Are there new biomarkers of the gastroduodenal microbiota useful in the diagnosis of coeliac disease in children? A pilot study.


Journal

Beneficial microbes
ISSN: 1876-2891
Titre abrégé: Benef Microbes
Pays: Netherlands
ID NLM: 101507616

Informations de publication

Date de publication:
23 Apr 2024
Historique:
received: 18 10 2023
accepted: 27 03 2024
medline: 24 4 2024
pubmed: 24 4 2024
entrez: 23 4 2024
Statut: aheadofprint

Résumé

The changing of microbiome could precede the development of coeliac disease (CeD). We compared the bacterial profile of microbiota of tissues collected simultaneously from the stomach and duodenum in newly diagnosed patients with CeD. Biopsies were collected from 60 children and adolescents aged 2-18 years: (1) 40 patients with CeD; (2) 20 children as control group. The evaluation of the bacterial microbiota was carried out by sequencing the V3-V4 regions of the 16S rRNA subunit, using next-generation sequencing (NGS). The composition of bacterial microbiota was correlated with clinical and blood parameters. The beta diversity analysis revealed a significant dissimilarity in the gastric samples between the CeD and control group (Bray-Curtis index, P = 0.008, and weighted UniFrac distance, P = 0.024). At L2 (phylum level), Campylobacterota was only present in the stomach of the CeD group. A comparison of the abundance of bacteria between the stomach and duodenum showed significant differences in 10 OTUs (operational taxonomic units) in the control and 9 OTUs in the CeD group at L6 (genus) and in 8 OTUs and in 6 OTUs, respectively, at L7 (species). A significant correlation was observed between the genus Novosphingobium in stomach of CeD group and possession of the DQ2.5 and DQ 8 allele, and in the duodenum - between the DQ 8 allele and the species Blautia wexlerae. Significant differences in selected, little-known genera of bacteria suggest their potential role as new biomarkers in the development of CeD. To fully understand the mechanism of CeD development in genetically predisposed individuals, it is necessary to take into account not only the abundance of a given genus or species of bacteria, but also the anatomical location of its occurrence.

Identifiants

pubmed: 38653476
doi: 10.1163/18762891-bja00009
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-13

Auteurs

D Salamon (D)

Department of Molecular Medical Microbiology, Division of Microbiology, Faculty of Medicine, 49573Jagiellonian University Medical College, ul. Czysta 18, 31-121 Krakow, Poland.

K Kowalska-Duplaga (K)

Department of Pediatrics, Gastroenterology and Nutrition, Faculty of Medicine, 49573Jagiellonian University Medical College, ul. Wielicka 265, 30-663 Krakow, Poland.

A Krawczyk (A)

Department of Molecular Medical Microbiology, Division of Microbiology, Faculty of Medicine, 49573Jagiellonian University Medical College, ul. Czysta 18, 31-121 Krakow, Poland.

M Duplaga (M)

Department of Health Promotion and e-Health, Institute of Public Health, Faculty of Health Sciences, 49573Jagiellonian University Medical College, ul. Skawińska 8, 31-066 Krakow, Poland.

A Gurgul (A)

Center for Experimental and Innovative Medicine, 49563University of Agriculture in Krakow, ul. Rędzina 1c, 30-248, Krakow, Poland.

T Gosiewski (T)

Microbiome Research Laboratory, Department of Molecular Medical Microbiology, Division of Microbiology, Faculty of Medicine, 49573Jagiellonian University Medical College, ul. Czysta 18, 31-121 Krakow, Poland.

Classifications MeSH