Aggregatibacter is inversely associated with inflammatory mediators in sputa of patients with chronic airway diseases and reduces inflammation in vitro.


Journal

Respiratory research
ISSN: 1465-993X
Titre abrégé: Respir Res
Pays: England
ID NLM: 101090633

Informations de publication

Date de publication:
12 Oct 2024
Historique:
received: 24 01 2024
accepted: 18 09 2024
medline: 13 10 2024
pubmed: 13 10 2024
entrez: 12 10 2024
Statut: epublish

Résumé

Chronic airway disease (CAD) is characterized by chronic airway inflammation and colonization of the lungs by pro-inflammatory pathogens. However, while various other bacterial species are present in the lower airways, it is not fully understood how they influence inflammation. We aimed to identify novel anti-inflammatory species present in lower airway samples of patients with CAD. Paired sputum microbiome and inflammatory marker data of adults with CAD across three separate cohorts (Australian asthma and bronchiectasis, Scottish bronchiectasis) was analyzed using Linear discriminant analysis Effect Size (LEfSE) and Spearman correlation analysis to identify species associated with a low inflammatory profile in patients. We identified the genus Aggregatibacter as more abundant in patients with lower levels of airway inflammatory markers in two CAD cohorts (Australian asthma and bronchiectasis). In addition, the relative abundance of Aggregatibacter was inversely correlated with sputum IL-8 (Australian bronchiectasis) and IL-1β levels (Australian asthma and bronchiectasis). Subsequent in vitro testing, using a physiologically relevant three-dimensional lung epithelial cell model, revealed that Aggregatibacter spp. (i.e. A. actinomycetemcomitans, A. aphrophilus) and their cell-free supernatant exerted anti-inflammatory activity without influencing host cell viability. These findings suggest that Aggregatibacter spp. might act to reduce airway inflammation in CAD patients.

Sections du résumé

BACKGROUND BACKGROUND
Chronic airway disease (CAD) is characterized by chronic airway inflammation and colonization of the lungs by pro-inflammatory pathogens. However, while various other bacterial species are present in the lower airways, it is not fully understood how they influence inflammation. We aimed to identify novel anti-inflammatory species present in lower airway samples of patients with CAD.
METHODS METHODS
Paired sputum microbiome and inflammatory marker data of adults with CAD across three separate cohorts (Australian asthma and bronchiectasis, Scottish bronchiectasis) was analyzed using Linear discriminant analysis Effect Size (LEfSE) and Spearman correlation analysis to identify species associated with a low inflammatory profile in patients.
RESULTS RESULTS
We identified the genus Aggregatibacter as more abundant in patients with lower levels of airway inflammatory markers in two CAD cohorts (Australian asthma and bronchiectasis). In addition, the relative abundance of Aggregatibacter was inversely correlated with sputum IL-8 (Australian bronchiectasis) and IL-1β levels (Australian asthma and bronchiectasis). Subsequent in vitro testing, using a physiologically relevant three-dimensional lung epithelial cell model, revealed that Aggregatibacter spp. (i.e. A. actinomycetemcomitans, A. aphrophilus) and their cell-free supernatant exerted anti-inflammatory activity without influencing host cell viability.
CONCLUSIONS CONCLUSIONS
These findings suggest that Aggregatibacter spp. might act to reduce airway inflammation in CAD patients.

Identifiants

pubmed: 39395980
doi: 10.1186/s12931-024-02983-z
pii: 10.1186/s12931-024-02983-z
doi:

Substances chimiques

Inflammation Mediators 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

368

Subventions

Organisme : Research Foundation Flanders
ID : 1S34622N
Organisme : National Health and Medical Research Council
ID : APP2008625
Organisme : Fonds Wetenschappelijk Onderzoek
ID : G024423N
Organisme : Fonds Wetenschappelijk Onderzoek
ID : 1SC3722N
Organisme : Ghent University Industrial Research Fund
ID : F2020/IOF-StarTT/103

Informations de copyright

© 2024. The Author(s).

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Auteurs

Ellen Goeteyn (E)

Laboratory of Pharmaceutical Microbiology, Ghent University, Ghent, Belgium.

Steven L Taylor (SL)

Microbiome and Host Health Programme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, Australia.
College of Medicine and Public Health, Flinders University, Adelaide, Australia.

Alison Dicker (A)

Scottish Centre for Respiratory Research, University of Dundee, Dundee, UK.

Laura Bollé (L)

Laboratory of Pharmaceutical Microbiology, Ghent University, Ghent, Belgium.
Respiratory Infection and Defense Lab (RIDL), Department of Internal Medicine and Paediatrics, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
Department of Respiratory Medicine, Ghent University Hospital, Ghent, Belgium.

Merel Wauters (M)

Laboratory of Pharmaceutical Microbiology, Ghent University, Ghent, Belgium.
VIB Center for Medical Biotechnology, VIB, Ghent, Belgium.

Marie Joossens (M)

Laboratory of Microbiology, Ghent University, Ghent, Belgium.

Eva Van Braeckel (E)

Respiratory Infection and Defense Lab (RIDL), Department of Internal Medicine and Paediatrics, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
Department of Respiratory Medicine, Ghent University Hospital, Ghent, Belgium.

Jodie L Simpson (JL)

Faculty of Health and Medicine, Priority Research Centre for Healthy Lungs, University of Newcastle, Newcastle, NSW, Australia.

Lucy Burr (L)

Department of Respiratory Medicine, Mater Health Sciences, South Brisbane, QLD, Australia.
Mater Research - University of Queensland, Aubigny Place, South Brisbane, QLD, Australia.

James D Chalmers (JD)

Scottish Centre for Respiratory Research, University of Dundee, Dundee, UK.

Geraint B Rogers (GB)

Microbiome and Host Health Programme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, Australia.
College of Medicine and Public Health, Flinders University, Adelaide, Australia.

Aurélie Crabbé (A)

Laboratory of Pharmaceutical Microbiology, Ghent University, Ghent, Belgium. aurelie.crabbe@ugent.be.

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