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一种用于隐孢子虫的细胞培养平台,能够进行长期培养,并为系统研究其生物学特性提供新工具。

A cell culture platform for Cryptosporidium that enables long-term cultivation and new tools for the systematic investigation of its biology.

机构信息

Laboratory of Molecular & Evolutionary Parasitology, RAPID Group, School of Biosciences, University of Kent, Canterbury, UK; School of Biosciences, University of Kent, Canterbury, UK.

Laboratory of Molecular & Evolutionary Parasitology, RAPID Group, School of Biosciences, University of Kent, Canterbury, UK; School of Biosciences, University of Kent, Canterbury, UK; Industrial Biotechnology Centre, School of Biosciences, University of Kent, Canterbury, UK.

出版信息

Int J Parasitol. 2018 Mar;48(3-4):197-201. doi: 10.1016/j.ijpara.2017.10.001. Epub 2017 Nov 28.

Abstract

Cryptosporidium parasites are a major cause of diarrhoea that pose a particular threat to children in developing areas and immunocompromised individuals. Curative therapies and vaccines are lacking, mainly due to lack of a long-term culturing system of this parasite. Here, we show that COLO-680N cells infected with two different Cryptosporidium parvum strains produce sufficient infectious oocysts to infect subsequent cultures, showing a substantial fold increase in production, depending on the experiment, over the most optimistic HCT-8 models. Oocyst identity was confirmed using a variety of microscopic- and molecular-based methods. This culturing system will accelerate research on Cryptosporidium and the development of anti-Cryptosporidium drugs.

摘要

隐孢子虫寄生虫是导致腹泻的主要原因,对发展中地区的儿童和免疫功能低下的个体构成特别威胁。目前缺乏有效的治疗方法和疫苗,主要是因为缺乏长期培养这种寄生虫的系统。在这里,我们展示了感染两种不同的微小隐孢子虫(Cryptosporidium parvum)株的 COLO-680N 细胞能够产生足够数量的感染性卵囊来感染后续的培养物,在实验中,与最乐观的 HCT-8 模型相比,产量显著增加,增加幅度取决于实验情况。通过多种基于显微镜和分子的方法确认了卵囊的身份。这种培养系统将加速对隐孢子虫的研究和抗隐孢子虫药物的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4da/5854368/acf0eacd86f8/fx1.jpg

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