Population genomics studies identify signatures of global dispersal and drug resistance in Plasmodium vivax
Jane Carlton, Daniel Neafsey and colleagues report a population genomics analysis of 182 Plasmodium vivax isolates from 11 countries. They find evidence of regional adaptation and signatures of selection at genes involved in antimalarial drug resistance. Plasmodium vivax is a major public health bur...
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Published in | Nature genetics Vol. 48; no. 8; pp. 953 - 958 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Nature Publishing Group US
01.08.2016
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 1061-4036 1546-1718 1546-1718 |
DOI | 10.1038/ng.3588 |
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Summary: | Jane Carlton, Daniel Neafsey and colleagues report a population genomics analysis of 182
Plasmodium vivax
isolates from 11 countries. They find evidence of regional adaptation and signatures of selection at genes involved in antimalarial drug resistance.
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. |
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Bibliography: | SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1061-4036 1546-1718 1546-1718 |
DOI: | 10.1038/ng.3588 |