The genetic diversity of Plasmodium vivax populations

Trends in Parasitology

Volumn 19, Issue 5, 2003, Pages 220-226

  Cui, Liwang ^a   Escalante, Ananias A ^b   Imwong, Mallika ^c   Snounou, Georges ^d  

^a PENNSYLVANIA STATE UNIVERSITY   (United States)

^b NATL CENTER FOR INFECTIOUS DISEASES   (United States)

^c MAHIDOL UNIVERSITY   (Thailand)

^d INSTITUT PASTEUR   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIGEN; APICAL MEMBRANE ANTIGEN 1; CIRCUMSPOROZOITE PROTEIN; GENE PRODUCT; MEROZOITE SURFACE PROTEIN 1; MEROZOITE SURFACE PROTEIN 2; UNCLASSIFIED DRUG;

ALLELISM; DISEASE CONTROL; GENE; GENETIC MARKER; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HOST; HUMAN; LIFE CYCLE; LIFESPAN; MALARIA; MOLECULAR EVOLUTION; NONHUMAN; PARASITE; PARASITE TRANSMISSION; PLASMODIUM VIVAX; POPULATION STRUCTURE; REVIEW;

PLASMODIUM VIVAX; PROTOZOA;

EID: 0037728538     PISSN: 14714922     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1471-4922(03)00085-0     Document Type: Review

References (65)

1. Mendis K.N., et al. The neglected burden of Plasmodium vivax malaria. Am. J. Trop. Med. Hyg. 64:2001;97-106.
2. Beg M.A., et al. Cerebral involvement in benign tertian malaria. Am. J. Trop. Med. Hyg. 67:2002;230-232.
3. Rieckmann K.H., et al. Plasmodium vivax resistance to chloroquine? Lancet ii. 1989;1183-1184.
4. Baird J.K., et al. Resistance to chloroquine by Plasmodium vivax in Irian Jaya, Indonesia. Am. J. Trop. Med. Hyg. 44:1991;547-552.
5. Li J., et al. Geographic subdivision of the range of the malaria parasite Plasmodium vivax. Emerg. Infect. Dis. 7:2001;35-42.
6. Babiker H.A., Walliker D. Current views on the population structure of Plasmodium falciparum: implications for control. Parasitol. Today. 13:1997;262-267.
7. Awadalla P., et al. The question of Plasmodium falciparum population structure. Trends Parasitol. 17:2001;351-353.
8. Myint-Oo. Isoenzyme variation in schizonts of Plasmodium vivax from Burma. Trans. R. Soc. Trop. Med. Hyg. 80:1986;1-4.
9. Udagama P.V., et al. Demonstration of antigenic polymorphism in Plasmodium vivax malaria with a panel of 30 monoclonal antibodies. Infect. Immun. 55:1987;2604-2611.
10. Golenda C., et al. Continuous in vitro propagation of the malaria parasite Plasmodium vivax. Proc. Natl. Acad. Sci. U. S. A. 94:1997;6786-6791.
11. Del Portillo H.A., et al. Primary structure of the merozoite surface antigen 1 of Plasmodium vivax reveals sequences conserved between different Plasmodium species. Proc. Natl. Acad. Sci. U. S. A. 88:1991;4030-4034.
12. Galinski M.R., et al. Plasmodium vivax merozoite surface protein-3 contains coiled-coil motifs in an alanine-rich central domain. Mol. Biochem. Parasitol. 101:1999;131-147.
13. Gibson H.L., et al. Structure and expression of the gene for Pv200, a major blood-stage surface antigen of Plasmodium vivax. Mol. Biochem. Parasitol. 50:1992;325-333.
14. Porto M., et al. Second form in a segment of the merozoite surface protein 1 gene of Plasmodium vivax among isolates from Rondônia (Brazil). Mol. Biochem. Parasitol. 54:1992;121-124.
15. Premawansa S., et al. Plasmodium vivax: recombination between potential allelic types of the merozoite surface protein MSP1 in parasites isolated from patients. Exp. Parasitol. 76:1993;192-199.
16. Mancilla L.I., et al. Plasmodium vivax: dimorphic DNA sequences from the MSP-1 gene code for regions that are immunogenic in natural infections. Exp. Parasitol. 79:1994;148-158.
17. Kolakovich K.A., et al. Plasmodium vivax: favored gene frequencies of the merozoite surface protein-1 and the multiplicity of infection in a malaria endemic region. Exp. Parasitol. 83:1996;11-18.
18. Putaporntip C., et al. Interallelic recombination in the merozoite surface protein 1 (MSP-1) gene of Plasmodium vivax from Thai isolates. Mol. Biochem. Parasitol. 84:1997;49-56.
19. Cheng Q., et al. Polymorphism in Plasmodium vivax MSA1 gene - the result of intragenic recombinations? Parasitology. 106:1993;335-345.
20. Gutierrez A., et al. Plasmodium vivax: polymorphism in the merozoite surface protein 1 gene from wild Colombian isolates. Exp. Parasitol. 95:2000;215-219.
21. Bruce M.C., et al. Polymorphism at the merozoite surface protein-3α locus of Plasmodium vivax: global and local diversity. Am. J. Trop. Med. Hyg. 61:1999;518-525.
22. Bruce M.C., et al. Genetic diversity and dynamics of Plasmodium falciparum and P. vivax populations in multiply infected children with asymptomatic malaria infections in Papua New Guinea. Parasitology. 121:2000;257-272.
23. Rayner J.C., et al. Extensive polymorphism in the Plasmodium vivax merozoite surface coat protein MSP-3α is limited to specific domains. Parasitology. 125:2002;393-405.
24. Cui, L. et al. Genetic diversity and multiple infections of Plasmodium vivax malaria in western Thailand. Am. J. Trop. Med. Hyg. (in press).
25. Cheng Q., Saul A.J. Sequence analysis of the apical membrane antigen I (AMA-1) of Plasmodium vivax. Mol. Biochem. Parasitol. 65:1994;183-187.
26. Figtree M., et al. Plasmodium vivax synonymous substitution frequencies, evolution and population structure deduced from diversity in AMA 1 and MSP 1 genes. Mol. Biochem. Parasitol. 108:2000;53-66.
27. Arnot D.E., et al. Circumsporozoite protein of Plasmodium vivax: gene cloning and characterization of the immunodominant epitope. Science. 230:1985;815-818.
28. Rosenberg R., et al. Circumsporozoite protein heterogeneity in the human malaria parasite Plasmodium vivax. Science. 245:1989;973-976.
29. Kain K.C., et al. Circumsporozoite genotyping of global isolates of Plasmodium vivax from dried blood specimens. J. Clin. Microbiol. 30:1992;1863-1866.
30. Qari S.H., et al. Polymorphism in the circumsporozoite protein of the human malaria parasite Plasmodium vivax. Mol. Biochem. Parasitol. 55:1992;105-113.
31. Kain K.C., Lanar D.E. Determination of genetic variation within Plasmodium falciparum by using enzymatically amplified DNA from filter paper disks impregnated with whole blood. J. Clin. Microbiol. 29:1991;1171-1174.
32. Burkot T.R., et al. The population dynamics in mosquitoes and humans of two Plasmodium vivax polymorphs distinguished by different circumsporozoite protein repeat regions. Am. J. Trop. Med. Hyg. 47:1992;778-786.
33. Rosenberg R., et al. Random mating of natural Plasmodium populations demonstrated from individual oocysts. Mol. Biochem. Parasitol. 53:1992;129-133.
34. Snewin V.A., et al. A new polymorphic marker for PCR typing of Plasmodium vivax parasites. Mol. Biochem. Parasitol. 71:1995;135-138.
35. Imwong M., et al. Plasmodium vivax: polymerase chain reaction amplification artifacts limit the suitability of pvgam1 as a genetic marker. Exp. Parasitol. 99:2001;175-179.
36. Eldin de Pécoulas P., et al. Sequence variation in the Plasmodium vivax dihydrofolate reductase-thymidylate synthase gene and their relationship with pyrimethamine resistance. Mol. Biochem. Parasitol. 92:1998;265-273.
37. Imwong M., et al. Association of genetic mutations in Plasmodium vivax dhfr with resistance to sulfadoxine-pyrimethamine: geographical and clinical correlates. Antimicrob. Agents Chemother. 45:2001;3122-3127.
38. Anderson T.J., et al. Microsatellite markers reveal a spectrum of population structures in the malaria parasite Plasmodium falciparum. Mol. Biol. Evol. 17:2000;1467-1482.
39. Urdaneta L., et al. Evidence for clonal propagation in natural isolates of Plasmodium falciparum from Venezuela. Proc. Natl. Acad. Sci. U. S. A. 98:2001;6725-6729.
40. Putaporntip C., et al. Diversity in the thrombospondin-related adhesive protein gene (TRAP) of Plasmodium vivax. Gene. 268:2001;97-104.
41. Lim C.S., et al. Analysis of Plasmodium vivax merozoite surface protein-1 gene sequences from resurgent Korean isolates. Am. J. Trop. Med. Hyg. 62:2000;261-265.
42. Mann V.H., et al. Sequence variation in the circumsporozoite protein gene of Plasmodium vivax appears to be regionally biased. Mol. Biochem. Parasitol. 68:1994;45-52.
43. Lim C.S., et al. The analysis of circumsporozoite-protein gene sequences from South Korean isolates of Plasmodium vivax. Ann. Trop. Med. Parasitol. 95:2001;229-235.
44. Gonzalez-Ceron L., et al. Differential susceptibilities of Anopheles albimanus and Anopheles pseudopunctipennis to infections with coindigenous Plasmodium vivax variants VK210 and VK247 in southern Mexico. Infect. Immun. 67:1999;410-412.
45. Rodriguez M.H., et al. Different prevalences of Plasmodium vivax phenotypes VK210 and VK247 associated with the distribution of Anopheles albimanus and Anopheles pseudopunctipennis in Mexico. Am. J. Trop. Med. Hyg. 62:2000;122-127.
46. Gonzalez-Ceron L., et al. Plasmodium vivax: ookinete destruction and oocyst development arrest are responsible for Anopheles albimanus resistance to circumsporozoite phenotype VK247 parasites. Exp. Parasitol. 98:2001;152-161.
47. Joshi H., et al. Genetic structure of Plasmodium vivax isolates in India. Trans. R. Soc. Trop. Med. Hyg. 91:1997;231-235.
48. Anderson T.J., et al. Do malaria parasites mate non-randomly in the mosquito midgut? Genet. Res. 75:2000;285-296.
49. Hughes M.K., Hughes A.L. Natural selection on Plasmodium surface proteins. Mol. Biochem. Parasitol. 71:1995;99-113.
50. Escalante A.A., et al. Genetic polymorphism and natural selection in the malaria parasite Plasmodium falciparum. Genetics. 149:1998;189-202.
51. Verra F., Hughes A.L. Evidence for ancient balanced polymorphism at the Apical Membrane Antigen-1 (AMA-1) locus of Plasmodium falciparum. Mol. Biochem. Parasitol. 105:2000;149-153.
52. Polley S.D., Conway D.J. Strong diversifying selection on domains of the Plasmodium falciparum apical membrane antigen 1 gene. Genetics. 158:2001;1505-1512.
53. Conway D.J. Natural selection on polymorphic malaria antigens and the search for a vaccine. Parasitol. Today. 13:1997;26-29.
54. Escalante A.A., et al. Polymorphism in the gene encoding the Pfs48/45 antigen of Plasmodium falciparum. XI. Asembo Bay Cohort Project. Mol. Biochem. Parasitol. 119:2002;17-22.
55. Escalante A.A., et al. Evolutionary origin of human and primate malarias: evidence from the circumsporozoite protein gene. Mol. Biol. Evol. 12:1995;616-626.
56. 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.
57. Snounou G., Beck H.-P. The use of PCR-genotyping in the assessment of recrudescence or reinfection after antimalarial treatment. Parasitol. Today. 14:1998;462-467.
58. Del Portillo H.A., et al. A superfamily of variant genes encoded in the subtelomeric region of Plasmodium vivax. Nature. 410:2001;839-842.
59. Boyd M.F. Malariology. 1949;W.B. Saunders Co.
60. Young M.D., Eyles D.E. Parasites resembling Plasmodium ovale in strains of Plasmodium vivax. J. Natl. Malaria Soc. 8:1949;219-223.
61. Field J.W., et al. The Microscopic Diagnosis of Human Malaria. 1956;Government Press.
62. Shortt H.E., Garnham P.C.C. The pre-erythrocytic development of Plasmodium cynomolgi and Plasmodium vivax. Trans. Roy. S. Trop. Med. Hyg. 41:1948;785-795.
63. Krotoski W.A., et al. Relapses in primate malaria: discovery of two populations of exoerythrocytic stages. Preliminary note. Br. Med. J. 280:1980;153-154.
64. Krotoski W.A., et al. Demonstration of hypnozoites in sporozoite-transmitted Plasmodium vivax infection. Am. J. Trop. Med. Hyg. 31:1982;1291-1293.
65. Mazier D. Cultivation of the liver forms of Plasmodium vivax in human hepatocytes. Nature. 307:1984;367-369.