Open Access

The implication of dihydrofolate reductase and dihydropteroate synthetase gene mutations in modification of Plasmodium falciparum characteristics

  • Ishraga E A-Elbasit1,
  • Michael Alifrangis2,
  • Insaf F Khalil2,
  • Ib C Bygbjerg2,
  • Emad M Masuadi3,
  • Mustafa I Elbashir1 and
  • Hayder A Giha1, 3Email author
Malaria Journal20076:108

DOI: 10.1186/1475-2875-6-108

Received: 31 May 2007

Accepted: 08 August 2007

Published: 08 August 2007



The Plasmodium falciparum dihydrofolate reductase (DHFR) and dihydropteroate synthetase (DHPS) are enzymes of central importance in parasite metabolism. The dhfr and dhps gene mutations are known to be associated with sulphadoxine/pyrimethamine (SP) resistance.


To investigate the effects of dhfr/dhps mutations on parasite characteristics other than SP resistance.


Parasite infections obtained from 153 Sudanese patients with uncomplicated falciparum malaria treated with SP or SP + chloroquine, were successfully genotyped at nine codons in the dhfr/dhps genes by PCR-ELISA.

Results & conclusion

Mutations were detected in dhfr at N51I, S108N and C59R, and in at dhps at A/S436F, A437G, K540E and A581G, the maximum number of mutations per infection were five. Based on number of mutant codons per infection (multiplicity of mutation, MOM), the infections were organized into six grades: wild-types (grade 0; frequency, 0.03) and infections with MOM grades of 1 to 5, with the following cumulative frequency; 0.97, 0.931, 0.866, 0.719, 0.121, respectively. There was no significant association between the MOM and SP response. Importantly, immunity, using age as a surrogate marker, contributed significantly to the clearance of parasites with multiple dhfr/dhps mutations. However, these mutations have a survival advantage as they were associated with increased gametocytogenesis. The above implications of dhfr/dhps mutations were associated with MOM 2 to 5, regardless of the gene/codon locus.


Falciparum malaria is still out of control, primarily because of the ability of the parasite to develop resistance against the used drugs. But, also the fast disseminations of the resistant parasites and possibly the accelerated ability of the parasite to develop resistance against new drugs, are important factors [1]. Sulphadoxine/pyrimethamine (SP), has been an alternative to CQ for treatment and control of uncomplicated malaria in endemic countries, it was effective, affordable and complying drug. The fixed combination in SP inhibits the action of two enzymes, dihydrofolate reductase (DHFR) and dihydropteroate synthetase (DHPS) in folate metabolism pathway [2, 3]. Mutations in the parasite genes coding for the two enzymes, dhfr and dhps, lead to SP resistance, however, the mutations also affect the parasite population, fitness and evolution [4, 5].

Although elimination of the asexual stages of Plasmodium falciparum is the focus of the treatment of individual symptomatic patients, at population level, reducing the carriage of gametocytes is necessary to limit the transmission of malaria parasites and the spread of anti-malarial drug resistance. In relation to SP treatment, the gametocyte carriage and infectivity to mosquitoes was found to be consistently higher in patients infected with drug resistant compared with drug sensitive malaria parasites [6].

In malaria endemic areas, the host immune system acts synergistically with chemotherapy in the clearance of parasites [7]. The susceptibility of parasites with mutations to the host immune mechanisms is largely unknown. In studies done in Mali, the term genotype-resistance index (GRI) was introduced to correct for the differences between the two arms of the equation; the treatment failure rate and the prevalence of parasite mutations [8]. This index is a proxy for the role of immunity, which varies between epidemiological settings, and in the same setting depends on the age. The hypothesis on which this study was based was a combination of two old observations, the association of drug resistance with dhfr/dhps mutation, and the implication of immunity in clearance of drug resistant parasites. That implies, the dhfr/dhps mutant parasites might be more susceptible than the wild variants to host immune clearance. Further more the study aim to investigate the relationship between the dhfr/dhps mutations and the parasite fitness in term of; in-vivo parasite growth and gametocytogenesis. This data is complementary to a previous report in which these parameters were analysed in relation to in-vivo drug response [9].


Study area, population and parasites

The study was carried out in Daraweesh and Kajara villages in Eastern Sudan, the details is mentioned elsewhere [9]. The major characteristics of this setting are seasonality and marked instability of malaria transmission, and susceptibility of people in all age groups to malaria infection. This study was conducted in 2003, one year before the official replacement of CQ with artesunate/SP combination therapy as first-line treatment for malaria.

All patients with uncomplicated P. falciparum malaria (n, 254) in all age groups were enrolled in the study, excluding pregnant women and severely ill patients. A modified protocol for assessment of drug resistance was used [10]. The study design, in-vivo results and classification of treatment outcome into: early treatment failure (ETF), late treatment failure (LTF), and adequate clinical and parasitological response (ACR), were presented before [9]. However, PCR was not done to confirm that all microscopically confirmed ACPR infections were not having sub-microscopic parasitaemia. Blood collected in filter papers during 28-day follow up was used for genotyping to confirm recrudescence.

A subset of 168 infections, obtained from patients with (TF, 82) and randomly selected patients with (ACR, 86), were genotyped in the P. falciparum genes dhfr and dhps. Only 153 parasite infections were successfully genotyped at all examined loci, 78 from patients with ACR and 75 from patients with TF (included 17 ETF, and the remaining were LTF). The informed consent of the patient or guardian was obtained, and institutional and national ethical clearance were obtained from the Sudan Ministry of Health.

DNA extraction, PCR and SSOP-ELISA for detection of drug-resistance-associated mutations

The parasite DNA was prepared from filter papers as described before [11]. Single nucleotide polymorphisms (SNP) and haplotypes of the SP resistance genes; dhfr and dhps (SP), were analysed by a recently developed PCR-SSOP-ELISA method [12]. The laboratory clones; 3D7, 7G8, Dd2, FCR3 and K1, and four field infections expressing the 164L of dhfr and 436/437AA, 436/437AG and 540E genotypes of dhps, respectively, were used as a standard positive control. Known SNPs of dhfr and dhps are represented in this panel of parasites. The nested PCR followed by SSOP-ELISA were performed as described before [12].

The multiplicity of mutations (MOM)

Based on the number of dhfr/dhps mutations regardless of their loci (multiplicity of mutations – MOM), parasite infections were grouped into six grades, wild infections (MOM = 0), and infections with 1, 2, 3, 4 or 5 mutations (MOM 1 to 5). Some parasite infections were negative for one or more of the examined dhfr/dhps loci (n = 15) and they were excluded from MOM grouping. The types of mutations in the different MOM grades are shown in Figure 1. In Table 1 a cumulative MOM classification was used to calculate the GRI and to estimate the prevalence of mutations in relation to the treatment outcome. Parasites of a cumulative MOM grade of 1, were parasites had at least one dhfr/dhps mutation, by definition this includes all parasites with any number of mutation (MOM 1–5), and parasites of cumulative MOM 2 includes parasites with MOM 2–5 and etc.
Figure 1

The distribution of the individual dhfr/dhps mutant codons (small bars with different shading grade) in parasites infections with different MOM (multiplicity of mutations) grades (multi-bar columns) was shown numerically in y-axis. The parasite infections were obtained from patients with uncomplicated malaria (n = 153), genotyped at dhfr/dhps loci, and grouped into five groups based on the number of mutations per parasite (MOM 1 – 5), as indicated by in x-axis. The type of mutant codons were shown in the key.

Table 1

The frequency of the different dhfr/dhps multiple mutations (multiplicity of mutations, MOM), in parasite infections obtained from patients with different treatment outcome, ACR and TF, following SP and CQ therapy, and the overall prevalence rate of MOM and the corresponding mutation/TF ratio.

Multiplicity of mutation (MOM)

Frequency of cumulative MOM

Overall prevalence of cumulative MOM

Mutation/TF ratio (GRI)


ACR (n,78)

TF (n,75)

P-value Chi-Square

measured N1 = 153

calculated N2 = 231


Null (wild)

0.038 (3)

0.013 (1)


2.6% (4)

03% (7)



0.962 (75)

0.987 (74)


97.4% (149)

97.0% (224)



0.910 (71)

0.973 (73)


94.1% (144)

93.1% (215)



0.846 (66)

0.907 (68)


87.6% (134)

86.6% (200)



0.679 (53)

0.800 (60)


73.9% (113)

71.9% (166)



0.103 (8)

0.160 (12)


13.1% (20)

12.1% (28)


ACR, adequate clinical response; TF, treatment failure; MOM, multiplicity of mutations; Mutation/TF ratio = prevalence of MOM (calculated)/TF rate (35.4)]. N1, number of genotyped samples; N2, total number of samples; GRI, genotype-resistance index

Statistical analysis

The Statistical Product and Service Solutions (SPSS; version 13) software was used for the statistical analysis. Independent T-test was used to compare between subgroups of patients infected by parasites with (MOM 0 to 5) but different response (ACR and TF) regarding parasite density and patient's age. ANOVA was used for comparing parasite densities between all study groups. The gametocyte prevalence and longevity was compared between parasite infections with different number of mutations by calculating the Odds Ratio and using Chi-Square Tests, respectively.


Clinical, parasitological and genotyping data

The clinical and parasitological data was presented before [9]. Briefly, the treatment response of the two treatment groups (SP and SP/CQ) was comparable, TF of SP alone (31.7%) and of SP plus CQ (36.6%) was similar, and the overall TF rate was 35.4% (90/254, PCR-corrected). The parasite infections used in this study were obtained from 168 patients treated with SP/CQ (n = 127; mean age 22.5 ± 16.4 Y) and SP alone (n = 41; 22.9 ± 15.5 Y). The prevalence of the individual dhfr mutations; 51I, 108N, 59R and 164L, were 0.89, 0.89, 0.005 and 0.0, respectively, and that of dhps; 437G, 540E, 581G, 436F and 613T, were; 0.88, 0.77, 0.13, 0.005 and 0.0 respectively.

Overall prevalence of MOM, and its relation with the treatment response

The subset of analysed samples (n, 153) represented most of the SP-resistant parasite and 45% of the SP-sensitive parasite population. Still, the MOM prevalence according to the analysed samples was similar to that calculated from the total parasite population (n, 231; the remaining 23 infections were the calculated to be negative in at least one of the examined loci, if all 254 infections were genotyped) (Table 1). The overall prevalence of infections with at least one, two, three, four or five mutations (cumulative MOM 1–5), as estimated from the total population, were: 0.97, 0.93, 0.87, 0.72 and 0.12, respectively. The prevalence of cumulative MOM 0–5 was comparable between the treatment outcome groups, the ACR and TF. Only four parasite infections (0.026) were found carrying wild-type alleles in all examined loci (Table 1). Alternatively, taking all patients infected with parasites of the same MOM grade together, the proportion of patients had TF was 25% and 20% in groups of patients infected with parasites had MOM 0 and 1, respectively, and 60% in patients had infections with MOM5. The proportions of the TF in infections of MOM 2–4 ranged between the above mentioned values (Figure 2A), however, all the differences were not significant. The frequency of the MOM 0–5 (non-cumulative) was also not different between the parasite infections obtained from patients with ACR and TF response, and between ETF and LTF (data not shown). The infections with single mutation (MOM 1) were few (n = 5) and comparable to the wild-type infections (MOM 0) in number (n = 4) and other characteristics as will be shown
Figure 2

Comparisons between parasite groups of different dhfr/dhps genotype profile; wild parasite infections and infections with different number of mutations (MOM 1 to MOM 5), and in each parasite group between infections obtained from patients attended adequate clinical response (ACR) (white bars) and those had treatment failure (TF) (back bars). The test parameters were; A. The proportions of patients with different treatment outcome in each group (upper) B. The mean ages of the parasite donors in years (middle). C. The pre-treatment parasite density (lower). The pattern in wild infections and infections with single mutation (MOM 1) was different from that in infections with MOM 2 to 5.

Multiplicity of mutations, age and immunity

Patients with a TF outcome were significantly younger in age than patients achieving an ACR (P > 0.001), but no significant difference in age between ETF and LTF (P = 0.193). Patients infected with parasites with different number of mutations including the wild-type parasites (MOM 0–5), were not different in age (P = 0.839, ANOVA) (Figure 2B, comparison between all double bars). However, for patients infected with parasites of the same MOM grade, patients achieved ACR were mostly significantly older in age than patients had TF (Figure 2B, comparison between black and white bars in each pair separately); MOM2: (P = 0.052), MOM3: (P = 0.34), MOM4: (0.042) and MOM5: (P = 0.019). But no significant difference between the two groups (ACR vs TF) when infections caused by wild parasites (P = 0.79) or parasites with a single mutation (P = 0.76).

The role of immunity in clearance of mutant parasites was estimated by calculation of the ratio of cumulative MOM prevalence to the corresponding TF rate, GRI, which varied between 2.03 and 2.74 (excluding MOM 5, prevalence less than TF rate), as shown in Table 1.

Multiplicity of mutations and pre-treatment (D0) parasitaemia

There was no significant difference in the pretreatment (D0) parasite density between ACR and TF donors of these samples (P = 0.143). However, there was a certain trend of differences in parasite density between patients infected with parasites with different dhfr/dhps mutations (MOM 0 to 5; P = 0.066, ANOVA). For infections of the same number of mutations (MOM), the parasite count was higher in patients with ACR outcome if the MOM grade was 0 or 1, and the reverse was true (i.e. higher count in TF) if the MOM grade was 2 to 5. However, the difference was only significant for MOM4 parasite infections, P = 0.022, Independent T-Test, (Figure 2C).

Multiplicity of mutations and gametocytogenesis

Gametogenesis, was defined as the ability of the infections to produce gametocytes at least once during follow up (D0, 3, 7, 14, 21 and 28), while gametocyte longevity, refers to the number of times gametocytes were detected during the follow up. The later was scaled from 0 (no gametocyte detected) to 6 (gametocytes detected in the 6 days of follow up). Both parameters are indices for gametocytogenesis in-vivo. None of the wild-type or MOM1 infections (n = 9) produced gametocytes during the follow up, while parasites with multiple mutations (MOM 2–5) had high rates of gametogenesis (60 – 70%), the difference was strongly significant (P = 0.004, Chi-Square Tests). The odd ratios confirmed the difference in gametogenesis between MOM 0 – 1 and MOM 2 – 5 parasite infections (Table 2). For the comparison of the gametocyte longevity in infections with parasites of different MOM grades, there was significant difference between infections with MOM 0 – 1 and MOM 2 – 5, (P = 0.002), Table 2.
Table 2

The gametocyte rate – gametogenesis – and gametocyte longevity (gametocytogenesis) in malaria infections caused by wild-type parasites and parasites with different number of dhfr/dhps mutations (MOM 1 – 5). The differences in gametogenesis between parasites with different MOM were estimated by calculation of the Odd ratios with reference to MOM5.




Gametocyte longevity




Odd Ratio

95% CI










6 (max)

*Wild (4)













*Single (5)













Double (10)













Triple (21)













Quadruple (93)













Quintuple (20)













* In the two groups the test parameters were significantly lower than in the other groups


The mutations of genes encoding important enzymes such as DHFR and DHPS, should affects parasite metabolism and indeed change certain parasite characteristics. The goal of this study is to understand the implications of gene mutations of the two enzymes in certain parasite characteristics, namely the susceptibility of the parasite to immune clearance (parasite fitness), sexual reproduction (gametocytogenesis) and asexual reproduction (parasite growth).

The dhfr/dhps gene mutations are known to be involved in parasite resistance to SP [2, 3], and in-vivo studies have shown that immunity is involved in clearance of drug resistant parasites [9, 13]. Taken together, the dhfr/dhps mutations are probably involved in immune clearance of SP resistant infections. In this study the ratio of TF to prevalence of the predominant quadruple dhfr/dhps mutations (MOM 4) was approximately 1: 2, that was a circumstantial evidence for the role of host immunity in clearance of mutant parasites. The supporting evidence was the higher age (a surrogate marker for immunity) of the successfully treated patients. Interestingly, the ratio of MOMs prevalence to the actual treatment failure (2.03 and 2.74) is similar to the GRI (genotype resistance index) in Mali (1.6 to 2.8), a region epidemiologically similar to this study site [14], although different drugs were used. The specific evidence for the increased suscebtibilty of the dhfr/dhps multi-mutant parasites to immune clearance was the difference in age of the patients infected with parasites with the same number of mutations (MOM grade) but had different treatment outcome. This difference in age (ACR vs TF) was limited to the parasite infections with multiple mutations (MOM 2–5), but not to infections with wild parasites and parasites with single mutation (Figure 2B). For identification of the most important mutations (loci), larger sample size is needed, however, in this study, 51I, 108N, 437G and 540E were the predominant mutations (Figure 1). Furthermore, the reduced resistance of multi-mutant parasites to host immunity is a sign of reduced fitness, supporting previous reports [4, 5, 15]. The degree of immunity which is required for clearance of parasite with specific number of mutation was estimated by the GRI value. The interpretation of this data indicates that, there are at least three factors directly contributing to parasite clearance (ACR): the drug (SP), immunity (represented by age) and parasite mutations (MOM > 1). The paradox is that, the dhfr/dhps mutations provide the parasite the ability to resist chemotherapy, while it renders it more susceptible to the host immunity.

The pre-treatment parasite density probably reflects the in-vivo parasite growth, assuming that sequestration is confined to severe malaria infection; and the peripheral parasitaemia represents the total parasite load. In this study, the parasite growth was influenced by dhfr/dhps mutations where growth of wild and parasites with single mutation (MOM 1) was relatively higher from that of multi-mutant parasites in patients achieved ACR and the reverse was true in case of TF (Figure 2C). However, these results (trends) need to be taken with precaution because the sample size was small and the accuracy of the microscopic estimation of parasitaemia is not high, in addition parasite sequestration is not confined to severe malaria. In a previous study in the same site it was found that, there was significant association between reduced parasite growth and dhfr/dhps mutations [15].

It is known that, the frequency of gametocytaemia increases with treatment failure [16], treatment with SP [17] and younger age [9]. In this study, the gametogenesis was significantly higher in parasites with multiple dhfr/dhps mutations compared to wild type and parasites with single mutation, as recognized in other studies [18, 19]. However, only two dhfr/dhps mutations (MOM2) were needed to enhance the gametocytogenesis significantly, with no additive effect for more mutations (MOM 3–5). In the in-vivo study, the patient achieved ACR had significantly lower frequency of gametocytaemia compared to patients who had TF. The association between gametocytogenesis and dhfr/dhps mutations was independent of the treatment outcome and the host age. That is because, there was no association between the treatment outcome and the mutations in this study, and the age of patients infected with wild-type parasite and parasites with MOM1 (median 13 years) was not different from the age of patients who had TF (median, 12 years). Also, the differences cannot be due to gametocytogenic effect of SP treatment, as all patients were treated with SP. Although, the gametocytogenesis is the corner stone in the spread of the resistant strains, there are only few studies that had evoked the issue at the molecular level [15, 19]. Finally, it is difficult to look at these parasite characteristics of gametocytogenesis, immune clearance and in-vivo parasite growth in isolation of drug resistance since they are not independent from each other, thus, further studies are needed for detailed molecular exploration.

In conclusion, the dhfr/dhps gene mutations in P. falciparum are probably affecting the parasite fitness by rendering the parasite more susceptible to immune clearance than the wild-type variants. The increased immune clearance of mutant parasites can explain the lack of association between the prevalence of dhfr/dhps mutations and the TF rate in this setting. Furthermore, there were indications that the in-vivo asexual growth of the dhfr/dhps multi-mutant parasites was lower compared to wild types, while the gametocytogenesis in the former group was significantly higher than in the later. That is more likely an evolutionary mechanism compensating for the reduced asexual reproduction, and also can explain the fast propagation of SP resistance. Finally, the above-mentioned implications need only two (double) mutations in the dhfr/dhps genes irrespective of their codon/gene locus, while it was reported, SP resistance is associated with higher number of mutations in specific loci.



The families in Daraweesh and Kajara villages, our research team; Adil Ameen, Faiz Omer and others are all acknowledged for making the field a success with meager facilities. This work would have not been done without the technical support of the Copenhagen team. Professor M. Hommel is thanked for the editing and for the remarks made to improve the manuscript. This investigation received technical and financial support from the joint WHO Eastern Mediterranean Region (EMRO), Division of Communicable Disease (DCD) and WHO Special Programme for Research and Training in Tropical Disease (TDR): The EMRO DCD/TDR Small Grants Scheme for Operational Research in Tropical and Other Communicable Disease, project number SGS02/110.

Authors’ Affiliations

Malaria Research Centre (MalRC), Department of Biochemistry, Faculty of Medicine, University of Khartoum
Centre for Medical Parasitology (CMP) at Institute of Medical Microbiology and Immunology and Institute of Public Health, University of Copenhagen
Department of Biochemistry, and Department of Family & Community Medicine, Faculty of Medicine and Medical Sciences, Arabian Gulf University (AGU)


  1. Le Bras J, Durand R: The mechanisms of resistance to antimalarial drugs in Plasmodium falciparum. Fundam Clin Pharmacol. 2003, 17: 147-153. 10.1046/j.1472-8206.2003.00164.x.View ArticlePubMedGoogle Scholar
  2. Peterson DS, Walliker D, Wellems TE: Evidence that a point mutation in dihydrofolate reductase-thymidylate synthase confers resistance to pyrimethamine in falciparum malaria. Proc Natl Acad Sci USA. 1988, 85: 9114-9118. 10.1073/pnas.85.23.9114.PubMed CentralView ArticlePubMedGoogle Scholar
  3. Triglia T, Menting JG, Wilson C, Cowman AF: Mutations in dihydropteroate synthase are responsible for sulfone and sulfonamide resistance in Plasmodium falciparum . Proc Natl Acad Sci USA. 1997, 94: 13944-13949. 10.1073/pnas.94.25.13944.PubMed CentralView ArticlePubMedGoogle Scholar
  4. Hastings IM, Donnelly MJ: The impact of antimalarial drug resistance mutations on parasite fitness, and its implications for the evolution of resistance. Drug Resist Updat. 2005, 8: 43-50. 10.1016/j.drup.2005.03.003.View ArticlePubMedGoogle Scholar
  5. Walliker D, Hunt P, Babiker H: Fitness of drug-resistant malaria parasites. Acta Trop. 2005, 94: 251-259.View ArticlePubMedGoogle Scholar
  6. Barnes KI, White NJ: Population biology and antimalarial resistance: The transmission of antimalarial drug resistance in Plasmodium falciparum . Acta Trop. 2005, 94: 230-240.View ArticlePubMedGoogle Scholar
  7. Francis D, Nsobya SL, Talisuna A, Yeka A, Kamya MR, Machekano R, Dokomajilar C, Rosenthal PJ, Dorsey G: Geographic differences in antimalarial drug efficacy in Uganda are explained by differences in endemicity and not by known molecular markers of drug resistance. J Infect Dis. 2006, 193: 978-986. 10.1086/500951.View ArticlePubMedGoogle Scholar
  8. Plowe CV: Monitoring antimalarial drug resistance: making the most of the tools at hand. J Exp Biol. 2003, 206: 3745-3752. 10.1242/jeb.00658.View ArticlePubMedGoogle Scholar
  9. A-Elbasit IE, Elbashir MI, Khalil IF, Alifrangis M, Giha HA: The efficacy of sulfadoxine-pyrimethamine alone and in combination with chloroquine for malaria treatment in rural Eastern Sudan: the interrelation between resistance, age and gametocytogenesis. Trop Med Int Health. 2006, 11: 604-612. 10.1111/j.1365-3156.2006.01616.x.View ArticlePubMedGoogle Scholar
  10. WHO: Assessment of therapeutic efficacy of antimalarial drugs for uncomplicated malaria in areas with intense transmission. 1996, WHO, Geneva, (WHO/MAL/96.1077)Google Scholar
  11. Pearce RJ, Drakeley C, Chandramohan D, Mosha F, Roper C: Molecular determination of point mutation haplotypes in the dihydrofolate reductase and dihydropteroate synthase of Plasmodium falciparum in three districts of northern Tanzania. Antimicrob Agents Chemother. 2003, 47: 1347-1354. 10.1128/AAC.47.4.1347-1354.2003.PubMed CentralView ArticlePubMedGoogle Scholar
  12. Alifrangis M, Enosse S, Pearce R, Drakeley C, Roper C, Khalil IF, Nkya WM, Ronn AM, Theander TG, Bygbjerg IC: A simple, high-throughput method to detect Plasmodium falciparum single nucleotide polymorphisms in dihydrofolate reductase, dihydropteroate synthase, and P. falciparum chloroquine resistence genes using polymerase chain reaction and enzyme-linked immunosorbent assay-based technology. Am J Trop Med Hyg. 2005, 72: 155-162.PubMedGoogle Scholar
  13. Djimde AA, Doumbo OK, Traore O, Guindo AB, Kayentao K, Diourte Y, Niare-Doumbo S, Coulibaly D, Kone AK, Cissoko Y, Tekete M, Fofana B, Dicko A, Diallo DA, Wellems TE, Kwiatkowski D, Plowe CV: Clearance of drug-resistant parasites as a model for protective immunity in Plasmodium falciparum malaria. Am J Trop Med Hyg. 2003, 69: 558-563.PubMedGoogle Scholar
  14. Djimde A, Doumbo OK, Cortese JF, Kayentao K, Doumbo S, Diourte Y, Dicko A, Su XZ, Nomura T, Fidock DA, Wellems TE, Plowe CV, Coulibaly D: A molecular marker for chloroquine-resistant falciparum malaria. N Engl J Med. 2001, 344: 257-263. 10.1056/NEJM200101253440403.View ArticlePubMedGoogle Scholar
  15. Osman ME, Mockenhaupt FP, Bienzle U, Elbashir MI, Giha H: Field-based evidence for linkage of mutations associated with chloroquine (pfcrt /pfmdr1) and sulfadoxine-pyrimethamine (pfdhfr/pfdhps) resistance and for the fitness cost of multiple mutations in P. falciparum. Infect Genet Evol. 2007, 7: 52-59. 10.1016/j.meegid.2006.03.008.View ArticlePubMedGoogle Scholar
  16. Bousema JT, Gouagna LC, Meutstege AM, Okech BE, Akim NI, Githure JI, Beier JC, Sauerwein RW: Treatment failure of pyrimethamine-sulphadoxine and induction of Plasmodium falciparum gametocytaemia in children in western Kenya. Trop Med Int Health. 2003, 8: 427-430. 10.1046/j.1365-3156.2003.01047.x.View ArticlePubMedGoogle Scholar
  17. von Seidlein L, Jawara M, Coleman R, Doherty T, Walraven G, Targett G: Parasitaemia and gametocytaemia after treatment with chloroquine, pyrimethamine/sulfadoxine, and pyrimethamine/sulfadoxine combined with artesunate in young Gambians with uncomplicated malaria. Trop Med Int Health. 2001, 6: 92-98. 10.1046/j.1365-3156.2001.00683.x.View ArticlePubMedGoogle Scholar
  18. Mendez F, Munoz A, Carrasquilla G, Jurado D, Arevalo-Herrera M, Cortese JF, Plowe CV: Determinants of treatment response to sulfadoxine-pyrimethamine and subsequent transmission potential in falciparum malaria. Am J Epidemiol. 2002, 156: 230-238. 10.1093/aje/kwf030.View ArticlePubMedGoogle Scholar
  19. Mockenhaupt FP, Teun Bousema J, Eggelte TA, Schreiber J, Ehrhardt S, Wassilew N, Otchwemah RN, Sauerwein RW, Bienzle U: Plasmodium falciparum dhfr but not dhps mutations associated with sulphadoxine-pyrimethamine treatment failure and gametocyte carriage in northern Ghana. Trop Med Int Health. 2005, 10: 901-908. 10.1111/j.1365-3156.2005.01471.x.View ArticlePubMedGoogle Scholar


© A-Elbasit et al; licensee BioMed Central Ltd. 2007

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.