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班氏巴贝斯虫,一种用于研究红细胞内寄生和新型抗寄生虫治疗策略的模式生物。

Babesia duncani, a Model Organism for Investigating Intraerythrocytic Parasitism and Novel Antiparasitic Therapeutic Strategies.

机构信息

Department of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, Connecticut, USA.

Department of Microbial Pathogenesis, Yale School of Medicine, New Haven, Connecticut, USA.

出版信息

J Infect Dis. 2024 Jul 25;230(1):263-270. doi: 10.1093/infdis/jiae191.

DOI:10.1093/infdis/jiae191
PMID:39052743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11272067/
Abstract

Pathogens such as Plasmodium, Babesia, and Theileria invade and multiply within host red blood cells, leading to the pathological consequences of malaria, babesiosis, and theileriosis. Establishing continuous in vitro culture systems and suitable animal models is crucial for studying these pathogens. This review spotlights the Babesia duncani in culture-in mouse (ICIM) model as a promising resource for advancing research on the biology, pathogenicity, and virulence of intraerythrocytic parasites. The model offers practical benefits, encompassing well-defined culture conditions, ease of manipulation, and a well-annotated genome. Moreover, B. duncani serves as a surrogate system for drug discovery, facilitating the evaluation of new antiparasitic drugs in vitro and in animals, elucidating their modes of action, and uncovering potential resistance mechanisms. The B. duncani ICIM model thus emerges as a multifaceted tool with profound implications, promising advancements in our understanding of parasitic biology and shaping the development of future therapies.

摘要

疟原虫、巴贝虫和泰勒虫等病原体在宿主的红细胞内入侵和繁殖,导致疟疾、巴贝斯虫病和泰勒虫病等病理后果。建立连续的体外培养系统和合适的动物模型对于研究这些病原体至关重要。本文重点介绍了在培养的鼠疟原虫(ICIM)模型中,巴贝虫属作为一种有前途的资源,可用于推进对红细胞内寄生虫的生物学、致病性和毒力的研究。该模型具有实际的优势,包括明确的培养条件、易于操作和注释良好的基因组。此外,巴贝虫属还可以作为药物发现的替代系统,便于在体外和动物中评估新的抗寄生虫药物,阐明其作用机制,并揭示潜在的耐药机制。因此,巴贝虫属 ICIM 模型是一种多方面的工具,具有深远的意义,有望增进我们对寄生虫生物学的理解,并为未来疗法的发展奠定基础。

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引用本文的文献

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本文引用的文献

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Tafenoquine-Atovaquone Combination Achieves Radical Cure and Confers Sterile Immunity in Experimental Models of Human Babesiosis.他非诺喹-阿托伐醌联合用药在人类巴贝斯虫病实验模型中实现了根治并赋予了无菌免疫。
J Infect Dis. 2024 Jan 12;229(1):161-172. doi: 10.1093/infdis/jiad315.
2
Babesia BdFE1 esterase is required for the anti-parasitic activity of the ACE inhibitor fosinopril.疟原虫 BdFE1 酯酶对于 ACE 抑制剂福辛普利的抗寄生虫活性是必需的。
J Biol Chem. 2023 Nov;299(11):105313. doi: 10.1016/j.jbc.2023.105313. Epub 2023 Oct 4.
3
Babesia duncani multi-omics identifies virulence factors and drug targets.班氏巴贝斯虫多组学鉴定毒力因子和药物靶点。
Nat Microbiol. 2023 May;8(5):845-859. doi: 10.1038/s41564-023-01360-8. Epub 2023 Apr 13.
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Continuous In Vitro Culture of in a Serum-Free Medium.无血清培养基中 的连续体外培养。
Cells. 2023 Feb 2;12(3):482. doi: 10.3390/cells12030482.
5
in Culture and in Mouse (ICIM) Model for the Advancement of Biology, Pathogenesis, and Therapy.用于生物学、发病机制和治疗进展的培养与小鼠(ICIM)模型
Bio Protoc. 2022 Nov 20;12(22). doi: 10.21769/BioProtoc.4549.
6
Development and Optimization of a Selective Whole-Genome Amplification To Study Plasmodium ovale Spp.开发和优化选择性全基因组扩增技术以研究卵形疟原虫 spp.
Microbiol Spectr. 2022 Oct 26;10(5):e0072622. doi: 10.1128/spectrum.00726-22. Epub 2022 Sep 13.
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