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Nasopharyngeal Microbiota as an early severity biomarker in COVID-19 hospitalised patients

This study aimed to analyse the diversity and taxonomic composition of the nasopharyngeal microbiota, to determine its association with COVID-19 clinical outcome. To study the microbiota, we utilized 16S rRNA sequencing of 177 samples that came from a retrospective cohort of COVID-19 hospitalized pa...

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Autores principales: Ventero, Maria Paz, Moreno-Perez, Oscar, Molina-Pardines, Carmen, Paytuví-Gallart, Andreu, Boix, Vicente, Escribano, Isabel, Galan, Irene, González-delaAleja, Pilar, López-Pérez, Mario, Sánchez-Martínez, Rosario, Merino, Esperanza, Rodríguez, Juan Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Infection Association. Published by Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709923/
https://www.ncbi.nlm.nih.gov/pubmed/34963638
http://dx.doi.org/10.1016/j.jinf.2021.12.030
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author Ventero, Maria Paz
Moreno-Perez, Oscar
Molina-Pardines, Carmen
Paytuví-Gallart, Andreu
Boix, Vicente
Escribano, Isabel
Galan, Irene
González-delaAleja, Pilar
López-Pérez, Mario
Sánchez-Martínez, Rosario
Merino, Esperanza
Rodríguez, Juan Carlos
author_facet Ventero, Maria Paz
Moreno-Perez, Oscar
Molina-Pardines, Carmen
Paytuví-Gallart, Andreu
Boix, Vicente
Escribano, Isabel
Galan, Irene
González-delaAleja, Pilar
López-Pérez, Mario
Sánchez-Martínez, Rosario
Merino, Esperanza
Rodríguez, Juan Carlos
author_sort Ventero, Maria Paz
collection PubMed
description This study aimed to analyse the diversity and taxonomic composition of the nasopharyngeal microbiota, to determine its association with COVID-19 clinical outcome. To study the microbiota, we utilized 16S rRNA sequencing of 177 samples that came from a retrospective cohort of COVID-19 hospitalized patients. Raw sequences were processed by QIIME2. The associations between microbiota, invasive mechanical ventilation (IMV), and all-cause mortality were analysed by multiple logistic regression, adjusted for age, gender, and comorbidity. The microbiota α diversity indexes were lower in patients with a fatal outcome, whereas the β diversity analysis showed a significant clustering in these patients. After multivariate adjustment, the presence of Selenomonas spp., Filifactor spp., Actinobacillus spp., or Chroococcidiopsis spp., was associated with a reduction of more than 90% of IMV. Higher diversity and the presence of certain genera in the nasopharyngeal microbiota seem to be early biomarkers of a favourable clinical evolution in hospitalized COVID-19 patients.
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spelling pubmed-87099232021-12-28 Nasopharyngeal Microbiota as an early severity biomarker in COVID-19 hospitalised patients Ventero, Maria Paz Moreno-Perez, Oscar Molina-Pardines, Carmen Paytuví-Gallart, Andreu Boix, Vicente Escribano, Isabel Galan, Irene González-delaAleja, Pilar López-Pérez, Mario Sánchez-Martínez, Rosario Merino, Esperanza Rodríguez, Juan Carlos J Infect Article This study aimed to analyse the diversity and taxonomic composition of the nasopharyngeal microbiota, to determine its association with COVID-19 clinical outcome. To study the microbiota, we utilized 16S rRNA sequencing of 177 samples that came from a retrospective cohort of COVID-19 hospitalized patients. Raw sequences were processed by QIIME2. The associations between microbiota, invasive mechanical ventilation (IMV), and all-cause mortality were analysed by multiple logistic regression, adjusted for age, gender, and comorbidity. The microbiota α diversity indexes were lower in patients with a fatal outcome, whereas the β diversity analysis showed a significant clustering in these patients. After multivariate adjustment, the presence of Selenomonas spp., Filifactor spp., Actinobacillus spp., or Chroococcidiopsis spp., was associated with a reduction of more than 90% of IMV. Higher diversity and the presence of certain genera in the nasopharyngeal microbiota seem to be early biomarkers of a favourable clinical evolution in hospitalized COVID-19 patients. The British Infection Association. Published by Elsevier Ltd. 2022-03 2021-12-25 /pmc/articles/PMC8709923/ /pubmed/34963638 http://dx.doi.org/10.1016/j.jinf.2021.12.030 Text en © 2022 The British Infection Association. Published by Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Ventero, Maria Paz
Moreno-Perez, Oscar
Molina-Pardines, Carmen
Paytuví-Gallart, Andreu
Boix, Vicente
Escribano, Isabel
Galan, Irene
González-delaAleja, Pilar
López-Pérez, Mario
Sánchez-Martínez, Rosario
Merino, Esperanza
Rodríguez, Juan Carlos
Nasopharyngeal Microbiota as an early severity biomarker in COVID-19 hospitalised patients
title Nasopharyngeal Microbiota as an early severity biomarker in COVID-19 hospitalised patients
title_full Nasopharyngeal Microbiota as an early severity biomarker in COVID-19 hospitalised patients
title_fullStr Nasopharyngeal Microbiota as an early severity biomarker in COVID-19 hospitalised patients
title_full_unstemmed Nasopharyngeal Microbiota as an early severity biomarker in COVID-19 hospitalised patients
title_short Nasopharyngeal Microbiota as an early severity biomarker in COVID-19 hospitalised patients
title_sort nasopharyngeal microbiota as an early severity biomarker in covid-19 hospitalised patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709923/
https://www.ncbi.nlm.nih.gov/pubmed/34963638
http://dx.doi.org/10.1016/j.jinf.2021.12.030
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