Literature DB >> 29624747

Fecal microbiome signatures are different in food-allergic children compared to siblings and healthy children.

Atoosa Kourosh1,2, Ruth A Luna3,4, Miriam Balderas3,4, Christina Nance1,2, Aikaterini Anagnostou1,2, Sridevi Devaraj3,4, Carla M Davis1,2.   

Abstract

BACKGROUND: Intestinal microbes have been shown to influence predisposition to atopic disease, including food allergy. The intestinal microbiome of food-allergic children may differ in significant ways from genetically similar non-allergic children and age-matched controls. The aim was to characterize fecal microbiomes to identify taxa that may influence the expression of food allergy.
METHODS: Stool samples were collected from children with IgE-mediated food allergies, siblings without food allergy, and non-allergic controls. Stool microbiome characterization was performed via next-generation sequencing (Illumina) of the V1V3 and V4 variable regions of the 16S rRNA gene. Bacterial diversity, evenness, richness, and relative abundance of the operational taxonomic units (OTUs) were evaluated using QIIME. ANOVA and Welch's t test were utilized to compare groups.
RESULTS: Sixty-eight children were included: food-allergic (n = 22), non-food-allergic siblings (n = 25), and controls (n = 21). When comparing fecal microbial communities across groups, differences were noted in Rikenellaceae (P = .035), Actinomycetaceae (P = .043), and Pasteurellaceae (P = .018), and nine other distinct OTUs. Food-allergic subjects had enrichment for specific microbes within the Clostridia class and Firmicutes phylum (Oscillobacter valericigenes, Lachnoclostridium bolteae, Faecalibacterium sp.) compared to siblings and controls. Identification of Clostridium sp. OTUs revealed differences in specific Clostridia drive the separation of the allergic from the siblings and controls. Alistipes sp. were enriched in non-allergic siblings.
CONCLUSIONS: Comparisons in the fecal microbiome of food-allergic children, siblings, and healthy children point to key differences in microbiome signatures, suggesting the role of both genetic and environmental contributors in the manifestation of food-allergic disease.
© 2018 EAACI and John Wiley and Sons A/S. Published by John Wiley and Sons Ltd.

Entities:  

Keywords:  T regulatory cells; environment; food allergy; genetics; microbiome

Mesh:

Substances:

Year:  2018        PMID: 29624747     DOI: 10.1111/pai.12904

Source DB:  PubMed          Journal:  Pediatr Allergy Immunol        ISSN: 0905-6157            Impact factor:   6.377


  26 in total

Review 1.  Immunomodulatory effects of breast milk on food allergy.

Authors:  Kirsi M Järvinen; Hayley Martin; Michiko K Oyoshi
Journal:  Ann Allergy Asthma Immunol       Date:  2019-04-29       Impact factor: 6.347

2.  Fecal microbiome and metabolome differ in healthy and food-allergic twins.

Authors:  Riyue Bao; Lauren A Hesser; Ziyuan He; Xiaoying Zhou; Kari C Nadeau; Cathryn R Nagler
Journal:  J Clin Invest       Date:  2021-01-19       Impact factor: 14.808

3.  Effects of Lactobacillus plantarum FZU3013-Fermented Laminaria japonica on Lipid Metabolism and Gut Microbiota in Hyperlipidaemic Rats.

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4.  [Features of intestinal flora in children with food protein-induced proctocolitis based on high-throughput sequencing].

Authors:  Shun-Li Chen; Zheng-Zhen Tang; Bo Huang; Xing-Yan Zhao; Shou-Shan Chen
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2022-05-15

Review 5.  Newly identified T cell subsets in mechanistic studies of food immunotherapy.

Authors:  Vanitha Sampath; Kari C Nadeau
Journal:  J Clin Invest       Date:  2019-04-01       Impact factor: 14.808

6.  Lower gut microbiome diversity and higher abundance of proinflammatory genus Collinsella are associated with biopsy-proven nonalcoholic steatohepatitis.

Authors:  Stuart Astbury; Edmond Atallah; Amrita Vijay; Guruprasad P Aithal; Jane I Grove; Ana M Valdes
Journal:  Gut Microbes       Date:  2019-11-07

Review 7.  Butyrate: A Link between Early Life Nutrition and Gut Microbiome in the Development of Food Allergy.

Authors:  Margherita Di Costanzo; Nicoletta De Paulis; Giacomo Biasucci
Journal:  Life (Basel)       Date:  2021-04-23

8.  Anxiety-like behavior and intestinal microbiota changes as strain-and sex-dependent sequelae of mild food allergy in mouse models of cow's milk allergy.

Authors:  Nicholas A Smith; Danielle L Germundson; Pan Gao; Junguk Hur; Angela M Floden; Kumi Nagamoto-Combs
Journal:  Brain Behav Immun       Date:  2021-03-09       Impact factor: 19.227

Review 9.  Immunologically Active Components in Human Milk and Development of Atopic Disease, With Emphasis on Food Allergy, in the Pediatric Population.

Authors:  Puja S Rajani; Antti E Seppo; Kirsi M Järvinen
Journal:  Front Pediatr       Date:  2018-08-07       Impact factor: 3.418

Review 10.  Resolving Clinical Phenotypes into Endotypes in Allergy: Molecular and Omics Approaches.

Authors:  Tesfaye B Mersha; Yashira Afanador; Elisabet Johansson; Steven P Proper; Jonathan A Bernstein; Marc E Rothenberg; Gurjit K Khurana Hershey
Journal:  Clin Rev Allergy Immunol       Date:  2021-04       Impact factor: 8.667

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