| Literature DB >> 33187958 |
Rory Gibb1, Lydia H V Franklinos1,2, David W Redding1,3, Kate E Jones4,3.
Abstract
Entities:
Mesh:
Year: 2020 PMID: 33187958 PMCID: PMC7662085 DOI: 10.1136/bmj.m3389
Source DB: PubMed Journal: BMJ ISSN: 0959-8138
Fig 1Effects of global environmental change on zoonotic disease hazards and risks. Inset boxes highlight key socioecological processes through which climate and land use changes can affect hazard, exposure, and vulnerability. For example, zoonotic hazard (underlying potential for pathogen spillover) is a consequence of changes in reservoir host and vector distributions, abundance, and host-pathogen dynamics (example shown for a hypothetical rodent species)
Zoonoses of known public health significance likely to be affected by future climatic and land use changes
| Disease | Reservoir host/vector | Pathogen | Main transmission route to humans | Annual global incidence (estimated cases) | Socioecological context and current trends | Potential sensitivity to climate and land change |
|---|---|---|---|---|---|---|
| Lassa fever | Rodent (single species) | Lassa arenavirus | Contact with rodent contaminated food and surfaces | 100 000-300 000 | Seasonally endemic in rural west Africa, where rodent reservoir host is common around fields and villages. Reported cases have steadily increased over past twodecades | Increasing rainfall and agricultural expansion across much of west Africa may expand suitable habitat for reservoir host. Future shifts in rainfall seasonality may affect reservoir host population cycles and seasonality of human risk |
| Leptospirosis | Rodents (numerous species) |
| Contact with rodent contaminated environment (water, soil) | ~1 million | Found in rodents globally, but human exposures and burden are highest in poor communities in the tropics | Climate change is increasing the frequency and intensity of extreme weather events. Agricultural expansion and unplanned urbanization can increase both rodent-human contact and susceptibility to flooding |
| Lyme borreliosis | Wild vertebrates (numerous species), ticks |
| Tick bite | Unknown but ~30 000 in US alone | Maintained in forested areas across Palaearctic in complex, multispecies transmission cycles. Disease in humans arises through infectious tick bites. Reported incidence increasing | Forest degradation and fragmentation often favors more competent host communities, increasing hazard for humans. |
| Zoonotic malaria | Primates, |
| Mosquito bite | Unknown; seems to be increasing | Maintained among macaques and mosquitoes in forests of South East Asia. Spillover to humans occurs through infectious mosquito bites, in forests and around forest edges. Human incidence rising in recent decades | Ongoing rapid deforestation and forest fragmentation in South East Asia is increasing human exposure |
| Rift Valley fever | Mosquitoes (several genera), ruminant livestock | Rift Valley fever phlebovirus | Mosquito bite, infected livestock body fluids | Variable; occurs in sporadic outbreaks | Maintained and transmitted by mosquitoes in Africa and Arabian peninsula. Periodic, explosive outbreaks occur in ruminant livestock (eg, cattle) and in humans through mosquito bites and contact with infectious livestock fluids (eg, through slaughtering) | Seasonal temperature and water availability shape mosquito populations and virus persistence. |
| Ebola virus disease | Bat reservoir (species unknown), primate and duiker intermediate hosts | Zaire ebolavirus | Contact with infectious body fluids (wildlife or people) | Variable; occurs in sporadic outbreaks | Ebola reservoir not definitively identified but most likely bat populations in central and west Africa. Following initial spillover event(s), epidemics driven by extended human-to-human transmission chains, with high case fatality rates | Warmer and wetter climates in Africa, forest fragmentation and expansion of plantation ecosystems, may increase habitat suitability for reservoir hosts and facilitate human-bat contact |
Policy areas where ecosystem perspectives could assist in reducing zoonotic disease risk driven by climate change
| Policy sector | Ecological contributions to policy | Examples of ecosystem based approaches to managing zoonotic risks |
|---|---|---|
| Urban planning | Understanding the ecology of urban adapted reservoir/vector species (eg, brown rat, | Future urban planning could aim for co-benefits of climate adaptation and disease reduction. Increasing the density of drainage networks and the provision of piped water can mitigate increased flooding and water shortage risks while also reducing reservoir or vector habitat. Green spaces can help to reduce urban heat island effects, which would otherwise provide warmer microclimates for vector breeding, and reduce heat stress for people |
| Agricultural (arable) | Evaluating how animal reservoir or vector populations respond to expansions of agriculture and to climate changes in human managed landscapes can identify high risk emerging interfaces for zoonotic transmission | Agricultural landscapes and practices could be designed to naturally regulate populations of synanthropic reservoir hosts (eg, rodents) or vectors, reduce pathogen or parasite transmission (eg, by reducing standing water), and regulate local microclimates. This could also help to benefit food security by reducing crop losses |
| Agricultural (pastoral) | Climate and land use change will influence occurrence and abundance of reservoir and vector species that can transmit pathogens to livestock and people, as well as influencing environmental suitability for livestock husbandry. Understanding how these interfaces will change can identify high risk areas for future outbreaks | Adopting methods from higher yield farming systems could enable more efficient use of land and reduce human-wildlife-livestock interfaces. Agricultural landscapes can be designed to reduce contact between livestock and wildlife reservoir species (eg, bat hosts of henipaviruses), lowering risks of livestock epizootics and spillover to humans |
| Public health and clinical planning | Early warning surveillance systems (eg, monitoring sentinel wildlife populations) or mapping and forecast models of reservoir populations, can inform targeted prevention and outbreak response for specific zoonoses | Modeling approaches can evaluate how future climate and land change scenarios may affect geographic trends in zoonotic hazard for multiple zoonoses. The outcomes from these models can inform targeted strengthening of national health systems and health information management, as well as long term planning for prevention and response |
| Habitat loss and degradation | Understanding and mapping habitat use by known or predicted hosts of priority pathogens (eg, betacoronaviruses, filoviruses), under present and future environmental conditions, can identify regions that may pose a high hazard of zoonotic emergence and outbreaks | Much deforestation and agricultural expansion is driven by upstream factors, including global trade. Identifying and addressing upstream drivers could reduce human exposure risks to emerging zoonoses while preserving biodiversity and other ecosystem functions |
| Wildlife trade and hunting | People hunting and trading in wild animal species can increase risks of exposure to zoonotic pathogens. Understanding and mitigating the environmental drivers (eg, climate, land use) that increase pathogen prevalence in reservoir species could help to reduce hazards. Policy interventions to protect species could in some cases reduce exposures | Hunting and wildlife trade are often driven by nutritional and financial needs, and bans would not eliminate these needs. Investment to increase opportunities for profitable alternative livelihoods that are resilient to future climate change could reduce reliance on wild animal products while benefiting food security and biodiversity conservation |