Figures
Abstract
North-east India, being a corridor to South-east Asia, is believed to play an important role in transmitting drug resistant Plasmodium falciparum malaria to India and South Asia. North-east India was the first place in India to record the emergence of drug resistance to chloroquine as well as sulphadoxine/pyrimethamine. Presently chloroquine resistance is widespread all over the North-east India and resistance to other anti-malarials is increasing. In this study both in vivo therapeutic efficacy and molecular assays were used to screen the spectrum of drug resistance to chloroquine and sulphadoxine/pyrimethamine in the circulating P. falciparum strains. A total of 220 P. falciparum positives subjects were enrolled in the study for therapeutic assessment of chloroquine and sulphadoxine/pyrimethamine and assessment of point mutations conferring resistances to these drugs were carried out by genotyping the isolates following standard methods. Overall clinical failures in sulphadoxine/pyrimethamine and chloroquine were found 12.6 and 69.5% respectively, while overall treatment failures recorded were 13.7 and 81.5% in the two arms. Nearly all (99.0%) the isolates had mutant pfcrt genotype (76T), while 68% had mutant pfmdr-1 genotype (86Y). Mutation in dhps 437 codon was the most prevalent one while dhfr codon 108 showed 100% mutation. A total of 23 unique haplotypes at the dhps locus and 7 at dhfr locus were found while dhps-dhfr combined loci revealed 49 unique haplotypes. Prevalence of double, triple and quadruple mutations were common while 1 haplotype was found with all five mutated codons (F/AGEGS/T) at dhps locus. Detection of quadruple mutants (51I/59R/108N/164L) in the present study, earlier recorded from Car Nicobar Island, India only, indicates the presence of high levels of resistance to sulphadoxine/pyrimethamine in north-east India. Associations between resistant haplotypes and the clinical outcomes and emerging resistance in sulphadoxine/pyrimethamine in relation to the efficacy of the currently used artemisinin combination therapy are discussed.
Citation: Mohapatra PK, Sarma DK, Prakash A, Bora K, Ahmed MA, Sarma B, et al. (2014) Molecular Evidence of Increased Resistance to Anti-Folate Drugs in Plasmodium falciparum in North-East India: A Signal for Potential Failure of Artemisinin Plus Sulphadoxine-Pyrimethamine Combination Therapy. PLoS ONE 9(9): e105562. https://doi.org/10.1371/journal.pone.0105562
Editor: Luzia Helena Carvalho, Centro de Pesquisa Rene Rachou/Fundação Oswaldo Cruz (Fiocruz-Minas), Brazil
Received: March 14, 2014; Accepted: July 24, 2014; Published: September 3, 2014
Copyright: © 2014 Mohapatra et al. 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 author and source are credited.
Data Availability: The authors confirm that, for approved reasons, some access restrictions apply to the data underlying the findings. We confirm that all data underlying the findings in this study are freely available in the manuscript. However, as per the institutional policy the ownership of the data lies with the Director, RMRC, NE (ICMR), Dibrugarh. The data can be made available freely upon request to – The Director, Regional Medical Research Centre, NE (Indian Council of Medical Research), Post Box no. 105, Dibrugarh, Assam (India).
Funding: The study was funded by Indian Council of Medical Research, Government of India. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Control of Plasmodium falciparum (Pf) malaria in the north-east India, reporting 0.15–0.2 million cases of malaria and over 100 deaths annually [1] is becoming challenging due to the widespread resistance to chloroquine (CQ) and increasing therapeutic failure to sulphadoxine/pyrimethamine (SP) [2]. Chloroquine resistance in Pf first appeared more or less simultaneously in Southeast Asia (Thai-Cambodian border) and South America (Colombia) in the late 1950s [3], [4]. In India, resistance to chloroquine in Pf was first detected in 1973 in Diphu area of Karbi-Anglong district of Assam state, north-east India [5] which gradually spread towards the east, west and south, covering almost entire country [6]. While resistance to SP was first reported again from Thai-Cambodian border in 1960s [7], initial reports of SP resistance in India, emerged in 1979, again in Karbi-Anglong district, Assam [8] and later documented in 1992 in Changlang district of Arunachal Pradesh, north-east India [9] indicating epidemiological importance of this region in spreading the drug resistant strains. Recently, treatment failure to CQ, SP and quinine, administered sequentially, was noted in 6% of Pf cases, indicating the presence of multidrug resistant Pf strains [10]. It has been observed that though the slide positivity rates (SPR) and slide falciparum rates (SFR) in north-east India have increased following emergence of drug resistance, the trend of progression of SFR over time has remained more or less linear, the case fatality rate (CFR) showed a steady increase (Figure S1 & Figure S2 as per north-east Indian states NVBDCP data).
Resistance to anti-folates (e.g. sulphadoxine/pyrimethamine) has been found associated with the point mutations at dihydrofolate reductase (dhfr) and dihydropteroate synthetase (dhps) genes and that of chloroquine with Pf chloroquine resistance transporter (Pfcrt) and Pf multidrug resistance (Pfmdr1) genes, [11], [12], [13]. Mutations at several amino acid positions of the Pfcrt gene from the chloroquine resistant parasite lines have been reported, of which mutation at 76 position from lysine to threonine (K76T) was consistently present among CQ-resistant P. falciparum isolates [14], making it a good marker to provide information on the Pf chloroquine resistance status. Additionally, point mutations at N86Y, Y184F, N1042D and D1246Y loci of pfmdr-1 gene are reported to reduce susceptibility to chloroquine [15], [16]. Pyrimethamine inhibits the parasite enzyme Pfdhfr involved in folate biosynthesis pathway [17], [18]. However, parasites with point mutations at codon position 51, 59, 108 and 164 of dhfr gene require higher amount of pyrimethamine to inhibit its activity and subsequently become resistant to pyrimethamine. The first mutation was found to be in position 108 (S108N). The drug sensitivity is reduced further if this mutation occurs along with mutations at N51I (Asn-Ile), C59R (Cys-Arg) or I164L (Ile-Leu). It was noted that the double mutation in dhfr gene (N51I+S108N or C59R+S108N) causes intermediate resistance while the triple mutation of the codons S108N+N51I+C59R confers high resistance [19]. However, an additional mutation at codon I164L leading to a quadruple mutation results in highest level of resistance to SP as well as to chloroproguanil dapsone and artesunate dapsone proguanil [20]. Sulphadoxine competes with the substrate that binds to the parasite enzyme Pfdhps. Mutations at several amino acid positions of this enzyme have shown reduction in its binding capacity to the drug. Mutations in pfdhps gene have been reported at five different amino acid positions (436, 437, 540, 580 and 613). In dhps mutation first starts at codon S436F/A (Ser-Ala/Phe) or at A437G (Ala-Gly) followed by mutations at other positions viz., K540E (Lys-Glu), A581G (Ala-Gly) and A613S/T (Ala-Ser/Thr) conferring more resistance [1], [21], [22], [23], [24], [25], [26]. The presence of mutations at codons 437 and 540 of pfdhps together with the triple mutation of pfdhfr [quintuple mutation] is a significant predictor of SP treatment failure [27].
CQ was the drug of choice in north-east India, except in some select areas where SP was used as the first line of treatment till 2008. Thorough assessment of the extent of anti-malarial drug resistance and therapeutic failure is required before taking a call on making any changes in the drug policy, particularly in highly endemic areas such as north-east India. In view of this, the present study was conducted during 2006–2007 in two districts of Assam state in north-east India covering two sites located at considerable distances to determine the therapeutic efficacy of CQ and SP against uncomplicated falciparum malaria. Further, the frequency of mutations associated with CQ and SP resistance were determined in circulating Pf strains to correlate their association with therapeutic efficacy.
Materials and Methods
Study sites and study design
The study was carried out in two malaria endemic districts of north-east Indian state of Assam viz., North Lakhimpur and Hailakandi (Figure 1). Fever cases attending the Primary Health Centre of these two study sites were screened for malaria infection using conventional microscopy by examining both thick and thin blood smears stained with 3% Giemsa. Uncomplicated falciparum malaria cases meeting the following inclusion criteria were included in the study (1) >6 months of age (2) initial parasite count within 1000–1,00,000 parasites/µl on Day 0 (3) not suffering from severe malnutrition (4) mono infection with P. falciparum (5) no signs of any other illness and other causes of febrile disease (6) axillary temperature ≥37.5°C (7) written informed consent for willingness to participate in the study (8) no history of allergic reactions to sulfa-containing drugs and (9) able to return to clinic for follow-up visits.
A total of 220 Pf positives subjects fulfilling above criteria were enrolled in the study at PHC Kathlicherra in Hailakandi district (n = 120) and PHC Nowboicha in North Lakhimpur district (n = 100) and the therapeutic assessment of CQ and SP was carried out. Both drugs were supplied by the Directorate of National Vector Borne Diseases Control Programme, Government of India. CQ was administered orally at 25 mg/kg body weight in three divided doses (10 mg/kg on Day 0, 10 mg/kg on Day 1 and 5 mg/kg on Day 2). SP was given orally as a single dose at 25 mg sulphadoxine and 1.25 mg pyrimethamine/kg body weight. Antimalarials were administered under direct supervision of the investigators and patients were followed-up for a period of 28 days for CQ and 42 days for SP. Patients showing failure were treated with parental quinine in 5% dextrose until they were able to take the drug orally. All patients were given 0.75 mg primaquine/kg body weight as a single dose, for radical cure, at the end of the study.
Clinical and Parasitological evaluation
The standard WHO protocol [28] for classification of response to anti-malarial treatment in low to moderate transmission areas was adopted. Blood smears were taken for parasite density count on day 0, 1, 2, 3, 7, 14, 21, 28 and 42 of recruitment along with the recording of axillary temperature and clinical assessment of the enrolled subjects. In addition, blood samples were collected from the willing subjects on filter paper on day 0 for molecular studies. The clinical response was classified as (i) early treatment failure (ETF) (ii) late clinical failure (LCF) (iii) late parasitological failure (LPF) and (iv) adequate clinical and parasitological response (ACPR).
Sample processing and DNA Isolation
Approximately 50 µl of blood from each fever case at the time of initial recruitment was spotted on Whatman no. 1filter paper, desiccated and transferred to the laboratory. Parasite DNA was extracted from 4–5 punches (3 mm diameter) cut from dried blood spot from each filter paper using QIAamp DNA Blood Mini Kit (Cat. 51106, QIAGEN, USA) following manufacturer's instructions. The parasite DNA was eluted in 50 µl volume and stored at 4°C for immediate use. The parasite species was determined using primers and method described earlier [29].
Parasite genotyping
P. falciparum mutations associated with CQ and SP resistance were typed by nested PCR-RFLP method as described and available on the web (http://medschool.umaryland.edu/CVD/plowe.html). In this study, the following codons and polymorphisms were analyzed: pfmdr 86, pfcrt 76; pfdhfr (16, 50, 51, 59, 108, 164) and pfdhps (436, 437, 540, 581, 613). All PCR amplifications were performed with MJ Mini thermal cycler (Bio-Red) in a reaction volume of 25 µl with Promega master mix. 5 µl of extracted DNA was used as a template in 1st round PCR while 1–2 µl of primary PCR product was used as a template for nested PCR. 5–8 µl of 2nd round PCR product was digested with 1 unit of respective restriction enzyme (NEB) in a 20 µl reaction volume using NEB buffer. Amplicons and fragments were separated on 2% or 3% agarose gels, stained with ethidium bromide and visualized under UV. The detailed description of sample size used for different aspects are outlined in Figure 2.
Data analyses
The data was double entered in SPSS V13.0. All statistical analyses were carried out using SPSS V13.0 and XLSTAT V-2012.5.02.
Mutations were determined on the basis of the presence or absence of the expected bands on ethidium bromide stained agarose gel analysis from PCR amplicon after restriction digestions. Site specific distribution of allele was expressed in percentage. dhps and dhfr haplotypes were counted separately and in combination and their prevalence recorded. Associations between dhfr/dhps alleles and SP therapeutic failure and pfcrt alleles and CQ therapeutic failure were assessed using an adjusted Odds ratios (OR) and the 95% confidence intervals. Appropriate statistical tests were carried out.
Ethical consideration
The study was approved by the Scientific Advisory Committee and Human Ethical Committee of Regional Medical Research Centre, Dibrugarh, Assam (India). All participants provided informed written consent. However, in case of a minor or children enrolled in the study, informed written consent was taken either from their parents or from their legal guardians, if parents were not available. As proposed by the Institutional Ethics Committee, Regional Medical Research Centre, Dibrugarh, Assam, all participants were informed about the objectives and intended use of the findings prior to their enrollment in the study as well as their right to withdraw from the study at any time without notification. The informed consent was translated into local language.
Results
Therapeutic efficacy of CQ and SP
A total of 200, among the 220 enrolled subjects with acute uncomplicated malaria, from the two sites were included in the study (50 for CQ and 50 for SP from each site) and treated with SP and CQ. Patients' characteristics, demographic data and treatment outcomes are shown in Table 1. Of these, 95 subjects each successfully completed the 28 days follow up for CQ and 42 days follow up for SP. The therapeutic efficacy study at the two sites revealed 86.3% and 19% ACPR response with SP and CQ respectively. Overall clinical failures in SP and CQ arms were 12.6 and 69.5% respectively, while overall treatment failures were 13.7 and 81.5% in the two arms. Hailakandi recorded the higher CQ failure while both the sites had almost similar rate of SP failure (Table 1).
Prevalence of pfcrt and pfmdr1 mutations
The status of pfcrt K76T and pfmdr-1 N86Y mutations was determined in 200 (119 from Hailakandi, 81 from North Lakhimpur) and 196 (Hailakandi = 119, North Lakhimpur = 77) isolates from the two locations. Based on pfcrt locus almost all isolates were found resistant to CQ at both the sites [North Lakhimpur 80/81 (98.8%), Hailakandi 118/119 (99.2%)], while at the pfmdr-1 locus 80% (61/77) isolates from North Lakimpur and 61% (72/119) isolates from Hailakandi were found resistant. Overall, 99% isolates had mutant pfcrt genotype (76T), while 68% had mutant pfmdr-1 genotype (86Y) locus (Figure 3).
Prevalence of dhps and dhfr mutations
The presence of five dhps mutations (S436F/A, A437G, K540E, A581G, and A613S/T) and six dhfr mutations (A16V, C50R N51I, C59R, S108N and I164L) known to be involved in resistance to SP were evaluated (Table 2). Mutation analysis was successful in 173 subjects for dhps codons and in 168 patients for dhfr codons.
Mutant codons were quite common at both the loci and study sites. Among all mutations studied, mutation in dhps 437 codon was the most prevalent, while mutation in dhps 581 codon was the least prevalent. Mutant alleles of dhps were more common in Hailakandi. The mutant dhfr 50 allele was completely absent while dhfr codon 108 showed 100% mutation (Table 2, Figure 4).
Distributions of dhps and dhfr haplotypes
The allelic pattern or haplotypes were constructed for dhps and dhfr loci individually as well as in combination. A total of 23 unique haplotypes at the dhps locus (Table 3) and 7 haplotypes at dhfr locus (Table 4) were found. In case of dhps, 40 isolates (23.1% of isolates) had all five sensitive codons (SAKAA). On the other hand 5 haplotypes (22.5%) with single mutation (SAKAS/T, SAKGA, SAEAA, SGKAA, F/AAKAA), 7 haplotypes (25.4%) with double mutations (SAKGS/T, SAEAS/T, SGKAS/T, SGKGA, SGEAA, F/AAEAA, F/AGKAA), 6 haplotypes (22.5%) with triple mutations (SGKGS/T, SGEAS/T, SGEGA, F/AAEAS/T, F/AGKAA, F/AGEAA), 3 haplotypes (5.8%) with quadruple mutations (SGEGS/T, F/AGEAS/T, F/AGEGA) and 1 haplotype (0.6%) with all five mutated codons (F/AGEGS/T) were found. Higher prevalence of resistant allele at codon 437 (14 haplotypes), codon 540 (12 haplotypes) and codon 613 (11 haplotypes) was noted suggesting that mutations first started at 437 codon position of dhps locus in NE India and subsequently associated with other mutations to confer resistance (Table 3).
At the dhfr locus, only 7 haplotypes were observed among 168 isolate (Table 4). No haplotype having all the 6 sensitive codons was observed. There was only 1 haplotype (1.8% of isolates) carrying single mutation (ACNCNI), 2 haplotypes (65.5%) with double mutations (ACNRNI, ACNCNL), 3 haplotypes (14.3%) with triple mutations (VCNRNI, ACIRNI and ACNRNL) and 1 haplotype (1.8%) with quadruple mutation (ACIRNL). The prevalence of haplotype ACNRNI containing mutations at codons 59 and 108 had the highest frequency (64.3%).
Construction of dhps-dhfr combined haplotypes among the 154 isolates, where PCR-RFLP results for all codons were available, revealed 49 unique haplotypes, of which SAKAA-ACNRNI (13.6%), SGKAA-ACNRNI (8.4%) and F/AGEAA-ACNRNI (7.1%) haplotypes had the higher frequencies (Table 5). Assessment of dhps/dhfr combined haplotypes with single or multiple mutations viz., S108N, N51I+S108N, C59R+S108N, N51I+C59R+S108N, C59R+S108N+I164L, N51I+C59R+S108N+I164L, N51I+C59R+S108N/A437G, N51I+C59R+S108N/K540E and N51I+C59R+S108N/A437G+K540E, considered as predictive for SP resistance or failure [26], revealed that C59R+S108N (n = 108; Hailakandi 65%, North Lakhimpur 59%), N51I+C59R+S108N (n = 31; Hailakandi 17.5%, North Lakhimpur 19%) and C59R+S108N+I164L (n = 19; Hailakandi 6%, North Lakhimpur 19%) combinations were the most prevalent ones (Figure 5).
Association between dhfr-dhps point mutations and treatment failure with SP and CQ
SP treatment failure was strongly associated with dhps-dhfr mutations and their combinations. It was found that 5 dhps-dhfr combined haplotypes were associated with 6 cases of early treatment failures of SP, while 25 dhps-dhfr combined haplotypes were associated with 33 cases of early treatment failure of CQ. Most of the treatment failure haplotypes were with mutations 59R+108N or 51I+59R+108N or 59R+108N+164L at the dhfr locus indicating their role in SP treatment failure in north-east India (Table 6). Among the CQ failure cases, 67% belonged to adult age group (>15 years), 24% to 5–15 years age and 9% were under 5 years of age. However, in case of SP treatment failures, 50% cases were below 5 years of age while >15 years and 5–15 years age groups represented 33% and 17% failure cases respectively. The dhfr double mutant ACNRNI (with mutations at 59 and 108 codon) with the highest frequency in the adult age group was associated with CQ treatment failure. However, in case of SP treatment failure, the same haplotype was found associated with treatment failure in adult cases (33.3%) as well as under 5 years of age (16.7%) while haplotype ACIRNL (with mutations at 51, 59, 108 and 164 codon) was solely associated with treatment failure cases in <5 years of age (Figure 6). Overall, the results were indicative of the presence of multi drug resistant strains of Pf in the study sites.
Discussion
Control of drug resistant P. falciparum malaria has become a challenging task globally. Except for artemisinin and its derivatives, anti-malarial resistance to P. falciparum has been reported in vivo for all drugs [30]. Chloroquine resistance to falciparum in South-east Asia originated from a single focus in Paillang region near Thai–Cambodia border during 1950s. Resistance to SP was detected in 1960s again from Thai-Cambodian border from where Pf strains resistant not only to CQ, but also to SP, mefloquine and quinine spread to surrounding countries [4]. This spread of anti-malarial resistance in South-east Asia apparently followed a pattern until 1978. Initially, it remained limited to tropical forested areas corresponding well with the geographical distribution of Anopheles dirus complex mosquitoes; thereafter, it moved out of the geographical limits of An. dirus. In India too, the same trend was witnessed where Pf strains resistant to CQ first appeared in 1973 [5] and to SP in 1987 [6] in An. dirus complex mosquito dominated areas of north-east India before moving to other parts of the country. Therefore, north-east India may be acting as the gateway to resistant falciparum strains in India. Increasing failure rates of anti-malarials in north-east India demands a close monitoring of the epidemiology and dynamics of the drug resistant Pf. Availability of easy and rapid molecular markers would greatly facilitate this process and allows overcoming difficulties in the use of traditional methods for characterizing anti-malarial drug resistance. Moreover, the molecular surveillance of drug resistance markers such as pfcrt, pfmdr-1, dhfr, dhps & pfatp-6 associated with anti-malarial treatment failure provides sufficient evidence to policy makers for a renewed thinking on the existing drug policy [31].
Genotyping of circulating Pf strains for CQ resistance revealed that almost all isolates were resistant at pfcrt locus, while 68% isolates showed resistance at pfmdr-1 locus. Simultaneous in vivo therapeutic study recorded 80% treatment failure to CQ. Age stratified analysis revealed that of all the CQ failure cases (77/95), 78% (25/32) belonged to <15 years of age including 100% cases (7/7) belonging to <5 years indicating the synergistic role of host immunity in the clearance of parasitaemia. Although treatment failure in the older age group (>15 years) was also pretty high (22%), it might partly be explained based on the fact that many adult subjects included in the study were not the permanent inhabitants of the study sites and had migrated from non/less endemic areas for temporary contractual works in search of livelihood and possibly had low immune status against malaria. Earlier studies in north-east India [2], [10] have also reported CQ resistance in more than 80% isolates of Pf indicating non-effectiveness of CQ over the region. Although pfmdr-1 has been thought to affect CQ resistance, however, no correlation between the prevalence of pfcrt mutation and pfmdr-1 point mutation was noted in the present study, which was also observed in earlier studies further strengthening the doubt over its involvement in CQ resistance [32], [33].
In case of dhps, though the prevalence of sensitive haplotype (SAKAA) was as high as 23%, double (25.4%), triple (22.5%) and quadruple (5.8%) mutant haplotypes were also present in good numbers along with a full box mutation (F/AGEGS/T) in one isolate from Hailakandi district. To the best of our knowledge this is the first study recording as many as 23 unique dhps haplotypes and a full box mutated haplotype anywhere in India. Earlier studies found 8 [34] and 15 [35] dhps haplotypes. Presence of the mutated codon 437G (frequency 60%) in most of our dhps haplotypes suggests that mutation in this locus started settling first at 437 position in north-east India, similar to the inference made by others [26].
At dhfr locus, codon 108 was found mutated in all the isolates while no mutation was seen in codon 50. Double, triple and quadruple mutations were noted resulting in 7 different but unique haplotypes of dhfr. Elsewhere in India, presence of double mutants (59R/108N) or single mutants (108N) were found to be common [22], [36]. Although the presence of triple mutants viz. 51I/59R/108N or 59R/108N/164L were observed from north-east India in ∼10% isolates [22], [37], no study has ever reported quadruple mutations (51I/59R/108N/164L) from this part of country. We found 3 isolates (∼2%) harboring quadruple mutants (51I/59R/108N/164L) in the present study (Table 4) which was earlier recorded only from Car Nicobar Island, India [37], [38]. We found the presence of double mutants of dhfr i.e., C59R/S108N or N51I/S108N associated with intermediate level of resistance to SP, while presence of triple mutant (N51I/C59R/S108N) was seen in 32% isolates of early treatment failure of SP in therapeutic assessment.
This study revealed high frequency of mutant codons at both dhps and dhfr loci that correlated well with the status of therapeutic response to SP in Pf malaria cases. Presence of haplotypes with mutations at codon position 437 and 540 in the dhps gene combined with triple and quadruple mutations in dhfr gene, seen in about 10% of isolates comprising of 8 haplotypes (Table 4), was predictive of early treatment failure of SP. Overall prevalence of mutated codons of dhps and dhfr in north-east India detected in our study matches well with the data available in the World Wide Antimalarial Resistance Network Molecular Surveyor (WWARN: http://www.wwarn.org/surveyor/) (Figure S3). From the distribution of the mutations, it can also be inferred that most of the mutations in dhps and dhfr loci are fixed in north-east India and is now spreading to other parts of India.
The present study provides important information not only on the resistance pattern of CQ and SP drugs to Pf in Assam state of north-east India (2006–2007) but also raises concern on the potential effectiveness of the current first line of the drug i.e. Artemisinin based combination therapy (ACT) along with highlighting the importance of constant molecular surveillance of drug resistance. ACT (Artesunate with SP) has been introduced in north-east India since 2008 as the first line of drug for treating uncomplicated P. falciparum cases. Present study indicates that although SP is therapeutically effective in treating uncomplicated Pf malaria cases in the study sites, yet fixation and prevalence of double, triple and even quadruple mutations at both the loci associated with its treatment failure was quite high.
Although we didn't explore pfatp6, the molecular marker for artemisinin resistance, in this study, as ACT was not in use during the study period, yet it can be speculated from the findings that due to wide spread occurrence of dhfr and dhps mutant codons in north- east India, the artesunate, that is combined with sulphadoxine-pyrimethamine in ACT, is probably acting as a monotherapy. Since artemisinin is a short acting drug with a rapid parasite reduction and a shorter half-life (in hours only), it is generally combined with a partner drug (such as SP) having longer half life with different mechanism of action. However, in areas of high transmission, like in north-east India, the partner drug may promote the proliferation of drug resistant parasites exposed to sub therapeutic levels of drug, which may result in decreased efficacy of ACT [39]. It is further speculated that the situation in north-east India might further worsen by changes in frequencies of mutant alleles with the passage of time due to the selective drug pressure which raises serious concern over using SP as a partner drug with artemisinin for the treatment of Pf cases. Therefore, current therapeutic efficacy studies of ACT in north-east India are urgently warranted. Although there is a paucity of data on the therapeutic efficacy of ACT from this part of India, yet a study on ACT involving 4 sites in the Myanmar bordering areas of north-east India carried out during 2004–2006 (long before ACT was introduced as a first line of drug for treating Pf cases in north-east India) recorded 95.5% ACPR of ACT with mean parasite clearance time of 55:17±14:26 hrs (RMRC unpublished data). It was significant that the study revealed 4.5% overall failure (Late clinical failure 2.1% and Late parasitological failure 2.4%). This might be due to the resistance of circulating Pf strain to SP, since most of the treatment failures in ACT is related to the failure of SP [40]. In the same study delayed parasite clearance time of 69:49±6:58 hrs was observed at one of study sites indicating relatively slower effectiveness of ACT in that area. Though delayed parasite clearance time is regarded as the most important surrogate signal for artemisinin resistance [41] in the absence of pharmaco-kinetic study, it is difficult to pin point whether increased parasite clearance time observed in that study was due to the resistance to artesunate or SP. However, more recently (in 2013) the National Vector Borne Disease Control Programme, Government of India has changed its drug policy to ACT-AL co-formulated tablet of artemether - Lumefantrine combination for three days regimen for the treatment of Pf cases of north-east India only [42] whereas in the rest of the country a status - quo of using ACT (artesunate and SP) for three days as before was maintained.
A very high level of resistance to CQ and growing resistance to SP, as evident in the present study through therapeutic evaluation and molecular characterization of circulating Pf strains, is a serious concern for malaria control in north-east India. In view of increasing resistance to SP, the partner drug in the ACT combination therapy used in north-east India, and considering this region as a gateway for the drug resistant Pf strains from South-east Asia to the South Asia, a close monitoring on the anti-malarial drug resistance status is necessary with a constant and area wide surveillance for the therapeutic efficacy study along with screening of additional molecular markers for artemisinin and multidrug resistance (such as pfatp6, pfmdr1 D1042N and pfmdr1 Y1246D etc.,) for overall assessment of the dynamics of therapeutic failure of anti-malarials and longitudinal resistance monitoring in north-east India to treat Pf malaria cases. Again the availability of the recently introduced new ACT-AL combination drugs and proper implementation of the new drug policy in NE India needs to be monitored from time to time to make the change more effective and to reduce the emergence of drug resistance as inappropriate use of drugs as well as strong suspicion of widespread use of substandard and/or spurious drugs in this region is believed to increase drug selection pressure and thus lead to development of drug resistance.
Supporting Information
Figure S1.
Epidemiological situation of malaria in NE India (1961–2012) (Source NVBDCP of NE States, India).
https://doi.org/10.1371/journal.pone.0105562.s001
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Figure S2.
Trend of SfR & CFR (10−5), NE India (1986–2012) (Source NVBDCP of NE States, India).
https://doi.org/10.1371/journal.pone.0105562.s002
(TIF)
Figure S3.
Prevalence of dhfr and dhps codon mutations in NE India (given in box) as found in present study compared to rest of Indian and SE Asian scenario (Curtsey: http://www.wwarn.org/surveyor).
https://doi.org/10.1371/journal.pone.0105562.s003
(TIF)
Acknowledgments
We appreciate the assistance of Late A.C. Rabha and D. Dutta. Logistic support provided by various officials of the Health Departments of Assam state is sincerely thanked.
Author Contributions
Conceived and designed the experiments: PKM JM AP DRB. Performed the experiments: MAA BS DKS BKG. Analyzed the data: DKS KB. Contributed reagents/materials/analysis tools: PKM JM AP DRB. Contributed to the writing of the manuscript: DKS PKM JM AP.
References
- 1.
NVBDCP (2013) Malaria situation in India. Available: http://www.nvbdcp.gov.in/Doc/mal-situation-July13.pdf. Accessed 2013 Sept 16.
- 2. Mohapatra PK, Prakash A, Taison K, Negmu K, Gohain AC, et al. (2005) Evaluation of chloroquine (CQ) and sulphadoxine/pyrimethamine (SP) therapy in uncomplicated falciparum malaria in Indo-Myanmar border areas. Trop Med Int Health 10: 478–483.
- 3. Young M, Moore D (1961) Chloroquine resistance in Plasmodium falciparum. Am J Trop Med Hyg 10: 317–320.
- 4. Wernsdorfer WH, Payne D (1991) The dynamics of drug resistance in Plasmodium falciparum. Pharmacol Ther 50 95–121.
- 5. Sehgal PN, Sharma MID, Sharma SL, Gogai S (1975) Resistance to chloroquine in falciparum malaria in Assam state, India. J Commun Dis 5: 175–180.
- 6. Farooq U, Mahajan RC (2004) Drug resistance in malaria. J Vector Borne Dis 41: 45–53.
- 7. Bjorkman A, Phillips-Howard PA (1990) The epidemiology of drug-resistant malaria. Trans R Soc Trop Med Hyg 84 177–80.
- 8. Das S, Barkakaty BN, Roy JR, Guha AK, Rastogi AC, et al. (1981) Pyrimethamine in combination with sulfadoxine or sulfalene in P. falciparum infected cases in India. Indian J Malariol 18: 109–116.
- 9.
NMEP (1997) Drug resistance and chemotherapy of malaria in India, an update. In: National Malaria Eradication Programme (Enhanced Malaria Control Project) (eds GPS Dhillon,GS Sonal, U Arora & J Nandi) Ministry of Health & Family Welfare, Government of India, New Delhi, pp. 14–18.
- 10. Mohapatra PK, Namchoom NS, Prakash A, Bhattacharyya DR, Goswami BK, et al. (2003) Therapeutic efficacy of antimalarials in Plasmodium falciparum malaria in an Indo-Myanmar border area of Arunachal Pradesh. Indian J Med Res 118: 71–76.
- 11. Ouellette M (2001) Biochemical and molecular mechanisms of drug resistance in parasites. Trop Med Int Health 6: 874–876.
- 12. Warhurst D (1999) Drug resistance in Plasmodium falciparum malaria. Infection 27: S55–58.
- 13. Wellems T, Plowe CV (2001) Chloroquine-resistant malaria. J Infect Dis 184: 770–776.
- 14. Fidock DA, Nomura T, Talley AK, Cooper RA, Dzekunov SM, et al. (2000) Mutations in the P. falciparum digestive vacuole transmembrane protein PfCRT and evidence for their role in chloroquine resistance. Mol Cell 6: 861–871.
- 15. Sa JM, Twu O, Hayton K, Reyes S, Fay MP, et al. (2009) Geographic patterns of Plasmodium falciparum drug resistance distinguished by differential responses to amodiaquine and chloroquine. Proc Natl Acad Sci U S A 106: 18883–18889.
- 16. Pickard AL, Wongsrichanalai C, Purfield A, Kamwendo D, Emery K, et al. (2003) Resistance to antimalarials in Southeast Asia and genetic polymorphisms in pfmdr1. Antimicrob Agents Chemother 47: 2418–2423.
- 17. Anderson AC (2005) Targeting DHFR in parasitic protozoa. Drug Discov Today 10: 121–128.
- 18. Gregson A, Plowe CV (2005) Mechanisms of resistance of malaria parasites to antifolates. Pharmacol Rev 57: 117–145.
- 19. Wu Y, Kirkman LA, Wellems TE (1996) Transformation of Plasmodium falciparum malaria parasites by homologous integration of plasmids that confer resistance to pyrimethamine. Proc Natl Acad Sci USA 93: 1130–1134.
- 20. Lynch C, Pearce R, Pota H, Cox J, Abeku TA, et al. (2008) Emergence of a dhfr mutation conferring high-level drug resistance in Plasmodium falciparum populations from southwest Uganda. J Infect Dis 197: 1598–1604.
- 21. Trigilia T, Menting JGT, Wilson C, Cowman AF (1997) Mutations in dihydropteroate synthase are responsible for sulfone and sulfonamide resistance in Plasmodium falciparum. Proc Natl Acad Sci USA 94: 13944–13949.
- 22. Biswas S, Escalante A, Chaiyaroj S, Angkasekwinai P, Lai AA (2000) Prevalence of point mutations in the dihydrofolate reductase and dihydropteroate synthetase genes of Plasmodium falciparum isolates from India and Thailand: a molecular epidemiologic study. Trop Med Int Health 5: 737–743.
- 23. Ndiaye D, Daily JP, Sarr O, Ndir O, Gaye O, et al. (2005) Mutations in Plasmodium falciparum dihydrofolate reductase and dihydropteroate synthase genes in Senegal. Trop Med Int Health 10: 1176–1179.
- 24. Fernandes N, Figueiredo P, do Rosário VE, Cravo P (2007) Analysis of sulphadoxine/pyrimethamine resistance-conferring mutations of Plasmodium falciparum from Mozambique reveals the absence of the dihydrofolate reductase 164L mutant. Malaria J 6: 35.
- 25. Figueiredo P, Benchimo C, Lopes D, Bernardino L, do Rosário VE, et al. (2008) Prevalence of pfmdr1, pfcrt, pfdhfr and pfdhps mutations associated with drug resistance, in Luanda, Angola. Malaria J 7: 236.
- 26. Sharma YD (2012) Molecular surveillance of drug-resistant malaria in India. Curr Sci 102: 696–703.
- 27.
WHO (2009) Report of Technical Consultation: Defining and validating a measure of parasite resistance to sulfadoxinepyrimethamine (SP) that would be indicative of the protective efficacy of SP for intermittent preventive treatment in infancy (SP-IPTi), Geneva: World Health Organization.
- 28.
WHO (2003) World Health Organization: Assessment and monitoring of antimalarial drug efficacy for the treatment of uncomplicated falciparum malaria. Geneva: World Health Organization.
- 29. Snounou G, Viriyakosol S, Zhu XP, Jarra W, Pinheiro L, et al. (1993) High sensitivity of detection of human malaria parasites by the use of nested polymerase chain reaction. Mol Biochem Parasitol 61: 315–320.
- 30. Shah NK, Dhillon GP, Dash AP, Arora U, Meshnick SR, et al. (2011) Antimalarial drug resistance of Plasmodium falciparum in India: changes over time and space. Lancet Infect Dis 11: 57–64.
- 31. Plowe CV, Roper C, Barnwell JW, Happi CT, Joshi HH, et al. (2007) World Antimalarial Resistance Network (WARN) III: molecular markers for drug resistant malaria. Malar J 6: 121.
- 32. Goswami D, Dhiman S, Rabha B, Kumar D, Baruah I, et al. (2014) Pfcrt mutant haplotypes may not correspond with chloroquine resistance. J Infect Dev Ctries 8: 768–773.
- 33. Zakeri S, Afsharpad M, Kazemzadeh T, Mehdizadeh K, Shabani A, et al. (2008) Association of pfcrt but not pfmdr1 alleles with chloroquine resistance in Iranian isolates of Plasmodium falciparum. Am J Trop Med Hyg 78: 633–640.
- 34. Lumb V, Das MK, Mittra P, Ahmed A, Kumar M, et al. (2009) Emergence of an unusual sulphadoxinepyrimethamine resistance pattern and a novel K540N mutation in dihydropteroate synthetase in Plasmodium falciparum isolates obtained from Car Nicobar Island, India, after the 2004 Tsunami. J Infect Dis 199: 1064–1073.
- 35. Ahmed A, Bararia D, Vinayak S, Yameen M, Biswas S, et al. (2004) Plasmodium falciparum isolates in India exhibit a progressive increase in mutations associated with sulphadoxine-pyrimethamine resistance. Antimicrob Agents Chemother 48: 879–889.
- 36. Biswas S (2004) Associations of antifolate resistance in vitro andpointmutations in dihydrofolate reductase and dihydropteroate synthetase genes of Plasmodium falciparum. J Postgrad Med 50: 17–20.
- 37. Ahmed A, Lumb V, Das MK, Dev V, Wajihullah, et al (2006) Prevalence of mutations associated with higher levels of sulfadoxine-pyrimethamine resistance in Plasmodium falciparum isolates from Car Nicobar Island and Assam, India. Antimicrob Agents Chemother 50: 3934–3938.
- 38. Ahmed A, Das MK, Dev V, Saifi MA, Wajihullah, et al (2006) Quadruple mutations in dihydrofolate reductase of Plasmodium falciparum isolates from Car Nicobar Island, India. Antimicrob Agents Chemother 50: 1546–1549.
- 39. Lin JT, Juliano JJ, Wongsrichanalai C (2010) Drug-Resistant Malaria: The Era of ACT. Curr Infect Dis Rep 12: 165–173.
- 40. Dondorp AM, Nosten F, Yi P, Das D, Phyo AP, et al. (2009) Artemisinin resistance in Plasmodium falciparum malaria. N Engl J Med 361: 455–467.
- 41. O'Brien C, Henrich PP, Passi N, Fidock DA (2011) Recent clinical and molecular insights into emerging artemisinin resistance in Plasmodium falciparum. Curr Opin Infect Dis 24: 570–577.
- 42.
National Vector Borne Disease Control Programme. National Drug Policy on malaria. Directorate of National Vector Borne Disease Control Programme, Directorate General of Health Services, Ministry of Health and Family Welfare, Government of India, 2013. Available: http://nvbdcp.gov.in/Doc/National-Drug-Policy-2013.pdf. Accessed 2014 Jul 19.