Malaria

Certainty Style Key
Hover over keys for definitions:
True   Likely   Speculative
Human Uniqueness Relative to "Great Apes": 
True
MOCA Domain: 
Medical Disease
MOCA Topic Authors: 

Among the human malarias, P. falciparum is the most virulent and associated with the largest number of deaths. Chimpanzees are hosts to a closely related pathogen (P. reichenowii) and can be experimentally infected with human P. falciparum without exhibiting any symptoms of severe disease. Conversely, an old study indicated that humans could not be infected by P. reichenowii. One study comparing the merozoite stage EBA-175 receptors of these two pathogens and their respective binding preferences to host target molecules on red blood cells indicates that human P. falciparum evolved to exploit the uniquely human sialic acid content of target attachment molecules - possibly explaining the difference in virulence of P. falciparum in humans and apes.  A more recent study has shown that all extant P. falciparum strains are likely derived from a single chimpanzee to human transfer event.  A likely explanation is that the loss of expression of the Neu5Gc sialic acid in hominin ancestors made them partially or completely resistant to the extant P. reichenowii, and that one strain later evolved to bind the Neu5Ac-rich erythrocytes of humans, eventually becoming P. falciparum

 

Timing

Timing of Appearance of the Difference in the Hominin Lineage.

For this entry assume that

  • the common ancestor of humans and old world monkeys was 25000 thousand (25 million) years ago
  • the common ancestor of humans and chimpanzees was 6000 thousand (6 million) years ago
  • the emergence of the genus Homo was 2000 thousand (2 million) years ago
  • the common ancestor of modern humans was 100 thousand years ago

 

Possible Appearance: 
3000 Thousand Years
Probable Appearance: 
1000 Thousand Years
Definite Appearance: 
50 Thousand Years
References: 

Martin, M.J., Rayner, J.C., Gagneux, P., Barnwell, J.W., and Varki, A. 2005. Evolution of human-chimpanzee differences in malaria susceptibility: relationship to human genetic loss of N-glycolylneuraminic acid. Proc Natl Acad Sci U S A. 102:12819-12824.
 
Rich, S.M., Leendertz, F.H., Xu, G., Lebreton, M., Djoko, C.F., Aminake, M.N., Takang, E.E., Diffo, J.L., Pike, B.L., Rosenthal, B.M., Formenty, P., Boesch, C., Ayala, F.J., and Wolfe, N.D. 2009. The origin of malignant malaria. Proc Natl Acad Sci U S A.
 
Varki A, Gagneux P. Human-specific evolution of sialic acid targets: Explaining the malignant malaria mystery?Proc Natl Acad Sci U S A. 106:14739-14740, 2009. PMID: 19717444