TY - JOUR
T1 - Major subpopulations of Plasmodium falciparum in sub-Saharan Africa
AU - Amambua-Ngwa, Alfred
AU - Amenga-Etego, Lucas
AU - Kamau, Edwin
AU - Amato, Roberto
AU - Ghansah, Anita
AU - Golassa, Lemu
AU - Randrianarivelojosia, Milijaona
AU - Ishengoma, Deus
AU - Apinjoh, Tobias
AU - Maïga-Ascofaré, Oumou
AU - Andagalu, Ben
AU - Yavo, William
AU - Bouyou-Akotet, Marielle
AU - Kolapo, Oyebola
AU - Mane, Karim
AU - Worwui, Archibald
AU - Jeffries, David
AU - Simpson, Vikki
AU - D’Alessandro, Umberto
AU - Kwiatkowski, Dominic
AU - Djimde, Abdoulaye A.
N1 - Publisher Copyright:
© 2017 The Authors.
PY - 2019/8/23
Y1 - 2019/8/23
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85071427056&partnerID=8YFLogxK
U2 - 10.1126/science.aav5427
DO - 10.1126/science.aav5427
M3 - Article
C2 - 31439796
AN - SCOPUS:85071427056
SN - 0036-8075
VL - 365
SP - 813
EP - 816
JO - Science
JF - Science
IS - 6455
ER -