Antibiotics-Induced Dysbiosis of Intestinal Microbiota Aggravates Atopic Dermatitis in Mice by Altered Short-Chain Fatty Acids
10.4168/aair.2020.12.1.137
- Author:
Ha Jung KIM
1
;
Seung Hwa LEE
;
Soo Jong HONG
Author Information
1. Department of Internal Medicine, College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
- Publication Type:Original Article
- Keywords:
Atopic dermatitis;
cytokines;
dysbiosis;
fatty acids;
intestines;
microbiota;
probiotics
- MeSH:
Animals;
Anti-Bacterial Agents;
Cytokines;
Dermatitis, Atopic;
Drinking Water;
Dysbiosis;
Fatty Acids;
Fatty Acids, Volatile;
Feces;
Gastrointestinal Microbiome;
Humans;
Immunoglobulin E;
Immunoglobulins;
Interleukins;
Intestines;
Lymphocytes;
Mice;
Microbiota;
Ovalbumin;
Ovum;
Phenotype;
Probiotics;
Skin;
T-Lymphocytes, Regulatory;
Water
- From:Allergy, Asthma & Immunology Research
2020;12(1):137-148
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Alterations in the intestinal microbiota in early life affects the development of atopic dermatitis (AD) in humans. This study aimed to further investigate the effects of gut dysbiosis in early life in an ovalbumin (OVA)-induced mouse model of AD. METHODS: The AD mouse model was developed by serial OVA sensitization and mice were treated with an antibiotic cocktail in their drinking water for 2 weeks before primary sensitization. Probiotics (Lactobacillus rhamnosus, 1 × 10⁹ CFU) or 100 µL of fresh fecal supernatant were orally administered daily from 1 week before the first sensitization until the end of the study. RESULTS: The AD mice which received antibiotics had significantly aggravated phenotypes, including clinical score, transepidermal water loss, and histopathology, compared to those treated with healthy feces or probiotics. Total systemic immunoglobulin E production and skin interleukin (IL) 4 levels were significantly increased in the antibiotic-treated mice compared to the other groups. Antibiotic treatment also increased the levels of IL17 and group 3 innate lymphoid cells (ILC3) in the gut and significantly suppressed the production of short-chain fatty acids (SCFAs) and decreased the number FOXP3⁺ cells. CONCLUSIONS: Our results suggest that the status of the gut microbiota in early life in the mouse may play a crucial role in AD development through intestinal SCFA production through regulate the numbers of CD4⁺IL17⁺/CD4⁺FOXP3⁺ regulatory T cells and ILC3s.
