4.7 Article

Metatranscriptomics yields new genomic resources and sensitive detection of infections for diverse blood parasites

期刊

MOLECULAR ECOLOGY RESOURCES
卷 20, 期 1, 页码 14-28

出版社

WILEY
DOI: 10.1111/1755-0998.13091

关键词

co-infection; Leucocytozoon; malaria parasite; Parahaemoproteus; Plasmodium; RNA-seq

资金

  1. American Museum of Natural History
  2. National Institutes of Health [1R03AI117223-01A1]
  3. Division of Biological Infrastructure [1811806]
  4. Federal Bureau of Land Management Rio Puerco Field Office
  5. New Mexico Ornithological Society
  6. Society of Systematic Biologists
  7. Explorers Club
  8. Richard Gilder Graduate Scool
  9. Div Of Biological Infrastructure
  10. Direct For Biological Sciences [1811806] Funding Source: National Science Foundation

向作者/读者索取更多资源

Metatranscriptomics is a powerful method for studying the composition and function of complex microbial communities. The application of metatranscriptomics to multispecies parasite infections is of particular interest, as research on parasite evolution and diversification has been hampered by technical challenges to genome-scale DNA sequencing. In particular, blood parasites of vertebrates are abundant and diverse although they often occur at low infection intensities and exist as multispecies infections, rendering the isolation of genomic sequence data challenging. Here, we use birds and their diverse haemosporidian parasites to illustrate the potential for metatranscriptome sequencing to generate large quantities of genome-wide sequence data from multiple blood parasite species simultaneously. We used RNA-sequencing of 24 blood samples from songbirds in North America to show that metatranscriptomes can yield large proportions of haemosporidian protein-coding gene repertoires even when infections are of low intensity (<0.1% red blood cells infected) and consist of multiple parasite taxa. By bioinformatically separating host and parasite transcripts and assigning them to the haemosporidian genus of origin, we found that transcriptomes detected similar to 23% more total parasite infections across all samples than were identified using microscopy and DNA barcoding. For single-species infections, we obtained data for >1,300 loci from samples with as low as 0.03% parasitaemia, with the number of loci increasing with infection intensity. In total, we provide data for 1,502 single-copy orthologous loci from a phylogenetically diverse set of 33 haemosporidian mitochondrial lineages. The metatranscriptomic approach described here has the potential to accelerate ecological and evolutionary research on haemosporidians and other diverse parasites.

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