TY - JOUR
T1 - Accelerated diversification of nonhuman primate malarias in Southeast Asia
T2 - Adaptive radiation or geographic speciation?
AU - Muehlenbein, Michael P.
AU - Pacheco, M. Andreina
AU - Taylor, Jesse E.
AU - Prall, Sean P.
AU - Ambu, Laurentius
AU - Nathan, Senthilvel
AU - Alsisto, Sylvia
AU - Ramirez, Diana
AU - Escalante, Ananias A.
N1 - Publisher Copyright:
© The Author 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Although parasitic organisms are found worldwide, the relative importance of host specificity and geographic isolation for parasite speciation has been explored in only a few systems. Here, we study Plasmodium parasites known to infect Asian nonhuman primates, a monophyletic group that includes the lineage leading to the human parasite Plasmodium vivax and several species used as laboratory models in malaria research. We analyze the available data together with new samples from three sympatric primate species from Borneo: The Bornean orangutan and the long-tailed and the pig-tailed macaques. We find several species of malaria parasites, including three putatively new species in this biodiversity hotspot. Among those newly discovered lineages, we report two sympatric parasites in orangutans. We find no differences in the sets of malaria species infecting each macaque species indicating that these species show no host specificity. Finally, phylogenetic analysis of these data suggests that the malaria parasites infecting Southeast Asian macaques and their relatives are speciating three to four times more rapidly than those with other mammalian hosts such as lemurs and African apes. We estimate that these events took place in approximately a 3-4-Ma period. Based on the genetic and phenotypic diversity of the macaque malarias, we hypothesize that the diversification of this group of parasites has been facilitated by the diversity, geographic distributions, and demographic histories of their primate hosts.
AB - Although parasitic organisms are found worldwide, the relative importance of host specificity and geographic isolation for parasite speciation has been explored in only a few systems. Here, we study Plasmodium parasites known to infect Asian nonhuman primates, a monophyletic group that includes the lineage leading to the human parasite Plasmodium vivax and several species used as laboratory models in malaria research. We analyze the available data together with new samples from three sympatric primate species from Borneo: The Bornean orangutan and the long-tailed and the pig-tailed macaques. We find several species of malaria parasites, including three putatively new species in this biodiversity hotspot. Among those newly discovered lineages, we report two sympatric parasites in orangutans. We find no differences in the sets of malaria species infecting each macaque species indicating that these species show no host specificity. Finally, phylogenetic analysis of these data suggests that the malaria parasites infecting Southeast Asian macaques and their relatives are speciating three to four times more rapidly than those with other mammalian hosts such as lemurs and African apes. We estimate that these events took place in approximately a 3-4-Ma period. Based on the genetic and phenotypic diversity of the macaque malarias, we hypothesize that the diversification of this group of parasites has been facilitated by the diversity, geographic distributions, and demographic histories of their primate hosts.
KW - host range
KW - macaques
KW - malaria
KW - orangutan
KW - parasite speciation
KW - phylogeny Plasmodium
KW - population structure
UR - http://www.scopus.com/inward/record.url?scp=84925125246&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84925125246&partnerID=8YFLogxK
U2 - 10.1093/molbev/msu310
DO - 10.1093/molbev/msu310
M3 - Article
C2 - 25389206
AN - SCOPUS:84925125246
SN - 0737-4038
VL - 32
SP - 422
EP - 439
JO - Molecular Biology and Evolution
JF - Molecular Biology and Evolution
IS - 2
ER -