» Articles » PMID: 37256857

Phylogenetic and Biogeographical Traits Predict Unrecognized Hosts of Zoonotic Leishmaniasis

Overview
Authors
Affiliations
Soon will be listed here.
Abstract

The spatio-temporal distribution of leishmaniasis, a parasitic vector-borne zoonotic disease, is significantly impacted by land-use change and climate warming in the Americas. However, predicting and containing outbreaks is challenging as the zoonotic Leishmania system is highly complex: leishmaniasis (visceral, cutaneous and muco-cutaneous) in humans is caused by up to 14 different Leishmania species, and the parasite is transmitted by dozens of sandfly species and is known to infect almost twice as many wildlife species. Despite the already broad known host range, new hosts are discovered almost annually and Leishmania transmission to humans occurs in absence of a known host. As such, the full range of Leishmania hosts is undetermined, inhibiting the use of ecological interventions to limit pathogen spread and the ability to accurately predict the impact of global change on disease risk. Here, we employed a machine learning approach to generate trait profiles of known zoonotic Leishmania wildlife hosts (mammals that are naturally exposed and susceptible to infection) and used trait-profiles of known hosts to identify potentially unrecognized hosts. We found that biogeography, phylogenetic distance, and study effort best predicted Leishmania host status. Traits associated with global change, such as agricultural land-cover, urban land-cover, and climate, were among the top predictors of host status. Most notably, our analysis suggested that zoonotic Leishmania hosts are significantly undersampled, as our model predicted just as many unrecognized hosts as unknown hosts. Overall, our analysis facilitates targeted surveillance strategies and improved understanding of the impact of environmental change on local transmission cycles.

Citing Articles

Enzootic transmission of Leishmania spp. in gallery forests of the Brazilian Cerrado.

Rapello A, Andrade A, Nitz N, Minuzzi-Sousa T, Vital T, Ferreira T Rev Bras Parasitol Vet. 2024; 33(4):e011624.

PMID: 39661812 PMC: 11756826. DOI: 10.1590/S1984-29612024073.


Nationwide cross-sectional surveillance of Leishmania donovani in phlebotomine sand flies and its impact on national kala-azar elimination in India.

Shah H, Fathima P, Ajithlal P, Kumar A, Rawani A, Thakur M Sci Rep. 2024; 14(1):28455.

PMID: 39557939 PMC: 11574011. DOI: 10.1038/s41598-024-78915-0.

References
1.
Sokolow S, Nova N, Pepin K, Peel A, Pulliam J, Manlove K . Ecological interventions to prevent and manage zoonotic pathogen spillover. Philos Trans R Soc Lond B Biol Sci. 2019; 374(1782):20180342. PMC: 6711299. DOI: 10.1098/rstb.2018.0342. View

2.
da Silva M, Portela J, Li W, Jackson M, Gonzalez-Juarrero M, Hidalgo A . Evidence of zoonotic leprosy in Pará, Brazilian Amazon, and risks associated with human contact or consumption of armadillos. PLoS Negl Trop Dis. 2018; 12(6):e0006532. PMC: 6023134. DOI: 10.1371/journal.pntd.0006532. View

3.
Goncalves N, Miranda C, da Costa R, Guedes J, Matsumura E, Costa S . Cutaneous leishmaniasis: Spatial distribution and environmental risk factors in the state of Pará, Brazilian Eastern Amazon. J Infect Dev Ctries. 2020; 13(10):939-944. DOI: 10.3855/jidc.11573. View

4.
Kennedy C, Oakleaf J, Theobald D, Baruch-Mordo S, Kiesecker J . Managing the middle: A shift in conservation priorities based on the global human modification gradient. Glob Chang Biol. 2019; 25(3):811-826. DOI: 10.1111/gcb.14549. View

5.
Lima A, de Lima I, Coutinho J, de Sousa U, Rodrigues M, Wilson M . Changing epidemiology of visceral leishmaniasis in northeastern Brazil: a 25-year follow-up of an urban outbreak. Trans R Soc Trop Med Hyg. 2018; 111(10):440-447. PMC: 5914331. DOI: 10.1093/trstmh/trx080. View