4.8 Article

Diversification of mammalian deltaviruses by host shifting

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2019907118

关键词

satellite virus; hepatitis delta virus; zoonosis; host shifting

资金

  1. Wellcome Trust [102507/Z/13/A, 102507/Z/13/Z]
  2. Human Frontier Science Program [RGP0013/2018]
  3. Medical Research Council [MC_UU_12014/12]
  4. NSF [DEB-1601052]
  5. Achievement Rewards for College Scientists Foundation
  6. Sigma Xi
  7. Animal Behavior Society
  8. Bat Conservation International
  9. American Society of Mammalogists
  10. Odum School of Ecology
  11. University of Georgia (UGA) Graduate School
  12. UGA Latin American and Caribbean Studies Institute
  13. UGA Biomedical and Health Sciences Institute
  14. Explorers Club
  15. Wellcome Trust [102507/Z/13/A, 102507/Z/13/Z] Funding Source: Wellcome Trust
  16. MRC [MC_UU_12014/12, MC_UU_12014/2] Funding Source: UKRI

向作者/读者索取更多资源

Research shows that deltaviruses diversify by transmitting between different mammalian species, with a recent diversification indicated within the Americas. Both bat and rodent-infecting deltaviruses were paraphyletic, and co-evolutionary modeling rejected cospeciation with mammalian hosts. A two-year field study revealed multiple introductions of divergent deltaviruses to common vampire bats in Peru, illustrating horizontal transmission within and between species.
Hepatitis delta virus (HDV) is an unusual RNA agent that replicates using host machinery but exploits hepatitis B virus (HBV) to mobilize its spread within and between hosts. In doing so, HDV enhances the virulence of HBV. How this seemingly improbable hyperparasitic lifestyle emerged is unknown, but it underpins the likelihood that HDV and related deltaviruses may alter other host-virus interactions. Here, we show that deltaviruses diversify by transmitting between mammalian species. Among 96,695 RNA sequence datasets, deltaviruses infected bats, rodents, and an artiodactyl from the Americas but were absent from geographically overrepresented Old World representatives of each mammalian order, suggesting a relatively recent diversification within the Americas. Consistent with diversification by host shifting, both bat and rodent-infecting deltaviruses were paraphyletic, and co-evolutionary modeling rejected cospeciation with mammalian hosts. In addition, a 2-y field study showed common vampire bats in Peru were infected by two divergent deltaviruses, indicating multiple introductions to a single host species. One vampire bat-associated deltavirus was detected in the saliva of up to 35% of individuals, formed phylogeographically compartmentalized clades, and infected a sympatric bat, illustrating horizontal transmission within and between species on ecological timescales. Consistent absence of HBV-like viruses in two deltavirus-infected bat species indicated acquisitions of novel viral associations during the divergence of bat and human-infecting deltaviruses. Our analyses support an American zoonotic origin of HDV and reveal prospects for future cross-species emergence of deltaviruses. Given their peculiar life history, deltavirus host shifts will have different constraints and disease outcomes compared to ordinary animal pathogens.

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