- Open Access
Identification of pyrimethamine- and chloroquine-resistant Plasmodium falciparum in Africa between 1984 and 1998: genotyping of archive blood samples
© Saito-Nakano et al; licensee BioMed Central Ltd. 2011
- Received: 27 September 2011
- Accepted: 31 December 2011
- Published: 31 December 2011
Understanding the geographical distribution of drug resistance of Plasmodium falciparum is important for the effective treatment of malaria. Drug resistance has previously been inferred mainly from records of clinical resistance. However, clinical resistance is not always consistent with the parasite's genetic resistance. Thus, molecular identification of the parasite's drug resistance is required. In Africa, clinical resistance to pyrimethamine (Pyr) and chloroquine (CQ) was evident before 1980 but few studies investigating the genetic resistance to these drugs were conducted before the late 1990s. In this study, genotyping of genes involved in resistance to Pyr and CQ was performed using archive blood samples from Africa between 1984 and 1998.
Parasite DNA was extracted from P. falciparum-infected blood smears collected from travellers returning to Japan from Africa between 1984 and 1998. Genotypes of the dihydrofolate reductase gene (dhfr) and CQ-resistance transporter gene (pfcrt) were determined by polymerase chain reaction amplification and sequencing.
Genotyping of dhfr and pfcrt was successful in 59 and 80 samples, respectively. One wild-type and seven mutant dhfr genotypes were identified. Three dhfr genotypes lacking the S108N mutation (NR SI, I CSI, IR SI; amino acids at positions 51, 59, 108, and 164 with mutations underlined) were highly prevalent before 1994 but reduced after 1995, accompanied by an increase in genotypes with the S108N mutation. The dhfr IRN I genotype was first identified in Nigeria in 1991 in the present samples, and its frequency gradually increased. However, two double mutants (I CN I and NRN I), the latter of which was exclusively found in West Africa, were more frequent than the IRN I genotype. Only two pfcrt genotypes were found, the wild-type and a Southeast Asian type (CVIET; amino acids at positions 72-76 with mutations underlined). The CVIET genotype was already present as early as 1984 in Tanzania and Nigeria, and appeared throughout Africa between 1984 and 1998.
This study is the first to report the molecular identification of Pyr- and CQ-resistant genotypes of P. falciparum in Africa before 1990. Genotyping of dhfr and pfcrt using archive samples has revealed new aspects of the evolutionary history of Pyr- and CQ-resistant parasites in Africa.
- Plasmodium falciparum
- Drug resistance
- Archive sample
Drug resistance of Plasmodium falciparum, the most virulent human malaria parasite, is imposing a serious problem for the effective treatment of malaria in almost all endemic areas. Thus it is imperative to understand the geographical distribution and origin of the parasite's drug resistance. In Africa, clinical resistance of falciparum malaria to chloroquine (CQ) was first reported in the late 1970s [1, 2]. In addition, while clinical resistance to pyrimethamine (Pyr) had been reported in limited endemic foci in the 1950s after mass drug treatment using Pyr [3, 4], highly resistant parasites became remarkably frequent and spread into endemic regions throughout Africa during the 1990s after the implementation of sulphadoxine/pyrimethamine (SP) as a first-line therapy in these regions . Clinical resistance is not always consistent with genetic resistance because drug resistance results from the interplay of the parasite, drug, and human host, and is largely influenced by immune factors. In highly endemic areas in Africa, where individuals often possess semi-immunity against malaria after repeated infections, this semi-immunity more or less strengthens efficacy of anti-malarial drugs to drug-resistant parasites [6, 7]. Thus, in Africa the timing of the first appearance of genetic resistance to CQ and Pyr and its subsequent spread in the continent remain to be explored.
The P. falciparum chloroquine-resistance transporter gene (pfcrt) was identified as a primary target gene for CQ resistance in 2000 . PfCRT is a transmembrane protein, localized to the parasite's food vacuole . An amino acid substitution at position 76 from lysine to threonine (K76T) in pfcrt confers resistance to CQ . Pyr inhibits a key enzyme in the folate biosynthetic pathway, dihydrofolate reductase (DHFR), which is encoded by the parasite dihydrofolate reductase gene (dhfr). Four major amino acid substitutions in dhfr have been widely recognised among Pyr-resistant parasites [10, 11]. A mutation at position 108 from serine to asparagine (S108N), leading to the NCN I dhfr genotype (amino acids at positions 51, 59, 108, and 164 with mutation underlined), is essential for conferring a mild resistance to Pyr in the parasite [10–13]. Additional point mutations at 51, 59, and 164 are associated with increased levels of Pyr resistance in vitro. Importantly, as the number of mutations in dhfr increases, levels of resistance to Pyr become higher . The IRNL dhfr genotype of the quadruple mutant shows so far the highest IC50 values to Pyr (1,111-fold as compared to that of the wild-type parasite) . The IRNL dhfr genotype is predominant in Southeast Asia and South America where the efficacy of SP has already reached unacceptable levels .
Recent molecular studies using microsatellite markers showed that the geographical origins of the mutant pfcrt genotypes were extremely restricted and resistant genotypes spread into almost all endemic regions, due to a selective sweep driven by treatment with CQ [14–17]. The CVIET (amino acids at positions 72-76 in pfcrt with mutations underlined) genotype represents the most common CQ-resistant type in Southeast Asia, which expanded to Africa. Similarly, a highly Pyr-resistant dhfr genotype (IRN I triple mutant) emerged from Southeast Asia and migrated to Africa, where it spread into endemic regions throughout Africa [14, 18, 19].
The identification of pfcrt and dhfr as target genes for drug resistance provides solid ground for exploring the geographical distribution and spread of CQ- and Pyr-resistant P. falciparum. However, previous reports of genetic resistance (but not clinical resistance) to these drugs are very limited before the 1990s, since the target genes for CQ- and Pyr-resistance were not identified until 2000 and 1988, respectively [8, 10, 20]. Indeed, studies on the genotypes of drug-resistant genes are scarce, with only one report each for pfcrt and dhfr in the late 1980s in Africa. Investigating the geographical distribution of pfcrt and dhfr genotypes in Africa before 1990 is undoubtedly crucial for tracing the evolutionary history of CQ- and Pyr-resistance in the continent, where both CQ- and Pyr-resistance was introduced from Southeast Asia. To address this issue, genotyping of archive blood samples was performed using samples collected from travellers who had returned from Africa between 1984 and 1998. Results show that in Africa the CQ-resistant pfcrt genotype was already widely prevalent in the 1980s, and the highly Pyr-resistant dhfr genotypes (double and triple mutants) increased after the mid-1990s.
Collection of samples and DNA extraction
The archive blood samples used in this study had been collected and stored as blood smears for the national surveillance system of imported malaria cases operating in 50 hospitals in Japan from 1984 to 1998 . Of the 588 malaria cases imported to Japan during the period, 122 Plasmodium falciparum cases were derived from 23 African countries. Parasite DNA was extracted from Giemsa-stained thin blood smears as previously described . Briefly, Giemsa-stained slides were dipped in xylene and then in methanol to remove the immersion oil and dye, respectively. Each blood smear was scraped off with the edge of a clean glass slide, and subjected to DNA purification using the QIAamp DNA Blood Mini Kit (Qiagen, Hilden, Germany). A non-infected blood smear was also used as a negative control in the DNA extraction and polymerase chain reaction (PCR) amplification procedures. In total, genotyping was successful for dhfr and/or pfcrt in 85 samples of the 122 samples examined [see Additional file 1].
For genotyping of the dhfr locus, amplification of a 350-base pair fragment covering the four polymorphic sites at positions 51, 59, 108 and 164 was unsuccessful, due primarily to severe fragmentation of the templates extracted from the methanol-fixed blood smears, which were not suitable for amplification of fragments greater than 200-base pairs [24, 25]. Thus, three 190-base pair fragments covering the polymorphic amino acid positions at 51 and 59, 108, and 164 were separately amplified by nested PCR . The PCR products were subjected to direct sequencing in both directions. In samples with mixed infections of different genotypes showing superimposed peaks on an electropherogram, the PCR products were cloned into pT7Blue vector (Merck, Darmstadt, Germany) and sequenced. More than 10 plasmid clones were sequenced to ascertain linkage of the polymorphisms at 51 and 59 in dhfr; those clones in which linkage was not confirmed were excluded from further analysis. For genotyping of the pfcrt locus, a 190-base pair fragment of pfcrt encoding the amino acid residues at positions 72-76 was amplified by nested PCR as previously described .
Comparisons between the prevalence of drug resistant genotypes before and after 1995 were examined using the Fisher exact test or Chi-square analysis. A p-value of less than 0.05 was considered to be statistically significant.
The IRN I genotype, which is currently predominant in many endemic regions in Africa , was first identified in Nigeria in 1991 in the present samples (Figure 2a). Since then, the frequency of IRN I genotype gradually increased (Figure 1a), but it was not highly predominant in both East Africa (16%) and West Africa (18%) in 1991-1998. Instead, the double mutant genotypes (I CN I and NRN I) were predominant during that period in the present sample set. The NRN I genotype was identified exclusively in West African countries: Nigeria, Ghana, Cote d'Ivoire, and Niger (Figure 2a). On the other hand, the I CN I genotype was prevalent in both East and West Africa.
Genotyping of pfcrt was successful in 80 of the 122 archive samples. Only two pfcrt genotypes were found; the wild-type (CVMNK) and the CQ-resistant genotype (CVIET) of Southeast Asia (Figure 1b). Mixed infections of wild-type and CVIET type were found in 22 (28%) samples. The S VMNT pfcrt genotype that originated in either Melanesia or South America was not detected. The CVIET genotype was already present as early as 1984 in Tanzania and Nigeria in the present samples (Figure 2b), and appeared throughout the studied period (1984-1998). There was no difference in the prevalence of the CQ-resistant pfcrt genotype (CVIET) before 1994 and after 1995 (p > 0.8, Chi-square analysis). The prevalence of CQ-resistant pfcrt genotype between West and East Africa was comparable (p > 0.48, Chi-square test).
The present study is the first to report pfcrt and dhfr genotypes in Africa before 1990 using archive samples. It was found that before the mid-1990s the predominant dhfr genotypes were wild-type (NCSI) and three mutant genotypes (NR SI, I CSI, IR SI), all of which lacked the S108N mutation. This is unexpected because it was believed that the initial mutation in dhfr was exclusively the S108N mutation, which confers weak resistance to Pyr on P. falciparum[10–13]. Experimental investigations have recently demonstrated that mutant genotypes lacking the S108N mutation (NR SI, I CSI, IR SI) are as sensitive to Pyr as the wild-type parasite [13, 27]. Notably, the prevalence of these three mutant genotypes (NR SI, I CSI, IR SI) lacking the S108N mutation, as well as the wild-type, was remarkably reduced after the mid-1990s. Instead, dhfr mutant genotypes possessing the S108N mutation became more frequent in the late 1990s than in the early 1990s. SP had been used as a secondary treatment for CQ-resistant falciparum malaria in limited African countries before the mid-1990s , but was widely deployed in many African countries following the first official introduction of SP as the first-line treatment for uncomplicated malaria in Malawi in 1993. Therefore it seems likely that increased Pyr pressure may have led to the increased prevalence of dhfr genotypes with the S108N mutation, and the observed reduction in the three Pyr-sensitive genotypes (NR SI, I CSI, IR SI) and wild-type (NCSI) in Africa.
This study also showed that the dhfr triple mutant (IRN I), a highly Pyr-resistant genotype, was already present in Central and West Africa in the early 1990s; Nigeria in 1991, Uganda in 1992, and Mali in 1993. The earliest appearance of the IRN I genotype, known to date, was in 1988 in Kenya , and this genotype was shown to have been introduced from Southeast Asia. Most of the IRN I genotype currently prevalent in Africa has been generated from this migrated resistant parasite lineage [14, 18, 19, 28], which arrived in East Africa then rapidly moved westwards. Thus, the identification of the IRN I genotype in Nigeria in 1991 supports the idea that the Southeast Asian resistant parasite had already migrated into Central/West Africa in the early 1990s, during which time treatment with Pyr was not common in Africa. However, this idea needs to be confirmed because migration of this type from Southeast Asia cannot be substantiated without the assessment of microsatellite haplotypes flanking dhfr[18, 19]. Indeed, an indigenous origin of the same triple mutant (IRN I) genotype, having microsatellite haplotypes distinctive from the Southeast Asian haplotypes, has recently been shown in Cameroon  and Kenya [14, 30]. In the present study, unfortunately, it was not feasible to determine the lineage of the resistant parasite with the triple mutant (IRN I) genotype, as sufficient amounts of DNA required to determine the microsatellite haplotypes could not be recovered from the Giemsa-stained thin blood smears. However, the recently discovered indigenous African parasite lineage was observed in low frequency compared to the Southeast Asian parasite lineage [14, 29]. Hence, it seems likely that the Southeast Asian parasite lineage had already migrated to Africa before SP was widely used in Africa, and subsequently spread across the continent after the increased use of SP.
The highest Pyr-resistant dhfr genotype, quadruple mutant (IRNL), was not identified in the present sample set. Consistently, the earliest record of the appearance of IRNL genotype in Africa was in 1999 from Uganda -in 2000 from Tanzania . However, the prevalence of the IRNL genotype is notably still low in many endemic countries in Africa  in spite of the intense usage of SP as a first-line therapy . This is in sharp contrast to a high prevalence of the IRNL genotype in Indochina, where the genotype has remarkably increased after the initial identification in the late 1980s [33, 34]. Many factors appear to be associated with the observed difference of the prevalence of the IRNL genotype between Africa and Indochina. One factor could be a level of acquired immunity against falciparum malaria. In many endemic areas in Africa, adults acquire semi-immunity after repeated infections. In those individuals SP is considered to be effective to not only Pyr-sensitive parasites but also Pyr-resistant parasites. Importantly, the IRNL genotype is reportedly not associated with SP treatment failure or in vivo resistance in individuals who have high levels of immunity to malaria [33, 35]. It is thus suggested that the IRNL genotype has not been strongly selected for by SP pressure in semi-immune African adults, and consequently the genotype has not expanded in Africa. Other factors that have retarded the expansion of the IRNL genotype in Africa cannot be excluded, and this issue needs to be clarified in the near future.
This study is the first to report the occurrence of the CVIET CQ-resistant pfcrt genotype as early as 1984 in Nigeria. Previously, the oldest identification of the pfcrt mutant genotype was in 1989 in East Africa  and in 1992 in West Africa . This strongly suggests that CQ resistance, which first arrived in East Africa from Southeast Asia, had already spread to West Africa by 1984. Around that time, however, CQ efficacy was satisfactory in the countries of western Africa, and several in vivo tolerance and resistance cases were reported only in non-immune individuals [37–39]. Acquired immunity against malaria in individuals in highly endemic areas in Africa may have strengthened the efficacy of CQ against the CQ-resistant parasites [6, 7] and probably masked the appearance of clinical CQ resistance.
In contrast to the mainland of Africa, where resistance to CQ and Pyr is widely spread, CQ and Pyr are still effective in Madagascar and Comoros in the south-western Indian Ocean . A recent report has shown that Pyr resistant genotypes found in Madagascar were introduced from Comoros . Unfortunately, the present sample set included only one sample from Madagascar, and thus it is difficult to infer when and from where drug resistant genotype was introduced to Madagascar and Comoros islands. Further molecular surveys of samples from African countries including Madagascar and Comoros are required for better understanding of the evolutionary history of drug resistance in the continent.
The present study used archive blood samples to reveal new aspects of the evolutionary history of Plasmodium falciparum resistance to Pyr and CQ in Africa. Pyr-sensitive mutant genotypes lacking the S108N mutation were frequently observed in the 1980s but were drastically reduced in the late 1990s, and instead, the frequency of highly Pyr-resistant genotypes (double and triple mutants) considerably increased after the mid-1990s. In addition, the CQ-resistant pfcrt genotype, CVIET, was identified as early as 1984 in West Africa. Further molecular epidemiological investigations using archive samples from diverse endemic areas would lead to a better understanding of the evolutionary history of drug resistance of P. falciparum.
We thank Eiko Nakasone for technical support. We also acknowledge the staff who participated in sample collection for the national surveillance system. This work was supported by a Grant-in-Aid from the Ministry of Health, Labour and Welfare of Japan (grant H20-Shinkou-ippan-013), a grant for Research on Emerging and Re-emerging Infectious Diseases from the Ministry of Health, Labour and Welfare of Japan (H23-Shinko-Ippan-014), and from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (22406012, 23590498, 23659211).
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