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肺孢子菌肺炎的遗传小鼠模型。

Genetic Mouse Models of Pneumocystis Pneumonia.

机构信息

AFRICA CMM Medical Mycology Research Unit, Institute of Infectious Disease and Molecular Medicine (IDM), Cape Town, South Africa.

Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

出版信息

Methods Mol Biol. 2023;2667:169-179. doi: 10.1007/978-1-0716-3199-7_13.

DOI:10.1007/978-1-0716-3199-7_13
PMID:37145284
Abstract

Pneumocystis jirovecii causes pneumonia in immunocompromised patients. A major challenge in drug susceptibility testing and in understanding host/pathogen interactions is that Pneumocystis spp. are not viable in vitro. Continuous culture of the organism is not currently available, and therefore, developing new drug targets is very limited. Due to this limitation, mouse models of Pneumocystis pneumonia have proven to be an invaluable resource to researchers. In this chapter, we provide an overview of selected methods used in mouse models of infection including, in vivo Pneumocystis murina propagation, routes of transmission, genetic mouse models available, a P. murina life form-specific model, a mouse model of PCP immune reconstitution inflammatory syndrome (IRIS), and the experimental parameters associated with these models.

摘要

肺孢子菌引起免疫功能低下患者的肺炎。药物敏感性测试和了解宿主/病原体相互作用的主要挑战是,肺孢子菌在体外不可存活。该生物的连续培养目前不可用,因此,新的药物靶点的开发非常有限。由于这一限制,肺孢子菌肺炎的小鼠模型已被证明是研究人员非常宝贵的资源。在本章中,我们提供了感染小鼠模型中使用的选定方法的概述,包括体内传播、传播途径、现有的遗传小鼠模型、肺孢子菌生活形态特异性模型、PCP 免疫重建炎症综合征 (IRIS) 的小鼠模型,以及与这些模型相关的实验参数。

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本文引用的文献

1
Pneumonia: Pitfalls and Hindrances to Establishing a Reliable Animal Model.肺炎:建立可靠动物模型的陷阱与障碍
J Fungi (Basel). 2022 Jan 27;8(2):129. doi: 10.3390/jof8020129.
2
The Persistent Challenge of Pneumocystis Growth Outside the Mammalian Lung: Past and Future Approaches.肺孢子菌在哺乳动物肺外生长的持续挑战:过去与未来的研究方法
Front Microbiol. 2021 May 20;12:681474. doi: 10.3389/fmicb.2021.681474. eCollection 2021.
3
The trophic life cycle stage of Pneumocystis species induces protective adaptive responses without inflammation-mediated progression to pneumonia.
肺孢子菌属的营养生命周期阶段可诱导保护性适应性反应,而不会因炎症介导发展为肺炎。
Med Mycol. 2018 Nov 1;56(8):994-1005. doi: 10.1093/mmy/myx145.
4
Genome analysis of three Pneumocystis species reveals adaptation mechanisms to life exclusively in mammalian hosts.对三种肺孢子菌的基因组分析揭示了其仅在哺乳动物宿主中生存的适应机制。
Nat Commun. 2016 Feb 22;7:10740. doi: 10.1038/ncomms10740.
5
B Lymphocytes Are Required during the Early Priming of CD4+ T Cells for Clearance of Pneumocystis Infection in Mice.清除小鼠肺孢子菌感染时,CD4+ T细胞早期启动阶段需要B淋巴细胞。
J Immunol. 2015 Jul 15;195(2):611-20. doi: 10.4049/jimmunol.1500112. Epub 2015 Jun 3.
6
Eosinophils Contribute to Early Clearance of Pneumocystis murina Infection.嗜酸性粒细胞有助于早期清除鼠肺孢子菌感染。
J Immunol. 2015 Jul 1;195(1):185-93. doi: 10.4049/jimmunol.1403162. Epub 2015 May 20.
7
Novel pneumocystis antigen discovery using fungal surface proteomics.利用真菌表面蛋白质组学发现新型肺孢子菌抗原。
Infect Immun. 2014 Jun;82(6):2417-23. doi: 10.1128/IAI.01678-13. Epub 2014 Mar 31.
8
Dectin immunoadhesins and pneumocystis pneumonia.Dectin 免疫黏附素与肺孢子菌肺炎。
Infect Immun. 2013 Sep;81(9):3451-62. doi: 10.1128/IAI.00136-13. Epub 2013 Jul 8.
9
Characterization of a distinct host response profile to Pneumocystis murina asci during clearance of pneumocystis pneumonia.在清除卡氏肺孢子虫肺炎期间,对卡氏肺孢子虫囊包体的独特宿主反应谱进行了表征。
Infect Immun. 2013 Mar;81(3):984-95. doi: 10.1128/IAI.01181-12. Epub 2013 Jan 14.
10
Memory CD4+ T cells are required for optimal NK cell effector functions against the opportunistic fungal pathogen Pneumocystis murina.记忆性 CD4+ T 细胞对于 NK 细胞针对机会性真菌病原体鼠肺囊虫发挥最佳效应功能是必需的。
J Immunol. 2013 Jan 1;190(1):285-95. doi: 10.4049/jimmunol.1200861. Epub 2012 Nov 30.