| Literature DB >> 27071123 |
Boris Makanga1, Patrick Yangari2, Nil Rahola2, Virginie Rougeron2, Eric Elguero3, Larson Boundenga4, Nancy Diamella Moukodoum4, Alain Prince Okouga4, Céline Arnathau3, Patrick Durand3, Eric Willaume5, Diego Ayala2, Didier Fontenille3, Francisco J Ayala6, François Renaud3, Benjamin Ollomo4, Franck Prugnolle7, Christophe Paupy7.
Abstract
Recent studies have highlighted the large diversity of malaria parasites infecting African great apes (subgenus Laverania) and their strong host specificity. Although the existence of genetic incompatibilities preventing the cross-species transfer may explain host specificity, the existence of vectors with a high preference for a determined host represents another possibility. To test this hypothesis, we undertook a 15-mo-long longitudinal entomological survey in two forest regions of Gabon, where wild apes live, at different heights under the canopy. More than 2,400 anopheline mosquitoes belonging to 18 species were collected. Among them, only three species of Anopheles were found infected with ape Plasmodium: Anopheles vinckei, Anopheles moucheti, and Anopheles marshallii Their role in transmission was confirmed by the detection of the parasites in their salivary glands. Among these species, An. vinckei showed significantly the highest prevalence of infection and was shown to be able to transmit parasites of both chimpanzees and gorillas. Transmission was also shown to be conditioned by seasonal factors and by the heights of capture under the canopy. Moreover, human landing catches of sylvan Anopheles demonstrated the propensity of these three vector species to feed on humans when available. Our results suggest therefore that the strong host specificity observed in the Laveranias is not linked to a specific association between the vertebrate host and the vector species and highlight the potential role of these vectors as bridge between apes and humans.Entities:
Keywords: African rainforest; Anopheles; Laverania; Plasmodium; ape-to-human infection
Mesh:
Year: 2016 PMID: 27071123 PMCID: PMC4868493 DOI: 10.1073/pnas.1603008113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205