High prevalence of mutations in the dihydrofolate reductase gene of Plasmodium falciparum in isolates from Tanzania without evidence of an association to clinical sulfadoxine/pyrimethamine resistance

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

High prevalence of mutations in the dihydrofolate reductase gene of Plasmodium falciparum in isolates from Tanzania without evidence of an association to clinical sulfadoxine/pyrimethamine resistance. / Jelinek, T; Rønn, A M; Curtis, J; Duraisingh, M T; Lemnge, M M; Mhina, J; Bygbjerg, I C; Warhurst, D C.

In: Tropical Medicine & International Health, Vol. 2, No. 11, 1997, p. 1075-9.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Jelinek, T, Rønn, AM, Curtis, J, Duraisingh, MT, Lemnge, MM, Mhina, J, Bygbjerg, IC & Warhurst, DC 1997, 'High prevalence of mutations in the dihydrofolate reductase gene of Plasmodium falciparum in isolates from Tanzania without evidence of an association to clinical sulfadoxine/pyrimethamine resistance', Tropical Medicine & International Health, vol. 2, no. 11, pp. 1075-9.

APA

Jelinek, T., Rønn, A. M., Curtis, J., Duraisingh, M. T., Lemnge, M. M., Mhina, J., Bygbjerg, I. C., & Warhurst, D. C. (1997). High prevalence of mutations in the dihydrofolate reductase gene of Plasmodium falciparum in isolates from Tanzania without evidence of an association to clinical sulfadoxine/pyrimethamine resistance. Tropical Medicine & International Health, 2(11), 1075-9.

Vancouver

Jelinek T, Rønn AM, Curtis J, Duraisingh MT, Lemnge MM, Mhina J et al. High prevalence of mutations in the dihydrofolate reductase gene of Plasmodium falciparum in isolates from Tanzania without evidence of an association to clinical sulfadoxine/pyrimethamine resistance. Tropical Medicine & International Health. 1997;2(11):1075-9.

Author

Jelinek, T ; Rønn, A M ; Curtis, J ; Duraisingh, M T ; Lemnge, M M ; Mhina, J ; Bygbjerg, I C ; Warhurst, D C. / High prevalence of mutations in the dihydrofolate reductase gene of Plasmodium falciparum in isolates from Tanzania without evidence of an association to clinical sulfadoxine/pyrimethamine resistance. In: Tropical Medicine & International Health. 1997 ; Vol. 2, No. 11. pp. 1075-9.

Bibtex

@article{46f2c580e61511ddbf70000ea68e967b,
title = "High prevalence of mutations in the dihydrofolate reductase gene of Plasmodium falciparum in isolates from Tanzania without evidence of an association to clinical sulfadoxine/pyrimethamine resistance",
abstract = "Recently the efficacy of sulfadoxine/pyrimethamine (S/P) in treatment of uncomplicated falciparum malaria in Tanzania has been seriously compromised by the development of resistance. The occurrence of active site mutations in the Plasmodium falciparum gene sequence coding for dihydrofolate reductase (DHFR) is known to confer resistance to pyrimethamine. This study investigates the occurrence of these mutations in infected blood samples taken from Tanzanian children before treatment with S/P and their relationship to parasite breakthrough by day 7. The results confirm the occurrence of one or more DHFR mutations in all the samples, but no relationship was found with the presence of parasites in the blood at day 7. The results suggest that alterations in the coding region for dihydropteroate synthetase (DHPS), the enzyme target for sulfadoxine, should be studied in order to predict resistance to the S/P combination. It has been proposed earlier that sulfadoxine could itself act on DHFR, because of a false dihydrofolate produced by drug metabolism through DHPS and dihydrofolate synthase. The results of this treatment study suggest that such a possibility is unlikely.",
author = "T Jelinek and R{\o}nn, {A M} and J Curtis and Duraisingh, {M T} and Lemnge, {M M} and J Mhina and Bygbjerg, {I C} and Warhurst, {D C}",
note = "Keywords: Animals; Antimalarials; Child; Child, Preschool; DNA, Protozoan; Drug Combinations; Drug Resistance; Female; Humans; Infant; Malaria, Falciparum; Male; Plasmodium falciparum; Point Mutation; Pyrimethamine; Sulfadoxine; Tanzania; Tetrahydrofolate Dehydrogenase",
year = "1997",
language = "English",
volume = "2",
pages = "1075--9",
journal = "Tropical Medicine & International Health",
issn = "1360-2276",
publisher = "Wiley-Blackwell",
number = "11",

}

RIS

TY - JOUR

T1 - High prevalence of mutations in the dihydrofolate reductase gene of Plasmodium falciparum in isolates from Tanzania without evidence of an association to clinical sulfadoxine/pyrimethamine resistance

AU - Jelinek, T

AU - Rønn, A M

AU - Curtis, J

AU - Duraisingh, M T

AU - Lemnge, M M

AU - Mhina, J

AU - Bygbjerg, I C

AU - Warhurst, D C

N1 - Keywords: Animals; Antimalarials; Child; Child, Preschool; DNA, Protozoan; Drug Combinations; Drug Resistance; Female; Humans; Infant; Malaria, Falciparum; Male; Plasmodium falciparum; Point Mutation; Pyrimethamine; Sulfadoxine; Tanzania; Tetrahydrofolate Dehydrogenase

PY - 1997

Y1 - 1997

N2 - Recently the efficacy of sulfadoxine/pyrimethamine (S/P) in treatment of uncomplicated falciparum malaria in Tanzania has been seriously compromised by the development of resistance. The occurrence of active site mutations in the Plasmodium falciparum gene sequence coding for dihydrofolate reductase (DHFR) is known to confer resistance to pyrimethamine. This study investigates the occurrence of these mutations in infected blood samples taken from Tanzanian children before treatment with S/P and their relationship to parasite breakthrough by day 7. The results confirm the occurrence of one or more DHFR mutations in all the samples, but no relationship was found with the presence of parasites in the blood at day 7. The results suggest that alterations in the coding region for dihydropteroate synthetase (DHPS), the enzyme target for sulfadoxine, should be studied in order to predict resistance to the S/P combination. It has been proposed earlier that sulfadoxine could itself act on DHFR, because of a false dihydrofolate produced by drug metabolism through DHPS and dihydrofolate synthase. The results of this treatment study suggest that such a possibility is unlikely.

AB - Recently the efficacy of sulfadoxine/pyrimethamine (S/P) in treatment of uncomplicated falciparum malaria in Tanzania has been seriously compromised by the development of resistance. The occurrence of active site mutations in the Plasmodium falciparum gene sequence coding for dihydrofolate reductase (DHFR) is known to confer resistance to pyrimethamine. This study investigates the occurrence of these mutations in infected blood samples taken from Tanzanian children before treatment with S/P and their relationship to parasite breakthrough by day 7. The results confirm the occurrence of one or more DHFR mutations in all the samples, but no relationship was found with the presence of parasites in the blood at day 7. The results suggest that alterations in the coding region for dihydropteroate synthetase (DHPS), the enzyme target for sulfadoxine, should be studied in order to predict resistance to the S/P combination. It has been proposed earlier that sulfadoxine could itself act on DHFR, because of a false dihydrofolate produced by drug metabolism through DHPS and dihydrofolate synthase. The results of this treatment study suggest that such a possibility is unlikely.

M3 - Journal article

C2 - 9391510

VL - 2

SP - 1075

EP - 1079

JO - Tropical Medicine & International Health

JF - Tropical Medicine & International Health

SN - 1360-2276

IS - 11

ER -

ID: 9830635