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Microbial signature in IgE-mediated food allergies
BACKGROUND: Multiple studies suggest a key role for gut microbiota in IgE-mediated food allergy (FA) development, but to date, none has studied it in the persistent state. METHODS: To characterize the gut microbiota composition and short-chain fatty acid (SCFAs) profiles associated with major food a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7592384/ https://www.ncbi.nlm.nih.gov/pubmed/33109272 http://dx.doi.org/10.1186/s13073-020-00789-4 |
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author | Goldberg, Michael R. Mor, Hadar Magid Neriya, Dafna Magzal, Faiga Muller, Efrat Appel, Michael Y. Nachshon, Liat Borenstein, Elhanan Tamir, Snait Louzoun, Yoram Youngster, Ilan Elizur, Arnon Koren, Omry |
author_facet | Goldberg, Michael R. Mor, Hadar Magid Neriya, Dafna Magzal, Faiga Muller, Efrat Appel, Michael Y. Nachshon, Liat Borenstein, Elhanan Tamir, Snait Louzoun, Yoram Youngster, Ilan Elizur, Arnon Koren, Omry |
author_sort | Goldberg, Michael R. |
collection | PubMed |
description | BACKGROUND: Multiple studies suggest a key role for gut microbiota in IgE-mediated food allergy (FA) development, but to date, none has studied it in the persistent state. METHODS: To characterize the gut microbiota composition and short-chain fatty acid (SCFAs) profiles associated with major food allergy groups, we recruited 233 patients with FA including milk (N = 66), sesame (N = 38), peanut (N = 71), and tree nuts (N = 58), and non-allergic controls (N = 58). DNA was isolated from fecal samples, and 16S rRNA gene sequences were analyzed. SCFAs in stool were analyzed from patients with a single allergy (N = 84) and controls (N = 31). RESULTS: The gut microbiota composition of allergic patients was significantly different compared to age-matched controls both in α-diversity and β-diversity. Distinct microbial signatures were noted for FA to different foods. Prevotella copri (P. copri) was the most overrepresented species in non-allergic controls. SCFAs levels were significantly higher in the non-allergic compared to the FA groups, whereas P. copri significantly correlated with all three SCFAs. We used these microbial differences to distinguish between FA patients and non-allergic healthy controls with an area under the curve of 0.90, and for the classification of FA patients according to their FA types using a supervised learning algorithm. Bacteroides and P. copri were identified as taxa potentially contributing to KEGG acetate-related pathways enriched in non-allergic compared to FA. In addition, overall pathway dissimilarities were found among different FAs. CONCLUSIONS: Our results demonstrate a link between IgE-mediated FA and the composition and metabolic activity of the gut microbiota. |
format | Online Article Text |
id | pubmed-7592384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75923842020-10-29 Microbial signature in IgE-mediated food allergies Goldberg, Michael R. Mor, Hadar Magid Neriya, Dafna Magzal, Faiga Muller, Efrat Appel, Michael Y. Nachshon, Liat Borenstein, Elhanan Tamir, Snait Louzoun, Yoram Youngster, Ilan Elizur, Arnon Koren, Omry Genome Med Research BACKGROUND: Multiple studies suggest a key role for gut microbiota in IgE-mediated food allergy (FA) development, but to date, none has studied it in the persistent state. METHODS: To characterize the gut microbiota composition and short-chain fatty acid (SCFAs) profiles associated with major food allergy groups, we recruited 233 patients with FA including milk (N = 66), sesame (N = 38), peanut (N = 71), and tree nuts (N = 58), and non-allergic controls (N = 58). DNA was isolated from fecal samples, and 16S rRNA gene sequences were analyzed. SCFAs in stool were analyzed from patients with a single allergy (N = 84) and controls (N = 31). RESULTS: The gut microbiota composition of allergic patients was significantly different compared to age-matched controls both in α-diversity and β-diversity. Distinct microbial signatures were noted for FA to different foods. Prevotella copri (P. copri) was the most overrepresented species in non-allergic controls. SCFAs levels were significantly higher in the non-allergic compared to the FA groups, whereas P. copri significantly correlated with all three SCFAs. We used these microbial differences to distinguish between FA patients and non-allergic healthy controls with an area under the curve of 0.90, and for the classification of FA patients according to their FA types using a supervised learning algorithm. Bacteroides and P. copri were identified as taxa potentially contributing to KEGG acetate-related pathways enriched in non-allergic compared to FA. In addition, overall pathway dissimilarities were found among different FAs. CONCLUSIONS: Our results demonstrate a link between IgE-mediated FA and the composition and metabolic activity of the gut microbiota. BioMed Central 2020-10-27 /pmc/articles/PMC7592384/ /pubmed/33109272 http://dx.doi.org/10.1186/s13073-020-00789-4 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Goldberg, Michael R. Mor, Hadar Magid Neriya, Dafna Magzal, Faiga Muller, Efrat Appel, Michael Y. Nachshon, Liat Borenstein, Elhanan Tamir, Snait Louzoun, Yoram Youngster, Ilan Elizur, Arnon Koren, Omry Microbial signature in IgE-mediated food allergies |
title | Microbial signature in IgE-mediated food allergies |
title_full | Microbial signature in IgE-mediated food allergies |
title_fullStr | Microbial signature in IgE-mediated food allergies |
title_full_unstemmed | Microbial signature in IgE-mediated food allergies |
title_short | Microbial signature in IgE-mediated food allergies |
title_sort | microbial signature in ige-mediated food allergies |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7592384/ https://www.ncbi.nlm.nih.gov/pubmed/33109272 http://dx.doi.org/10.1186/s13073-020-00789-4 |
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