The origin and age of Plasmodium vivax

Trends in Parasitology

Volumn 22, Issue 12, 2006, Pages 558-563

  Cornejo, Omar E ^a   Escalante, Ananias A ^b  

^a EMORY UNIVERSITY   (United States)

^b ARIZONA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ASIA; HOMINID; HUMAN; MACACA; MEDICAL RESEARCH; NONHUMAN; PARASITE; PARASITE ISOLATION; PHYLOGENY; PLASMODIUM; PLASMODIUM VIVAX; SAMPLING;

ANIMALS; ASIA, SOUTHEASTERN; DNA, MITOCHONDRIAL; DNA, PROTOZOAN; EVOLUTION, MOLECULAR; HAPLOTYPES; HUMANS; MACACA; MALARIA, VIVAX; PHYLOGENY; PLASMODIUM VIVAX; POLYMORPHISM, GENETIC; VARIATION (GENETICS);

HOMINIDAE; MACACA; PLASMODIUM VIVAX; PRIMATES;

EID: 33750835869     PISSN: 14714922     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pt.2006.09.007     Document Type: Article

References (32)

1. Snow R.W., et al. The global distribution of clinical episodes of Plasmodium falciparum malaria. Nature 434 (2005) 214-217
2. Garnham P.C.C. Malaria Parasites and Other Haemosporidia (1966), Blackwell Scientific Publications
3. Coatney R.G., et al. The Primate Malaria (1971), US Government Printing Office
4. Hartl D.L. The origin of malaria: mixed messages from genetic diversity. Nat. Rev. Microbiol. 2 (2004) 15-22
5. Joy D.A., et al. Early origin and recent expansion of Plasmodium falciparum. Science 300 (2003) 318-321
6. Hughes A.L., and Verra F. Very large long-term effective population size in the virulent human malaria parasite Plasmodium falciparum. Proc. Biol. Sci. 268 (2001) 1855-1860
7. Escalante A.A., et al. Assessing the effect of natural selection in malaria parasites. Trends Parasitol. 20 (2004) 388-395
8. Mendis K., et al. The neglected burden of Plasmodium vivax malaria. Am. J. Trop. Med. Hyg. 64 (2001) 97-106
9. Escalante A.A., et al. The evolution of primate malaria parasites based on the gene encoding cytochrome b from the linear mitochondrial genome. Proc. Natl. Acad. Sci. U. S. A. 95 (1998) 8124-8129
10. Escalante A.A., et al. A monkey's tale: the origin of Plasmodium vivax as a human malaria parasite. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 1980-1985
11. Mu J., et al. Host switch leads to emergence of Plasmodium vivax malaria in humans. Mol. Biol. Evol. 22 (2005) 1686-1693
12. Jongwutiwes S., et al. Mitochondrial genome sequences support ancient population expansion in Plasmodium vivax. Mol. Biol. Evol. 22 (2005) 1733-1739
13. McCutchan T.F., et al. Evolutionary relatedness of Plasmodium species as determined by the structure of DNA. Science 225 (1984) 808-811
14. Severini C., et al. Risk of Plasmodium vivax malaria reintroduction in Uzbekistan: genetic characterization of parasites and status of potential malaria vectors in the Surkhandarya region. Trans. R. Soc. Trop. Med. Hyg. 98 (2004) 585-592
15. Rodriguez-Morales A.J., et al. Impact of imported malaria on the burden of disease in northeastern Venezuela. J. Travel Med. 13 (2006) 15-20
16. Centers for Disease Control and Prevention (2004) Multifocal autochthonous transmission of malaria - Florida. MMWR Morb. Mortal. Wkly. Rep. 53, 412-413
17. Roos C., et al. Molecular phylogeny of Mentawai macaques: taxonomic and biogeographic implications. Mol. Phylogenet. Evol. 29 (2003) 139-150
18. Jablonski N.G., et al. The influence of life history and diet on the distribution of catarrhine primates during the Pleistocene in eastern Asia. J. Hum. Evol. 39 (2000) 131-157
19. Nordborg M., and Krone S. Separation of time scales and convergence to the coalescent in structured populations. In: Slatkin M., and Veuille M. (Eds). Modern Developments in Theoretical Population Genetics (2002), Oxford University Press 194-232
20. Sjödin P., et al. On the meaning and existence of an effective population size. Genetics 169 (2005) 1061-1070
21. Weir B.S., and Cockerham C.C. Estimating F-statistics for the analysis of population structure. Evolution Int. J. Org. Evolution 38 (1984) 1358-1370
22. Excoffier L.G., et al. Arlequin ver. 3.0: an integrated software package for population genetics data analysis. Evol. Bioinform. Online 1 (2005) 47-50
23. Bahlo M., and Griffiths R.C. Inference from gene trees in a subdivided population. Theor. Popul. Biol. 57 (2000) 79-95
24. Tajima F. Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123 (1989) 585-589
25. Hammer M.F., et al. Human population structure and its effects on sampling Y chromosome sequence variation. Genetics 164 (2003) 1495-1509
26. Imwong M., et al. Microsatellite variation, repeat array length and population history of Plasmodium vivax. Mol. Biol. Evol. 23 (2006) 1016-1018
27. Excoffier L. Patterns of DNA sequence diversity and genetic structure after a range expansion: lessons from the infinite-island model. Mol. Ecol. 13 (2004) 853-864
28. Huelsenbeck J.P., and Ronquist F. MRBAYES: Bayesian inference of phylogeny. Bioinformatics 17 (2001) 754-755
29. Saitou N., and Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol. Biol. Evol. 4 (1987) 406-425
30. Kumar S., et al. MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment. Brief. Bioinform. 5 (2004) 150-163
31. Nei M., and Kumar S. Molecular Evolution and Phylogenetics (2000), Oxford University Press
32. Bandelt H.J., et al. Median-joining networks for inferring intraspecific phylogenies. Mol. Biol. Evol. 16 (1999) 37-48