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本文引用的文献

1
Intestinal fungi are causally implicated in microbiome assembly and immune development in mice.肠道真菌与小鼠微生物组组装和免疫发育有因果关系。
Nat Commun. 2020 May 22;11(1):2577. doi: 10.1038/s41467-020-16431-1.
2
Fungal Trans-kingdom Dynamics Linked to Responsiveness to Fecal Microbiota Transplantation (FMT) Therapy in Ulcerative Colitis.真菌跨界动态与溃疡性结肠炎对粪便微生物群移植 (FMT) 治疗的反应性相关。
Cell Host Microbe. 2020 May 13;27(5):823-829.e3. doi: 10.1016/j.chom.2020.03.006. Epub 2020 Apr 15.
3
Fungal Dysbiosis and Intestinal Inflammation in Children With Beta-Cell Autoimmunity.真菌失调与β细胞自身免疫儿童的肠道炎症
Front Immunol. 2020 Mar 19;11:468. doi: 10.3389/fimmu.2020.00468. eCollection 2020.
4
T Cell Antifungal Immunity and the Role of C-Type Lectin Receptors.T 细胞抗真菌免疫与 C 型凝集素受体的作用。
Trends Immunol. 2020 Jan;41(1):61-76. doi: 10.1016/j.it.2019.11.007. Epub 2019 Dec 5.
5
The Candida albicans exotoxin candidalysin promotes alcohol-associated liver disease.白色念珠菌外毒素白念珠菌溶素促进酒精相关性肝病。
J Hepatol. 2020 Mar;72(3):391-400. doi: 10.1016/j.jhep.2019.09.029. Epub 2019 Oct 10.
6
The fungal mycobiome promotes pancreatic oncogenesis via activation of MBL.真菌微生物组通过激活 MBL 促进胰腺发生癌变。
Nature. 2019 Oct;574(7777):264-267. doi: 10.1038/s41586-019-1608-2. Epub 2019 Oct 2.
7
Gene-diet interactions associated with complex trait variation in an advanced intercross outbred mouse line.基因-饮食相互作用与先进的互交近交系小鼠中复杂性状变异相关。
Nat Commun. 2019 Sep 10;10(1):4097. doi: 10.1038/s41467-019-11952-w.
8
Candidalysin Is Required for Neutrophil Recruitment and Virulence During Systemic Candida albicans Infection.白色念珠菌细胞溶素在系统性白色念珠菌感染期间中性粒细胞募集和毒力中是必需的。
J Infect Dis. 2019 Sep 26;220(9):1477-1488. doi: 10.1093/infdis/jiz322.
9
Microbial genes and pathways in inflammatory bowel disease.炎症性肠病中的微生物基因和途径。
Nat Rev Microbiol. 2019 Aug;17(8):497-511. doi: 10.1038/s41579-019-0213-6.
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Intestinal Fungal Dysbiosis and Systemic Immune Response to Fungi in Patients With Alcoholic Hepatitis.酒精性肝炎患者肠道真菌失调与真菌的全身免疫反应。
Hepatology. 2020 Feb;71(2):522-538. doi: 10.1002/hep.30832. Epub 2019 Aug 20.

从出生到生命全程:营养和代谢健康中的真菌微生物组。

From Birth and Throughout Life: Fungal Microbiota in Nutrition and Metabolic Health.

机构信息

Gastroenterology and Hepatology Division, Joan and Sanford I. Weill Department of Medicine; The Jill Roberts Institute for Research in Inflammatory Bowel Disease, Weill Cornell Medicine, Cornell University, New York, NY 10021, USA; email:

Department of Microbiology and Immunology and Immunology and Microbial Pathogenesis Program, Weill Cornell Graduate School of Medical Sciences, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.

出版信息

Annu Rev Nutr. 2020 Sep 23;40:323-343. doi: 10.1146/annurev-nutr-013120-043659. Epub 2020 Jul 17.

DOI:10.1146/annurev-nutr-013120-043659
PMID:32680437
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7529963/
Abstract

The human gastrointestinal tract is home to a vibrant, diverse ecosystem of prokaryotic and eukaryotic microorganisms. The gut fungi (mycobiota) have recently risen to prominence due to their ability to modulate host immunity. Colonization of the gut occurs through a combination of vertical transmission from the maternal mycobiota and environmental and dietary exposure. Data from human and animal studies demonstrate that nutrition strongly affects the mycobiota composition and that changes in the fungal communities can aggravate metabolic diseases. The mechanisms pertaining to the mycobiota's influence on host health, pathology, and resident gastrointestinal communities through intrakingdom, transkingdom, and immune cross talk are beginning to come into focus, setting the stage for a new chapter in microbiota-host interactions. Herein, we examine the inception, maturation, and dietary modulation of gastrointestinal and nutritional fungal communities and inspect their impact on metabolic diseases in humans.

摘要

人类胃肠道是原核生物和真核微生物的一个充满活力且多样化的生态系统。由于其能够调节宿主免疫功能,肠道真菌(真菌群落)最近受到了关注。肠道的定植是通过母体真菌群落的垂直传播以及环境和饮食暴露的共同作用实现的。来自人类和动物研究的数据表明,营养强烈影响真菌群落的组成,而真菌群落的变化可能会加重代谢疾病。有关真菌群落通过种内、种间和免疫串扰对宿主健康、病理学和常驻胃肠道群落的影响的机制开始成为焦点,为微生物群-宿主相互作用的新篇章奠定了基础。在此,我们研究了胃肠道和营养真菌群落的起源、成熟和饮食调节,并检查了它们对人类代谢疾病的影响。