Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Apr 27;118(17):e2023540118.
doi: 10.1073/pnas.2023540118.

Impacts of biodiversity and biodiversity loss on zoonotic diseases

Affiliations

Impacts of biodiversity and biodiversity loss on zoonotic diseases

Felicia Keesing et al. Proc Natl Acad Sci U S A. .

Abstract

Zoonotic diseases are infectious diseases of humans caused by pathogens that are shared between humans and other vertebrate animals. Previously, pristine natural areas with high biodiversity were seen as likely sources of new zoonotic pathogens, suggesting that biodiversity could have negative impacts on human health. At the same time, biodiversity has been recognized as potentially benefiting human health by reducing the transmission of some pathogens that have already established themselves in human populations. These apparently opposing effects of biodiversity in human health may now be reconcilable. Recent research demonstrates that some taxa are much more likely to be zoonotic hosts than others are, and that these animals often proliferate in human-dominated landscapes, increasing the likelihood of spillover. In less-disturbed areas, however, these zoonotic reservoir hosts are less abundant and nonreservoirs predominate. Thus, biodiversity loss appears to increase the risk of human exposure to both new and established zoonotic pathogens. This new synthesis of the effects of biodiversity on zoonotic diseases presents an opportunity to articulate the next generation of research questions that can inform management and policy. Future studies should focus on collecting and analyzing data on the diversity, abundance, and capacity to transmit of the taxa that actually share zoonotic pathogens with us. To predict and prevent future epidemics, researchers should also focus on how these metrics change in response to human impacts on the environment, and how human behaviors can mitigate these effects. Restoration of biodiversity is an important frontier in the management of zoonotic disease risk.

Keywords: biodiversity; disease; disease ecology; zoonoses; zoonotic disease.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interest.

Figures

Fig. 1.
Fig. 1.
Alternative conceptual models linking host biodiversity to zoonotic emergence in humans. (A) Total host diversity: In this model, the overall diversity of hosts leads to a pool of pathogens, any one of which could jump to humans. Research assuming this model typically involves comparisons of large geographic areas with innate variation in biodiversity (e.g., along latitudinal gradients or between countries). (B) Zoonotic host diversity: In this model, some species are more likely to host zoonotic pathogens, and it is the diversity of these zoonotic hosts that is most important in determining the risk of zoonotic emergence. Research using the zoonotic host diversity model typically focuses on the distribution or characteristics of a particular taxon (e.g., bats or primates). (C) Zoonotic host diversity and abundance: In this model, the diversity and the abundance of zoonotic hosts determine the risk of zoonotic emergence. Research using this model typically focuses on the effects of changes in natural biodiversity (e.g., through human impacts, on zoonotic pathogens). Modified from an illustration in Ostfeld and Keesing (7).
Fig. 2.
Fig. 2.
Relative importance of five major mammalian Orders as hosts of zoonotic viruses based on different metrics. (A) Mean number of viruses per host for all species in the Order. (B) Mean number of viruses per host for species that host at least one virus. (C) Proportion of all species that host at least one virus. (D) Total number of species in the Order that host at least one virus. The variety of metrics used in different studies is a source of confusion in competing claims about taxonomic importance. Plotted from data made available in the supplemental material from Johnson et al. (21); see caveats about these and similar data in SI Appendix.
Fig. 3.
Fig. 3.
Proportion of species in each conservation category for nonhosts, hosts, and superhosts in the five Orders of mammals that host the majority of zoonotic viruses. “Non-hosts” harbor no known zoonotic viruses, “Hosts” harbor one to two, and “Super-hosts” harbor three or more. For all five Orders, hosts and superhosts are more likely to be in the conservation category of least concern. Plotted from data made available in supplementary materials from Johnson et al. (21); see caveats about these and similar data in SI Appendix. Species for which data needed to assign a conservation status were unavailable have been excluded.
Fig. 4.
Fig. 4.
The paradigm and the reality for research on spillover of zoonotic pathogens into humans. (A) The paradigm emphasizes a single animal host species for a zoonotic pathogen and an original spillover event, though the event and the species are rarely identified. (B) In reality, most zoonotic pathogens have multiple host species whose specific roles in transmission to and from humans are rarely known. (C) The number of viral zoonotic diseases that have 1, 2 to 5, 6 to 10, or 11+ known animal host species other than humans. Plotted from data made available in supplementary materials from Johnson et al. (21); see caveats about these and similar data in SI Appendix.

References

    1. Centers for Disease Control and Prevention , MicrobeNet (2020). https://www.cdc.gov/microbenet/index.html. Accessed 24 August 2020.
    1. Geoghegan J. L., Senior A. M., Di Giallonardo F., Holmes E. C., Virological factors that increase the transmissibility of emerging human viruses. Proc. Natl. Acad. Sci. U.S.A. 113, 4170–4175 (2016). - PMC - PubMed
    1. Janbon G., Quintin J., Lanternier F., d’Enfert C., Studying fungal pathogens of humans and fungal infections: Fungal diversity and diversity of approaches. Genes Immun. 20, 403–414 (2019). - PubMed
    1. Wolfe N. D., Dunavan C. P., Diamond J., Origins of major human infectious diseases. Nature 447, 279–283 (2007). - PMC - PubMed
    1. Jones K. E., et al. ., Global trends in emerging infectious diseases. Nature 451, 990–993 (2008). - PMC - PubMed

Publication types

LinkOut - more resources