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Acute SARS-CoV-2 infection is associated with an increased abundance of bacterial pathogens, including Pseudomonas aeruginosa in the nose
Research conducted on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pathogenesis and coronavirus disease 2019 (COVID-19) generally focuses on the systemic host response, especially that generated by severely ill patients, with few studies investigating the impact of acute SARS-CoV-2 a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s).
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361213/ https://www.ncbi.nlm.nih.gov/pubmed/34433082 http://dx.doi.org/10.1016/j.celrep.2021.109637 |
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author | Rhoades, Nicholas S. Pinski, Amanda N. Monsibais, Alisha N. Jankeel, Allen Doratt, Brianna M. Cinco, Isaac R. Ibraim, Izabela Messaoudi, Ilhem |
author_facet | Rhoades, Nicholas S. Pinski, Amanda N. Monsibais, Alisha N. Jankeel, Allen Doratt, Brianna M. Cinco, Isaac R. Ibraim, Izabela Messaoudi, Ilhem |
author_sort | Rhoades, Nicholas S. |
collection | PubMed |
description | Research conducted on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pathogenesis and coronavirus disease 2019 (COVID-19) generally focuses on the systemic host response, especially that generated by severely ill patients, with few studies investigating the impact of acute SARS-CoV-2 at the site of infection. We show that the nasal microbiome of SARS-CoV-2-positive patients (CoV(+), n = 68) at the time of diagnosis is unique when compared to CoV(−) healthcare workers (n = 45) and CoV(−) outpatients (n = 21). This shift is marked by an increased abundance of bacterial pathogens, including Pseudomonas aeruginosa, which is also positively associated with viral RNA load. Additionally, we observe a robust host transcriptional response in the nasal epithelia of CoV(+) patients, indicative of an antiviral innate immune response and neuronal damage. These data suggest that the inflammatory response caused by SARS-CoV-2 infection is associated with an increased abundance of bacterial pathogens in the nasal cavity that could contribute to increased incidence of secondary bacterial infections. |
format | Online Article Text |
id | pubmed-8361213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Author(s). |
record_format | MEDLINE/PubMed |
spelling | pubmed-83612132021-08-13 Acute SARS-CoV-2 infection is associated with an increased abundance of bacterial pathogens, including Pseudomonas aeruginosa in the nose Rhoades, Nicholas S. Pinski, Amanda N. Monsibais, Alisha N. Jankeel, Allen Doratt, Brianna M. Cinco, Isaac R. Ibraim, Izabela Messaoudi, Ilhem Cell Rep Report Research conducted on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pathogenesis and coronavirus disease 2019 (COVID-19) generally focuses on the systemic host response, especially that generated by severely ill patients, with few studies investigating the impact of acute SARS-CoV-2 at the site of infection. We show that the nasal microbiome of SARS-CoV-2-positive patients (CoV(+), n = 68) at the time of diagnosis is unique when compared to CoV(−) healthcare workers (n = 45) and CoV(−) outpatients (n = 21). This shift is marked by an increased abundance of bacterial pathogens, including Pseudomonas aeruginosa, which is also positively associated with viral RNA load. Additionally, we observe a robust host transcriptional response in the nasal epithelia of CoV(+) patients, indicative of an antiviral innate immune response and neuronal damage. These data suggest that the inflammatory response caused by SARS-CoV-2 infection is associated with an increased abundance of bacterial pathogens in the nasal cavity that could contribute to increased incidence of secondary bacterial infections. The Author(s). 2021-08-31 2021-08-13 /pmc/articles/PMC8361213/ /pubmed/34433082 http://dx.doi.org/10.1016/j.celrep.2021.109637 Text en © 2021 The Author(s) 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 | Report Rhoades, Nicholas S. Pinski, Amanda N. Monsibais, Alisha N. Jankeel, Allen Doratt, Brianna M. Cinco, Isaac R. Ibraim, Izabela Messaoudi, Ilhem Acute SARS-CoV-2 infection is associated with an increased abundance of bacterial pathogens, including Pseudomonas aeruginosa in the nose |
title | Acute SARS-CoV-2 infection is associated with an increased abundance of bacterial pathogens, including Pseudomonas aeruginosa in the nose |
title_full | Acute SARS-CoV-2 infection is associated with an increased abundance of bacterial pathogens, including Pseudomonas aeruginosa in the nose |
title_fullStr | Acute SARS-CoV-2 infection is associated with an increased abundance of bacterial pathogens, including Pseudomonas aeruginosa in the nose |
title_full_unstemmed | Acute SARS-CoV-2 infection is associated with an increased abundance of bacterial pathogens, including Pseudomonas aeruginosa in the nose |
title_short | Acute SARS-CoV-2 infection is associated with an increased abundance of bacterial pathogens, including Pseudomonas aeruginosa in the nose |
title_sort | acute sars-cov-2 infection is associated with an increased abundance of bacterial pathogens, including pseudomonas aeruginosa in the nose |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361213/ https://www.ncbi.nlm.nih.gov/pubmed/34433082 http://dx.doi.org/10.1016/j.celrep.2021.109637 |
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