Literature DB >> 29426044

Dysbiosis of Inferior Turbinate Microbiota Is Associated with High Total IgE Levels in Patients with Allergic Rhinitis.

Dong-Wook Hyun1,2, Hyun Jin Min3, Min-Soo Kim1,2, Tae Woong Whon1,2, Na-Ri Shin1,2, Pil Soo Kim1,2, Hyun Sik Kim1,2, June Young Lee1,2, Woorim Kang1,2, Augustine M K Choi4, Joo-Heon Yoon5, Jin-Woo Bae6,2.   

Abstract

Abnormalities in the human microbiota are associated with the etiology of allergic diseases. Although disease site-specific microbiota may be associated with disease pathophysiology, the role of the nasal microbiota is unclear. We sought to characterize the microbiota of the site of allergic rhinitis, the inferior turbinate, in subjects with allergic rhinitis (n = 20) and healthy controls (n = 12) and to examine the relationship of mucosal microbiota with disease occurrence, sensitized allergen number, and allergen-specific and total IgE levels. Microbial dysbiosis correlated significantly with total IgE levels representing combined allergic responses but not with disease occurrence, the number of sensitized allergens, or house dust mite allergen-specific IgE levels. Compared to the populations in individuals with low total IgE levels (group IgElow), low microbial biodiversity with a high relative abundance of Firmicutes phylum (Staphylococcus aureus) and a low relative abundance of Actinobacteria phylum (Propionibacterium acnes) was observed in individuals with high total serum IgE levels (group IgEhigh). Phylogeny-based microbial functional potential predicted by the 16S rRNA gene indicated an increase in signal transduction-related genes and a decrease in energy metabolism-related genes in group IgEhigh as shown in the microbial features with atopic and/or inflammatory diseases. Thus, dysbiosis of the inferior turbinate mucosa microbiota, particularly an increase in S. aureus and a decrease in P. acnes, is linked to high total IgE levels in allergic rhinitis, suggesting that inferior turbinate microbiota may be affected by accumulated allergic responses against sensitized allergens and that site-specific microbial alterations play a potential role in disease pathophysiology.
Copyright © 2018 American Society for Microbiology.

Entities:  

Keywords:  Propionibacterium acnes; Staphylococcus aureus; allergic rhinitis; commensal microbiota; immunoglobulin E; inferior turbinate; multiple-allergen simultaneous test; nasal mucosa; skin prick test

Mesh:

Substances:

Year:  2018        PMID: 29426044      PMCID: PMC5865026          DOI: 10.1128/IAI.00934-17

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


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