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Longitudinal disease-associated gut microbiome differences in infants with food protein-induced allergic proctocolitis
BACKGROUND: Complex interactions between the gut microbiome and immune cells in infancy are thought to be part of the pathogenesis for the marked rise in pediatric allergic diseases, particularly food allergies. Food protein-induced allergic proctocolitis (FPIAP) is commonly the earliest recognized...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503280/ https://www.ncbi.nlm.nih.gov/pubmed/36138438 http://dx.doi.org/10.1186/s40168-022-01322-y |
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author | Martin, Victoria M. Virkud, Yamini V. Dahan, Ehud Seay, Hannah L. Itzkovits, Dvir Vlamakis, Hera Xavier, Ramnik Shreffler, Wayne G. Yuan, Qian Yassour, Moran |
author_facet | Martin, Victoria M. Virkud, Yamini V. Dahan, Ehud Seay, Hannah L. Itzkovits, Dvir Vlamakis, Hera Xavier, Ramnik Shreffler, Wayne G. Yuan, Qian Yassour, Moran |
author_sort | Martin, Victoria M. |
collection | PubMed |
description | BACKGROUND: Complex interactions between the gut microbiome and immune cells in infancy are thought to be part of the pathogenesis for the marked rise in pediatric allergic diseases, particularly food allergies. Food protein-induced allergic proctocolitis (FPIAP) is commonly the earliest recognized non-immunoglobulin E (IgE)-mediated food allergy in infancy and is associated with atopic dermatitis and subsequent IgE-mediated food allergy later in childhood. Yet, a large prospective longitudinal study of the microbiome of infants with FPIAP, including samples prior to symptom onset, has not been done. RESULTS: Here, we analyzed 954 longitudinal samples from 160 infants in a nested case-control study (81 who developed FPIAP and 79 matched controls) from 1 week to 1 year of age by 16S rRNA ribosomal gene sequencing as part of the Gastrointestinal Microbiome and Allergic Proctocolitis (GMAP) study. We found key differences in the microbiome of infants with FPIAP, most strongly a higher abundance of a genus of Enterobacteriaceae and a lower abundance of a family of Clostridiales during the symptomatic period. We saw some of these significant taxonomic differences even prior to symptom onset. There were no consistent longitudinal differences in richness or stability diversity metrics between infants with FPIAP and healthy controls. CONCLUSIONS: This study is the first to identify differences in the infant gut microbiome in children who develop FPIAP, some even before they develop symptoms, and provides a foundation for more mechanistic investigation into the pathogenesis of FPIAP and subsequent food allergic diseases in childhood. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01322-y. |
format | Online Article Text |
id | pubmed-9503280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95032802022-09-24 Longitudinal disease-associated gut microbiome differences in infants with food protein-induced allergic proctocolitis Martin, Victoria M. Virkud, Yamini V. Dahan, Ehud Seay, Hannah L. Itzkovits, Dvir Vlamakis, Hera Xavier, Ramnik Shreffler, Wayne G. Yuan, Qian Yassour, Moran Microbiome Research BACKGROUND: Complex interactions between the gut microbiome and immune cells in infancy are thought to be part of the pathogenesis for the marked rise in pediatric allergic diseases, particularly food allergies. Food protein-induced allergic proctocolitis (FPIAP) is commonly the earliest recognized non-immunoglobulin E (IgE)-mediated food allergy in infancy and is associated with atopic dermatitis and subsequent IgE-mediated food allergy later in childhood. Yet, a large prospective longitudinal study of the microbiome of infants with FPIAP, including samples prior to symptom onset, has not been done. RESULTS: Here, we analyzed 954 longitudinal samples from 160 infants in a nested case-control study (81 who developed FPIAP and 79 matched controls) from 1 week to 1 year of age by 16S rRNA ribosomal gene sequencing as part of the Gastrointestinal Microbiome and Allergic Proctocolitis (GMAP) study. We found key differences in the microbiome of infants with FPIAP, most strongly a higher abundance of a genus of Enterobacteriaceae and a lower abundance of a family of Clostridiales during the symptomatic period. We saw some of these significant taxonomic differences even prior to symptom onset. There were no consistent longitudinal differences in richness or stability diversity metrics between infants with FPIAP and healthy controls. CONCLUSIONS: This study is the first to identify differences in the infant gut microbiome in children who develop FPIAP, some even before they develop symptoms, and provides a foundation for more mechanistic investigation into the pathogenesis of FPIAP and subsequent food allergic diseases in childhood. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01322-y. BioMed Central 2022-09-23 /pmc/articles/PMC9503280/ /pubmed/36138438 http://dx.doi.org/10.1186/s40168-022-01322-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Martin, Victoria M. Virkud, Yamini V. Dahan, Ehud Seay, Hannah L. Itzkovits, Dvir Vlamakis, Hera Xavier, Ramnik Shreffler, Wayne G. Yuan, Qian Yassour, Moran Longitudinal disease-associated gut microbiome differences in infants with food protein-induced allergic proctocolitis |
title | Longitudinal disease-associated gut microbiome differences in infants with food protein-induced allergic proctocolitis |
title_full | Longitudinal disease-associated gut microbiome differences in infants with food protein-induced allergic proctocolitis |
title_fullStr | Longitudinal disease-associated gut microbiome differences in infants with food protein-induced allergic proctocolitis |
title_full_unstemmed | Longitudinal disease-associated gut microbiome differences in infants with food protein-induced allergic proctocolitis |
title_short | Longitudinal disease-associated gut microbiome differences in infants with food protein-induced allergic proctocolitis |
title_sort | longitudinal disease-associated gut microbiome differences in infants with food protein-induced allergic proctocolitis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503280/ https://www.ncbi.nlm.nih.gov/pubmed/36138438 http://dx.doi.org/10.1186/s40168-022-01322-y |
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