TY - JOUR
T1 - Molecular epidemiology of drug-resistant malaria in western Kenya highlands
AU - Zhong, Daibin
AU - Afrane, Yaw
AU - Githeko, Andrew
AU - Cui, Liwang
AU - Menge, David M.
AU - Yan, Guiyun
N1 - Funding Information:
The authors thank Hong Chen, Emmanuel A. Temu, Thomas Loescher, David Warhurst and two anonymous reviewers for constructive comments on the manuscript. The work was supported by NIH grants R01 A150243, D43 TW01505, and R03 TW007360.
PY - 2008/7/3
Y1 - 2008/7/3
N2 - Background: Since the late 1980s a series of malaria epidemics has occurred in western Kenya highlands. Among the possible factors that may contribute to the highland malaria epidemics, parasite resistance to antimalarials has not been well investigated. Methods: Using parasites from highland and lowland areas of western Kenya, we examined key mutations associated with Plasmodium falciparum resistance to sulfadoxine - pyrimethamine and chloroquine, including dihydrofolate reductase (pfdhfr) and dihydropteroate synthetase (pfdhps), chloroquine resistance transporter gene (pfcrt), and multi-drug resistance gene 1 (pfmdr1). Results: We found that >70% of sam ples harbored 76T pfcrt mutations and over 80% of samples harbored quintuple mutations (51I/59R/108N pfdhfr and 437G/540E pfdhps) in both highland and lowland samples. Further, we did not detect significant difference in the frequencies of these mutations between symptomatic and asymptomatic malaria volunteers, and between highland and lowland samples. Conclusion: These findings suggest that drug resistance of malaria parasites in the highlands could be contributed by the mutations and their high frequencies as found in the lowland. The results are discussed in terms of the role of drug resistance as a driving force for malaria outbreaks in the highlands.
AB - Background: Since the late 1980s a series of malaria epidemics has occurred in western Kenya highlands. Among the possible factors that may contribute to the highland malaria epidemics, parasite resistance to antimalarials has not been well investigated. Methods: Using parasites from highland and lowland areas of western Kenya, we examined key mutations associated with Plasmodium falciparum resistance to sulfadoxine - pyrimethamine and chloroquine, including dihydrofolate reductase (pfdhfr) and dihydropteroate synthetase (pfdhps), chloroquine resistance transporter gene (pfcrt), and multi-drug resistance gene 1 (pfmdr1). Results: We found that >70% of sam ples harbored 76T pfcrt mutations and over 80% of samples harbored quintuple mutations (51I/59R/108N pfdhfr and 437G/540E pfdhps) in both highland and lowland samples. Further, we did not detect significant difference in the frequencies of these mutations between symptomatic and asymptomatic malaria volunteers, and between highland and lowland samples. Conclusion: These findings suggest that drug resistance of malaria parasites in the highlands could be contributed by the mutations and their high frequencies as found in the lowland. The results are discussed in terms of the role of drug resistance as a driving force for malaria outbreaks in the highlands.
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U2 - 10.1186/1471-2334-8-105
DO - 10.1186/1471-2334-8-105
M3 - Article
C2 - 18671871
AN - SCOPUS:51649106416
SN - 1471-2334
VL - 8
JO - BMC Infectious Diseases
JF - BMC Infectious Diseases
M1 - 105
ER -