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体外感染模型研究真菌-宿主相互作用。

In vitro infection models to study fungal-host interactions.

机构信息

Department of Microbial Pathogenicity Mechanisms, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute, Beutenbergstrasse 11a, 07745, Jena, Germany.

Center for Sepsis Control and Care (CSCC), Jena University Hospital, Am Klinikum 1, 07747, Jena, Germany.

出版信息

FEMS Microbiol Rev. 2021 Sep 8;45(5). doi: 10.1093/femsre/fuab005.

DOI:10.1093/femsre/fuab005
PMID:33524102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8498566/
Abstract

Fungal infections (mycoses) affect over a billion people per year. Approximately, two million of these infections are life-threatening, especially for patients with a compromised immune system. Fungi of the genera Aspergillus, Candida, Histoplasma and Cryptococcus are opportunistic pathogens that contribute to a substantial number of mycoses. To optimize the diagnosis and treatment of mycoses, we need to understand the complex fungal-host interplay during pathogenesis, the fungal attributes causing virulence and how the host resists infection via immunological defenses. In vitro models can be used to mimic fungal infections of various tissues and organs and the corresponding immune responses at near-physiological conditions. Furthermore, models can include fungal interactions with the host-microbiota to mimic the in vivo situation on skin and mucosal surfaces. This article reviews currently used in vitro models of fungal infections ranging from cell monolayers to microfluidic 3D organ-on-chip (OOC) platforms. We also discuss how OOC models can expand the toolbox for investigating interactions of fungi and their human hosts in the future.

摘要

真菌感染(真菌病)每年影响超过 10 亿人。其中,约有 200 万人的感染是危及生命的,尤其是对免疫系统受损的患者。曲霉属、假丝酵母属、组织胞浆菌属和隐球菌属等真菌是机会致病菌,它们导致了大量的真菌病。为了优化真菌病的诊断和治疗,我们需要了解发病机制过程中复杂的真菌-宿主相互作用、导致毒力的真菌特性以及宿主如何通过免疫防御来抵抗感染。体外模型可用于模拟各种组织和器官的真菌感染以及相应的免疫反应,接近生理条件。此外,模型还可以包括真菌与宿主微生物群的相互作用,以模拟皮肤和粘膜表面的体内情况。本文综述了目前用于真菌感染的体外模型,从单层细胞到微流控 3D 器官芯片(OOC)平台。我们还讨论了 OOC 模型如何在未来扩展研究真菌与其人类宿主相互作用的工具包。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff97/8498566/70eefa3d9edd/fuab005fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff97/8498566/f8f22bfd380c/fuab005fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff97/8498566/70eefa3d9edd/fuab005fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff97/8498566/f8f22bfd380c/fuab005fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff97/8498566/70eefa3d9edd/fuab005fig2.jpg

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T cell immunity to commensal fungi.T 细胞对共生真菌的免疫。
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Survival Strategies of Pathogenic Species in Human Blood Show Independent and Specific Adaptations.致病物种在人类血液中的生存策略表现出独立和特定的适应性。
mBio. 2020 Oct 6;11(5):e02435-20. doi: 10.1128/mBio.02435-20.
3
Lysosome Fusion Maintains Phagosome Integrity during Fungal Infection.溶酶体融合在真菌感染过程中维持吞噬体的完整性。
DMEM和EMEM是合适的替代培养基,可用于模拟宿主环境并利用工具扩展钩端螺旋体发病机制研究。
bioRxiv. 2025 Jan 24:2025.01.22.634353. doi: 10.1101/2025.01.22.634353.
4
Integrated multi-omics identifies pathways governing interspecies interaction between A. fumigatus and K. pneumoniae.整合多组学鉴定了烟曲霉和肺炎克雷伯菌种间相互作用的调控途径。
Commun Biol. 2024 Nov 12;7(1):1496. doi: 10.1038/s42003-024-07145-x.
5
Shining a light on -induced epithelial damage with a luciferase reporter.用荧光素酶报告基因观察光诱导的上皮损伤。
mSphere. 2024 Nov 21;9(11):e0050924. doi: 10.1128/msphere.00509-24. Epub 2024 Oct 16.
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Candida albicans translocation through the intestinal epithelial barrier is promoted by fungal zinc acquisition and limited by NFκB-mediated barrier protection.白色念珠菌通过肠道上皮屏障的易位是由真菌锌的摄取所促进的,同时受到 NFκB 介导的屏障保护的限制。
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