Abstract

The origin of Plasmodium falciparum, the etiological agent of the most dangerous forms of human malaria, remains controversial. Although investigations of homologous parasites in African Apes are crucial to resolve this issue, studies have been restricted to a chimpanzee parasite related to P. falciparum, P. reichenowi, for which a single isolate was available until very recently. Using PCR amplification, we detected Plasmodium parasites in blood samples from 18 of 91 individuals of the genus Pan, including six chimpanzees (three Pan troglodytes troglodytes, three Pan t. schweinfurthii) and twelve bonobos (Pan paniscus). We obtained sequences of the parasites' mitochondrial genomes and/or from two nuclear genes from 14 samples. In addition to P. reichenowi, three other hitherto unknown lineages were found in the chimpanzees. One is related to P. vivax and two to P. falciparum that are likely to belong to distinct species. In the bonobos we found P. falciparum parasites whose mitochondrial genomes indicated that they were distinct from those present in humans, and another parasite lineage related to P. malariae. Phylogenetic analyses based on this diverse set of Plasmodium parasites in African Apes shed new light on the evolutionary history of P. falciparum. The data suggested that P. falciparum did not originate from P. reichenowi of chimpanzees (Pan troglodytes), but rather evolved in bonobos (Pan paniscus), from which it subsequently colonized humans by a host-switch. Finally, our data and that of others indicated that chimpanzees and bonobos maintain malaria parasites, to which humans are susceptible, a factor of some relevance to the renewed efforts to eradicate malaria.

Highlights

  • Malaria infections have influenced the development of human civilizations, and have shaped the genetic make-up of current human populations

  • Blood samples were obtained from 49 chimpanzees, Pan troglodytes, in Uganda and the Democratic Republic of the Congo (DRC), and from 42 bonobos, Pan paniscus, in the DRC

  • Since we were interested in lineages related to P. falciparum, we used oligonucleotides based on sequences from P. falciparum to target two nuclear genes: dihydrofolate reductase-thymidylate synthase, and the gene encoding the merozoite surface protein 2 because this gene is not known to have orthologues outside P. falciparum and P. reichenowi [15]

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Summary

Introduction

Malaria infections have influenced the development of human civilizations, and have shaped the genetic make-up of current human populations. Molecular phylogenetic analyses have demonstrated that these four parasites are not monophyletic [1,2], indicating that they independently colonised hominids [3,4,5,6] The timing of their appearance in Homo sapiens, remains unresolved. Several evolutionary genetic approaches rely on reliable phylogenetic information to detect putative adaptive genetic variation, thereby identifying genes that might be involved in pathogenesis or in the evasion of host immune responses. Addressing these issues is a Author Summary

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