» Articles » PMID: 28636590

Host and Viral Traits Predict Zoonotic Spillover from Mammals

Overview
Journal Nature
Specialty Science
Date 2017 Jun 22
PMID 28636590
Citations 475
Authors
Affiliations
Soon will be listed here.
Abstract

The majority of human emerging infectious diseases are zoonotic, with viruses that originate in wild mammals of particular concern (for example, HIV, Ebola and SARS). Understanding patterns of viral diversity in wildlife and determinants of successful cross-species transmission, or spillover, are therefore key goals for pandemic surveillance programs. However, few analytical tools exist to identify which host species are likely to harbour the next human virus, or which viruses can cross species boundaries. Here we conduct a comprehensive analysis of mammalian host-virus relationships and show that both the total number of viruses that infect a given species and the proportion likely to be zoonotic are predictable. After controlling for research effort, the proportion of zoonotic viruses per species is predicted by phylogenetic relatedness to humans, host taxonomy and human population within a species range-which may reflect human-wildlife contact. We demonstrate that bats harbour a significantly higher proportion of zoonotic viruses than all other mammalian orders. We also identify the taxa and geographic regions with the largest estimated number of 'missing viruses' and 'missing zoonoses' and therefore of highest value for future surveillance. We then show that phylogenetic host breadth and other viral traits are significant predictors of zoonotic potential, providing a novel framework to assess if a newly discovered mammalian virus could infect people.

Citing Articles

Host ecology and phylogeny shape the temporal dynamics of social bee viromes.

Doublet V, Doyle T, Carvell C, Brown M, Wilfert L Nat Commun. 2025; 16(1):2207.

PMID: 40044660 PMC: 11882784. DOI: 10.1038/s41467-025-57314-7.


Understanding ecological systems using knowledge graphs: an application to highly pathogenic avian influenza.

Robertson H, Han B, Castellanos A, Rosado D, Stott G, Zimmerman R Bioinform Adv. 2025; 5(1):vbaf016.

PMID: 40041112 PMC: 11879169. DOI: 10.1093/bioadv/vbaf016.


Translational lessons from the balanced immune system in bats.

Ng W, Wang L Dis Model Mech. 2025; 18(9).

PMID: 39968756 PMC: 11876839. DOI: 10.1242/dmm.050763.


Bat genomes illuminate adaptations to viral tolerance and disease resistance.

Morales A, Dong Y, Brown T, Baid K, Kontopoulos D, Gonzalez V Nature. 2025; 638(8050):449-458.

PMID: 39880942 PMC: 11821529. DOI: 10.1038/s41586-024-08471-0.


Domestic Dogs Exposed to Orthopoxvirus in Urban Areas of Brazil.

de Meneses D, Stoffella-Dutra A, Blaso V, de Almeida I, Dias K, Domingos I Viruses. 2025; 17(1).

PMID: 39861920 PMC: 11768714. DOI: 10.3390/v17010131.


References
1.
Luis A, Hayman D, OShea T, Cryan P, Gilbert A, Pulliam J . A comparison of bats and rodents as reservoirs of zoonotic viruses: are bats special?. Proc Biol Sci. 2013; 280(1756):20122753. PMC: 3574368. DOI: 10.1098/rspb.2012.2753. View

2.
Woolhouse M, Haydon D, Antia R . Emerging pathogens: the epidemiology and evolution of species jumps. Trends Ecol Evol. 2006; 20(5):238-44. PMC: 7119200. DOI: 10.1016/j.tree.2005.02.009. View

3.
Brierley L, Vonhof M, Olival K, Daszak P, Jones K . Quantifying Global Drivers of Zoonotic Bat Viruses: A Process-Based Perspective. Am Nat. 2016; 187(2):E53-64. PMC: 9516484. DOI: 10.1086/684391. View

4.
Poulin R, Krasnov B, Mouillot D . Host specificity in phylogenetic and geographic space. Trends Parasitol. 2011; 27(8):355-61. DOI: 10.1016/j.pt.2011.05.003. View

5.
Pulliam J, Dushoff J . Ability to replicate in the cytoplasm predicts zoonotic transmission of livestock viruses. J Infect Dis. 2009; 199(4):565-8. PMC: 7110041. DOI: 10.1086/596510. View