org/10.3390/microorganisms8111717 |
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