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Complete development and long-term maintenance of Cryptosporidium parvum human and cattle genotypes in cell culture.在细胞培养中完成微小隐孢子虫人源和牛源基因型的全面发育及长期维持。
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Short report: possible Cryptosporidium muris infection in humans.简短报告:人类可能感染微小隐孢子虫
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Attachment of Cryptosporidium parvum sporozoites to MDCK cells in vitro.微小隐孢子虫子孢子在体外与犬肾细胞(MDCK细胞)的附着。
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微小隐孢子虫在人胃腺癌细胞系中的体外培养

In vitro culture of Cryptosporidium muris in a human stomach adenocarcinoma cell line.

作者信息

Choi Min-Ho, Hong Sung-Tae, Chai Jong-Yil, Park Woo-Yoon, Yu Jae-Ran

机构信息

Department of Parasitology and Tropical Medicine, Institute of Endemic Diseases, Seoul National University College of Medicine, Medical Research Center, Seoul 110-799, Republic of Korea.

出版信息

Korean J Parasitol. 2004 Mar;42(1):27-34. doi: 10.3347/kjp.2004.42.1.27.

DOI:10.3347/kjp.2004.42.1.27
PMID:15060337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2717336/
Abstract

We investigated the optimal culture conditions for Cryptosporidium muris in a human stomach adenocarcinoma (AGS) cell line by determining the effects of medium pH and of selected supplements on the development of C. muris. The optimum pH of the culture medium required for the development of C. muris was determined to be 6.6. The number of parasites significantly increased during cultivation for 72 hr (p < 0.05) at this level. On the other hand, numbers decreased linearly after 24 hr of incubation at pH 7.5. When cultured in different concentrations of serum, C. muris in media containing 5% FBS induced 4-7 times more parasites than in 1% or 10% serum. Of the six medium supplements examined, only 1 mM pyruvate enhanced the number of C. muris in vitro. Transmission electron microscopic observation showed the developmental stages of C. muris in the cytoplasm of the cells, not in an extracytoplasmic location. The growth of C. muris in AGS cells provides a means of investigating its biological characteristics and of testing its response to therapeutic agents. However, a more optimized culture system is needed for the recovery of oocysts on a large scale in vitro.

摘要

我们通过测定培养基pH值和选定添加物对微小隐孢子虫发育的影响,研究了微小隐孢子虫在人胃腺癌细胞系(AGS)中的最佳培养条件。确定微小隐孢子虫发育所需培养基的最佳pH值为6.6。在此pH水平下培养72小时期间,寄生虫数量显著增加(p<0.05)。另一方面,在pH 7.5孵育24小时后,数量呈线性下降。当在不同浓度血清中培养时,含5%胎牛血清(FBS)的培养基中微小隐孢子虫诱导产生的寄生虫数量比含1%或10%血清的培养基多4至7倍。在所检测的六种培养基添加物中,只有1 mM丙酮酸能在体外增加微小隐孢子虫的数量。透射电子显微镜观察显示微小隐孢子虫的发育阶段存在于细胞胞质内,而非胞质外位置。微小隐孢子虫在AGS细胞中的生长为研究其生物学特性和测试其对治疗药物的反应提供了一种方法。然而,需要一个更优化的培养系统以便在体外大规模回收卵囊。