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  1. Daszak P, Zambrana-Torrelio C, Bogich TL, Fernandez M, Epstein JH, Murray KA, et al.
    Proc Natl Acad Sci U S A, 2013 Feb 26;110 Suppl 1:3681-8.
    PMID: 22936052 DOI: 10.1073/pnas.1201243109
    Emerging infectious diseases (EIDs) pose a significant threat to human health, economic stability, and biodiversity. Despite this, the mechanisms underlying disease emergence are still not fully understood, and control measures rely heavily on mitigating the impact of EIDs after they have emerged. Here, we highlight the emergence of a zoonotic Henipavirus, Nipah virus, to demonstrate the interdisciplinary and macroecological approaches necessary to understand EID emergence. Previous work suggests that Nipah virus emerged due to the interaction of the wildlife reservoir (Pteropus spp. fruit bats) with intensively managed livestock. The emergence of this and other henipaviruses involves interactions among a suite of anthropogenic environmental changes, socioeconomic factors, and changes in demography that overlay and interact with the distribution of these pathogens in their wildlife reservoirs. Here, we demonstrate how ecological niche modeling may be used to investigate the potential role of a changing climate on the future risk for Henipavirus emergence. We show that the distribution of Henipavirus reservoirs, and therefore henipaviruses, will likely change under climate change scenarios, a fundamental precondition for disease emergence in humans. We assess the variation among climate models to estimate where Henipavirus host distribution is most likely to expand, contract, or remain stable, presenting new risks for human health. We conclude that there is substantial potential to use this modeling framework to explore the distribution of wildlife hosts under a changing climate. These approaches may directly inform current and future management and surveillance strategies aiming to improve pathogen detection and, ultimately, reduce emergence risk.
  2. Watts N, Amann M, Arnell N, Ayeb-Karlsson S, Beagley J, Belesova K, et al.
    Lancet, 2021 Jan 09;397(10269):129-170.
    PMID: 33278353 DOI: 10.1016/S0140-6736(20)32290-X
    For the Chinese, French, German, and Spanish translations of the abstract see Supplementary Materials section.
  3. Romanello M, McGushin A, Di Napoli C, Drummond P, Hughes N, Jamart L, et al.
    Lancet, 2021 Oct 30;398(10311):1619-1662.
    PMID: 34687662 DOI: 10.1016/S0140-6736(21)01787-6
  4. Romanello M, Di Napoli C, Drummond P, Green C, Kennard H, Lampard P, et al.
    Lancet, 2022 Nov 05;400(10363):1619-1654.
    PMID: 36306815 DOI: 10.1016/S0140-6736(22)01540-9
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