韩国食物过敏儿童肠道菌群多样性和组成的改变

IF 4.6 2区 医学 Q2 ALLERGY
Minyoung Jung, Ji Young Lee, Sukyung Kim, Jeongmin Song, Sehun Jang, Sanghee Shin, Min Hee Lee, Mi Jin Kim, Jiwon Kim, Han Byul Lee, Yeonghee Kim, Kangmo Ahn, Minji Kim, Jihyun Kim
{"title":"韩国食物过敏儿童肠道菌群多样性和组成的改变","authors":"Minyoung Jung,&nbsp;Ji Young Lee,&nbsp;Sukyung Kim,&nbsp;Jeongmin Song,&nbsp;Sehun Jang,&nbsp;Sanghee Shin,&nbsp;Min Hee Lee,&nbsp;Mi Jin Kim,&nbsp;Jiwon Kim,&nbsp;Han Byul Lee,&nbsp;Yeonghee Kim,&nbsp;Kangmo Ahn,&nbsp;Minji Kim,&nbsp;Jihyun Kim","doi":"10.1002/clt2.70036","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>This study aimed to comprehensively characterize the gut microbiome and identify individual and grouped gut microbes associated with food allergy (FA) using 16S rRNA gene sequencing.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Fecal samples were collected from children with IgE-mediated FA and from sex- and age-matched controls. The V3–V4 variable regions of the 16S rRNA gene of the gut microbiome were profiled using next-generation sequencing (Illumina, USA). Bacterial species richness, intracommunity diversity, and intergroup dissimilarity were evaluated. Functional profiles were predicted using Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) and the Minimal Set of Pathways (MinPath) algorithm.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Fecal samples were collected from children with IgE-mediated FA (<i>n</i> = 66) and from sex- and age-matched controls (<i>n</i> = 22). Gut microbiome richness (<i>p</i> &lt; 0.0001), intra-community diversity (<i>p</i> &lt; 0.0001), and inter-community diversity (<i>p</i> = 0.0004) were higher in the healthy group than in the FA group. Patients with FA were enriched in <i>Blautia</i>, <i>Fusicatenibacter</i>, and <i>Ruminococcus_g5</i> compared with healthy control individuals (all <i>p</i> &lt; 0.05). Healthy control individuals were significantly enriched in <i>Oscillibacter</i> and <i>Ruminococcus</i> compared with patients with FA (all <i>p</i> &lt; 0.05). Functional pathway analysis identified enrichment in pathways related to endoglucanase in healthy controls and the ATP-binding cassette (ABC) transport system in FA patients.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>The gut microbiomes of patients with FA and healthy control individuals had different taxonomic abundances, and the microbiome richness and diversity of the bacterial flora of patients with FA were reduced compared with controls.</p>\n </section>\n </div>","PeriodicalId":10334,"journal":{"name":"Clinical and Translational Allergy","volume":"15 3","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/clt2.70036","citationCount":"0","resultStr":"{\"title\":\"Altered diversity and composition of gut microbiota in Korean children with food allergy\",\"authors\":\"Minyoung Jung,&nbsp;Ji Young Lee,&nbsp;Sukyung Kim,&nbsp;Jeongmin Song,&nbsp;Sehun Jang,&nbsp;Sanghee Shin,&nbsp;Min Hee Lee,&nbsp;Mi Jin Kim,&nbsp;Jiwon Kim,&nbsp;Han Byul Lee,&nbsp;Yeonghee Kim,&nbsp;Kangmo Ahn,&nbsp;Minji Kim,&nbsp;Jihyun Kim\",\"doi\":\"10.1002/clt2.70036\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>This study aimed to comprehensively characterize the gut microbiome and identify individual and grouped gut microbes associated with food allergy (FA) using 16S rRNA gene sequencing.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Fecal samples were collected from children with IgE-mediated FA and from sex- and age-matched controls. The V3–V4 variable regions of the 16S rRNA gene of the gut microbiome were profiled using next-generation sequencing (Illumina, USA). Bacterial species richness, intracommunity diversity, and intergroup dissimilarity were evaluated. Functional profiles were predicted using Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) and the Minimal Set of Pathways (MinPath) algorithm.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Fecal samples were collected from children with IgE-mediated FA (<i>n</i> = 66) and from sex- and age-matched controls (<i>n</i> = 22). Gut microbiome richness (<i>p</i> &lt; 0.0001), intra-community diversity (<i>p</i> &lt; 0.0001), and inter-community diversity (<i>p</i> = 0.0004) were higher in the healthy group than in the FA group. Patients with FA were enriched in <i>Blautia</i>, <i>Fusicatenibacter</i>, and <i>Ruminococcus_g5</i> compared with healthy control individuals (all <i>p</i> &lt; 0.05). Healthy control individuals were significantly enriched in <i>Oscillibacter</i> and <i>Ruminococcus</i> compared with patients with FA (all <i>p</i> &lt; 0.05). Functional pathway analysis identified enrichment in pathways related to endoglucanase in healthy controls and the ATP-binding cassette (ABC) transport system in FA patients.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>The gut microbiomes of patients with FA and healthy control individuals had different taxonomic abundances, and the microbiome richness and diversity of the bacterial flora of patients with FA were reduced compared with controls.</p>\\n </section>\\n </div>\",\"PeriodicalId\":10334,\"journal\":{\"name\":\"Clinical and Translational Allergy\",\"volume\":\"15 3\",\"pages\":\"\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-03-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/clt2.70036\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical and Translational Allergy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/clt2.70036\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ALLERGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and Translational Allergy","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/clt2.70036","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0

摘要

本研究旨在通过16S rRNA基因测序,全面表征肠道微生物组,鉴定与食物过敏(FA)相关的个体和肠道微生物群。方法收集ige介导的FA患儿和性别、年龄相匹配的对照组的粪便样本。使用下一代测序(Illumina, USA)对肠道微生物组16S rRNA基因的V3-V4可变区进行了分析。对细菌种类丰富度、群落内多样性和群间差异性进行了评价。利用重构未观察状态(PICRUSt)和最小路径集(MinPath)算法对群落的系统发育调查进行了功能预测。结果收集了ige介导的FA患儿(n = 66)和性别和年龄匹配的对照组(n = 22)的粪便样本。肠道菌群丰富度(p <;0.0001),群落内多样性(p <;0.0001),健康组的群落间多样性(p = 0.0004)高于FA组。与健康对照组相比,FA患者中Blautia、Fusicatenibacter和Ruminococcus_g5含量丰富(p <;0.05)。与FA患者相比,健康对照个体的Oscillibacter和Ruminococcus显著富集(p <;0.05)。功能通路分析发现,健康对照中与内切葡聚糖酶相关的通路富集,FA患者中与atp结合盒(ABC)运输系统相关的通路富集。结论FA患者与健康对照者肠道菌群的分类丰度存在差异,FA患者肠道菌群的丰富度和多样性均低于对照组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Altered diversity and composition of gut microbiota in Korean children with food allergy

Altered diversity and composition of gut microbiota in Korean children with food allergy

Background

This study aimed to comprehensively characterize the gut microbiome and identify individual and grouped gut microbes associated with food allergy (FA) using 16S rRNA gene sequencing.

Methods

Fecal samples were collected from children with IgE-mediated FA and from sex- and age-matched controls. The V3–V4 variable regions of the 16S rRNA gene of the gut microbiome were profiled using next-generation sequencing (Illumina, USA). Bacterial species richness, intracommunity diversity, and intergroup dissimilarity were evaluated. Functional profiles were predicted using Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) and the Minimal Set of Pathways (MinPath) algorithm.

Results

Fecal samples were collected from children with IgE-mediated FA (n = 66) and from sex- and age-matched controls (n = 22). Gut microbiome richness (p < 0.0001), intra-community diversity (p < 0.0001), and inter-community diversity (p = 0.0004) were higher in the healthy group than in the FA group. Patients with FA were enriched in Blautia, Fusicatenibacter, and Ruminococcus_g5 compared with healthy control individuals (all p < 0.05). Healthy control individuals were significantly enriched in Oscillibacter and Ruminococcus compared with patients with FA (all p < 0.05). Functional pathway analysis identified enrichment in pathways related to endoglucanase in healthy controls and the ATP-binding cassette (ABC) transport system in FA patients.

Conclusions

The gut microbiomes of patients with FA and healthy control individuals had different taxonomic abundances, and the microbiome richness and diversity of the bacterial flora of patients with FA were reduced compared with controls.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Clinical and Translational Allergy
Clinical and Translational Allergy Immunology and Microbiology-Immunology
CiteScore
7.50
自引率
4.50%
发文量
117
审稿时长
12 weeks
期刊介绍: Clinical and Translational Allergy, one of several journals in the portfolio of the European Academy of Allergy and Clinical Immunology, provides a platform for the dissemination of allergy research and reviews, as well as EAACI position papers, task force reports and guidelines, amongst an international scientific audience. Clinical and Translational Allergy accepts clinical and translational research in the following areas and other related topics: asthma, rhinitis, rhinosinusitis, drug hypersensitivity, allergic conjunctivitis, allergic skin diseases, atopic eczema, urticaria, angioedema, venom hypersensitivity, anaphylaxis, food allergy, immunotherapy, immune modulators and biologics, animal models of allergic disease, immune mechanisms, or any other topic related to allergic disease.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信