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基于干细胞的平台可实现体外完整隐孢子虫发育和遗传操作性。

A Stem-Cell-Derived Platform Enables Complete Cryptosporidium Development In Vitro and Genetic Tractability.

机构信息

Department of Molecular Microbiology, Washington University School of Medicine, 660 S. Euclid Ave, St Louis, MO 63130, USA.

Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Ave, St Louis, MO 63130, USA.

出版信息

Cell Host Microbe. 2019 Jul 10;26(1):123-134.e8. doi: 10.1016/j.chom.2019.05.007. Epub 2019 Jun 20.

Abstract

Despite being a frequent cause of severe diarrheal disease in infants and an opportunistic infection in immunocompromised patients, Cryptosporidium research has lagged due to a lack of facile experimental methods. Here, we describe a platform for complete life cycle development and long-term growth of C. parvum in vitro using "air-liquid interface" (ALI) cultures derived from intestinal epithelial stem cells. Transcriptomic profiling revealed that differentiating epithelial cells grown under ALI conditions undergo profound changes in metabolism and development that enable completion of the parasite life cycle in vitro. ALI cultures support parasite expansion > 100-fold and generate viable oocysts that are transmissible in vitro and to mice, causing infection and animal death. Transgenic parasite lines created using CRISPR/Cas9 were used to complete a genetic cross in vitro, demonstrating Mendelian segregation of chromosomes during meiosis. ALI culture provides an accessible model that will enable innovative studies into Cryptosporidium biology and host interactions.

摘要

尽管隐孢子虫是导致婴儿严重腹泻病的常见原因,也是免疫功能低下患者的机会性感染,但由于缺乏简便的实验方法,其研究进展缓慢。在这里,我们描述了一种使用源自肠上皮干细胞的“气液界面”(ALI)培养物在体外进行完整生命周期发育和长期生长的平台。转录组分析显示,在 ALI 条件下分化的上皮细胞在代谢和发育方面发生了深刻的变化,从而使寄生虫在体外完成生命周期。ALI 培养物支持寄生虫扩增超过 100 倍,并产生有活力的卵囊,可在体外和小鼠体内传播,导致感染和动物死亡。使用 CRISPR/Cas9 构建的转基因寄生虫系被用于在体外完成遗传杂交,证明减数分裂过程中染色体的孟德尔分离。ALI 培养物提供了一种易于接近的模型,将能够对隐孢子虫生物学和宿主相互作用进行创新性研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df14/6617391/491f4c41cf9b/fx1.jpg

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