Scully E. J., Liu W. M., Li Y. Y., Ndjango J. B. N., Peeters Martine, Kamenya S., Pusey A. E., Lonsdorf E. V., Sanz C. M., Morgan D. B., Piel A. K., Stewart F. A., Gonder M. K., Simmons N., Asiimwe C., Zuberbuhler K., Koops K., Chapman C. A., Chancellor R., Rundus A., Huffman M. A., Wolfe N. D., Duraisingh M. T., Hahn B. H., Wrangham R. W. (2022). The ecology and epidemiology of malaria parasitism in wild chimpanzee reservoirs. Communications Biology, 5 (1), p. 1020 [14 p.].
Titre du document
The ecology and epidemiology of malaria parasitism in wild chimpanzee reservoirs
Année de publication
2022
Auteurs
Scully E. J., Liu W. M., Li Y. Y., Ndjango J. B. N., Peeters Martine, Kamenya S., Pusey A. E., Lonsdorf E. V., Sanz C. M., Morgan D. B., Piel A. K., Stewart F. A., Gonder M. K., Simmons N., Asiimwe C., Zuberbuhler K., Koops K., Chapman C. A., Chancellor R., Rundus A., Huffman M. A., Wolfe N. D., Duraisingh M. T., Hahn B. H., Wrangham R. W.
Source
Communications Biology, 2022,
5 (1), p. 1020 [14 p.]
Chimpanzees (Pan troglodytes) harbor rich assemblages of malaria parasites, including three species closely related to P. falciparum (sub-genus Laverania), the most malignant human malaria parasite. Here, we characterize the ecology and epidemiology of malaria infection in wild chimpanzee reservoirs. We used molecular assays to screen chimpanzee fecal samples, collected longitudinally and cross-sectionally from wild populations, for malaria parasite mitochondrial DNA. We found that chimpanzee malaria parasitism has an early age of onset and varies seasonally in prevalence. A subset of samples revealed Hepatocystis mitochondrial DNA, with phylogenetic analyses suggesting that Hepatocystis appears to cross species barriers more easily than Laverania. Longitudinal and cross-sectional sampling independently support the hypothesis that mean ambient temperature drives spatiotemporal variation in chimpanzee Laverania infection. Infection probability peaked at similar to 24.5 degrees C, consistent with the empirical transmission optimum of P. falciparum in humans. Forest cover was also positively correlated with spatial variation in Laverania prevalence, consistent with the observation that forest-dwelling Anophelines are the primary vectors. Extrapolating these relationships across equatorial Africa, we map spatiotemporal variation in the suitability of chimpanzee habitat for Laverania transmission, offering a hypothetical baseline indicator of human exposure risk.
Plan de classement
Santé : généralités [050]
;
Entomologie médicale / Parasitologie / Virologie [052]
;
Sciences du monde animal [080]
Description Géographique
OUGANDA ; ZONE EQUATORIALE ; KIBALE PARC NATIONAL
Localisation
Fonds IRD [F B010086307]
Identifiant IRD
fdi:010086307
