Disordered development of gut microbiome interferes with the establishment of the gut ecosystem during early childhood with atopic dermatitis. (31st December 2022)

• Record Type: Journal Article
• Authors: Lee, Min-Jung; Park, Yoon Mee; Kim, Byunghyun; Tae, in Hwan; Kim, Nam-Eun; Pranata, Marina; Kim, Taewon; Won, Sungho; Kang, Nam Joo; Lee, Yun Kyung; Lee, Dong-Woo; Nam, Myung Hee; Hong, Soo-Jong; Kim, Bong-Soo
• Is Part Of: Gut microbes. Volume 14:Isuse 1(2022)
• Publication Date: 2022-12-31
• Subjects: Gut -- microbiome -- atopic dermatitis -- development -- homeostasis; Gastrointestinal system -- Microbiology -- Periodicals; Microbiology -- Periodicals; Intestine, Small -- Periodicals; 616.3
• DOI: 10.1080/19490976.2022.2068366
• Languages: English
• ISSNs: 1949-0984

Abstract

ABSTRACT: The gut microbiome influences the development of allergic diseases during early childhood. However, there is a lack of comprehensive understanding of microbiome-host crosstalk. Here, we analyzed the influence of gut microbiome dynamics in early childhood on atopic dermatitis (AD) and the potential interactions between host and microbiome that control this homeostasis. We analyzed the gut microbiome in 346 fecal samples (6–36 months; 112 non-AD, 110 mild AD, and 124 moderate to severe AD) from the Longitudinal Cohort for Childhood Origin of Asthma and Allergic Disease birth cohort. The microbiome-host interactions were analyzed in animal and in vitro cell assays. Although the gut microbiome maturated with age in both AD and non-AD groups, its development was disordered in the AD group. Disordered colonization of short-chain fatty acids (SCFA) producers along with age led to abnormal SCFA production and increased IgE levels. A butyrate deficiency and downregulation of GPR109A and PPAR-γ genes were detected in AD-induced mice. Insufficient butyrate decreases the oxygen consumption rate of host cells, which can release oxygen to the gut and perturb the gut microbiome. The disordered gut microbiome development could aggravate balanced microbiome-host interactions, including immune responses during early childhood with AD.