4.7 Article

Predicting the zoonotic capacity of mammals to transmit SARS-CoV-2

Journal

Publisher

ROYAL SOC
DOI: 10.1098/rspb.2021.1651

Keywords

COVID-19; ecological traits; zoonotic; spillback; machine learning; structural modelling

Funding

  1. NSF EEID program [DEB 1717282]
  2. DARPA PREEMPT program [D18AC00031]
  3. CREATE-NEO, a member of the NIH NIAID CREID program [1U01 AI151807-01]
  4. NVIDIA Corporation GPU grant program
  5. NSF Polar program [OPP 1935870, 1947040]
  6. NIH NIGMS [R35GM122543]
  7. Directorate For Geosciences
  8. Office of Polar Programs (OPP) [1947040] Funding Source: National Science Foundation

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Transmission of SARS-CoV-2 between humans and animals can lead to establishment of virus reservoirs in wildlife, posing a threat to efforts to control COVID-19 and protect vulnerable animal populations. By combining ecological and biological traits of species with modeling of host-virus interactions using machine learning, predictions about the zoonotic capacity of SARS-CoV-2 for over 5000 mammals were made, revealing enhanced transmission risk from common mammals and geographic overlap with global COVID-19 hotspots.
Back and forth transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) between humans and animals will establish wild reservoirs of virus that endanger long-term efforts to control COVID-19 in people and to protect vulnerable animal populations. Better targeting surveillance and laboratory experiments to validate zoonotic potential requires predicting high-risk host species. A major bottleneck to this effort is the few species with available sequences for angiotensin-converting enzyme 2 receptor, a key receptor required for viral cell entry. We overcome this bottleneck by combining species' ecological and biological traits with three-dimensional modelling of host-virus protein-protein interactions using machine learning. This approach enables predictions about the zoonotic capacity of SARS-CoV-2 for greater than 5000 mammals-an order of magnitude more species than previously possible. Our predictions are strongly corroborated by in vivo studies. The predicted zoonotic capacity and proximity to humans suggest enhanced transmission risk from several common mammals, and priority areas of geographic overlap between these species and global COVID-19 hotspots. With molecular data available for only a small fraction of potential animal hosts, linking data across biological scales offers a conceptual advance that may expand our predictive modelling capacity for zoonotic viruses with similarly unknown host ranges.

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