首页> 外文期刊>Journal of Parasitology >EVALUATION OF TWO MODIFIED CULTURE MEDIA FOR LEISHMANIA INFANTUM CULTIVATION VERSUS DIFFERENT CULTURE MEDIA
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EVALUATION OF TWO MODIFIED CULTURE MEDIA FOR LEISHMANIA INFANTUM CULTIVATION VERSUS DIFFERENT CULTURE MEDIA

机译:两种改良的利什曼原虫培养相对于不同培养基的培养培养基的评价

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The aim of this study is to improve the cultivation of Leishmania promastigotes without the use of common, semisolid culture media such as Evans' modified Tobie's medium (EMTM), liquid RPMI 1640, and Peptone-yeast extract medium (P-Y). Although EMTM medium permits the growth of a high number of parasites, it is technically difficult to prepare as it requires the use of fresh rabbit blood from animals bred on farms, while RPMI 1640 and P-Y show lower growth rates than the EMTM. There is, therefore, a need to develop new blood-free and time-saving culture systems. The aim of this paper is to propose new modified microbiological media, named RPMI-PY and Tobie-PY, to isolate Leishmania and cultivate parasites for research and diagnostic purposes. This study compares classic culture media to the new media, RPMI-PY and Tobie-PY, and demonstrates that the new media have superior performance in terms of time and parasitic load. The growth rate of the parasite was significantly higher at 24, 48, and 72 hr cultivation, based on counts using Burker's chambers, when compared to classic media. This study was carried out at the National References Centre for Leishmaniasis (C. Re. Na. L.) where the isolation procedures are conducted daily from a number of different biological matrices.
机译:这项研究的目的是在不使用常见的半固体培养基如Evans改良的Tobie培养基(EMTM),液体RPMI 1640和蛋白ept-酵母抽提培养基(P-Y)的情况下改善利什曼原虫前鞭毛体的培养。尽管EMTM培养基允许大量寄生虫生长,但由于需要使用农场中饲养的动物新鲜的兔血,因此在技术上很难制备,而RPMI 1640和P-Y的生长速度低于EMTM。因此,需要开发新的无血和省时的培养系统。本文的目的是提出一种新的改良微生物培养基,分别称为RPMI-PY和Tobie-PY,以分离利什曼原虫并培养用于研究和诊断目的的寄生虫。这项研究将经典文化媒体与新媒体RPMI-PY和Tobie-PY进行了比较,并证明了新媒体在时间和寄生负载方面均具有出色的性能。与传统培养基相比,根据使用伯克氏培养箱进行的计数,在培养24、48和72小时时,寄生虫的生长速度明显更高。这项研究是在利什曼病国家参考中心(C. Re。Na。L.)进行的,每天从许多不同的生物基质中进行分离操作。

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