Analysis of κ and ω repeats of the cg2 gene and chloroquine susceptibility in isolates of Plasmodium falciparum from sub-Saharan Africa

Molecular and Biochemical Parasitology

Volumn 101, Issue 1-2, 1999, Pages 185-197

  Durand, Rémy ^a   Gabbett, Elizabeth ^a   Di Piazza, Jean Philippe ^a   Delabre, Jean François ^a   Le Bras, Jacques ^a  

^a ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

Author keywords

cg2 gene; Chloroquine susceptibility; Plasmodium falciparum

Indexed keywords

CHLOROQUINE;

ADULT; AFRICA; AGED; ARTICLE; CHILD; CONTROLLED STUDY; DNA SEQUENCE; DRUG RESISTANCE; DRUG SENSITIVITY; FEMALE; GENE SEQUENCE; GENE STRUCTURE; GENETIC ANALYSIS; HUMAN; MALE; NONHUMAN; NUCLEOTIDE SEQUENCE; PLASMODIUM FALCIPARUM; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ADOLESCENT; ADULT; AFRICA SOUTH OF THE SAHARA; AGED; ANIMALS; ANTIMALARIALS; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CHLOROQUINE; FEMALE; GENES, PROTOZOAN; HUMANS; MALARIA, FALCIPARUM; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; PLASMODIUM FALCIPARUM; POLYMORPHISM, GENETIC; PROTOZOAN PROTEINS; REPETITIVE SEQUENCES, NUCLEIC ACID; SEQUENCE ANALYSIS, DNA;

PLASMODIUM FALCIPARUM;

EID: 0033066723     PISSN: 01666851     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0166-6851(99)00073-0     Document Type: Article

References (35)

1. World Health Organization. Management of uncomplicated malaria and the use of antimalarial drugs for the protection of travellers. In: World Health Organization publication no. WHO/MAL/96.1075. Geneva: World Health Organization, 1996.
2. World Health Organization. World malaria situation in 1993. Wkly. Epidemiol. Rec. 1996: 17-22; 25-29; 37-39; 41-48.
3. Payne D. Spread of chloroquine resistance in Plasmodium falciparum. Parasitol. Today. 3:1987;241-246.
4. Ginsburg H., Stein W.D. Kinetic modeling of chloroquine uptake by malaria-infected erythrocytes. Biochem. Pharmacol. 41:1991;1463-1470.
5. Krogstad D.J., Gluzman I.Y., Kyle D.E., Oduola A.M., Martin S.K., Milhous W.K., Schlesinger P.H. Efflux of chloroquine from Plasmodium falciparum: mechanism of chloroquine resistance. Science. 238:1987;1283-1285.
6. Martin S.K., Oduola A.M.J., Milhous W.K. Reversal of chloroquine resistance in Plasmodium falciparum by verapamil. Science. 235:1987;899-901.
7. Riordan J.R., Deuchars K., Kartner N., Alon N., Trent J., Ling V. Amplification of P-glycoprotein genes in multidrug-resistant mammalian cell lines. Nature. 316:1985;817-819.
8. Wilson C.M., Serrano A.E., Wasley A., Bogenschutz M.P., Shankar A.H., Wirth D.F. Amplification of a gene related to mammalian mdr genes in drug resistant Plasmodium falciparum. Science. 244:1989;1184-1186.
9. Foote S.J., Kyle D.E., Martin R.K., Oduola A.M.J., Forsyth K., Kemp D.J., Cowman A.F. Several alleles of the multidrug-resistance gene are closely linked to chloroquine resistance in Plasmodium falciparum. Nature. 345:1990;255-258.
10. Awad-El-Kariem F.M., Miles M.A., Warhurst D.C. Chloroquine resistant Plasmodium falciparum isolates from the Sudan lack two mutations in the pfmdr 1 gene thought to be associated with chloroquine resistance. Trans. R. Soc. Trop. Med. Hyg. 86:1992;587-589.
11. Basco L.K., Le Bras J., Rhoades Z., Wilson M.C. Analysis of pfmdr 1 and drug susceptibility in fresh isolates of Plasmodium falciparum from sub-Saharan Africa. Mol. Biochem. Parasitol. 74:1995;157-166.
12. Wellems T.E., Walker-Jonah A., Panton L.J. Genetic mapping of the chloroquine-resistance locus on Plasmodium falciparum chromosome 7. Proc. Natl. Acad. Sci. USA. 88:1991;3382-3386.
13. Su X.Z., Kirkman L.A., Fujioka H., Wellems T.E. Complex polymorphisms in an ≈330 kDA protein are linked to chloroquine-resistant P. falciparum in Southeast Asia and Africa. Cell. 91:1997;593-603.
14. Le Bras J., Deloron P., Ricour A., Andrieu B., Savel J., Coulaud J.P. Plasmodium falciparum: drug sensitivity in vitro of isolates before and after adaptation to continuous culture. Exp. Parasitol. 56:1983;9-14.
15. Le Bras J., Deloron P. In vitro study of drug sensitivity of Plasmodium falciparum: an evaluation of a new semi-micro test. Am. J. Trop. Med. Hyg. 32:1983;447-451.
16. Durand R., Ramiliarisoa O., Sécardin Y., Eldin de Pécoulas P., Basco L.K., Le Bras J. DHFR gene point mutation as a predictor of Plasmodium falciparum resistance to cycloguanil in malaria cases from Africa imported to France. Trans. R. Soc. Trop. Med. Hyg. 91:1997;460-461.
17. Higuchi R. Rapid, efficient DNA extraction for PCR from cells or blood. Amplification. 2:1989;1-3.
18. Bretagne S., Costa J.M., Vidaud M., Tran Van Nhieu J., Fleury-Feith J. Detection of Toxoplasma gondii by competitive DNA amplification of bronchoalveolar lavage samples. J. Inf. Dis. 168:1993;1585-1588.
19. Le Bras J., Durand R., Di Piazza J.P., Pradines B., Longuet C., Parzy D. Prise en compte des disparités de résistance de Plasmodium falciparum en Afrique dans la décision chimioprophylactique. Presse Med. 27:1998;1419-1423.
20. Creasey A., Fenton B., Walker A., Thaitong S., Oliveira S., Mutambu S., Walliker D. Genetic diversity of Plasmodium falciparum shows geographical variation. Am. J. Trop. Med. Hyg. 42:1990;403-413.
21. Conway D.J., Mc Bride J.S. Population genetics of Plasmodium falciparum within a malaria hyperendemic area. Parasitology. 109:1991;7-16.
22. Babiker H.A., Lines J., Hill W.G., Walliker D. Population structure of Plasmodium falciparum in villages with different malaria endemicity in east Africa. Am. J. Trop. Med. Hyg. 56:1997;141-147.
23. Paul R.E.L., Packer M.J., Walmsley M., Lagog M., Randford-Cartwright L.C., Paru R., Day K.P. Mating patterns in malaria parasite populations of Papua New Guinea. Science. 269:1995;1709-1711.
24. Ntoumi F., Contamin H., Rogier C., Bonnefoy S., Trape J.F., Mercereau-Puijalon O. Age-dependent carriage of multiple Plasmodium falciparum merozoite surface antigen-2 alleles in asymptomatic malaria infections. Am. J. Trop. Med. Hyg. 52:1995;81-88.
25. Luxemburger C., Thwai K.L., White N.J., Webster H.K., Kyle D.E., Maelankirri L., Chongsuphajaisiddhi T., Nosten F. The epidemiology of malaria in a Karen population on the western border of Thailand. Trans. R. Soc. Trop. Med. Hyg. 90:1996;105-111.
26. Tibayrenc M. Beyond strain typing and molecular epidemiology: integrated genetic epidemiology of infectious diseases. Parasitol. Today. 14:1998;323-329.
27. Conway D.J., Greenwood B.M., McBride J.S. The epidemiology of multiple-clone Plasmodium falciparum infections in Gambian patients. Parasitology. 103:1991;1-6.
28. Wooden J., Gould E.E., Paull A.T., Sibley C.H. Plasmodium falciparum: a simple polymerase chain reaction method for differentiating strains. Exp. Parasitol. 75:1992;207-212.
29. Viriyakosol S., Siripoon N., Petcharapirat C., Jarra W., Thaithong S., Brown K.N., Snounou G. Genotyping of Plasmodium falciparum isolates by the polymerase chain reaction and potential uses in epidemiological studies. Bull. World Health Organ. 73:1993;85-95.
30. Contamin H., Fandeur T., Bonnefoy S., Skoury F., Ntoumi F., Mercereau-Puijalon O. PCR typing of field isolates of Plasmodium falciparum. J. Clin. Microbiol. 33:1995;944-951.
31. Ohrt C., Mirabelli-Primdahl L., Karnasuta C., Chantakulkij S., Kain K.C. Distinguishing Plasmodium falciparum treatment failures from re-infections by restriction fragment length polymorphism and polymerase chain reaction genotyping. Am. J. Trop. Med. Hyg. 57:1997;430-437.
32. Willet G.P., Milhous W.K., Gerena L., Oduola A.M.J. Mixed population dynamics in human malaria parasite cultures. Trans. R. Soc. Trop. Med. Hyg. 85:1991;33-34.
33. Durand R, Di Piazza JP, Longuet C, Sécardin Y, Clain J, Le Bras J. Increased incidence of cycloguanil resistance in malaria cases entering France from Africa, determined as point mutations in parasites' dihydrofolate-reductase genes. Ann. Trop. Med. Parasitol. 1999;93:25-30.
34. + exchanger of Plasmodium falciparum? Cell 1998;92:601-602 (letter).
35. + exchangers. Cell. 94:1998;285-286.