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Modeling malaria genomics reveals transmission decline and rebound in Senegal

Daniels, Rachel F., Schaffner, Stephen F., Wenger, Edward A., Proctor, Joshua L., Chang, Hsiao-Han, Wong, Wesley, Baro, Nicholas, Ndiaye, Daouda, Fall, Fatou Ba, Ndiop, Medoune, Ba, Mady, Milner, Danny A., Taylor, Terrie E., Neafsey, Daniel E., Volkman, Sarah K., Eckhoff, Philip A., Hartl, Daniel L., Wirth, Dyann F.
Proceedings of the National Academy of Sciences of the United States of America 2015 v.112 no.22 pp. 7067-7072
Culicidae, alleles, malaria, metagenomics, models, parasites, Senegal
To study the effects of malaria-control interventions on parasite population genomics, we examined a set of 1,007 samples of the malaria parasite Plasmodium falciparum collected in Thiès, Senegal between 2006 and 2013. The parasite samples were genotyped using a molecular barcode of 24 SNPs. About 35% of the samples grouped into subsets with identical barcodes, varying in size by year and sometimes persisting across years. The barcodes also formed networks of related groups. Analysis of 164 completely sequenced parasites revealed extensive sharing of genomic regions. In at least two cases we found first-generation recombinant offspring of parents whose genomes are similar or identical to genomes also present in the sample. An epidemiological model that tracks parasite genotypes can reproduce the observed pattern of barcode subsets. Quantification of likelihoods in the model strongly suggests a reduction of transmission from 2006–2010 with a significant rebound in 2012–2013. The reduced transmission and rebound were confirmed directly by incidence data from Thiè̀s. These findings imply that intensive intervention to control malaria results in rapid and dramatic changes in parasite population genomics. The results also suggest that genomics combined with epidemiological modeling may afford prompt, continuous, and cost-effective tracking of progress toward malaria elimination.