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Infant gut bacterial community composition and food-related manifestation of atopy in early childhood

BACKGROUND: Immunoglobulin E–mediated food allergy (IgE-FA) has emerged as a global public health concern. Immune dysregulation is an underlying mechanism for IgE-FA, caused by “dysbiosis” of the early intestinal microbiota. We investigated the association between infant gut bacterial composition an...

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Autores principales: Joseph, Christine LM, Sitarik, Alexandra R., Kim, Haejin, Huffnagle, Gary, Fujimura, Kei, Yong, Germaine Jia Min, Levin, Albert M., Zoratti, Edward, Lynch, Susan, Ownby, Dennis R., Lukacs, Nicholas W., Davidson, Brent, Barone, Charles, Johnson, Christine Cole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301652/
https://www.ncbi.nlm.nih.gov/pubmed/34811824
http://dx.doi.org/10.1111/pai.13704
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author Joseph, Christine LM
Sitarik, Alexandra R.
Kim, Haejin
Huffnagle, Gary
Fujimura, Kei
Yong, Germaine Jia Min
Levin, Albert M.
Zoratti, Edward
Lynch, Susan
Ownby, Dennis R.
Lukacs, Nicholas W.
Davidson, Brent
Barone, Charles
Johnson, Christine Cole
author_facet Joseph, Christine LM
Sitarik, Alexandra R.
Kim, Haejin
Huffnagle, Gary
Fujimura, Kei
Yong, Germaine Jia Min
Levin, Albert M.
Zoratti, Edward
Lynch, Susan
Ownby, Dennis R.
Lukacs, Nicholas W.
Davidson, Brent
Barone, Charles
Johnson, Christine Cole
author_sort Joseph, Christine LM
collection PubMed
description BACKGROUND: Immunoglobulin E–mediated food allergy (IgE-FA) has emerged as a global public health concern. Immune dysregulation is an underlying mechanism for IgE-FA, caused by “dysbiosis” of the early intestinal microbiota. We investigated the association between infant gut bacterial composition and food-related atopy at age 3–5 years using a well-characterized birth cohort. METHODS: The study definition of IgE-FA to egg, milk, or peanut was based on physician panel retrospective review of clinical and questionnaire data collected from birth through age 3–5 years. Using 16S rRNA sequencing, we profiled the bacterial gut microbiota present in stool specimens collected at 1 and 6 months of age. RESULTS: Of 447 infants with data for analysis, 44 (9.8%) met physician panel review criteria for IgE-FA to ≥1 of the three allergens. Among children classified as IgE-FA at 3–5 years, infant stool samples showed significantly less diversity of the gut microbiota compared with the samples of children classified as no IgE-FA at age 3–5 years, especially for milk and peanut (all covariate-adjusted p’s for alpha metrics <.007). Testing of individual operational taxonomic units (OTUs) revealed 6-month deficiencies in 31 OTUs for IgE-FA compared with no IgE-FA, mostly in the orders Lactobacillales, Bacteroidales, and Clostridiales. CONCLUSIONS: Variations in gut microbial composition in infant stool were associated with a study definition of IgE-FA at 3–5 years of age. This included evidence of a lack of bacterial diversity, deficiencies in specific OTUs, and delayed microbial maturation. Results support dysbiosis in IgE-FA pathogenesis.
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spelling pubmed-93016522022-07-21 Infant gut bacterial community composition and food-related manifestation of atopy in early childhood Joseph, Christine LM Sitarik, Alexandra R. Kim, Haejin Huffnagle, Gary Fujimura, Kei Yong, Germaine Jia Min Levin, Albert M. Zoratti, Edward Lynch, Susan Ownby, Dennis R. Lukacs, Nicholas W. Davidson, Brent Barone, Charles Johnson, Christine Cole Pediatr Allergy Immunol Article BACKGROUND: Immunoglobulin E–mediated food allergy (IgE-FA) has emerged as a global public health concern. Immune dysregulation is an underlying mechanism for IgE-FA, caused by “dysbiosis” of the early intestinal microbiota. We investigated the association between infant gut bacterial composition and food-related atopy at age 3–5 years using a well-characterized birth cohort. METHODS: The study definition of IgE-FA to egg, milk, or peanut was based on physician panel retrospective review of clinical and questionnaire data collected from birth through age 3–5 years. Using 16S rRNA sequencing, we profiled the bacterial gut microbiota present in stool specimens collected at 1 and 6 months of age. RESULTS: Of 447 infants with data for analysis, 44 (9.8%) met physician panel review criteria for IgE-FA to ≥1 of the three allergens. Among children classified as IgE-FA at 3–5 years, infant stool samples showed significantly less diversity of the gut microbiota compared with the samples of children classified as no IgE-FA at age 3–5 years, especially for milk and peanut (all covariate-adjusted p’s for alpha metrics <.007). Testing of individual operational taxonomic units (OTUs) revealed 6-month deficiencies in 31 OTUs for IgE-FA compared with no IgE-FA, mostly in the orders Lactobacillales, Bacteroidales, and Clostridiales. CONCLUSIONS: Variations in gut microbial composition in infant stool were associated with a study definition of IgE-FA at 3–5 years of age. This included evidence of a lack of bacterial diversity, deficiencies in specific OTUs, and delayed microbial maturation. Results support dysbiosis in IgE-FA pathogenesis. 2022-01 2021-12-05 /pmc/articles/PMC9301652/ /pubmed/34811824 http://dx.doi.org/10.1111/pai.13704 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This Article is brought to you for free and open access by the Public Health Sciences at Henry Ford Health Scholarly Commons. It has been accepted for inclusion in Public Health Sciences Articles by an authorized administrator of Henry Ford Health Scholarly Commons.
spellingShingle Article
Joseph, Christine LM
Sitarik, Alexandra R.
Kim, Haejin
Huffnagle, Gary
Fujimura, Kei
Yong, Germaine Jia Min
Levin, Albert M.
Zoratti, Edward
Lynch, Susan
Ownby, Dennis R.
Lukacs, Nicholas W.
Davidson, Brent
Barone, Charles
Johnson, Christine Cole
Infant gut bacterial community composition and food-related manifestation of atopy in early childhood
title Infant gut bacterial community composition and food-related manifestation of atopy in early childhood
title_full Infant gut bacterial community composition and food-related manifestation of atopy in early childhood
title_fullStr Infant gut bacterial community composition and food-related manifestation of atopy in early childhood
title_full_unstemmed Infant gut bacterial community composition and food-related manifestation of atopy in early childhood
title_short Infant gut bacterial community composition and food-related manifestation of atopy in early childhood
title_sort infant gut bacterial community composition and food-related manifestation of atopy in early childhood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301652/
https://www.ncbi.nlm.nih.gov/pubmed/34811824
http://dx.doi.org/10.1111/pai.13704
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