| Literature DB >> 27348298 |
Daniel N Hupalo1, Zunping Luo1, Alexandre Melnikov2, Patrick L Sutton1, Peter Rogov2, Ananias Escalante3, Andrés F Vallejo4, Sócrates Herrera4, Myriam Arévalo-Herrera4,5, Qi Fan6, Ying Wang7, Liwang Cui8, Carmen M Lucas9, Salomon Durand9, Juan F Sanchez9, G Christian Baldeviano9, Andres G Lescano9, Moses Laman10, Celine Barnadas11,12, Alyssa Barry13,14, Ivo Mueller13,14,15, James W Kazura16, Alex Eapen17, Deena Kanagaraj17, Neena Valecha18, Marcelo U Ferreira19, Wanlapa Roobsoong20, Wang Nguitragool21, Jetsumon Sattabonkot20, Dionicia Gamboa22,23, Margaret Kosek24, Joseph M Vinetz22,23,25, Lilia González-Cerón26, Bruce W Birren2, Daniel E Neafsey2, Jane M Carlton1.
Abstract
Plasmodium vivax is a major public health burden, responsible for the majority of malaria infections outside Africa. We explored the impact of demographic history and selective pressures on the P. vivax genome by sequencing 182 clinical isolates sampled from 11 countries across the globe, using hybrid selection to overcome human DNA contamination. We confirmed previous reports of high genomic diversity in P. vivax relative to the more virulent Plasmodium falciparum species; regional populations of P. vivax exhibited greater diversity than the global P. falciparum population, indicating a large and/or stable population. Signals of natural selection suggest that P. vivax is evolving in response to antimalarial drugs and is adapting to regional differences in the human host and the mosquito vector. These findings underline the variable epidemiology of this parasite species and highlight the breadth of approaches that may be required to eliminate P. vivax globally.Entities:
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Year: 2016 PMID: 27348298 PMCID: PMC5347536 DOI: 10.1038/ng.3588
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330