Nasopharyngeal Microbiota as an early severity biomarker in COVID-19 hospitalised patients
Copyright © 2021. Published by Elsevier Ltd..
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.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2022 |
---|---|
Erschienen: |
2022 |
Enthalten in: |
Zur Gesamtaufnahme - volume:84 |
---|---|
Enthalten in: |
The Journal of infection - 84(2022), 3 vom: 15. März, Seite 329-336 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Ventero, Maria Paz [VerfasserIn] |
---|
Links: |
---|
Themen: |
Biomarker |
---|
Anmerkungen: |
Date Completed 09.03.2022 Date Revised 22.03.2022 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1016/j.jinf.2021.12.030 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM334994705 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM334994705 | ||
003 | DE-627 | ||
005 | 20231225224856.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2022 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.jinf.2021.12.030 |2 doi | |
028 | 5 | 2 | |a pubmed24n1116.xml |
035 | |a (DE-627)NLM334994705 | ||
035 | |a (NLM)34963638 | ||
035 | |a (PII)S0163-4453(21)00647-2 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Ventero, Maria Paz |e verfasserin |4 aut | |
245 | 1 | 0 | |a Nasopharyngeal Microbiota as an early severity biomarker in COVID-19 hospitalised patients |
264 | 1 | |c 2022 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 09.03.2022 | ||
500 | |a Date Revised 22.03.2022 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2021. Published by Elsevier Ltd. | ||
520 | |a 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 | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Biomarker | |
650 | 4 | |a COVID-19 | |
650 | 4 | |a Microbiota | |
650 | 4 | |a Prognosis | |
650 | 4 | |a SARS-COV-2 | |
650 | 4 | |a Severity | |
650 | 7 | |a Biomarkers |2 NLM | |
650 | 7 | |a RNA, Ribosomal, 16S |2 NLM | |
700 | 1 | |a Moreno-Perez, Oscar |e verfasserin |4 aut | |
700 | 1 | |a Molina-Pardines, Carmen |e verfasserin |4 aut | |
700 | 1 | |a Paytuví-Gallart, Andreu |e verfasserin |4 aut | |
700 | 1 | |a Boix, Vicente |e verfasserin |4 aut | |
700 | 1 | |a Escribano, Isabel |e verfasserin |4 aut | |
700 | 1 | |a Galan, Irene |e verfasserin |4 aut | |
700 | 1 | |a González-delaAleja, Pilar |e verfasserin |4 aut | |
700 | 1 | |a López-Pérez, Mario |e verfasserin |4 aut | |
700 | 1 | |a Sánchez-Martínez, Rosario |e verfasserin |4 aut | |
700 | 1 | |a Merino, Esperanza |e verfasserin |4 aut | |
700 | 1 | |a Rodríguez, Juan Carlos |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t The Journal of infection |d 1982 |g 84(2022), 3 vom: 15. März, Seite 329-336 |w (DE-627)NLM012791822 |x 1532-2742 |7 nnns |
773 | 1 | 8 | |g volume:84 |g year:2022 |g number:3 |g day:15 |g month:03 |g pages:329-336 |
856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.jinf.2021.12.030 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 84 |j 2022 |e 3 |b 15 |c 03 |h 329-336 |