Candida gut commensalism and inflammatory disease

Zi-Qi Gu, Kuo-Yao Tseng, Yu-Huan Tsai
{"title":"Candida gut commensalism and inflammatory disease","authors":"Zi-Qi Gu,&nbsp;Kuo-Yao Tseng,&nbsp;Yu-Huan Tsai","doi":"10.1016/j.medmic.2020.100008","DOIUrl":null,"url":null,"abstract":"<div><p>The mammalian intestine harbors a collection of microbes ranging from viruses, archaea, protozoa, helminths, bacteria to fungi. This trans-kingdom community, the microbiota, has been demonstrated to modulate host immunity in health and disease. While bacterial components in this community have been extensively studied in the last two decades, the impact and composition of the fungal community in the gut, the mycobiome, have been recently unraveled. Multiple inflammatory diseases have been shown to link to change of gut mycobiome composition, predominantly the abundance of <em>Candida</em> species in the feces. While <em>Candida</em> species as a major colonizer in immunocompetent human beings are mostly supposed not harmful, they can cause life-threatening systemic infection under immunocompromised situation. Here we review the recent advances about the impact of <em>Candida</em> gut colonization on host immunity and development of inflammatory diseases in the absence of infections. We also discuss potential gaps in understanding the role of <em>Candida</em> species in inflammatory disease and the future perspective.</p></div>","PeriodicalId":36019,"journal":{"name":"Medicine in Microecology","volume":"3 ","pages":"Article 100008"},"PeriodicalIF":0.0000,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.medmic.2020.100008","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicine in Microecology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590097820300057","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 6

Abstract

The mammalian intestine harbors a collection of microbes ranging from viruses, archaea, protozoa, helminths, bacteria to fungi. This trans-kingdom community, the microbiota, has been demonstrated to modulate host immunity in health and disease. While bacterial components in this community have been extensively studied in the last two decades, the impact and composition of the fungal community in the gut, the mycobiome, have been recently unraveled. Multiple inflammatory diseases have been shown to link to change of gut mycobiome composition, predominantly the abundance of Candida species in the feces. While Candida species as a major colonizer in immunocompetent human beings are mostly supposed not harmful, they can cause life-threatening systemic infection under immunocompromised situation. Here we review the recent advances about the impact of Candida gut colonization on host immunity and development of inflammatory diseases in the absence of infections. We also discuss potential gaps in understanding the role of Candida species in inflammatory disease and the future perspective.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
念珠菌肠道寄生和炎症性疾病
哺乳动物的肠道孕育着一系列微生物,从病毒、古生菌、原生动物、蠕虫、细菌到真菌。这种跨界群落,即微生物群,已被证明在健康和疾病中调节宿主免疫。虽然在过去的二十年里,这个群落中的细菌成分已经被广泛研究,但真菌群落在肠道中的影响和组成,即真菌群落,最近才被揭示出来。多种炎症性疾病已被证明与肠道菌群组成的变化有关,主要是粪便中念珠菌种类的丰度。念珠菌作为免疫正常人群的主要定植菌,通常被认为是无害的,但在免疫功能低下的情况下,念珠菌可引起危及生命的全身性感染。在这里,我们回顾了念珠菌肠道定植对宿主免疫和炎症性疾病发展的影响的最新进展。我们还讨论了理解念珠菌在炎症性疾病中的作用和未来前景的潜在差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Medicine in Microecology
Medicine in Microecology Medicine-Gastroenterology
CiteScore
5.60
自引率
0.00%
发文量
16
审稿时长
76 days
期刊最新文献
Altered gut microbiome in fibromyalgia: Systematic review of genomic and metabolomic bacterial findings In-silico analysis, molecular docking and dynamic simulation of anti-cancer metabolites derived from Bacillus velezensis Phytomolecule and microbiota-modulation based therapeutic strategies for MDR-Tuberculosis: Mechanistic interplay and translational perspectives Pilot study of Raman-deep learning integration for rapid detection of antibiotic-resistant Escherichia coli: A proof-of-concept analysis Intranasal immunization with recombinant Omp34 and its derivative engineered construct, rOmp34L3×5, against Acinetobacter baumannii pulmonary infection
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1