
Ape Origins of Human Malaria
Author(s) -
Paul M. Sharp,
Lindsey J. Plenderleith,
Beatrice H. Hahn
Publication year - 2020
Publication title -
annual review of microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.817
H-Index - 192
eISSN - 1545-3251
pISSN - 0066-4227
DOI - 10.1146/annurev-micro-020518-115628
Subject(s) - plasmodium (life cycle) , biology , nonsynonymous substitution , lineage (genetic) , genetic diversity , malaria , plasmodium vivax , plasmodium malariae , population , plasmodium falciparum , gorilla , evolutionary biology , genetics , parasite hosting , gene , immunology , genome , demography , sociology , world wide web , computer science , paleontology
African apes harbor at least twelve Plasmodium species, some of which have been a source of human infection. It is now well established that Plasmodium falciparum emerged following the transmission of a gorilla parasite, perhaps within the last 10,000 years, while Plasmodium vivax emerged earlier from a parasite lineage that infected humans and apes in Africa before the Duffy-negative mutation eliminated the parasite from humans there. Compared to their ape relatives, both human parasites have greatly reduced genetic diversity and an excess of nonsynonymous mutations, consistent with severe genetic bottlenecks followed by rapid population expansion. A putative new Plasmodium species widespread in chimpanzees, gorillas, and bonobos places the origin of Plasmodium malariae in Africa. Here, we review what is known about the origins and evolutionary history of all human-infective Plasmodium species, the time and circumstances of their emergence, and the diversity, host specificity, and zoonotic potential of their ape counterparts.