The age of P. falciparum is also highly disputed, with previous estimates for the time to the most recent common ancestor (TMRCA) spanning more than an order of magnitude with values ranging from about 10,000 years to over 300,000 years. With P. falciparum being an exclusively human parasite with no known animal reservoir, we hypothesized that if P. falciparum had been associated with humans for over 50,000 to 60,000 years (the estimated date for the out-of-Africa migration of anatomically modern humans), its current population structure could still carry a signal of human settlement history.
Within-population genetic diversity of native human populations decreases smoothly with geographic distance measured through landmasses from a sub-Saharan African origin, and genetic differentiation between populations also increases steadily with physical distance along landmasses.
These smooth patterns in the distribution of human genetic diversity have been ascribed to sequential bottlenecks of small amplitude during the colonization of the world by our ancestors from an African cradle. In contrast, the parasite population structure may primarily depend on variation in epidemiological settings between populations. In particular, P. falciparum populations are characterized by high variability in variation in transmission intensity, which could have affected local genetic diversity. Selective pressure imposed by antimalaria interventions that used drugs and insecticides might, likewise, have locally reduced genetic diversity.
Further reading
Mapping malaria transmission intensity using geographical information systems (GIS): an example from Kenya.
Defining the relationship between Plasmodium falciparum parasite rate and clinical disease: statistical models for disease burden estimation
The entomological inoculation rate and Plasmodium falciparum infection in African children (Real Science copy)