Changes in upper airways microbiota in ventilator-associated pneumonia.

16S-rRNA microbial profiling Cohort study Mechanical ventilation Upper airways microbiota VAP Ventilator-associated pneumonia

Journal

Intensive care medicine experimental
ISSN: 2197-425X
Titre abrégé: Intensive Care Med Exp
Pays: Germany
ID NLM: 101645149

Informations de publication

Date de publication:
02 Mar 2023
Historique:
received: 14 10 2022
accepted: 03 02 2023
entrez: 2 3 2023
pubmed: 3 3 2023
medline: 3 3 2023
Statut: epublish

Résumé

The role of upper airways microbiota and its association with ventilator-associated pneumonia (VAP) development in mechanically ventilated (MV) patients is unclear. Taking advantage of data collected in a prospective study aimed to assess the composition and over-time variation of upper airway microbiota in patients MV for non-pulmonary reasons, we describe upper airway microbiota characteristics among VAP and NO-VAP patients. Exploratory analysis of data collected in a prospective observational study on patients intubated for non-pulmonary conditions. Microbiota analysis (trough 16S-rRNA gene profiling) was performed on endotracheal aspirates (at intubation, T0, and after 72 h, T3) of patients with VAP (cases cohort) and a subgroup of NO-VAP patients (control cohort, matched according to total intubation time). Samples from 13 VAP patients and 22 NO-VAP matched controls were analyzed. At intubation (T0), patients with VAP revealed a significantly lower microbial complexity of the microbiota of the upper airways compared to NO-VAP controls (alpha diversity index of 84 ± 37 and 160 ± 102, in VAP and NO_VAP group, respectively, p-value < 0.012). Furthermore, an overall decrease in microbial diversity was observed in both groups at T3 as compared to T0. At T3, a loss of some genera (Prevotella 7, Fusobacterium, Neisseria, Escherichia-Shigella and Haemophilus) was found in VAP patients. In contrast, eight genera belonging to the Bacteroidetes, Firmicutes and Fusobacteria phyla was predominant in this group. However, it is unclear whether VAP caused dysbiosis or dysbiosis caused VAP. In a small sample size of intubated patients, microbial diversity at intubation was less in patients with VAP compared to patients without VAP.

Sections du résumé

BACKGROUND BACKGROUND
The role of upper airways microbiota and its association with ventilator-associated pneumonia (VAP) development in mechanically ventilated (MV) patients is unclear. Taking advantage of data collected in a prospective study aimed to assess the composition and over-time variation of upper airway microbiota in patients MV for non-pulmonary reasons, we describe upper airway microbiota characteristics among VAP and NO-VAP patients.
METHODS METHODS
Exploratory analysis of data collected in a prospective observational study on patients intubated for non-pulmonary conditions. Microbiota analysis (trough 16S-rRNA gene profiling) was performed on endotracheal aspirates (at intubation, T0, and after 72 h, T3) of patients with VAP (cases cohort) and a subgroup of NO-VAP patients (control cohort, matched according to total intubation time).
RESULTS RESULTS
Samples from 13 VAP patients and 22 NO-VAP matched controls were analyzed. At intubation (T0), patients with VAP revealed a significantly lower microbial complexity of the microbiota of the upper airways compared to NO-VAP controls (alpha diversity index of 84 ± 37 and 160 ± 102, in VAP and NO_VAP group, respectively, p-value < 0.012). Furthermore, an overall decrease in microbial diversity was observed in both groups at T3 as compared to T0. At T3, a loss of some genera (Prevotella 7, Fusobacterium, Neisseria, Escherichia-Shigella and Haemophilus) was found in VAP patients. In contrast, eight genera belonging to the Bacteroidetes, Firmicutes and Fusobacteria phyla was predominant in this group. However, it is unclear whether VAP caused dysbiosis or dysbiosis caused VAP.
CONCLUSIONS CONCLUSIONS
In a small sample size of intubated patients, microbial diversity at intubation was less in patients with VAP compared to patients without VAP.

Identifiants

pubmed: 36862343
doi: 10.1186/s40635-023-00496-5
pii: 10.1186/s40635-023-00496-5
pmc: PMC9981834
doi:

Types de publication

Journal Article

Langues

eng

Pagination

17

Subventions

Organisme : Italian Ministry of Health
ID : RF GR-2018-12365988
Organisme : SITA
ID : https://www.sitaonline.net/2017/11/vincitori-bando-lassegnazione-contributi-ricerca-2017

Informations de copyright

© 2023. The Author(s).

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Auteurs

Laura Alagna (L)

Infectious Diseases Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy. laura.alagna@policlinico.mi.it.

Leonardo Mancabelli (L)

Department of Medicine and Surgery, University of Parma, Parma, Italy.
Interdepartmental Research Centre Microbiome Research Hub, University of Parma, Parma, Italy.

Federico Magni (F)

Neurointensive Care Unit, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.

Liliane Chatenoud (L)

Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.

Gabriele Bassi (G)

Intensive Care, ASST GOM Niguarda, Milan, Italy.

Silvia Del Bianco (S)

Neurointensive Care Unit, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.

Roberto Fumagalli (R)

School of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy.

Francesca Turroni (F)

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Interdepartmental Research Centre Microbiome Research Hub, University of Parma, Parma, Italy.

Davide Mangioni (D)

Infectious Diseases Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.

Guglielmo M Migliorino (GM)

Infectious Diseases Unit, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.

Christian Milani (C)

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Interdepartmental Research Centre Microbiome Research Hub, University of Parma, Parma, Italy.

Antonio Muscatello (A)

Infectious Diseases Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Giovanni Nattino (G)

Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.

Edoardo Picetti (E)

Department of Anesthesia and Intensive Care, Parma University Hospital, Parma, Italy.

Riccardo Pinciroli (R)

School of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy.

Sandra Rossi (S)

Department of Anesthesia and Intensive Care, Parma University Hospital, Parma, Italy.

Tommaso Tonetti (T)

Department of Anesthesia and Intensive Care, Parma University Hospital, Parma, Italy.

Alessia Vargiolu (A)

Neurointensive Care Unit, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
School of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy.

Alessandra Bandera (A)

Infectious Diseases Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.

Marco Ventura (M)

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Interdepartmental Research Centre Microbiome Research Hub, University of Parma, Parma, Italy.

Giuseppe Citerio (G)

Neurointensive Care Unit, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
School of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy.

Andrea Gori (A)

Infectious Diseases Unit, Department of Internal Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.

Classifications MeSH