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Review
. 2021 Feb 17:11:625162.
doi: 10.3389/fcimb.2021.625162. eCollection 2021.

Salivary Microbiome in Pediatric and Adult Celiac Disease

Affiliations
Review

Salivary Microbiome in Pediatric and Adult Celiac Disease

Dimitri Poddighe et al. Front Cell Infect Microbiol. .

Abstract

The human salivary microbiota includes hundreds of bacterial species. Alterations in gut microbiota have been explored in Celiac Disease (CD), but fewer studies investigated the characteristics of salivary microbiome in these patients, despite the potential implications in its pathogenesis. Indeed, some recent studies suggested that the partial digestion of gluten proteins by some bacteria may affect the array of gluten peptides reaching the gut and the way by which those are presented to the intestinal immune system. The available clinical studies investigating the salivary microbiota in children and adults, are insufficient to make any reliable conclusion, even though some bacterial species/phyla differences have been reported between celiac patients and controls. However, the salivary microbiome could correlate better with the duodenal microbiota, than the fecal one. Therefore, further clinical studies on salivary microbiome by different and independent research groups and including different populations, are advisable in order to explore the usefulness of the salivary microbiome analysis and understand some aspects of CD pathogenesis with potential clinical and practical implications.

Keywords: adults; celiac disease; children; microbiome; salivary microbiota.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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References

    1. Acar S., Yetkıner A. A., Ersın N., Oncag O., Aydogdu S., Arıkan C. (2012). Oral findings and salivary parameters in children with celiac disease: a preliminary study. Med. Princ Pract. 21, 129–133. 10.1159/000331794 - DOI - PubMed
    1. Caminero A., Galipeau H. J., McCarville J. L., Johnston C. W., Bernier S. P., Russell A. K., et al. . (2016). Duodenal Bacteria From Patients With Celiac Disease and Healthy Subjects Distinctly Affect Gluten Breakdown and Immunogenicity. Gastroenterology 151, 670–683. 10.1053/j.gastro.2016.06.041 - DOI - PubMed
    1. Caminero A., McCarville J. L., Galipeau H. J., Deraison C., Bernier S. P., Constante M., et al. . (2019). Duodenal bacterial proteolytic activity determines sensitivity to dietary antigen through protease-activated receptor-2. Nat. Commun. 10, 1198. 10.1038/s41467-019-09037-9 - DOI - PMC - PubMed
    1. Capittini C., De Silvestri A., Rebuffi C., Tinelli C., Poddighe D. (2019). Relevance of HLA-DQB1*02 Allele in the Genetic Predisposition of Children with Celiac Disease: Additional Cues from a Meta-Analysis. Medicina (Kaunas) 55, 190. 10.3390/medicina55050190 - DOI - PMC - PubMed
    1. Catassi C., Doloretta Macis M., Rätsch I. M., De Virgiliis S., Cucca F. (2001). The distribution of DQ genes in the Saharawi population provides only a partial explanation for the high celiac disease prevalence. Tissue Antigens 58, 402–406. 10.1034/j.1399-0039.2001.580609.x - DOI - PubMed

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