Videvall Elin, Cornwallis Charlie K, Palinauskas Vaidas, Valkiūnas Gediminas, Hellgren Olof
Department of Biology, Lund University, Lund, Sweden
Department of Biology, Lund University, Lund, Sweden.
Mol Biol Evol. 2015 May;32(5):1255-67. doi: 10.1093/molbev/msv016. Epub 2015 Jan 29.
Malaria parasites are highly virulent pathogens which infect a wide range of vertebrates. Despite their importance, the way different hosts control and suppress malaria infections remains poorly understood. With recent developments in next-generation sequencing techniques, however, it is now possible to quantify the response of the entire transcriptome to infections. We experimentally infected Eurasian siskins (Carduelis spinus) with avian malaria parasites (Plasmodium ashfordi), and used high-throughput RNA-sequencing to measure the avian transcriptome in blood collected before infection (day 0), during peak parasitemia (day 21 postinfection), and when parasitemia was decreasing (day 31). We found considerable differences in the transcriptomes of infected and uninfected individuals, with a large number of genes differentially expressed during both peak and decreasing parasitemia stages. These genes were overrepresented among functions involved in the immune system, stress response, cell death regulation, metabolism, and telomerase activity. Comparative analyses of the differentially expressed genes in our study to those found in other hosts of malaria (human and mouse) revealed a set of genes that are potentially involved in highly conserved evolutionary responses to malaria infection. By using RNA-sequencing we gained a more complete view of the host response, and were able to pinpoint not only well-documented host genes but also unannotated genes with clear significance during infection, such as microRNAs. This study shows how the avian blood transcriptome shifts in response to malaria infection, and we believe that it will facilitate further research into the diversity of molecular mechanisms that hosts utilize to fight malaria infections.
疟原虫是极具毒性的病原体,可感染多种脊椎动物。尽管它们很重要,但不同宿主控制和抑制疟疾感染的方式仍知之甚少。然而,随着下一代测序技术的最新发展,现在有可能量化整个转录组对感染的反应。我们用禽疟原虫(阿什福德疟原虫)对欧亚金翅雀(黄雀)进行实验性感染,并使用高通量RNA测序来测量在感染前(第0天)、寄生虫血症高峰期(感染后第21天)以及寄生虫血症下降时(第31天)采集的血液中的鸟类转录组。我们发现感染和未感染个体的转录组存在显著差异,在寄生虫血症高峰期和下降期都有大量基因差异表达。这些基因在免疫系统、应激反应、细胞死亡调控、代谢和端粒酶活性等功能中占比过高。将我们研究中差异表达的基因与在其他疟疾宿主(人类和小鼠)中发现的基因进行比较分析,揭示了一组可能参与对疟疾感染高度保守的进化反应的基因。通过使用RNA测序,我们对宿主反应有了更全面的了解,不仅能够确定有充分记录的宿主基因,还能确定在感染过程中具有明确意义的未注释基因,如微小RNA。这项研究展示了鸟类血液转录组如何因疟疾感染而发生变化,我们相信它将有助于进一步研究宿主对抗疟疾感染所利用的分子机制的多样性。