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组织培养中弓形虫的维持:一种培养RH速殖子的新有效方法。

Toxoplasma gondii maintenance in tissue culture: a new efficient method for culturing RH tachyzoites.

作者信息

Noriega F R, Hauser W E

机构信息

Evans Memorial Department for Clinical Research, Boston University Medical Center, Massachusetts 02118.

出版信息

J Parasitol. 1988 Jun;74(3):495-9.

PMID:3379531
Abstract

We describe here a new tissue culture method for prolonged laboratory maintenance of tachyzoites of the highly virulent RH strain of Toxoplasma gondii. Using a rapidly proliferating murine tumor cell line (YAC-1), the method described is easy to perform and is as or more efficient (both in terms of yield and cost) than other traditional methods for maintenance of the parasite. Furthermore, upon prolonged maintenance (greater than 160 days) in YAC-1 tissue culture, the pathogenicity of the parasite, as well as its capacity to elicit an immune response, are comparable to that of organisms maintained in mice. We conclude therefore, that the method described herein is a suitable alternative to the traditional method of maintenance of virulent RH strain T. gondii tachyzoites.

摘要

我们在此描述一种新的组织培养方法,用于在实验室中长期维持高毒力的刚地弓形虫RH株速殖子。使用快速增殖的鼠肿瘤细胞系(YAC-1),所述方法易于操作,并且在产量和成本方面与其他传统的寄生虫维持方法一样高效或更高效。此外,在YAC-1组织培养中长时间维持(超过160天)后,该寄生虫的致病性及其引发免疫反应的能力与在小鼠体内维持的生物体相当。因此,我们得出结论,本文所述方法是维持强毒RH株刚地弓形虫速殖子传统方法的合适替代方法。

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