| Literature DB >> 24557500 |
Weimin Liu1, Yingying Li1, Katharina S Shaw2, Gerald H Learn1, Lindsey J Plenderleith3, Jordan A Malenke1, Sesh A Sundararaman4, Miguel A Ramirez1, Patricia A Crystal1, Andrew G Smith1, Frederic Bibollet-Ruche1, Ahidjo Ayouba5, Sabrina Locatelli5, Amandine Esteban5, Fatima Mouacha5, Emilande Guichet5, Christelle Butel5, Steve Ahuka-Mundeke6, Bila-Isia Inogwabini7, Jean-Bosco N Ndjango8, Sheri Speede9, Crickette M Sanz10, David B Morgan11, Mary K Gonder12, Philip J Kranzusch13, Peter D Walsh14, Alexander V Georgiev15, Martin N Muller16, Alex K Piel17, Fiona A Stewart14, Michael L Wilson18, Anne E Pusey19, Liwang Cui20, Zenglei Wang20, Anna Färnert21, Colin J Sutherland22, Debbie Nolder22, John A Hart23, Terese B Hart23, Paco Bertolani24, Amethyst Gillis25, Matthew LeBreton25, Babila Tafon26, John Kiyang27, Cyrille F Djoko25, Bradley S Schneider25, Nathan D Wolfe25, Eitel Mpoudi-Ngole28, Eric Delaporte5, Richard Carter29, Richard L Culleton30, George M Shaw4, Julian C Rayner31, Martine Peeters5, Beatrice H Hahn4, Paul M Sharp32.
Abstract
Plasmodium vivax is the leading cause of human malaria in Asia and Latin America but is absent from most of central Africa due to the near fixation of a mutation that inhibits the expression of its receptor, the Duffy antigen, on human erythrocytes. The emergence of this protective allele is not understood because P. vivax is believed to have originated in Asia. Here we show, using a non-invasive approach, that wild chimpanzees and gorillas throughout central Africa are endemically infected with parasites that are closely related to human P. vivax. Sequence analyses reveal that ape parasites lack host specificity and are much more diverse than human parasites, which form a monophyletic lineage within the ape parasite radiation. These findings indicate that human P. vivax is of African origin and likely selected for the Duffy-negative mutation. All extant human P. vivax parasites are derived from a single ancestor that escaped out of Africa.Entities:
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Year: 2014 PMID: 24557500 PMCID: PMC4089193 DOI: 10.1038/ncomms4346
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919