Specific microbiome profile in Takayasu's arteritis and giant cell arteritis.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
15 03 2021
Historique:
received: 12 05 2020
accepted: 29 12 2020
entrez: 16 3 2021
pubmed: 17 3 2021
medline: 15 12 2021
Statut: epublish

Résumé

Recent studies have provided evidence of a close link between specific microbiota and inflammatory disorders. While the vessel wall microbiota has been recently described in large vessel vasculitis (LVV) and controls, the blood microbiome in these diseases has not been previously reported (LVV). We aimed to analyse the blood microbiome profile of LVV patients (Takayasu's arteritis [TAK], giant cell arteritis [GCA]) and healthy blood donors (HD). We studied the blood samples of 13 patients with TAK (20 samples), 9 patients with GCA (11 samples) and 15 HD patients. We assessed the blood microbiome profile by sequencing the 16S rDNA blood bacterial DNA. We used linear discriminant analysis (LDA) coupled with linear discriminant effect size measurement (LEfSe) to investigate the differences in the blood microbiome profile between TAK and GCA patients. An increase in the levels of Clostridia, Cytophagia and Deltaproteobacteria and a decrease in Bacilli at the class level were found in TAK patients compared with HD patients (LDA > 2, p < 0.05). Active TAK patients had significantly lower levels of Staphylococcus compared with inactive TAK patients. Samples of GCA patients had an increased abundance of Rhodococcus and an unidentified member of the Cytophagaceae family. Microbiota of TAK compared with GCA patients was found to show higher levels of Candidatus Aquiluna and Cloacibacterium (LDA > 2; p < 0.05). Differences highlighted in the blood microbiome were also associated with a shift of bacterial predicted metabolic functions in TAK in comparison with HD. Similar results were also found in patients with active versus inactive TAK. In conclusion, patients with TAK were found to present a specific blood microbiome profile in comparison with healthy donors and GCA subjects. Significant changes in the blood microbiome profiles of TAK patients were associated with specific metabolic functions.

Identifiants

pubmed: 33723291
doi: 10.1038/s41598-021-84725-5
pii: 10.1038/s41598-021-84725-5
pmc: PMC7961033
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5926

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Auteurs

Anne Claire Desbois (AC)

INSERM, UMR_S 959, Inflammation-Immunopathology-Biotherapy Department, Sorbonne Université, UPMC University of Paris, Paris, France. anneclaire.desbois@aphp.fr.
Department of Internal Medicine and Clinical Immunology, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France. anneclaire.desbois@aphp.fr.
Department of Internal Medicine and Laboratory I3 "Immunology, Immunopathology, Immunotherapy" UMR 7211 (CNRS/UPMC) INSERM U959, Hôpital Pitié-Salpêtrière, 47-83 boulevard de l'Hôpital, 75013, Paris, France. anneclaire.desbois@aphp.fr.

Dragos Ciocan (D)

INSERM U996, Inflammation Chemokines and Immunopathology, DHU Hépatinov, Faculté de Médecine-Univ Paris-Sud, Université Paris-Saclay, Clamart, France.
APHP-Hepatogastroenterology and Nutrition, Hôpital Antoine-Béclère, Clamart, France.

David Saadoun (D)

INSERM, UMR_S 959, Inflammation-Immunopathology-Biotherapy Department, Sorbonne Université, UPMC University of Paris, Paris, France.
Department of Internal Medicine and Clinical Immunology, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

Gabriel Perlemuter (G)

INSERM U996, Inflammation Chemokines and Immunopathology, DHU Hépatinov, Faculté de Médecine-Univ Paris-Sud, Université Paris-Saclay, Clamart, France.
APHP-Hepatogastroenterology and Nutrition, Hôpital Antoine-Béclère, Clamart, France.

Patrice Cacoub (P)

INSERM, UMR_S 959, Inflammation-Immunopathology-Biotherapy Department, Sorbonne Université, UPMC University of Paris, Paris, France.
Department of Internal Medicine and Clinical Immunology, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

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