| Literature DB >> 31439796 |
Alfred Amambua-Ngwa1, Lucas Amenga-Etego2, Edwin Kamau3,4, Roberto Amato5,6, Anita Ghansah7, Lemu Golassa8, Milijaona Randrianarivelojosia9, Deus Ishengoma10, Tobias Apinjoh11, Oumou Maïga-Ascofaré12, Ben Andagalu3, William Yavo13, Marielle Bouyou-Akotet14, Oyebola Kolapo1,15, Karim Mane1, Archibald Worwui1, David Jeffries1, Vikki Simpson4,6, Umberto D'Alessandro1, Dominic Kwiatkowski5,6, Abdoulaye A Djimde16,17.
Abstract
Understanding genomic variation and population structure of Plasmodium falciparum across Africa is necessary to sustain progress toward malaria elimination. Genome clustering of 2263 P. falciparum isolates from 24 malaria-endemic settings in 15 African countries identified major western, central, and eastern ancestries, plus a highly divergent Ethiopian population. Ancestry aligned to these regional blocs, overlapping with both the parasite's origin and with historical human migration. The parasite populations are interbred and shared genomic haplotypes, especially across drug resistance loci, which showed the strongest recent identity-by-descent between populations. A recent signature of selection on chromosome 12 with candidate resistance loci against artemisinin derivatives was evident in Ghana and Malawi. Such selection and the emerging substructure may affect treatment-based intervention strategies against P. falciparum malaria.Entities:
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Year: 2019 PMID: 31439796 DOI: 10.1126/science.aav5427
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728