4.5 Article

Hologenomic adaptations underlying the evolution of sanguivory in the common vampire bat

Journal

NATURE ECOLOGY & EVOLUTION
Volume 2, Issue 4, Pages 659-668

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41559-018-0476-8

Keywords

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Funding

  1. Lundbeck Foundation [R52-A5062]
  2. ERC Consolidator Grant [681396]
  3. Danish National Research Foundation [DNRF94]
  4. Deutsche Forschungsgemeinschaft (DFG) [GR 3924/9-1]
  5. Consejo Nacional de Ciencia y Tecnologia (CONACyT)
  6. German Academic Exchange Service (DAAD) [311664]
  7. European Research Council under FP7/ERC [614725-PATHPHYLODYN]
  8. Royal Society
  9. Bing-Mooney Fellowship in Environmental Science and Conservation
  10. US National Science Foundation [DEB-1020966]
  11. Sir Henry Dale Fellowship - Wellcome Trust [102507/Z/13/Z]
  12. Sir Henry Dale Fellowship - Royal Society [102507/Z/13/Z]
  13. Stanford Woods Institute for the Environment Environmental Venture Project
  14. MRC [MC_UU_12014/8] Funding Source: UKRI

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Adaptation to specialized diets often requires modifications at both genomic and microbiome levels. We applied a hologenomic approach to the common vampire bat (Desmodus rotundus), one of the only three obligate blood-feeding (sanguivorous) mammals, to study the evolution of its complex dietary adaptation. Specifically, we assembled its high-quality reference genome (scaffold N50 = 26.9 Mb, contig N50 = 36.6 kb) and gut metagenome, and compared them against those of insectivorous, frugivorous and carnivorous bats. Our analyses showed a particular common vampire bat genomic landscape regarding integrated viral elements, a dietary and phylogenetic influence on gut microbiome taxonomic and functional profiles, and that both genetic elements harbour key traits related to the nutritional (for example, vitamin and lipid shortage) and non-nutritional (for example, nitrogen waste and osmotic homeostasis) challenges of sanguivory. These findings highlight the value of a holistic study of both the host and its microbiota when attempting to decipher adaptations underlying radical dietary lifestyles.

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