Critically ill patients with COVID-19 show lung fungal dysbiosis with reduced microbial diversity in patients colonized with Candida spp.


Journal

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
ISSN: 1878-3511
Titre abrégé: Int J Infect Dis
Pays: Canada
ID NLM: 9610933

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 06 11 2021
revised: 03 02 2022
accepted: 06 02 2022
pubmed: 13 2 2022
medline: 31 3 2022
entrez: 12 2 2022
Statut: ppublish

Résumé

The COVID-19 pandemic has intensified interest in how the infection affects the lung microbiome of critically ill patients and how it contributes to acute respiratory distress syndrome (ARDS). We aimed to characterize the lower respiratory tract mycobiome of critically ill patients with COVID-19 in comparison to patients without COVID-19. We performed an internal transcribed spacer 2 (ITS2) profiling with the Illumina MiSeq platform on 26 respiratory specimens from patients with COVID-19 as well as from 26 patients with non-COVID-19 pneumonia. Patients with COVID-19 were more likely to be colonized with Candida spp. ARDS was associated with lung dysbiosis characterized by a shift to Candida species colonization and a decrease of fungal diversity. We also observed higher bacterial phylogenetic distance among taxa in colonized patients with COVID-19. In patients with COVID-19 not colonized with Candida spp., ITS2 amplicon sequencing revealed an increase of Ascomycota unassigned spp. and 1 Aspergillus spp.-positive specimen. In addition, we found that corticosteroid therapy was frequently associated with positive Galactomannan cell wall component of Aspergillus spp. among patients with COVID-19. Our study underpins that ARDS in patients with COVID-19 is associated with lung dysbiosis and that an increased density of Ascomycota unassigned spp. is present in patients not colonized with Candida spp.

Sections du résumé

BACKGROUND BACKGROUND
The COVID-19 pandemic has intensified interest in how the infection affects the lung microbiome of critically ill patients and how it contributes to acute respiratory distress syndrome (ARDS). We aimed to characterize the lower respiratory tract mycobiome of critically ill patients with COVID-19 in comparison to patients without COVID-19.
METHODS METHODS
We performed an internal transcribed spacer 2 (ITS2) profiling with the Illumina MiSeq platform on 26 respiratory specimens from patients with COVID-19 as well as from 26 patients with non-COVID-19 pneumonia.
RESULTS RESULTS
Patients with COVID-19 were more likely to be colonized with Candida spp. ARDS was associated with lung dysbiosis characterized by a shift to Candida species colonization and a decrease of fungal diversity. We also observed higher bacterial phylogenetic distance among taxa in colonized patients with COVID-19. In patients with COVID-19 not colonized with Candida spp., ITS2 amplicon sequencing revealed an increase of Ascomycota unassigned spp. and 1 Aspergillus spp.-positive specimen. In addition, we found that corticosteroid therapy was frequently associated with positive Galactomannan cell wall component of Aspergillus spp. among patients with COVID-19.
CONCLUSION CONCLUSIONS
Our study underpins that ARDS in patients with COVID-19 is associated with lung dysbiosis and that an increased density of Ascomycota unassigned spp. is present in patients not colonized with Candida spp.

Identifiants

pubmed: 35150910
pii: S1201-9712(22)00088-1
doi: 10.1016/j.ijid.2022.02.011
pmc: PMC8828296
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

233-240

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Elisa Viciani (E)

Wellmicro s.r.l, Via Piero Gobetti, 101, 40129 Bologna, Italy. Electronic address: elisa.viciani@wellmicro.com.

Paolo Gaibani (P)

Microbiology Unit, IRCCS S. Orsola-Malpighi Hospital, 40138 Bologna, Italy.

Andrea Castagnetti (A)

Wellmicro s.r.l, Via Piero Gobetti, 101, 40129 Bologna, Italy.

Andrea Liberatore (A)

Wellmicro s.r.l, Via Piero Gobetti, 101, 40129 Bologna, Italy.

Michele Bartoletti (M)

Department of Medical and Surgical Sciences, University of Bologna, Infectious Diseases Unit, IRCCS S. Orsola-Malpighi Hospital, 40138 Bologna, Italy.

Pierluigi Viale (P)

Department of Medical and Surgical Sciences, University of Bologna, Infectious Diseases Unit, IRCCS S. Orsola-Malpighi Hospital, 40138 Bologna, Italy.

Tiziana Lazzarotto (T)

Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Microbiology Unit, IRCCS S. Orsola-Malpighi Hospital, 40138 Bologna, Italy.

Simone Ambretti (S)

Wellmicro s.r.l, Via Piero Gobetti, 101, 40129 Bologna, Italy.

Russell Lewis (R)

Department of Medical and Surgical Sciences, University of Bologna, Infectious Diseases Unit, IRCCS S. Orsola-Malpighi Hospital, 40138 Bologna, Italy; Center for Applied Biomedical Research (CRBA), University of Bologna, 40138, Bologna, Italy.

Monica Cricca (M)

Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Microbiology Unit, IRCCS S. Orsola-Malpighi Hospital, 40138 Bologna, Italy; Center for Applied Biomedical Research (CRBA), University of Bologna, 40138, Bologna, Italy. Electronic address: monica.cricca3@unibo.it.

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