Skip to main content
Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1995 Apr;33(4):944–951. doi: 10.1128/jcm.33.4.944-951.1995

PCR typing of field isolates of Plasmodium falciparum.

H Contamin 1, T Fandeur 1, S Bonnefoy 1, F Skouri 1, F Ntoumi 1, O Mercereau-Puijalon 1
PMCID: PMC228073  PMID: 7790466

Abstract

We report on an analysis of the constraints of PCR typing of field Plasmodium falciparum isolates by using a few highly polymorphic markers, MSA-1, MSA-2, TRAP, and CS. We show that the reactions are specific for the P. falciparum species. The detection threshold (minimum number of parasites required to detect a visible band by ethidium bromide) differed from one marker to the other and, within one locus, from one primer combination to the other. Importantly, the various MSA-1 and MSA-2 reference alleles were amplified with the same efficiency. Amplification from reconstituted allele mixtures indicated that at certain allele ratios, the most abundant allele interfered with the amplification of the less abundant one. An analysis of nine isolates collected from patients with acute malaria in Dielmo, Senegal, during a transmission season when the inoculation rate was one infective bite every second night is presented and discussed. All samples contained more than one parasite type. A significant polymorphism was observed for the four markers. Novel TaqI restriction fragment length polymorphisms were found for the TRAP gene, and TRAP gene typing alone allowed a distinction between the various isolates. MSA-1 and MSA-2 gave multiple band patterns specific for each sample.

Full Text

The Full Text of this article is available as a PDF (384.9 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arnot D. E., Roper C., Bayoumi R. A. Digital codes from hypervariable tandemly repeated DNA sequences in the Plasmodium falciparum circumsporozoite gene can genetically barcode isolates. Mol Biochem Parasitol. 1993 Sep;61(1):15–24. doi: 10.1016/0166-6851(93)90154-p. [DOI] [PubMed] [Google Scholar]
  2. Babiker H. A., Creasey A. M., Fenton B., Bayoumi R. A., Arnot D. E., Walliker D. Genetic diversity of Plasmodium falciparum in a village in eastern Sudan. 1. Diversity of enzymes, 2D-PAGE proteins and antigens. Trans R Soc Trop Med Hyg. 1991 Sep-Oct;85(5):572–577. doi: 10.1016/0035-9203(91)90347-2. [DOI] [PubMed] [Google Scholar]
  3. Barker R. H., Jr, Banchongaksorn T., Courval J. M., Suwonkerd W., Rimwungtragoon K., Wirth D. F. A simple method to detect Plasmodium falciparum directly from blood samples using the polymerase chain reaction. Am J Trop Med Hyg. 1992 Apr;46(4):416–426. doi: 10.4269/ajtmh.1992.46.416. [DOI] [PubMed] [Google Scholar]
  4. Carter R., McGregor I. A. Enzyme variation in Plasmodium falciparum in the Gambia. Trans R Soc Trop Med Hyg. 1973;67(6):830–837. doi: 10.1016/0035-9203(73)90011-4. [DOI] [PubMed] [Google Scholar]
  5. Conway D. J., Greenwood B. M., McBride J. S. Longitudinal study of Plasmodium falciparum polymorphic antigens in a malaria-endemic population. Infect Immun. 1992 Mar;60(3):1122–1127. doi: 10.1128/iai.60.3.1122-1127.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Conway D. J., Greenwood B. M., McBride J. S. The epidemiology of multiple-clone Plasmodium falciparum infections in Gambian patients. Parasitology. 1991 Aug;103(Pt 1):1–6. doi: 10.1017/s0031182000059217. [DOI] [PubMed] [Google Scholar]
  7. Conway D. J., McBride J. S. Population genetics of Plasmodium falciparum within a malaria hyperendemic area. Parasitology. 1991 Aug;103(Pt 1):7–16. doi: 10.1017/s0031182000059229. [DOI] [PubMed] [Google Scholar]
  8. Creasey A., Fenton B., Walker A., Thaithong S., Oliveira S., Mutambu S., Walliker D. Genetic diversity of Plasmodium falciparum shows geographical variation. Am J Trop Med Hyg. 1990 May;42(5):403–413. doi: 10.4269/ajtmh.1990.42.403. [DOI] [PubMed] [Google Scholar]
  9. Dame J. B., Williams J. L., McCutchan T. F., Weber J. L., Wirtz R. A., Hockmeyer W. T., Maloy W. L., Haynes J. D., Schneider I., Roberts D. Structure of the gene encoding the immunodominant surface antigen on the sporozoite of the human malaria parasite Plasmodium falciparum. Science. 1984 Aug 10;225(4662):593–599. doi: 10.1126/science.6204383. [DOI] [PubMed] [Google Scholar]
  10. Fandeur T., Bonnefoy S., Mercereau-Puijalon O. In vivo and in vitro derived Palo Alto lines of Plasmodium falciparum are genetically unrelated. Mol Biochem Parasitol. 1991 Aug;47(2):167–178. doi: 10.1016/0166-6851(91)90176-7. [DOI] [PubMed] [Google Scholar]
  11. Fenton B., Clark J. T., Khan C. M., Robinson J. V., Walliker D., Ridley R., Scaife J. G., McBride J. S. Structural and antigenic polymorphism of the 35- to 48-kilodalton merozoite surface antigen (MSA-2) of the malaria parasite Plasmodium falciparum. Mol Cell Biol. 1991 Feb;11(2):963–971. doi: 10.1128/mcb.11.2.963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Galinski M. R., Medina C. C., Ingravallo P., Barnwell J. W. A reticulocyte-binding protein complex of Plasmodium vivax merozoites. Cell. 1992 Jun 26;69(7):1213–1226. doi: 10.1016/0092-8674(92)90642-p. [DOI] [PubMed] [Google Scholar]
  13. Kemp D. J., Cowman A. F., Walliker D. Genetic diversity in Plasmodium falciparum. Adv Parasitol. 1990;29:75–149. doi: 10.1016/s0065-308x(08)60105-0. [DOI] [PubMed] [Google Scholar]
  14. Kimura E., Mattei D., di Santi S. M., Scherf A. Genetic diversity in the major merozoite surface antigen of Plasmodium falciparum: high prevalence of a third polymorphic form detected in strains derived from malaria patients. Gene. 1990 Jul 2;91(1):57–62. doi: 10.1016/0378-1119(90)90162-k. [DOI] [PubMed] [Google Scholar]
  15. Kyes S., Craig A. G., Marsh K., Newbold C. I. Plasmodium falciparum: a method for the amplification of S antigens and its application to laboratory and field samples. Exp Parasitol. 1993 Dec;77(4):473–483. doi: 10.1006/expr.1993.1108. [DOI] [PubMed] [Google Scholar]
  16. Lockyer M. J., Marsh K., Newbold C. I. Wild isolates of Plasmodium falciparum show extensive polymorphism in T cell epitopes of the circumsporozoite protein. Mol Biochem Parasitol. 1989 Dec;37(2):275–280. doi: 10.1016/0166-6851(89)90159-x. [DOI] [PubMed] [Google Scholar]
  17. Marshall V. M., Anthony R. L., Bangs M. J., Purnomo, Anders R. F., Coppel R. L. Allelic variants of the Plasmodium falciparum merozoite surface antigen 2 (MSA-2) in a geographically restricted area of Irian Jaya. Mol Biochem Parasitol. 1994 Jan;63(1):13–21. doi: 10.1016/0166-6851(94)90004-3. [DOI] [PubMed] [Google Scholar]
  18. Marshall V. M., Coppel R. L., Martin R. K., Oduola A. M., Anders R. F., Kemp D. J. A Plasmodium falciparum MSA-2 gene apparently generated by intragenic recombination between the two allelic families. Mol Biochem Parasitol. 1991 Apr;45(2):349–351. doi: 10.1016/0166-6851(91)90104-e. [DOI] [PubMed] [Google Scholar]
  19. McBride J. S., Welsby P. D., Walliker D. Serotyping Plasmodium falciparum from acute human infections using monoclonal antibodies. Trans R Soc Trop Med Hyg. 1984;78(1):32–34. doi: 10.1016/0035-9203(84)90167-6. [DOI] [PubMed] [Google Scholar]
  20. Mercereau-Puijalon O., Fandeur T., Bonnefoy S., Jacquemot C., Sarthou J. L. A study of the genomic diversity of Plasmodium falciparum in Senegal. 2. Typing by the use of the polymerase chain reaction. Acta Trop. 1991 Sep;49(4):293–304. doi: 10.1016/0001-706x(91)90080-4. [DOI] [PubMed] [Google Scholar]
  21. Miller L. H., Roberts T., Shahabuddin M., McCutchan T. F. Analysis of sequence diversity in the Plasmodium falciparum merozoite surface protein-1 (MSP-1). Mol Biochem Parasitol. 1993 May;59(1):1–14. doi: 10.1016/0166-6851(93)90002-f. [DOI] [PubMed] [Google Scholar]
  22. Nussenzweig R. S., Yoshida N. Variation of T cell epitopes of the Plasmodium falciparum CS protein: its occurrence, extent and relevance. Immunol Lett. 1990 Aug;25(1-3):21–22. doi: 10.1016/0165-2478(90)90084-4. [DOI] [PubMed] [Google Scholar]
  23. Prescott N., Stowers A. W., Cheng Q., Bobogare A., Rzepczyk C. M., Saul A. Plasmodium falciparum genetic diversity can be characterised using the polymorphic merozoite surface antigen 2 (MSA-2) gene as a single locus marker. Mol Biochem Parasitol. 1994 Feb;63(2):203–212. doi: 10.1016/0166-6851(94)90056-6. [DOI] [PubMed] [Google Scholar]
  24. Ranford-Cartwright L. C., Balfe P., Carter R., Walliker D. Genetic hybrids of Plasmodium falciparum identified by amplification of genomic DNA from single oocysts. Mol Biochem Parasitol. 1991 Dec;49(2):239–243. doi: 10.1016/0166-6851(91)90067-g. [DOI] [PubMed] [Google Scholar]
  25. Robson K. J., Hall J. R., Davies L. C., Crisanti A., Hill A. V., Wellems T. E. Polymorphism of the TRAP gene of Plasmodium falciparum. Proc Biol Sci. 1990 Dec 22;242(1305):205–216. doi: 10.1098/rspb.1990.0126. [DOI] [PubMed] [Google Scholar]
  26. Saiki R. K., Scharf S., Faloona F., Mullis K. B., Horn G. T., Erlich H. A., Arnheim N. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science. 1985 Dec 20;230(4732):1350–1354. doi: 10.1126/science.2999980. [DOI] [PubMed] [Google Scholar]
  27. Schriefer M. E., Sacci J. B., Jr, Wirtz R. A., Azad A. F. Detection of polymerase chain reaction-amplified malarial DNA in infected blood and individual mosquitoes. Exp Parasitol. 1991 Oct;73(3):311–316. doi: 10.1016/0014-4894(91)90102-3. [DOI] [PubMed] [Google Scholar]
  28. Sethabutr O., Brown A. E., Panyim S., Kain K. C., Webster H. K., Echeverria P. Detection of Plasmodium falciparum by polymerase chain reaction in a field study. J Infect Dis. 1992 Jul;166(1):145–148. doi: 10.1093/infdis/166.1.145. [DOI] [PubMed] [Google Scholar]
  29. Smythe J. A., Coppel R. L., Day K. P., Martin R. K., Oduola A. M., Kemp D. J., Anders R. F. Structural diversity in the Plasmodium falciparum merozoite surface antigen 2. Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1751–1755. doi: 10.1073/pnas.88.5.1751. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Snewin V. A., Herrera M., Sanchez G., Scherf A., Langsley G., Herrera S. Polymorphism of the alleles of the merozoite surface antigens MSA1 and MSA2 in Plasmodium falciparum wild isolates from Colombia. Mol Biochem Parasitol. 1991 Dec;49(2):265–275. doi: 10.1016/0166-6851(91)90070-m. [DOI] [PubMed] [Google Scholar]
  31. Snounou G., Viriyakosol S., Jarra W., Thaithong S., Brown K. N. Identification of the four human malaria parasite species in field samples by the polymerase chain reaction and detection of a high prevalence of mixed infections. Mol Biochem Parasitol. 1993 Apr;58(2):283–292. doi: 10.1016/0166-6851(93)90050-8. [DOI] [PubMed] [Google Scholar]
  32. Snounou G., Viriyakosol S., Zhu X. P., Jarra W., Pinheiro L., do Rosario V. E., Thaithong S., Brown K. N. High sensitivity of detection of human malaria parasites by the use of nested polymerase chain reaction. Mol Biochem Parasitol. 1993 Oct;61(2):315–320. doi: 10.1016/0166-6851(93)90077-b. [DOI] [PubMed] [Google Scholar]
  33. Tanabe K., Mackay M., Goman M., Scaife J. G. Allelic dimorphism in a surface antigen gene of the malaria parasite Plasmodium falciparum. J Mol Biol. 1987 May 20;195(2):273–287. doi: 10.1016/0022-2836(87)90649-8. [DOI] [PubMed] [Google Scholar]
  34. Tirasophon W., Tassanakajon A., Boonsaeng V., Panyim S., Wilairat P. Sensitive detection of Plasmodium falciparum in blood and mosquito by DNA amplification. Parassitologia. 1993 Jul;35 (Suppl):117–120. [PubMed] [Google Scholar]
  35. Trape J. F., Rogier C., Konate L., Diagne N., Bouganali H., Canque B., Legros F., Badji A., Ndiaye G., Ndiaye P. The Dielmo project: a longitudinal study of natural malaria infection and the mechanisms of protective immunity in a community living in a holoendemic area of Senegal. Am J Trop Med Hyg. 1994 Aug;51(2):123–137. doi: 10.4269/ajtmh.1994.51.123. [DOI] [PubMed] [Google Scholar]
  36. Wataya Y., Arai M., Kubochi F., Mizukoshi C., Kakutani T., Ohta N., Ishii A. DNA diagnosis of falciparum malaria using a double PCR technique: a field trial in the Solomon Islands. Mol Biochem Parasitol. 1993 Mar;58(1):165–167. doi: 10.1016/0166-6851(93)90101-3. [DOI] [PubMed] [Google Scholar]
  37. Wooden J., Gould E. E., Paull A. T., Sibley C. H. Plasmodium falciparum: a simple polymerase chain reaction method for differentiating strains. Exp Parasitol. 1992 Sep;75(2):207–212. doi: 10.1016/0014-4894(92)90180-i. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Clinical Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES