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鸟类血孢子虫的激光显微切割显微镜技术与单细胞聚合酶链反应

Laser microdissection microscopy and single cell PCR of avian hemosporidians.

作者信息

Palinauskas Vaidas, Dolnik Olga V, Valkiūnas Gediminas, Bensch Staffan

机构信息

Institute of Ecology, Vilnius University, Vilnius, Lithuania.

出版信息

J Parasitol. 2010 Apr;96(2):420-4. doi: 10.1645/GE-2247.1.

Abstract

Avian malaria parasites (Plasmodium spp.) and related species of Haemoproteus constitute a remarkably diverse and species rich group of blood parasites. Analyses of the mitochondrial cytochrome b gene of these hemosporidians have demonstrated unexpected patterns of host distribution, host shifts, and host sharing. However, deeper insights into these patterns require access to multiple genetic markers and genetic analyses of single parasite cells. In the present study, we demonstrate the potential of laser microdissection microscopy (Olympus/MMI CellCut microdissection system) for solving these 2 problems. This technique was used for isolation of single blood stages and ookinetes of avian Haemoproteus and Plasmodium spp., which were then successfully used for DNA isolation, amplification, and sequencing. The methods of single cell dissection of hemosporidian parasites and PCR-based analyses with dissected single cells are described. These methods can be used to isolate substantial quantities of pure hemosporidian parasite DNA for large-scale sequencing, essential information when designing primers for developing multiple nuclear genetic markers. Such markers can then be applied to isolated single parasite cells for identification of parasites in mixed infections and deciphering mechanisms behind apparent reproductive isolation between parasite lineages. This method can be used in the molecular investigation of blood parasites of birds, reptiles, and fish because it enables removing the parasite DNA from the overpowering host DNA, which is present in red blood cells.

摘要

禽类疟原虫(疟原虫属)和血变原虫的相关物种构成了一组极为多样且物种丰富的血液寄生虫。对这些血孢子虫线粒体细胞色素b基因的分析揭示了宿主分布、宿主转移和宿主共享的意外模式。然而,要更深入地了解这些模式,需要获取多个遗传标记并对单个寄生虫细胞进行遗传分析。在本研究中,我们展示了激光显微切割显微镜(奥林巴斯/MMI CellCut显微切割系统)解决这两个问题的潜力。该技术用于分离禽类血变原虫和疟原虫属的单个血液阶段和动合子,随后成功用于DNA分离、扩增和测序。描述了血孢子虫寄生虫的单细胞切割方法以及基于PCR的切割后单个细胞的分析方法。这些方法可用于分离大量纯血孢子虫寄生虫DNA以进行大规模测序,这是设计用于开发多个核遗传标记的引物时的重要信息。然后,此类标记可应用于分离的单个寄生虫细胞,以鉴定混合感染中的寄生虫,并解读寄生虫谱系之间明显生殖隔离背后的机制。该方法可用于鸟类、爬行动物和鱼类血液寄生虫的分子研究,因为它能够从红细胞中占主导地位的宿主DNA中去除寄生虫DNA。

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