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Mol Biol Evol. 2015 May;32(5):1255-67. doi: 10.1093/molbev/msv016. Epub 2015 Jan 29.

The avian transcriptome response to malaria infection.

Author information

1
Department of Biology, Lund University, Lund, Sweden elin.videvall@biol.lu.se olof.hellgren@biol.lu.se.
2
Department of Biology, Lund University, Lund, Sweden.
3
Institute of Ecology, Nature Research Centre, Vilnius, Lithuania.

Abstract

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.

KEYWORDS:

Plasmodium; RNA-seq; experimental infection; host response; immune defense; transcriptome

PMID:
25636457
PMCID:
PMC4408411
DOI:
10.1093/molbev/msv016
[Indexed for MEDLINE]
Free PMC Article

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