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一种改良的体外诱导疟原虫配子体分化为动合子的方法。

An improved method for the in vitro differentiation of Plasmodium falciparum gametocytes into ookinetes.

机构信息

Johns Hopkins University School of Public Health, Dept. of Molecular Microbiology and Immunology, Malaria Research Institute, Baltimore, MD 21205, USA.

出版信息

Malar J. 2010 Jul 8;9:194. doi: 10.1186/1475-2875-9-194.

Abstract

BACKGROUND

Ookinete is the form of the malaria parasite that invades the mosquito midgut epithelium to initiate sporogony. Differentiation of ingested gametocytes into ookinetes in the mosquito midgut lumen and subsequent interaction with the lumenal surface of the midgut epithelium in preparation for invasion is a complex and multi-stepped process. To facilitate the study of these events in detail it is necessary to produce sufficient numbers of pure, fully mature and functional ookinetes. However, production of even a small number of Plasmodium falciparum ookinetes in vitro has proven to be a daunting task. Consequently, over the past four decades our collective understanding of the biology of this parasite form remains sorely deficient. This article reports on investigations of five different ookinete media, in an effort to improve the in vitro transformation efficiency of P. falciparum gametocytes into mature ookinetes and their infectivity of the mosquito midgut.

METHODS

Five different ookinete media were evaluated for their ability to support the differentiation of gametocytes into gametes and further into mature stage V ookinetes. Moreover, infectivity of the in vitro-transformed ookinetes was evaluated by feeding them to vector mosquitoes and measuring their ability to traverse the midgut and form oocysts.

RESULTS

One of the five media (medium E) was clearly superior in that the cultured ookinetes produced the largest number of oocysts when fed to mosquitoes. Key components were additions of human serum, human red blood cell lysate and mosquito pupal extract, resulting in the production of larger numbers of ookinetes able to develop into oocysts when fed to mosquitoes.

CONCLUSION

This simple and practical improvement over the prevailing methodology will facilitate the investigation of how this important human malaria parasite initiates its development in the mosquito and will contribute to the understanding of its transmission biology.

摘要

背景

动合子是疟原虫侵入蚊子中肠上皮细胞引发孢子增殖的形式。在蚊中肠腔中,摄入的配子体分化为动合子,随后与中肠上皮的腔面相互作用,为入侵做准备,这是一个复杂的多步骤过程。为了详细研究这些事件,有必要产生足够数量的纯、完全成熟和功能的动合子。然而,在体外产生少量的恶性疟原虫动合子已被证明是一项艰巨的任务。因此,在过去的四十年里,我们对这种寄生虫形式的生物学的集体理解仍然严重不足。本文报道了对五种不同动合子培养基的研究,以努力提高恶性疟原虫配子体在体外转化为成熟动合子的效率及其对蚊子中肠的感染力。

方法

评估了五种不同的动合子培养基,以确定它们支持配子体分化为配子体,进一步分化为成熟的第五期动合子的能力。此外,通过喂食媒介蚊子并测量它们穿透中肠和形成卵囊的能力来评估体外转化的动合子的感染力。

结果

五种培养基中的一种(培养基 E)明显更优越,因为培养的动合子在喂食蚊子时产生了最多的卵囊。关键成分是添加人血清、人红细胞裂解物和蚊子蛹提取物,从而产生了更多数量的能够发育成卵囊的动合子,当喂食蚊子时。

结论

与现行方法相比,这种简单实用的改进将促进对这种重要的人类疟原虫如何在蚊子中开始其发育的研究,并有助于理解其传播生物学。

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